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Review

Beetroot Juice and Exercise for Clinical Health and Athletic Performance: A Narrative Review

1
Physical Activity and Performance Institute, Konkuk University, Seoul 05029, Republic of Korea
2
Department of Sports Medicine and Science, Graduate School, Konkuk University, Seoul 05029, Republic of Korea
3
Department of Physical Education, Konkuk University, Seoul 05029, Republic of Korea
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Nutrients 2026, 18(1), 151; https://doi.org/10.3390/nu18010151 (registering DOI)
Submission received: 29 November 2025 / Revised: 28 December 2025 / Accepted: 29 December 2025 / Published: 1 January 2026
(This article belongs to the Special Issue Linking Fruit and Vegetable Bioactives to Human Health and Wellness)

Abstract

Beetroot juice (BRJ), a concentrated dietary source of nitrate alongside betalains and polyphenols, influences physiology through enhanced nitrate–nitrite–NO bioavailability, antioxidant activity, and interactions with oral and gut nitrate-reducing microbiota. The efficiency of these mechanisms depends on dose, timing, and preservation of oral bacteria, with antibacterial mouthwash or thiocyanate-rich foods potentially blunting NO2 generation. Acute BRJ ingestion consistently elevates circulating nitrate and nitrite, yet its impact on glucose, insulin, and lipid regulation is modest; chronic intake may reinforce nitrate-reduction capacity, improve redox balance, and shift microbial composition, though long-term metabolic outcomes remain variable. Cardiovascular adaptations appear more coherent, with acute reductions in systolic blood pressure and improved endothelial function complemented in some cases by microvascular enhancements during multi-week supplementation. Neuromuscular and cognitive effects are less uniform; BRJ does not reliably increase maximal strength or global cognition but may support electrophysiological recovery after muscle-damaging exercise and improve executive performance under fatigue. In exercise settings, dose and timing are critical, as BRJ most consistently benefits endurance performance by reducing oxygen cost, improving exercise economy, and enhancing time-trial or time-to-exhaustion outcomes, whereas effects on sprint, power, and team-sport tasks are more sensitive to contraction duration, recovery intervals, and athlete training status. Overall, available evidence supports a role for NO-mediated vascular and metabolic pathways in the physiological effects of BRJ, although marked inter-individual variability highlights the need for responder-focused dosing strategies and further mechanistic investigation integrating metabolic, microbial, and performance-related outcomes.

1. Introduction

Beetroot juice (BRJ) has attracted growing interest across health and performance research due to its substantial content of inorganic nitrate (NO3) along with betalains, polyphenols, and other bioactive compounds [1,2]. The reduction of dietary NO3 to nitrite and nitric oxide (NO) through the nitrate–nitrite–NO pathway is now well established, and this mechanism enables NO generation even under low-oxygen or acidic conditions typical of exercise [3]. Because NO influences vascular tone, oxidative balance, mitochondrial efficiency, and muscle contractile behavior, BRJ has become a promising nutritional strategy in several physiological domains [4,5,6]. Initial clinical research highlighted BRJ’s potential through observations of blood pressure reductions and improvements in endothelial function [7,8]. Subsequent studies broadened this perspective by reporting effects on mitochondrial efficiency [9], muscle performance characteristics [10], and changes in cerebral blood flow and cognitive responses [11]. In exercise science, BRJ has been explored for its ability to reduce the oxygen cost of submaximal work, delay fatigue in high-intensity tasks, and modify recovery dynamics [12,13]. At the same time, findings have not been uniform; the magnitude of response depends on exercise modality, supplementation dose and duration, and the individual’s training background [14]. More recently, researchers have emphasized that BRJ’s effects cannot be explained solely by nitrate intake. The timing of supplementation, the integrity of the oral microbiota, dietary habits, and factors such as age or cardiometabolic status all shape the degree to which NO3 is converted to NO2 and ultimately to NO [8,15]. These interactions underscore the need to interpret BRJ research within a broader physiological and behavioral context.
Therefore, the aim of this narrative review is to synthesize current evidence on the physiological actions of BRJ and to comprehensively examine human studies spanning metabolic, cardiovascular, neuromuscular, cognitive, and exercise-performance outcomes. By considering findings from both acute and chronic supplementation trials, this review explores how dosing strategies, timing, individual characteristics, and contextual factors shape the physiological and functional responses to BRJ. Through this broad evaluation, we summarize the potential applications, practical considerations, and known limitations of BRJ supplementation within both health-related and exercise settings.
This narrative review was designed to provide a broad overview of human evidence on the physiological and functional effects of beetroot juice across health- and exercise-related domains. Relevant literature was identified through searches of PubMed, Scopus, and Web of Science, including English-language studies available up to November 2025, using combinations of keywords related to beetroot juice, dietary nitrate, exercise performance, metabolic health, cardiovascular function, neuromuscular outcomes, immune responses, and cognitive function. Studies investigating the ingestion of isolated dietary nitrate or nitrate salts without beetroot juice were excluded. With the exception of the mechanistic section, which incorporates supporting in vivo and in vitro evidence, this narrative review primarily focuses on human intervention studies directly examining the effects of beetroot juice consumption. Meta-analyses and systematic reviews are cited only in the main text to provide contextual background and are not included in the tables, which summarize individual human intervention trials. As a narrative review, this work does not aim to systematically integrate or quantitatively synthesize findings; therefore, formal inclusion/exclusion criteria and risk-of-bias assessments were not applied. Instead, the review emphasizes broad coverage and descriptive synthesis of relevant studies across the topic.

2. Physiological Mechanisms Underlying the Effects of Beetroot Juice

NO is known to be produced endogenously through the oxidation of L-arginine catalyzed by nitric oxide synthase (NOS) [16,17,18]. This oxygen-dependent enzymatic pathway involves three major NOS isoforms—neuronal NOS, inducible NOS, and endothelial NOS —each contributing to essential physiological functions such as vascular tone regulation, glucose uptake, and skeletal muscle blood flow [3,17]. However, recent evidence has identified an alternative, oxygen-independent nitrate–nitrite–NO pathway activated by dietary nitrate (NO3), such as that obtained from BRJ [1,2]. Following ingestion, NO3 is absorbed in the small intestine and enters systemic circulation, where approximately 20–25% undergoes entero-salivary recirculation and is concentrated in the salivary glands. In the oral cavity, anaerobic bacteria (e.g., Neisseria, Veillonella) reduce NO3 to nitrite (NO2) [19]. The resulting NO2 is further reduced to NO through non-enzymatic reactions in the highly acidic environment of the stomach (pH 1–3), where nitrous acid decomposes to NO and other reactive nitrogen species [2]. A portion of NO2 enters systemic circulation and is enzymatically reduced to NO by deoxygenated hemoglobin (deoxy-Hb), deoxygenated myoglobin (deoxy-Mb), xanthine oxidoreductase (XOR), and mitochondrial respiratory chain enzymes—processes that are further enhanced under hypoxic or acidic conditions [20]. Thus, NO production can be maintained even when NOS activity is impaired.
Once produced, NO diffuses into vascular smooth muscle cells (SMCs) and activates soluble guanylate cyclase (sGC), leading to increased cyclic guanosine monophosphate (cGMP) concentrations, decreased intracellular Ca2+, and smooth muscle relaxation, ultimately inducing vasodilation [21,22]. Activation of this NO–sGC–cGMP signaling pathway supports endothelial function, enhances vascular compliance, lowers blood pressure, and promotes capillary recruitment and microvascular perfusion, thereby augmenting oxygen delivery and muscle oxygenation at the tissue level [23,24].
NO also exerts antiplatelet, antithrombotic, and endothelial-protective effects [8,25]. Furthermore, by inhibiting nicotinamide adenine dinucleotide phosphate oxidase and the nuclear factor-kappa B (NF-κB) signaling pathway, NO reduces oxidative stress and inflammatory responses, contributing to an overall improvement in cardiovascular function [4,26,27]. Beyond nitrate, BRJ contains several bioactive compounds—including betalains, betaine, and polyphenols—that provide complementary antioxidant and anti-inflammatory mechanisms [5]. Betalains (e.g., betanin, vulgaxanthin) act as potent antioxidants by directly scavenging reactive oxygen species (ROS), and by activating nuclear factor erythroid 2–related factor 2 (Nrf2). Through the antioxidant response element ARE, Nrf2 upregulates Phase II detoxification enzymes and endogenous antioxidant enzymes, thus attenuating oxidative stress [28,29,30,31]. Betalains and polyphenols further suppress inflammatory mediators—including NF-κB, cyclooxygenase-2, tumor necrosis factor-alpha, and interleukin-6 (IL-6)—thereby reinforcing endothelial protection [5,32].
Betaine acts as a methyl donor to reduce homocysteine concentrations and provides additional anti-inflammatory support to maintain cardiovascular stability [33]. At the skeletal muscle level, NO–cGMP signaling activates protein kinase G (PKG), which modulates intracellular Ca2+ homeostasis, enhances sarcoplasmic reticulum Ca2+ reuptake, and increases mitochondrial oxidative efficiency [10,34]. These adaptations improve contraction efficiency, reduce oxygen utilization, lower whole-body oxygen consumption (VO2), and enhance fatigue resistance [9,35]. Notably, NO competes with oxygen at cytochrome c oxidase (Complex IV), reducing the oxygen cost of ATP production and improving energy efficiency [9,36]. Understanding these physiological pathways (Figure 1) underscores the importance of factors such as nitrate dose, timing of ingestion, population characteristics, and oral microbiome integrity, all of which critically shape the magnitude of BRJ’s effects and are examined in the following section.

3. Practical Considerations for Beetroot Juice Supplementation

3.1. Timing Strategies for Exercise Settings

Most trials reporting benefits in vascular reactivity or exercise performance have aligned BRJ ingestion with the rise in circulating NO3 and NO2, which typically show their largest increases 2–3 h after intake [1,12]. This window corresponds to a period when NO formation is more strongly supported by the nitrate–nitrite pathway, and it is also when reductions in oxygen cost during submaximal work have most consistently been observed. Some studies have tested longer intervals, particularly in protocols involving prolonged exercise, yet the 2–3 h timing has remained sufficiently robust across different exercise modalities. When BRJ is consumed across several days or weeks, circulating nitrate gradually stabilizes at a higher baseline, and the exact timing becomes less sensitive; however, maintaining daily ingestion appears essential because the effect dissipates within 24–30 h without continued intake [37]. Testing schedules that diverge markedly from these pharmacokinetic patterns often show weaker results, suggesting that timing is an important contributor to variability in the literature.

3.2. Dose–Response and Population-Specific Responsiveness

The nitrate content of commercially available BRJ varies widely, but doses approximating 5–9 mmol of NO3 have repeatedly produced measurable changes in NO2 levels and improvements in hemodynamic or exercise outcomes [38,39]. Larger doses may be necessary for individuals with higher body mass or reduced vascular or metabolic function due to differences in nitrate distribution volume or impaired conversion efficiency. Still, responses do not scale linearly with dose, and several studies suggest diminishing returns when nitrate intake exceeds the capacity of oral bacteria or systemic pathways to reduce it. Training status adds another layer of complexity. Recreationally active individuals tend to show clearer benefits in VO2 kinetics, exercise economy, and blood pressure regulation, whereas highly trained endurance athletes often show minimal or inconsistent improvements, likely because their baseline physiological state already reflects high NO availability and efficient mitochondrial function [14,40]. Dietary background also matters; individuals habitually consuming nitrate-rich vegetables may exhibit blunted responses to supplementation because their baseline nitrite pool is already elevated. These population-specific factors help explain why responses to BRJ vary even when dosing protocols are similar.

3.3. Considerations Related to Oral Microbiome Preservation

The reduction of NO3 to NO2 relies almost entirely on oral nitrate-reducing bacteria, making the composition and activity of the oral microbiome one of the most influential determinants of how effectively BRJ intake translates into physiological changes. The suppressive effect of antibacterial mouthwash is well documented; regular use can markedly lower bacterial nitrate reduction and blunt the expected rise in circulating NO2, diminishing the improvements in blood pressure and vascular function reported in many supplementation studies [8,15]. Daily oral-hygiene habits, such as brushing immediately before ingestion or using certain toothpaste ingredients, can also transiently affect nitrate metabolism, although the magnitude of these effects varies. Dietary choices add another layer of nuance. Cruciferous vegetables such as broccoli, cauliflower, and red cabbage—along with related varieties like kale, Brussels sprouts, and Bok choy—contain appreciable amounts of thiocyanate, a compound that can compete with nitrate reduction under some conditions. While their influence is generally weaker than that of antimicrobial rinses, frequent or high intake may alter the oral environment enough to shift NO2 formation in sensitive individuals. Because these microbial and dietary factors operate at the first step of nitrate metabolism, even small disruptions can propagate downstream and partly explain the heterogeneous responses often seen across BRJ trials. Preserving the typical activity of oral nitrate-reducing bacteria is therefore essential when interpreting findings or advising individuals on how to use BRJ for vascular, metabolic, or performance-related purposes.

4. Effects of Beetroot Juice in Health and Exercise

The physiological actions of BRJ extend across multiple systems, and human studies have examined these effects in metabolic, cardiovascular, neuromuscular, immune, and cognitive domains. Although the magnitude of response varies across individuals and study designs, patterns in the literature suggest that changes in NO availability, microvascular function, mitochondrial efficiency, and redox balance are thought to contribute to several of the reported outcomes. However, the magnitude and consistency of these effects vary substantially across studies, reflecting heterogeneity in participant characteristics, supplementation protocols, and outcome measures. Figure 2 provides an overview of acute and chronic responses across organ systems and illustrates how these physiological pathways align with the findings summarized in this section.

4.1. Metabolic Health

Metabolic health encompasses glucose and insulin regulation, lipid profiles, oxidative balance, and contributions from the oral–gut microbiome. BRJ contains inorganic nitrate alongside betalains, polyphenols, and organic acids, allowing multiple routes of metabolic influence. Key findings from acute interventions are summarized in Table 1, while chronic adaptations are presented in Table 2.
Acute BRJ ingestion reliably raises circulating nitrate and nitrite [41,42]. Compared with sodium nitrate, beetroot juice uniquely increases betaine and choline [42], reflecting its broader composition. Despite clear biochemical changes, acute supplementation produces minimal effects on body composition or lipid markers [39,43,44,45,46,47,48]. Glucose-related outcomes remain stable in healthy adults [46], although reductions in total glucose exposure have been reported in type 2 diabetes (T2D) without concurrent changes in insulin [45]. Metabolomics analyses describe characteristic fingerprints—including dopamine-3-O-sulfate and 4-methylpyridine-2-carboxylic acid—that further increase during exercise [49].
Chronic BRJ ingestion yields patterns distinct from acute responses. Long-term intake preserves acute nitrite responsiveness and elevates fasting nitrate [39]. Four-week supplementation increased Neisseria and reduced Veillonella, correlating with higher plasma nitrate/nitrite [50]. Older adults show blunted nitrite responses, with greater ceruloplasmin-related NO scavenging [51]. Gut microbial shifts—including increased Akkermansia, decreased Bacteroides fragilis, and higher short-chain fatty acids (SCFAs) levels—have also been observed [52]. Chronic intake reduces oxidative stress and maintains NO availability even with impaired renal clearance [43]. In contrast, fasting glucose, insulin, homeostatic model assessment-insulin resistance (HOMA-IR), and postprandial responses largely remain unchanged [46,47,48]. These metabolic patterns vary with supplementation duration, dose, and individual microbial profiles, and the specific physiological relevance may differ across populations.
Table 1. Acute effects of beetroot juice supplementation on metabolic health outcomes.
Table 1. Acute effects of beetroot juice supplementation on metabolic health outcomes.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Fuchs et al. [44] M, obese, insulin-resistant
(n = 16)
EC1: BRJ
EC2: CON
EC1: BRJ 70 mL/day (4.8 mmol) (180 min before)/1 dayBeet It
(James White Drinks Ltd., Ipswich, UK)
Glucose homeostasis, Conduit Artery Blood Flow, Vascular occlusion plethysmography, NIRS, BPVascular resistance ↓
Postprandial glucose ↔
Postprandial insulin ↔
Garnacho-Castaño et al. [41]M, healthy with ≥ 2 years of crossfit experience
(n = 12)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (180 min before)/1 dayBeet It
(James White Drinks Ltd., Ipswich, UK)
Workout of the day Test (CrossFit),
Blood Sampling,
SpO2, CMJ
(1st) Number of Repetitions ↑
(2nd) Number of Repetitions ↔
Serum Cortisol
SpO2
Muscle Fatigue ↓
Serum Testosterone ↔
Testosterone/cortisol Ratio ↔
Blood Lactate ↔
Giampaoli et al. [49]M (n = 2) and W (n = 5) healthy adult
(n = 7)
EC1: BRJ
EC2: BRJ + EXE
EC3: PLA + EXE
EC1: BRJ 200 mL/day (9.7 mmol) (60 min before)/1 day
EC2: BRJ 200 mL/day (9.7 mmol) (60 min before)/1 day
EC3: BRJ 20 mL/day (1.8 mmol) (60 min before)/1 day
Commercial BRJ
(Aureli Mario SS Agricola, Ortucchio, Italy)
Cycle Ergometer,
Urine Sampling,
Gas Exchange
Dopamin-3-O-sulfate ↑
4-methylpyridine-2-carboxylic acid ↔
Heredia-Martínez et al. [43]M (n = 7) and W (n = 8)
hemodialysis (n = 8) and healthy adult
(n = 15)
EC1: BRJ (HD)
EC2: BRJ
EC3: PLA (HD)
EC4: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (NR)/1 day
EC2: BRJ 70 mL/day (6.4 mmol) (NR)/1 day
Beetroot Juice (James White Drinks Ltd., Ipswich, UK)Blood Sampling,
Dialysate Sampling, Saliva Sampling, BP
(EC1 vs. EC2) Plasma NO2 & NO3
(EC1 vs. EC2) Plasma NO2 AUClast ↑
(EC1) Plasma NO2 AUClast & t ½ ↑
(EC1 vs. EC2) BP and Plasma cGMP ↔
(EC1) Potassium and Safety and Tolerability ↔
Jurga et al. [42]M (n = 3) and W (n = 5) healthy adult
(n = 8)
EC1: BRJ
EC2: NIT
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (60 min before)/1 dayBeet It Sport
(James White Drinks)
Blood Sampling,
Flow-mediated skin fluorescence
Plasma NOx
Plasma Betaine/Choline ↑
Trimethylamine/
Trimethylamine N-oxide ↔
Rowland et al. [53]M, healthy adult
(n = 12)
EC1: BRJ (MORN)
EC2: BRJ (AFT)
EC3: BRJ (EVE)
EC4: PLA (MORN)
EC5: PLA (AFT)
EC6: PLA (EVE)
EC1: BRJ 2 × 70 mL/day (13 mmol) (morning)/1 day
EC2: BRJ 2 × 70 mL/day (13 mmol) (mid-day)/1 day
EC3: BRJ 2 × 70 mL/day (13 mmol) (evening)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
Cycle Ergometer Severe-Intensity Exercise, TTE,
Urine Sampling,
Saliva Sampling, BP, PWV
(EC1 & EC2 & EC3) NO3 Metabolism ↑
(Time) NO3 Metabolism ↔
(EC1 & EC2 & EC3) Central SBP ↓
(Time) SBP ↔
(EC1 & EC2 & EC3 vs. Time) Brachial SBP ↔
(EC1 & EC2 & EC3 vs. Time) TTE ↔
Shepherd et al. [46]M (n = 19) and W (n = 12)
healthy younger and older
(n = 31)
EC1: BRJ (YN)
EC: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 140 mL/day (11.9 mmol) (morning)/1 day
EC2: BRJ 140 mL/day (11.9 mmol) (morning)/1 day
Beet It
(James White Drinks., Ipswich, UK)
Magnetic resonance imaging, Incretin and C-peptide, Blood Sampling(EC1 & EC2) Plasma NO2
(EC1 & EC2) Plasma NO2
(EC1 & EC2) Portal vein flux

(EC1) Portal vein velocity ↓
(EC2) Portal vein velocity ↔
(EC1 & EC2) Plasma glucose, Total GLP-1, Active GLP-1, C-peptide, SBP, DBP ↔
Tyler et al. [45]M (n = 2) and W (n = 5)
T2D adult
(n = 7)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (120 min before)/1 dayBeetroot Juice
(James White Drinks, Ipswich., UK)
Blood Sampling,
OGTT, BP
Glucose AUG ↓
ΔSVR ↓
Salivary NO2 & NO3
SBP & DBP ↔
HOMA-IR & QUICKI ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 2. Chronic effects of beetroot juice supplementation on metabolic health outcomes.
Table 2. Chronic effects of beetroot juice supplementation on metabolic health outcomes.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Alharbi et al. [48] M (n = 7) and W (n = 22) obesity mid-age and older
(n = 29)
EC1: CR + BRJ
EC2: CR
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/2 weeksBeet It
(James White Ltd., Ashbocking, Suffolk, UK)
BP, REE,
Handgrip Strength,
Skin microvascular blood flow, IPAQ,
Urine Sampling,
Saliva Sampling
Average Microvascular Flux ↑
NO-dependent Endothelial Activity ↑
SBP ↓
Cognitive Function ↑
Oxidative Stress ↑
NO bioavailability ↑
Physical Strength ↑
Metabolic Adaptation ↔
Body composition ↔
Babateen et al. [47]M (n = 24) and
W (n = 38)
overweight/obese older adults
(n = 62)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning, evening)/13 weeks
EC2: BRJ 70 mL/day (6.45 mmol) (evening)/13 weeks
EC3: BRJ 35 mL/day (3.23 mmol) (evening)/13 weeks
Beet It Sports (James White Drinks, UK)Blood Sampling,
Urine Sampling
(EC1, EC2) Plasma NO3
(EC3) Plasma NO3
(EC1, EC3) Plasma NO2
(EC2) Plasma NO2
(EC1, EC2) Saliva NO3
(EC3) Saliva NO3
(EC1, EC2) Saliva NO2
(EC3) Saliva NO2
(EC1, EC2) Urine NO3
(EC3, time points) Urine NO3
(EC1, EC2, EC3) Urine NO2
Fejes et al. [54]M (NR) and W (NR) hypertension older
(n = 15)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (NR)/4 weeksBeet It
(James White Drinks Ltd., Ipswich, UK)
Blood Sampling, Salivary nitrate, FBF, Clinic BP, Home BP(3H post) Plasma NO3, NO2
Salivary NO3, NO2
FBF AUC ratio ↑
BP ↔
(4-week post) Plasma NO3, NO2
Salivary NO3, NO2
FBF AUC ratio ↔
BP ↔
Miller et al. [39]M (n = 3) and W (n = 10)
healthy middle-aged and older
(n = 13)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.1 mmol) (morning)/12 weeksBeet It Sports
(James White Drinks Ltd.; Ipswich, UK)
Blood Sampling(90 min) Plasma NO3
(90 min) Plasma NO2
Fasting Plasma NO3
Fasting Plasma NO2
Plasma NO2 Change Variability ↑
Vanhatalo et al. [51]M (NR) and W (NR) healthy younger and older
(n = 75)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 2 × 70 mL/day (12.1 mmol) (morning and evening)/2 weeks
EC2: BRJ 2 × 70 mL/day (12.1 mmol) (morning and evening)/2 weeks
Beetroot JuiceTongue Scarping,
Blood Sampling,
Peripheral blood pressure, Central blood pressure, FMD
(EC2) MAP ↓
(EC1) MAP ↔
(EC2) ΔNO2
(EC1) ΔNO2
(EC2, EC4) ΔMAP & ΔNO2
(EC1, EC3) ΔMAP & ΔNO2
(EC2, EC4) NO2 and oral microbes ↔
(EC1, EC3) NO2 and oral microbes ↔
Wang et al. [52]M (NR) and W (NR) healthy adults
(n = 18)
EC1: BRJEC1: BRJ 270 mL/day (2.7 mmol) (morning and evening)/2 weeksRed Beetroot Juice
(Hartley Wintney, UK)
Stool Sampling(Day3) Akkermansia muciniphila ↑
(Day3) Bacteroides fragilis ↓
(Day3, Day14) Total SCFAs ↑
(Day3, Day14) Butyric acid ↑
α- & β-diversity ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.

4.2. Cardiovascular Health

Cardiovascular health encompasses a broad set of physiological processes, including blood pressure regulation, endothelial function, macrovascular and microvascular responses, peripheral and cerebral hemodynamics, and autonomic reflex activity. Acute findings are summarized in Table 3, with longer-term adaptations detailed in Table 4.
Across this literature, BRJ consistently increases circulating nitrate and nitrite, yet the magnitude and expression of downstream vascular effects depend heavily on baseline vascular status, task context, and the heterogeneity of outcome measures used across studies. Acute ingestion produces rapid hemodynamic adjustments largely attributed to increased NO formation. Meta-analytic estimates report systolic blood pressure (SBP) reductions of approximately 5–10 mmHg following a single dose [55]. These findings are supported by trials in healthy younger adults showing comparable decreases [56]. Improvement in endothelial responsiveness represents another frequently observed acute outcome. Increases in flow-mediated dilation (FMD) have been reported in pregnant women [57], while trials examining postprandial vascular function documented reduced vascular resistance [44]. Exercise studies further demonstrate elevated skeletal muscle blood flow [58], implying that BRJ may facilitate nutrient and oxygen delivery during physiological stress. Several studies additionally describe more stable systemic and cerebral hemodynamics following acute ingestion [59], although the precise mechanisms underlying these responses remain incompletely defined. Acute effects on autonomic responses appear more selective. Cardiovagal baroreflex sensitivity and indices of cerebral autoregulation generally remain unchanged [60,61]. In contrast, reduced peripheral chemoreflex sensitivity has been documented [62], suggesting that BRJ may influence oxygen-sensing pathways more readily than central autonomic control. Heart rate and HRV typically show minimal changes [60,61], and acute supplementation rarely alters structural vascular indices such as arterial stiffness [59].
Chronic BRJ ingestion has been associated with broader and more sustained cardiovascular adaptations, particularly in individuals with elevated baseline risk. Several meta-analyses report reproducible SBP reductions among hypertensive adults, with interventions lasting ≥14 days yielding more consistent effects [63,64]. In contrast, normotensive adults or older adults taking antihypertensive medications tend to exhibit smaller or more variable blood pressure changes [54,56]. Improvements in endothelial function have been documented across multiple chronic trials. Older adults showed increased FMD after one to four weeks of supplementation [65,66], and studies combining BRJ with dietary modification demonstrated enhanced NO-dependent microvascular regulation [48]. In individuals with mild cognitive impairment, supplementation increased cerebral microvascular responsiveness [67], suggesting that BRJ may exert more pronounced effects in populations with impaired vascular control. Extended supplementation also appears to affect peripheral vascular and oxygenation responses. A 12-week high-nitrate BRJ intervention was associated with concurrent improvements in lower-limb FMD, skeletal muscle microvascular function, and angiogenic potential [68]. Similar patterns have been observed in studies examining exercising muscle perfusion and tissue oxygen delivery [58,59,69]. These effects suggest the possibility that microvascular adaptation may precede structural modifications in larger vessels, although direct longitudinal evidence remains limited. Chronic intake also contributes to sustained changes in NO metabolism. Plasma nitrate and nitrite reliably increase over time [70], accompanied by shifts in oral nitrate-reducing bacteria and reductions in oxidative stress markers [71]. Despite these biochemical modifications, metrics such as HR, HRV, and arterial stiffness generally remain unchanged [65,71]. Selective autonomic effects have been observed, including reduced peripheral chemoreflex sensitivity [62], though these do not appear to generalize across broader autonomic domains. Across studies, chronic BRJ supplementation shows variable effects on cardiovascular physiology. Substantial improvements are typically observed in groups with compromised endothelial function or elevated cardiometabolic risk, while responses in younger, healthy, or already normotensive individuals are more modest. Accordingly, these findings should be interpreted in light of population-specific baseline risk and differences in study design, rather than as uniform effects across all groups.

4.3. Neuromuscular Function

Neuromuscular function includes strength, power, motor unit behavior, muscle excitability, fatigue resistance, and recovery capacity. Findings are summarized in Table 5.
Across studies, acute BRJ ingestion produces minimal changes in maximal voluntary contraction (MVC), rate of force development, or peak strength in sport climbers [72], tennis and basketball athletes [73], and female hockey players [74]. Similar patterns are reported in eccentric-exercise protocols, where MVC recovery and subjective soreness do not differ from placebo [26]. Power- and sprint-based performance outcomes also show limited responsiveness, although one study in semi-professional female rugby players documented an improvement in countermovement jump height [75]. Dose–response work adds nuance, suggesting that lower nitrate doses may influence the rate of torque development, whereas higher doses may affect peak torque [76]. Motor unit–level findings indicate that neural activation patterns remain largely unchanged following nitrate ingestion. Studies by Esen et al. show no alterations in motor unit firing rate, recruitment threshold, or motor unit potential area [77,78]. However, consistent reductions in motor unit potential duration suggest faster restoration of muscle fiber membrane conduction velocity, particularly during ischemic contractions, where BRJ improves the recovery of peripheral muscle excitability [77]. Functional indices of recovery—including MVC, countermovement jump, and pain thresholds—have improved in some studies even when biochemical markers of muscle damage (Creatine kinase (CK), C-reactive protein (CRP), IL-6) do not change [26,79].
Longer-term supplementation has produced few measurable changes in neuromuscular performance. Extended nitrate ingestion improved exercise tolerance in one trial but did not modify MVC, electromyography (EMG) amplitude, or fatigability [53]. Other multi-week interventions similarly report no changes in muscle strength, power, EMG-based activation, or motor unit recruitment strategies [80,81]. Across chronic trials, contractile properties and central neural control appear largely unaffected, and performance outcomes remain stable regardless of dose or supplementation duration. Taken across studies, BRJ’s neuromuscular effects appear most evident in contexts involving fatigue or recovery, where improvements in functional performance and muscle fiber conduction properties are occasionally observed. The degree to which these responses occur varies by supplementation dose, muscle group tested, and the specific physiological demands of the task being evaluated. Nevertheless, the available evidence remains limited in scope, and conclusions are primarily based on a relatively small number of heterogeneous studies.
Table 3. Acute effects of beetroot juice supplementation on cardiovascular health.
Table 3. Acute effects of beetroot juice supplementation on cardiovascular health.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Benjamim et al. [82] W, systemic arterial hypertension postmenopausal adult
(n = 14)
EC1: BRJ (1st D)
EC2: BRJ
EC1: BRJ 2 × 70 mL/day (12.8 mmol) (morning)/1 week
EC2: BRJ 70 mL/day (6.4 mmol) (morning)/1 week
Beet It Sports
(James White Drinks Ltd., Ipswich, UK)
FMD, HRV, HR, BP,
Blood Sampling
(EC1) SBP ↓
(EC2) SBP ↔
(EC1 vs. EC2) FMD ↑
(EC1 vs. EC2) HRV ↑
(EC1 vs. EC2) HR ↔
(EC1 & EC2) Plasma NO3
(EC1 & EC2) Plasma NO2
Curry et al. [59]W, healthy adult
(n = 10)
EC1: BRJ
EC2: Orange Juice
EC1: BRJ 500 mL/day (12 mmol) (120 min before)/1 dayBeetroot Juice
(CAJ Food Products, Inc., Fishers, IN, USA)
Electronically braked leg cycle ergometer (40 & 80% VO2peak for 5 min),
BP, HR, Transcranial Doppler, CO
Blood NO ↑
SBP ↓
DBP & HR ↔
CAIx ↓
(Rest) CAIx ↔
PIx & RIx ↔
Chapman et al. [61]M (n = 7) and W (n = 7) healthy adult
(n = 14)
EC1: BRJ
EC2: PLA
EC1: BRJ 500 mL/day (9.68 mmol) (180 min before)/1 dayCommercial BRJ
(Biotta Beet Juice, Fishers, IN, USA)
Breathe CO2 for 5 min, Treadmill Walking Test, BP, Microcirculatory endothelial functionRenal/Segmental Artery blood velocity ↔
Vascular resistance ↔
Microcirculatory endothelial function ↔
Engan et al. [83]M (n = 5) and W (n = 3)
healthy adult
(n = 8)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (5 mmol) (120 min before)/1 dayBeetroot Juice
(James White Drinks Ltd., Ipswich, UK)
Apnea Test, SpO2,
HR, Spleen Maximal Diameters, Blood Sampling
Spleen Volume ↓
Hb Concentration ↑
Apnea Apleen Concentration ↔
Elevated Hb during Apnea ↔
Max Apnea Duration ↔
HR Drop during Apnea ↔
SpO2 Max ↔
Fejes et al. [71]M (n = 10) and W (n = 5) older adults with medically treated hypertension
(n = 15)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/1 dayBeet It
(James White Drinks Ltd., Ipswich, UK)
Blood Sampling, FMD, BPPlasma NO2
Plasma NO3
SBP, DBP ↔
Cardiovascular function ↔
Fuchs et al. [44]M, obese, insulin-resistant
(n = 16)
EC1: BRJ
EC2: CON
EC1: BRJ 70 mL/day (4.8 mmol) (180 min before)/1 dayBeet It
(James White Drinks Ltd., Ipswich, UK)
Glucose homeostasis,
Conduit Artery Blood Flow,
Vascular occlusion plethysmography, NIRS, BP
Vascular resistance ↓
Postprandial glucose ↔
Postprandial insulin ↔
Hayes et al. [84]M, healthy adult
(n = 15)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (14 mmol) (morning)/1 dayBeet It Sport
(James White Drinks Ltd., Ipswich, UK)
Blood Sampling,
BP
Plasma NO3
Plasma NO2
SBP ↓
DBP ↓
Heredia-Martinez et al. [43]M (n = 7) and W (n = 8)
hemodialysis (n = 8) and healthy adult
(n = 15)
EC1: BRJ(HD)
EC2: BRJ
EC3: PLA(HD)
EC4: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (NR)/1 day
EC2: BRJ 70 mL/day (6.4 mmol) (NR)/1 day
Beetroot Juice (James White Drinks Ltd., Ipswich, UK)Blood Sampling,
Dialysate Sampling,
Saliva Sampling,
BP
(EC1 vs. EC2) Plasma NO2& NO3
(EC1 vs. EC2) Plasma NO2 AUClast ↑
(EC1) Plasma NO2 AUClast & t ½ ↑
(EC1 vs. EC2) BP & Plasma cGMP ↔
(EC1) Potassium & Safety and Tolerability ↔
Horiuchi et al. [85]M, healthy adult
(n = 12)
EC1: BRJ (Normoxia)
EC2: BRJ (Hypoxia)
EC3: PLA (Normoxia)
EC4: PLA (Hypoxia)
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (NR)/4 days
EC2: BRJ 2 × 70 mL/day (12.9 mmol) (NR)/4 days
Beet It
(James White Drinks, Ipswich, UK)
Blood Sampling,
DCA, Internal carotid artery, SpO2, MAP, VE, PETCO2
(EC1, EC2 vs. EC3, EC4) Circulating NO3
(EC2, EC4 vs. EC1, EC3) DCA-RoR ↓
(EC1 vs. EC3) DCA-RoR ↔
(EC2 vs. EC4) DCA-RoR ↔
(EC2, EC4 vs. EC1, EC3) Internal carotid artery Diameter, Velocity, or Flow ↔
Jurga et al. [42]M (n = 3) and W (n = 5) healthy adult
(n = 8)
EC1: BRJ
EC2: NIT
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (60 min before)/1 dayBeet It Sport
(James White Drinks)
Blood Sampling,
Flow-mediated skin fluorescence
Plasma NOx ↑
Plasma Betaine/Choline ↑
Trimethylamine/
Trimethylamine N-oxide ↔
Kelly et al. [86]M (n = 6) and W (n = 6)
healthy older adult
(n = 12)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (9.6 mmol) (morning and mid-day)/1 dayBeet It Sports
(James White Drinks, Ipswich, UK)
Moderate Treadmill Walking,
Low/High-Intensity Kness Extension,
6MWT,
Blood Sampling,
BP,
HR,
Serial Sevens Subtraction Test
(EC1) SBP ↓
(EC1) DBP ↓
(EC1 & EC2) MAP ↓
(EC1) VO2 Mean Response Time ↓
6MWT, Muscle Metabolism, Cognition, Brain Metabolism ↔
Londono-Hoyos et al. [87]M (n = 14) and W (n = 2)
HFpEF Patients
(n = 16)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (120 min before)/1 dayBeet It Sport
(James White Drinks Ltd., Ipswich, UK
Echo, Doppler ultrasound, BPMAP, HR, CSA, Acute hemodynamic, Carotid Hydraulic Power, Carotid Power Penetration, Carotid Energy Penetration ↔
CO ↓
Pedrinolla et al. [67]M (NR) and W (NR)
younger (n = 10) and older (n = 10) and AD (n = 10)
(n = 30)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: BRJ (AD)
EC4: PLA (YN)
EC5: PLA (OLD)
EC6: PLA (AD)
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/1 day
EC2: BRJ 70 mL/day (6.4 mmol) (morning)/1 day
EC3: BRJ 70 mL/day (6.4 mmol) (morning)/1 day
Beet It Sports
(James White Drinks, Ipswich, UK)
Blood Sampling(EC3 vs. EC1, EC2) Baseline Plasma NO3
(EC2 vs. EC1) Baseline Plasma NO3
(EC1) Baseline Plasma NO3
(EC3, EC1, EC2) Baseline Plasma NO2
(EC3, EC1, EC2) Δ Plasma NO3
(EC3, EC1, EC2) Δ Plasma NO2
(EC3, EC1, EC2) Δ Vascular Responsiveness ↑
(EC3 vs EC1, EC2) Absolute Vascular Responsiveness ↓
(EC2 vs EC1) Absolute Vascular Responsiveness ↔
(EC1) Absolute Vascular Responsiveness ↔
Raubenheimer et al. [88]M (n = 5) and W (n = 7)
healthy older adults
(n = 12)
EC1: High BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (morning)/1 dayBeet It
(James White Drinks, UK)
BP,
Flow cytometry,
Thromboelastometry,
Blood Sampling
(3 h EC1) SBP ↓, DBP ↓, MAP ↓
(3 h) Monocyte-platelet aggregates ↓
(3 h) CD11b+ granulocytes ↓
(3 h) Intrinsic pathway ↓
(6 h) Aprotinin-test ↓
Richards et al. [58]M (n = 11) and W (n = 7)
healthy young adults
(n = 18)
EC1: BRJ-280
EC2: BRJ-210
EC3: PLA-280
EC4: PLA-210
EC1: BRJ 280 mL/day (16.8 mmol) (120 min before)/1 day
EC2: BRJ 210 mL/day (12.6 mmol) (12 min before)/1 day
Beet It Sports
(James White Drinks, Ipswich, UK)
FBF, Forced vital capacity,
Forearm VO2,
Handgrip Exercise
FBF ↑
Forced vital capacity ↑
Forearm VO2
Rogerson et al. [89]M (NR) and W (NR) younger (n = 18) and older (n = 7)
(n = 25)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 70 mL/day (6.4 mmol) (NR)/1 dayBeetroot Juice
(James White Drinks Company suffolk, UK)
Blood Sampling,
Urine Sampling,
BP, Microcirculatory endothelial function
(3 h, EC1 & EC2) NO3 Metabolism ↑
(24 h, EC1) NO3 Metabolism ↑
(EC1 & EC2) SBP, DBP ↔
(EC1 & EC2) Microcirculatory endothelial function ↔
Rowland et al. [53]M, healthy adult
(n = 12)
EC1: BRJ (MORN)
EC2: BRJ (AFT)
EC3: BRJ (EVE)
EC4: PLA (MORN)
EC5: PLA (AFT),
EC6: PLA (EVE),
EC1: BRJ 2 × 70 mL/day (13 mmol) (morning)/1 day
EC2: BRJ 2 × 70 mL/day (13 mmol) (mid-day)/1 day
EC3: BRJ 2 × 70 mL/day (13 mmol) (evening)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
Cycle Ergometer Severe-Intensity Exercise, TTE,
Urine Sampling,
Saliva Sampling,
BP, PWV
(EC1 & EC2 & EC3) NO3 Metabolism ↑
(Time) NO3 Metabolism ↔
(EC1 & EC2 & EC3) Central SBP ↓
(Time) SBP ↔
(EC1 & EC2 & EC3 vs. Time) Brachial SBP ↔
(EC1 & EC2 & EC3 vs. Time) TTE ↔
Stanaway et al. [70]M (n = 12) and W (n = 12)
healthy younger and older
(n = 24)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 150 mL/day (10.5 mmol) (morning)/1 day
EC2: BRJ 150 mL/day (10.5 mmol) (morning)/1 day
Beetroot JuiceTreadmill Walking (low-intensity aerobic exercise),
Blood Sampling,
Cognitive Measurements, BP,
Choice Reaction Test,
RVIP, Stroop test,
Mood and Perceptual
(EC1 & EC2) SBP ↓
(EC2) DBP ↓
(EC1 & EC2 & EC3 & EC4) Stroop reaction time ↑
(EC1 & EC2) Plasma NO3
(EC1 & EC2) Plasma NO2
(EC1 & EC2) Cognitive Function ↑
Tyler et al. [45]M (n = 2) and W (n = 5)
T2D adult
(n = 7)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (120 min before)/1 dayBeetroot Juice
(James White Drinks, Ipswich., UK)
Blood Sampling,
OGTT, BP
Glucose AUG ↓
ΔSVR ↓
Salivary NO2 & NO3
SBP & DBP ↔
HOMA-IR & QUICKI ↔
Vanhatalo et al. [51]M (NR) and W (NR) healthy younger and older
(n = 75)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 2 × 70 mL/day (12.1 mmol) (morning and evening)/2 weeks
EC2: BRJ 2 × 70 mL/day (12.1 mmol) (morning and evening)/2 weeks
Beetroot JuiceTongue Scarping,
Blood Sampling,
Peripheral blood pressure, Central blood pressure, FMD
(EC2) MAP ↓
(EC1) MAP ↔
(EC2) ΔNO2
(EC1) ΔNO2
(EC2, EC4) ΔMAP & ΔNO2
(EC1, EC3) ΔMAP & ΔNO2
(EC2, EC4) NO2 and oral microbes ↔
(EC1, EC3) NO2 and oral microbes ↔
van der Avoort et al. [56]M (n = 15) and W (n = 15)
healthy adults
(n = 30)
EC1: BRJ
EC2: VEG
EC1: BRJ (NR) (6.5 mmol) (mid-day)/1 weekBeet It
(James White Drinks, UK)
Blood Sampling,
BP
Plasma NO3/NO2
SBP ↓
DBP ↓
Volino-Souza et al. [57]W, Healthy pregnant
(n = 12)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (8.95 mmol) (150 min before)/1 dayBeetroot Juice
(processed in-lab)
Urine Sampling,
FMD, NIRS
FMD ↑
Urinary NO3
StO2
Wei et al. [76]M (n = 8) and W (n = 3)
healthy adult
(n = 11)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 210 mL/day (19.2 mmol) (150 min before)/1 day
EC2: BRJ 140 mL/day (12.8 mmol) (150 min before)/1 day
EC3: BRJ 70 mL/day (6.4 mmol) (150 min before)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
BP,
5 min all-out maximal voluntary knee extension test
(EC1) SBP ↓
(EC2, EC3) SBP ↔
(EC1) DBP ↓
(EC1, EC2) DBP ↔
(EC1) MAP ↓
(EC1, EC2) MAP ↔
(EC1, EC2) Peak Torque ↑
(EC3) Peak Torque ↔
(EC1, EC2) Torque Impulse ↑
(EC1, EC2) Torque Impulse ↑
(EC3) RTD ↑
(EC1, EC2) RTD ↓
Whole Blood[S-nitrosothiol] ↑
RBC[S-nitrosothiol] ↑
(EC1, EC2, EC3) Muscle NO3
(EC1, EC2, EC3) Muscle NO2
Worley et al. [60]M (n = 8) and W (n = 5)
healthy adult
(n = 13)
EC1: BRJ
EC2: PLA
EC1: 500 m/day (12.1 mmol) (180 min before)/1 dayBeetroot Juice
(Biotta, Carmel, IN, USA)
LBNP, Cerebral artery blood velocity,
HR, BP, cBRS
VLF Coherence ↑
VLF Phase ↔
VLF Gain ↔
LF Coherence ↔
LF Phase ↔
LF Gain ↓
Static-LBNP ↔
cBRS ↔
Wylie et al. [35]M, healthy adult
(n = 10)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 280 mL/day (16.8 mmol) (150 min before)/1 day
EC2: BRJ 140 mL/day (8.4 mmol) (150 min before)/1 day
EC3: BRJ 70 mL/day (4.2 mmol) (150 min before)/1 day
Beet It
(James White Drinks, Ipswich, UK)
Moderate- and severe-intensity cycling, BP, Blood Sampling(EC1, EC2, EC3) Plasma NO3
(EC1, EC2, EC3) Plasma NO2
SBP ↓
DBP ↓
MAP ↓
(EC1, EC2, EC3) VO2 amplitude ↓
(EC1, EC2, EC3) Time to task ↑
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 4. Chronic effects of beetroot juice supplementation on cardiovascular health.
Table 4. Chronic effects of beetroot juice supplementation on cardiovascular health.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Alharbi et al. [48]M (n = 7) and W (n = 22) obesity mid-age and older
(n = 29)
EC1: CR + BRJ
EC2: CR
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/2 weeksBeet It
(James White Ltd., Ashbocking, Suffolk, UK)
BP, REE,
Handgrip Strength,
Skin microvascular blood flow, IPAQ,
Urine Sampling,
Saliva Sampling
Average Microvascular Flux ↑
NO-dependent Endothelial Activity ↑
SBP ↓
Cognitive Function ↑
Oxidative Stress ↑
NO bioavailability ↑
Physical Strength ↑
Metabolic Adaptation ↔
Body composition ↔
Babateen et al. [47]M (n = 24) and
W (n = 38)
overweight/obese older adults
(n = 62)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning, evening)/13 weeks
EC2: BRJ 70 mL/day (6.45 mmol) (evening)/13 weeks
EC3: BRJ 35 mL/day (3.23 mmol) (evening)/13 weeks
Beet It Sports (James White Drinks, UK)Blood Sampling,
Urine Sampling
(EC1, EC2) Plasma NO3
(EC3) Plasma NO3
(EC1, EC3) Plasma NO2
(EC2) Plasma NO2
(EC1, EC2) Saliva NO3
(EC3) Saliva NO3
(EC1, EC2) Saliva NO2
(EC3) Saliva NO2
(EC1, EC2) Urine NO3
(EC3, time points) Urine NO3
(EC1, EC2, EC3) Urine NO2
Babateen et al. [90]M (n = 24) and
W (n = 38)
Overweight/Obese older adults
(n = 62)
EC1: High BRJ,
EC2: Medium BRJ,
EC3: Low BRJ,
EC4: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning, evening)/13 weeks
EC2: BRJ 70 mL/day (6.45 mmol) (evening)/13 weeks
EC3: BRJ 35 mL/day (3.23 mmol)/13 weeks
Beetroot Juice
(James White Company, UK)
BP, Endothelial Function(EC2, EC3) SBP ↓
(EC1) SBP ↔
(EC1, EC2, EC3) DBP ↔
(EC1, EC2, EC3) Home BP ↔
(EC2, EC3) Endothelial function ↑
(EC1) Endothelial function ↔
Bock et al. [62]M (n = 12) and W (n = 11)
healthy younger and older
(n = 23)
EC1: BRJ
EC2: PLA
EC1: BRJ 190 mL/day (4 mmol) (NR)/4 weeksSuperbeets
(HumanN Inc., Austin, TX, USA)
BP, HR, BP,
cBRS,
Peripheral chemoreceptor sensitivity
(EC1, post) Plasma NO3
(EC2 post) Plasma NO3
(EC1) SBP ↓
(EC2) SBP ↔
(EC1) MAP ↓
(EC2) MAP ↔
(EC1, EC2) HR ↔
(EC1) Chemoreflex sensitivity Ve ↓
(EC2) Chemoreflex sensitivity Ve ↔
(EC1, EC2) Chemoreflex sensitivity HR ↔
(EC1, EC2) cBRS ↔
Delgado Spicuzza et al. [66]W, early & late-postmenopausal adult
(n = 25)
EC1: BRJ (EPM)
EC2: BRJ (LPM)
EC3: PLA (EPM)
EC4: PLA (LPM)
EC1: BRJ 70 mL/day (6.4 mmol) (NR)/1 week
EC2: BRJ 70 mL/day (6.4 mmol) (NR)/1 week
Beet It Organic
(James White Drinks Ltd., Ipswich, UK)
BP, HR, baPWV,
Blood Sampling,
Macrovascular Function
(Rest, EC1, EC2 vs. EC3, EC4) ΔFMD ↑
(Rest, 24 h pre) ΔFMD ↑
(EC1, EC2 vs EC3, EC4) SBP/DBP ↔
(24 h pre) SBP/DBP↔
(EC1, EC2 vs EC3, EC4) Plasma NO3
(24 h pre) Plasma NO2
(EC1, EC2 vs EC3, EC4) Plasma NO2
(24 h pre) Plasma NO2
(EC1, EC2 vs EC3, EC4) Ischemia–reperfusion injury FMD ↔
(24 h pre) Ischemia–reperfusion injury FMD ↔
Fejes, Pilat et al. [71]M (n = 10) and W (n = 5)
hypertension older
(n = 15)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning and evening)/4 weeksBeetroot JuiceBP, Urine Sampling, Fasting Blood(4WK POST) oxLDL/NOx ratio ↓
GSH/GSSG ratio ↑
(vs. Baseline) High-sensitivity CRP ↓
Fejes et al. [50]M (n = 10) and W (n = 5) hypertension older
(n = 15)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning and evening)/4 weeksBeet It
(James White Drinks Ltd., Ipswich, UK)
BP, FBF,
Blood Sampling,
24 h Ambulatory BP monitoring
Plasma NO3 /NO2
Salivary NO3/ NO2
Acetylcholine, Nitroglycerin ↔
FBF-AUC Ratio ↔
SBP, MAP ↔
Home BP ↔
24 h Ambulatory BP monitoring ↔
Jones et al. [65]M (NR) and W (NR) healthy older
(n = 20)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/4 weeksBeet It Sport
(James White Drinks Ltd., Ipswich, UK)
BP FMD, Microvascular function, Tongue Scarping, Blood SamplingFMD ↑
SBP ↓
DBP ↓
Microvascular function ↔
Osman et al. [69]W, planning to conceive
(n = 29)
EC1: BRJ
EC2: BRJ + EXE
EC3: EXE
EC4: CON
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/12 weeks
EC2: BRJ 70 mL/day (6.4 mmol) (morning)/12 weeks
BRJ Supplementation Juice
(James White Drinks Ltd., Ipswich, UK)
Resistance and Endurance exercise,
BP, CO, TPR
(EC3) TPR ↓
(EC3) CO ↑
(EC2) DBP ↓
(EC2) CO ↑
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 5. Effects of beetroot juice supplementation on neurological function.
Table 5. Effects of beetroot juice supplementation on neurological function.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Acute
Berlanga et al. [72]M, amateur sports climber
(n = 10)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (150 min before)/1 dayBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
Maximal Isometric Half Crimp Test,
Pull-Up Failure Test,
IHS, CMJ, SJ,
Saliva Sampling
CMJ height ↔
SJ height ↔
IHS ↔
Pull-up test to failure ↔
Half crimp test ↔
Salivary NO3 and NO2
Clifford et al. [26]M, healthy, recreationally active
(n = 29)
EC1: High BRJ
EC2: Low BRJ
EC3: PLA
EC1: BRJ 250 mL/day (4 mmol) (morning and evening)/3 days
EC2: BRJ 250 mL/day (2 mmol) (morning and evening)/3 days
Love Beets Super Tasty Beet Juice
(Gs Fresh Ltd., Cambridgeshire, UK)
Drop Jump, MIVC, CMJ, PPT, CK(EC1, EC2) MIVC recovery ↑
CMJ recovery ↑
CK ↓
PPT ↓
Garnacho-Castano et al. [41]M, healthy with ≥ 2 years of crossfit experience
(n = 12)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (180 min before)/1 dayBeet It
(James White Drinks Ltd., Ipswich, UK)
Workout of the day Test (CrossFit),
Blood Sampling,
SpO2, CMJ
(1st) Number of Repetitions ↑
(2nd) Number of Repetitions ↔
Serum Cortisol
SpO2
Muscle Fatigue ↓
Serum Testosterone ↔
Testosterone/cortisol Ratio ↔
Blood Lactate ↔
Lopez-Samanes et al. [91]M, young basketball player
(n = 10)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (180 min before)/1 dayBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
Simulated Basketball game and Neuromuscular Performance Test(EC1 vs. EC2) CMJ ↑
(EC1 vs. EC2) Sprint ↑
(EC1 vs. EC2) Handgrip ↑
(EC1 vs. EC2) Agility T-test ↑
match physical activity ↔
Lopez-Samanes et al. [73]M, highly competitive tennis player
(n = 13)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (180 min before)/1 dayBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
RPE, Serve velocity test, CMJ, ISH, 5-0-5 agility, 10 mServe velocity test ↑
CMJ ↑
IHS ↑
5-0-5 agility dominant ↓
5-0-5 agility non-dominant side↓
10 m ↓
Lopez-Samanes et al. [75]W, semi-professional rugby player
(n = 14)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (150 min before)/1 dayBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
CMJ, IHS,
10 m and 30 m Sprint Test,
Modified agility T-test, Bronco endurance test
CMJ ↑
IHS ↔
10 m & 30 m Sprint ↔
Agility T-test ↔
Bronco endurance test ↔
Lopez-Samanes et al. [74]W, elite field hockey player
(n = 11)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (180 min before)/1 dayBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
CMJ,
IHS,
20 m-sprint,
RSA
CMJ ↔
Handgrip ↔
20 m Sprint ↔
RSA ↔
Match GPS metrics ↔
Rowland et al. [53]M, healthy adult
(n = 12)
EC1: BRJ (MORN)
EC2: BRJ (AFT)
EC3: BRJ (EVE)
EC4: PLA (MORN)
EC5: PLA (AFT)
EC6: PLA (EVE)
EC1: BRJ 2 × 70 mL/day (13 mmol) (morning)/1 day
EC2: BRJ 2 × 70 mL/day (13 mmol) (mid-day)/1 day
EC3: BRJ 2 × 70 mL/day (13 mmol) (evening)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
Cycle Ergometer Severe-Intensity Exercise, TTE,
Urine Sampling,
Saliva Sampling,
BP, PWV
(EC1 & EC2 & EC3) NO3 Metabolism ↑
(Time) NO3 Metabolism ↔
(EC1 & EC2 & EC3) Central SBP ↓
(Time) SBP ↔
(EC1 & EC2 & EC3 vs. Time) Brachial SBP ↔
(EC1 & EC2 & EC3 vs. Time) TTE ↔
Tan et al. [81]M, healthy and resistance-trained
(n = 18)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 4 × 70 mL/day (24 mmol) (150 min before)/1 day
EC2: BRJ 2 × 70 mL/day (12 mmol) (150 min before)/1 day
EC3: BRJ 70 mL/day (6 mmol) (150 min before)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
CMJ: 1 set × 5 reps (40% 1RM) Squat & Bench: 1 set × 3 reps (50% 1RM) + 1 set × 3 reps (75% 1RM), Liner position transducer, Blood Sampling, Brunel mood scaleCMJ ↔
Squat ↔
Bench Press ↔
(EC1, EC2, EC3) Plasma NO3
(EC1, EC2, EC3) Plasma NO2
Mood ↔
Wei et al. [76]M (n = 8) and W (n = 3)
healthy adult
(n = 11)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 210 mL/day (19.2 mmol) (150 min before)/1 day
EC2: BRJ 140 mL/day (12.8 mmol) (150 min before)/1 day
EC3: BRJ 70 mL/day (6.4 mmol) (150 min before)/1 day
Beet It
(James White Drinks Ltd., Ipswich, UK)
BP, 5 min all-out maximal voluntary knee extension test,(EC1) SBP ↓
(EC2, EC3) SBP ↔
(EC1) DBP ↓
(EC1, EC2) DBP ↔
(EC1) MAP ↓
(EC1, EC2) MAP ↔
(EC1, EC2) Peak Torque ↑
(EC3) Peak Torque ↔
(EC1, EC2) Torque Impulse ↑
(EC1, EC2) Torque Impulse ↑
(EC3) RTD ↑
(EC1, EC2) RTD ↓
Whole Blood[S-nitrosothiol] ↑
RBC[S-nitrosothiol] ↑
(EC1, EC2, EC3) Muscle NO3
(EC1, EC2, EC3) Muscle NO2
Wylie et al. [35]M, healthy adult
(n = 10)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 280 mL/day (16.8 mmol) (150 min before)/1 day
EC2: BRJ 140 mL/day (8.4 mmol) (150 min before)/1 day
EC3: BRJ 70 mL/day (4.2 mmol) (150 min before)/1 day
Beet It
(James White Drinks, Ipswich, UK)
Moderate- and severe-intensity cycling, BP, Blood Sampling(EC1, EC2, EC3) Plasma NO3
(EC1, EC2, EC3) Plasma NO2
SBP ↓
DBP ↓
MAP ↓
(EC1, EC2, EC3) VO2 amplitude ↓
(EC1, EC2, EC3) Time to task (severe) ↑
Chronic
Daab et al. [92]M, semi-professional soccer player
(n = 13)
EC1: BRJ
EC2: PLA
EC1: 2 × 150 mL/day (8 mmol) (morning and evening)/1 weekNatural Beetroot Juice (Homemade, freshly processed)Intermittent Shuttle Running, MVC, Qtw,pot, Voluntary activationMVC ↓
Qtw,pot
Voluntary activation ↓
Esen et al. [78]M (n = 10) and W (n = 6)
healthy, physically active young adult
(n = 16)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (12.8 mmol) (morning and evening)/5 daysBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
Isometric knee extension at 25% MVC with BFRPlasma NO2
MUP duration ↓
MUFR, MUP area ↔
Esen et al. [77]M, healthy, recreationally active
(n = 14)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (12.8 mmol) (morning and evening)/5 daysBeet It
(James White Drinks, Ipswich, UK)
Kness-Entensor Strength Test, Intramuscular EMG, Isometric contractions, Blood SamplingMUP duration ↓
Area, MUFR ↔
Plasma NO2
Munoz et al. [80]M, semi-professional handball player
(n = 12)
EC1: BRJ
EC2: PLA
EC1: 70 mL/day (6.4 mmol) (mid-day)/3 daysBeet-It Pro Elite Shot
(James White Drinks Ltd., Ipswich, UK)
IHS, CMJ, Throwing velocity, Agility T-test, RSAIHS ↑
CMJ Height ↑
Throwing velocity ↔
Agility T-test↔
RSA ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.

4.4. Brain Health and Cognitive Function

Neuromuscular outcomes reported in human trials (summarized in Table 5) show that acute BRJ ingestion rarely alters maximal strength, rate of force development, or high-intensity neuromuscular output across diverse populations.
Studies in sport climbers [72], tennis athletes [73], and female hockey players [74] consistently show unchanged MVC, handgrip force, pull-up performance, and short-duration power tasks. Eccentric-exercise protocols likewise report no differences in soreness, MVC recovery, or inflammatory markers [26]. Power- and sprint-based measures also tend to remain stable, although an increase in Countermovement jump (CMJ) height was observed in semi-professional female rugby players following acute supplementation [75]. Dose–response evidence further suggests that lower nitrate doses may enhance the rate of torque development, whereas higher doses influence peak torque [76], indicating that specific neuromuscular parameters may respond differently to nitrate availability. At the electrophysiological level, studies by Esen et al. demonstrate that motor unit firing rate, recruitment threshold, and MUP area remain unchanged following nitrate ingestion [77,78], yet repeated reductions in MUP duration point toward faster restoration of muscle fiber membrane conduction velocity. This effect is especially apparent under ischemic conditions, where nitrate improves the recovery of MUP duration and peripheral excitability without altering central activation strategies [77]. Functional recovery outcomes—such as restored MVC, improved CMJ, and increased pain thresholds—have been observed in some trials even when biochemical markers of muscle damage (CK, CRP, IL-6) do not change, suggesting that BRJ may support neuromuscular recovery through mechanisms not captured by standard damage biomarkers [26,79].
Chronic supplementation produces fewer measurable neuromuscular adaptations. Multi-week interventions show improved exercise tolerance in one study but little change in MVC, EMG amplitude, fatigability, or muscle contractile properties [53]. Similar null findings have been reported for strength, power, EMG-based activation, and motor unit recruitment after prolonged ingestion across different nitrate doses [80,81]. The available chronic evidence therefore suggests limited effects on central neuromuscular mechanisms or structural muscle function, although peripheral electrophysiological responses—such as faster restoration of membrane conduction—seen in acute studies may still be relevant depending on task demands. Together, the current literature indicates that BRJ does not consistently enhance maximal neuromuscular performance but may influence peripheral muscle excitability or functional recovery under specific physiological conditions, with responses varying according to muscle group, supplementation dose, and the characteristics of the activity performed.

5. Effects of Beetroot Juice and Exercise on Athletic Performance

The mechanisms through which beetroot juice (BRJ) influences physiological responses to exercise—illustrated in Figure 3—form the basis for understanding its potential effects on athletic performance. Building on these mechanistic pathways, this section synthesizes findings from studies that administered BRJ acutely or over periods of sustained supplementation and evaluates how performance responses differ across endurance- based exercise, short-duration sprint and power tasks, and the intermittent, multidirectional demands typical of team sports. Because outcomes vary considerably with factors such as training status, exercise modality, and supplementation timing, the following subsections outline these performance domains separately to clarify when and under what conditions BRJ intake translates into measurable ergogenic effects (Table 6).
Table 6. Effects of beetroot juice supplementation on brain health and cognitive outcomes.
Table 6. Effects of beetroot juice supplementation on brain health and cognitive outcomes.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Acute
Curry et al. [59]W, healthy
(n = 10)
EC1: BRJ
EC2: Orange Juice
EC1: BRJ 500 mL/day (12 mmol) (120 min before)/1 dayBeetroot Juice
(CAJ Food Products, Inc., Fishers, IN, USA)
Electronically braked leg cycle ergometer (40 & 80% VO2peak for 5 min),
BP, HR, Transcranial Doppler, CO
Blood NO ↑
SBP ↓
DBP & HR ↔
CAIx ↓
(Rest) CAIx ↔
PIx & RIx ↔
Horiuchi et al. [85]M, healthy adult
(n = 12)
EC1: BRJ (Normoxia),
EC2: BRJ (Hypoxia)
EC3: PLA (Normoxia)
EC4: PLA (Hypoxia)
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (NR)/4 days
EC2: BRJ 2 × 70 mL/day (12.9 mmol) (NR)/4 days
Beet It
(James White Drinks, UK)
Blood Sampling,
DCA, Internal carotid artery, SpO2, MAP, VE, PETCO2
(EC1, EC2 vs. EC3, EC4) Circulating NO3
(EC2, EC4 vs. EC1, EC3) DCA-RoR ↓
(EC1 vs. EC3) DCA-RoR ↔
(EC2 vs. EC4) DCA-RoR ↔
(EC2, EC4 vs. EC1, EC3) Internal carotid artery Diameter, Velocity, or Flow ↔
Londono-Hoyos et al. [87]M (n = 14) and W (n = 2)
HFpEF patients
(n = 16)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (120 min before)/1 dayBeet It Sport
(James White Drinks Ltd., UK)
Echo, Echo, BPMAP, HR, CSA, Acute hemodynamic, Carotid Hydraulic Power, Carotid Power Penetration, Carotid Energy Penetration ↔
Cardiac Output ↓
Miraftabi et al. [93]M, trained taekwondo athletes
(n = 8)
EC1: BRJ-800
EC2: BRJ-400
EC3: PLA
EC4: CON
EC1: BRJ 120 mL/day (12.9 mmol) (150 min before)/1 day
EC2: BRJ 120 mL/day (6.4 mmol) (150 min before)/1 day
Red Beet Vinitrox Shot
(Sponsor Ltd., Germany)
High-intensity Intermittent Exercise,
PSTT, Multiple frequency speed of kick test, CMJ,
Stroop Test, Finger-Prick Blood Sampling
PSTT, Multiple frequency speed of kick test ↔
(EC2, after PSTT) Stroop test ↑
CMJ Height ↔
HR ↔
RPE ↔
Blood Lactate ↔
Pedrinolla et al. [67]M (NR) and W (NR)
younger (n = 10) and older (n = 10) and AD (n = 10)
(n = 30)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: BRJ (AD)
EC4: PLA (YN)
EC5: PLA (OLD)
EC6: PLA (AD)
EC1: BRJ 70 mL/day (5.0 mmol) (morning)/1 day
EC2: BRJ 70 mL/day (5.0 mmol) (morning)/1 day
EC3: BRJ 70 mL/day (5.0 mmol) (morning)/1 day
Beet It Sports
(James White Drinks, Ipswich, UK)
Blood Sampling(EC3 vs. EC1, EC2) Baseline Plasma NO3
(EC2 vs. EC1) Baseline Plasma NO3
(EC1) Baseline Plasma NO3
(EC3, EC1, EC2) Baseline Plasma NO2
(EC3, EC1, EC2) Δ Plasma NO3
(EC3, EC1, EC2) Δ Plasma NO2
(EC3, EC1, EC2) Δ Vascular Responsiveness ↑
(EC3 vs EC1, EC2) Absolute Vascular Responsiveness ↓
(EC2 vs EC1) Absolute Vascular Responsiveness ↔
(EC1) Absolute Vascular Responsiveness ↔
Stanaway et al. [70]M (n = 12) and W (n = 12)
healthy younger and older
(n = 24)
EC1: BRJ (YN)
EC2: BRJ (OLD)
EC3: PLA (YN)
EC4: PLA (OLD)
EC1: BRJ 150 mL/day (10.5 mmol) (morning)/1 day
EC2: BRJ 150 mL/day (10.5 mmol) (morning)/1 day
Beetroot JuiceTreadmill Walking (low-intensity aerobic exercise),
Blood Sampling,
Cognitive Measurements, BP, RVIP,
Stroop test, Mood and Perceptual
(EC1, EC2) SBP ↓
(EC2) DBP ↓
(EC1, EC2, EC3, EC4) Stroop reaction time ↑
(EC1, EC2) Plasma NO3
(EC1, EC2) Plasma NO2
(EC1, EC2) Cognitive Function ↑
Thompson et al. [94]M, healthy and active
(n = 16)
EC1: BRJ
EC2: PLA
EC1: BRJ 450 mL/day (5 mmol) (90 min before)/1 dayBeet It
(James White Ltd., Ipswich, UK)
Electronically Braked leg Cycle Ergometer (RPE,
Brunel mood scale, BP, Finger-Prick Blood Sampling, Cerebral NIRS,
Muscle NIRS, Intramuscular EMG, RVIP) Stroop Test
Plasma Nitrate ↑
SBP ↓
VO2
HHb muscle ↓
HHb cerebral ↓
TTE ↑
RVIP ↔
RPE ↔
Mental Fatigue ↔
(pre-EXE) Lactate ↑
Wightman et al. [11]M (n = 12) and W (n =28)
healthy adult
(n = 40)
EC1: BRJ
EC2: PLA
EC1: 450 mL/day (5.5 mmol) (at test onset)Beet It
(James White Ltd., Ipswich, UK)
NIRS, Blood Sampling, RVIPPlasma NO3
Cognitive Performance ↑
(pre) Cerebral blood flow ↑
(post) Cerebral blood flow ↓
(Total Hb during RVIP) Cerebral blood flow ↓
Deoxy-Hb ↔
SBP/DBP ↔
HR ↔
Worley et al. [60]M (n = 8) and W (n = 5)
healthy adult
(n = 13)
EC1: BRJ
EC2: PLA
EC1: 500 m/day (12.1 mmol) (180 min before)/1 dayBeetroot Juice
(Biotta, Carmel, IN, USA)
LBNP, Cerebral artery blood velocity,
HR, BP, cBRS
VLF Coherence ↑
VLF Phase ↔
VLF Gain ↔
LF Coherence ↔
LF Phase ↔
LF Gain ↓
Static-LBNP ↔
cBRS ↔
Chronic
Alharbi et al. [48]M (n = 7) and W (n = 22) obesity mid-age and older
(n = 29)
EC1: CR + BRJ
EC2: CR
EC1: BRJ 70 mL/day (6.4 mmol) (morning)/2 weeksBeet It
(James White Ltd., Ashbocking, Suffolk, UK)
BP, REE, Handgrip Strength, Skin microvascular blood flow, IPAQ, Urine Sampling, Saliva SamplingAverage Microvascular Flux ↑
NO-dependent Endothelial
Activity ↑
SBP ↓
Cognitive Function ↑
Oxidative Stress ↑
NO bioavailability ↑
Physical Strength ↑
Metabolic Adaptation ↔
Body composition ↔
Babateen et al. [47]M (n = 24) and
W (n = 38)
overweight/obese older adults
(n = 62)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning, evening)/13 weeks
EC2: BRJ 70 mL/day (6.45 mmol) (evening)/13 weeks
EC3: BRJ 35 mL/day (3.23 mmol) (evening)/13 weeks
Beet It Sports (James White Drinks, UK)Blood Sampling,
Urine Sampling
(EC1, EC2) Plasma NO3
(EC3) Plasma NO3
(EC1, EC3) Plasma NO2
(EC2) Plasma NO2
(EC1, EC2) Saliva NO3
(EC3) Saliva NO3
(EC1, EC2) Saliva NO2
(EC3) Saliva NO2
(EC1, EC2) Urine NO3
(EC3, time points) Urine NO3
(EC1, EC2, EC3) Urine NO2
Babateen et al. [95]M (n = 24) and
W (n = 38)
overweight/obese older adults
(n = 62)
EC1: High BRJ
EC2: Medium BRJ
EC3: Low BRJ
EC4: PLA
EC1: BRJ 2 × 70 mL/day (12.9 mmol) (morning, evening)/13 weeks
EC2: BRJ 70 mL/day (6.45 mmol) (evening)/13 weeks
EC3: BRJ 35 mL/day (3.23 mmol)/13 weeks
Beetroot Juice
(James White Company, Ashbocking, Suffolk, UK)
qNIRS,
Cognitive Function
Cognitive Function ↔
Cerebral blood flow ↔
(EC3) Plasma NO3
(EC1, EC3) Plasma NO2
Kelly et al. [86]M (n = 6) and W (n = 6)
healthy older adult
(n = 12)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (9.6 mmol) (morning and mid-day)/1 dayBeet It Sports
(James White Drinks, UK)
Moderate Treadmill Walking, Low/High-Intensity Kness Extension, 6MWT,
Blood Sampling,
BP, HR, Serial Sevens, Subtraction Test
(EC1) SBP ↓, (EC1) DBP ↓
(EC1 & EC2) MAP, (EC1) VO 2 Mean Response Time ↓
6MWT, Muscle Metabolism,
Cognition, Brain Metabolism ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.

5.1. Endurance Athletes

Research on endurance performance shows the most consistent improvements with BRJ supplementation, reflecting its influence on oxygen cost, exercise economy, and tolerance to prolonged or high-intensity exertion. Findings summarized in Table 7 (acute) and Table 8 (chronic) demonstrate that BRJ can enhance aerobic performance across cycling, running, rowing, swimming, and other endurance-based activities.
Meta-analytic evidence indicates reductions in the oxygen cost of submaximal exercise, improved mitochondrial and contractile efficiency, and enhanced NO-mediated vasodilation, which together contribute to better exercise economy [96]. In trained cyclists, acute supplementation shortened 4 km and 16.1 km time-trial performance by 2.7–2.8% and increased the ratio of power output to oxygen consumption (PO/VO2) [14]. Similar benefits have been documented in rowing, where a single BRJ dose improved 2000 m time-trial performance and increased VO2max in master rowers [97], and in alpine skiing, where slalom completion time improved following supplementation [98]. Running performance also shows positive responses, with improvements of ~1.9% in 1500 m time trials following acute ingestion [99]. BRJ also demonstrates clear benefits for exercise economy and tolerance during sustained or intermittent efforts. In low-fitness individuals, four days of supplementation reduced submaximal oxygen consumption at 45% and 60% VO2max, whereas high-fitness individuals showed no change [100]. Competitive swimmers exhibited reduced aerobic energy cost and higher workloads at the anaerobic threshold after six days of BRJ ingestion [101]. During prolonged moderate-intensity cycling, BRJ preserved elevated plasma nitrite concentrations and attenuated the rise in oxygen uptake, reflecting improved submaximal economy when taken both before and during exercise [102]. Improvements in time to exhaustion (TTE) have been consistently reported across populations. Adolescents with obesity showed a ~23% increase in TTE after six days of supplementation, accompanied by reductions in the VO2 slow component [103]. Intermittent endurance capacity responds similarly, with single-dose BRJ increasing Yo-Yo IR1 performance [13] and three-day supplementation increasing total work and number of bouts completed during supramaximal intermittent cycling [104]. Cardiorespiratory variables may also improve under certain conditions; in female endurance athletes, acute intake increased VO2max by ~4.8% and improved ventilatory efficiency [105], although other studies in rowers observed performance benefits without changes in ventilatory responses [97]. Performance gains are not universal, particularly among elite endurance athletes whose physiological systems may already operate near their maximal NO-related capacity [106]. In highly trained 1500 m runners, BRJ supplementation did not affect running economy or time-trial performance [107], and in competitive swimmers, acute ingestion did not enhance repeated interval performance [101]. These heterogeneous responses indicate that the ergogenic effects of BRJ are more likely to emerge in athletes whose oxygen cost, mitochondrial efficiency, or NO-mediated vasodilation retain greater capacity for improvement.

5.2. Sprint and Power Athletes

The effects of BRJ supplementation on sprint and power performance are mixed and strongly context dependent, with improvements appearing in certain explosive tasks but not consistently expressed across protocols or athlete groups. In short-duration maximal efforts, several studies have reported clear benefits. A single dose of BRJ increased peak and mean power and shortened the time to reach peak power during a 30 s all-out Wingate sprint in resistance-trained men [108]. Maximal cycling sprints lasting 3–4 s have shown ~6% increases in peak power and higher optimal pedaling rates following BRJ ingestion [109]. In physically active women, supplementation improved CMJ height, power output, and barbell velocity during back squats, along with better repetition performance at 75% 1RM [110]. Similar improvements in explosive strength and Special Judo Fitness Test (SJFT) scores have been observed in elite adolescent judo athletes [111], suggesting that very brief, Type II fiber–dominant efforts may be particularly responsive to BRJ. Benefits have also been documented during repeated high-intensity resistance tasks. In healthy men, BRJ increased mean and peak power during sets performed at 60–80% 1RM, accompanied by higher barbell velocity and less power decline across repetitions [108]. Recovery-related outcomes demonstrate a similar pattern. After exercise-induced muscle damage, supplementation reduced muscle soreness and thigh swelling and helped restore static muscular endurance [112]. A systematic review has likewise shown improvements in muscle function recovery—especially MVC and CMJ—within 24–72 h [79]. These findings may reflect enhanced perfusion, improved metabolic efficiency, and NO-mediated support for excitation–contraction processes. At the same time, several well-controlled trials show minimal or no benefit. In some resistance-trained or sport-trained populations, BRJ has failed to meaningfully change peak force, movement velocity, repetition performance, or maximal isometric strength. These neutral outcomes are often observed in highly trained athletes whose neuromuscular systems are already operating near their mechanical and metabolic limits, leaving less opportunity for supplementation to influence contractile performance. BRJ appears to influence discrete components of sprint and power performance—particularly maximal power expression over very short durations, the maintenance of power during repeated efforts, and aspects of recovery from muscle-damaging activity—while showing limited effects on traditional strength measures or tasks requiring prolonged neuromuscular output. The available findings for acute and chronic protocols are summarized in Table 9 and Table 10.

5.3. Team-Sport Athletes

Team sports impose a distinct set of physiological and technical demands—continuous alternation between aerobic and anaerobic efforts, frequent changes in direction, contact situations, and decision-making under fatigue. These characteristics make the performance responses to BRJ supplementation different from those observed in isolated sprint or power protocols. Studies relevant to team sports from the current evidence base are summarized in Table 11, and their main findings are outlined below.
Across several investigations, repeated-sprint performance itself did not consistently improve, yet partial benefits appeared in recovery-related outcomes and in the preservation of function under fatigue. For example, in a study examining recovery between sprint bouts, BRJ ingestion facilitated better restoration of muscle function and reduced soreness, even though sprint performance per se remained unchanged [112]. In team-sport athletes such as basketball players, acute BRJ supplementation did not improve neuromuscular performance or match-play activity, supporting the notion that improvements in explosive actions may be context-dependent [91].
Some studies have reported performance enhancements under more specific conditions. In an intermittent-exercise model relevant to team sports, 7 days of BRJ supplementation increased total work performed during an 80 min protocol and helped maintain cognitive reaction speed in later stages, indicating protection of decision-making capacity under fatigue [113]. By contrast, protocols involving very high-intensity efforts with minimal recovery demonstrate a different response pattern. In an intermittent sprint task consisting of repeated 8 s all-out sprints with 30 s active recovery, a single dose of BRJ resulted in fewer completed sprints and lower total work, while mean and peak power, heart rate, blood lactate, and perceived exertion were unaffected [114]. BRJ supplementation in team-sport athletes appears to offer benefits in selected areas—such as recovery of muscle function, attenuation of soreness, maintenance of work output during prolonged intermittent exercise, and preservation of cognitive performance under fatigue—while showing inconsistent effects on key sport-specific outcomes including sprint speed, repeated-sprint ability, change-of-direction performance, and high-speed running. These variable responses likely reflect interactions among exercise structure, technical demands, recovery duration, athlete training status, and supplementation parameters, which together shape whether and how performance improvements emerge in team-sport environments.
Table 7. Acute effects of beetroot juice supplementation on endurance performance.
Table 7. Acute effects of beetroot juice supplementation on endurance performance.
ReferenceParticipantsExperimental
Conditions
Supplementation ProtocolSupplement SourceVariablesResults
Ahmadpour et al. [98]M, expert alpine Skiers (n = 10)EC1: BRJ
EC2: PLA
EC1: BRJ 220 mL/day (8.9 mmol) (150 min before)/1 dayBeetroot Juice
(Zarghan, Lepoi Fars, Shiraz, Iran)
90 s box jump, Hexagonal agility jump, wall-sit test, slalom runs at 15 min intervals90 s box jump ↑
Wall-sit endurance ↑
Hex jump time ↓
Slalom run time ↔
Aucouturier et al. [104]M, physically Active (n = 12)EC1: BRJ
EC2: PLA
EC1: BRJ 500 mL/day (9.3 mmol) (120 min before)/3 daysBeetroot juice (Pajottenlander, Belgium)15 s at 170% MAP + 30 s passive rest repeated to exhaustion (Number of repetitions to exhaustion, RBC, VO2, lactate, MVC)Number of repetitions to exhaustion ↑
RBC ↑
VO2, lactate, MVC ↔
Garnacho-Castaño et al. [97]M, master rowers (n = 10)EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (180 min before)/1 dayBeet it (James White Drinks Ltd., Ipswich, UK)2000 m rowing ergometer test (TT time, mean power output, strokes/min, meters/stroke, VO2 (absolute & relative), HR max & mean, VE·VCO2−1 slope, blood lactate, SpO2, RPE)TT time ↓
VO2 (absolute & relative) ↑
HR max & HR mean ↑
VE·VCO2−1 slope ↔
Blood lactate ↔
SpO2
RPE ↔
Mean power output ↔
Strokes/min ↔
Meters/stroke ↔
Lansley et al. [14]M, competitive cyclists (n = 9)EC1: BRJ
EC2: PLA
EC1: BRJ 500 mL/day (6.2 mmol) (180 min before)/1 day,
EC2: BRJ 500 mL/day (0.0047 mmol) (180 min before)/1 day
Beet It (James White Drinks Ltd., UK)4 km and 16.1 km cycling time-trial
(TT time, power output, VO2, HR, RPE)
TT time ↓
Power output ↑
VO2
HR ↔
RPE ↔
Moreno et al. [115]M (n = 7) and
W (n = 6)
competitive swimmers
(n = 13)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (180 min before)/1 day
EC2: BRJ 70 mL/day (0.04 mmol) (180 min before)/1 day
Beet-It-Pro Elite Shot (James White Drinks Ltd., Ipswich, UK)6 × 100 m repeated maximal-effort swimming test (front-crawl) with 7 min rest between sprints
(Time per 100 m, RPE, TQR scale, blood lactate concentration
Time per 100 m ↔
RPE ↓
TQR ↑
Blood lactate ↔
Moreno-Heredero et al. [116]M (n = 9) and
W (n = 9)
competitive swimmers
(n = 18)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (120 min before)/1 day
EC2: PLA 70 mL/day (0.04 mmol) (120 min before)/1 day
Beet-It-Pro Elite Shot; James White Drinks Ltd., Ipswich, UK6 × 100 m front-crawl interval swimming with 5 min rest between repetitions
(time per 100 m, RPE, TQR, HR, blood lactate)
Time per 100 m ↔
RPE ↔
TQR ↔
HR ↔
Blood lactate ↔
Zhang et al. [117]W, recreationally active young
(n = 13)
EC1: High BRJ
EC2: Low BRJ
EC3: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (150 min before)/1 day
EC2: BRJ 140 mL/day (6.45 mmol) (150 min before)/1 day
Beet It Sport (James White Drinks Ltd., Suffolk, England, UK)High intensity interval training (PPO, HR, RPE, Plasma NO3·NO2)(EC1, EC2)
PPO ↔
TTE ↔
HR ↓
RPE ↓
Plasma NO3, NO2
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 8. Chronic effects of beetroot juice supplementation on endurance performance.
Table 8. Chronic effects of beetroot juice supplementation on endurance performance.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Boorsma et al. [107]M, elite 1500 m runners (n = 8)EC1: BRJ
EC2: PLA
EC1: BRJ 210 mL (19.5 mmol NO3) 150 min before on days 1 and 8 + 140 mL/day (13.0 mmol NO3) on days 2–7 (8 days total).
EC2: PLA 140 mL (0.065-mmol NO3) on 2–7 day
Beet It Sport (James White Drinks,
Ipswich, UK)
Submaximal treadmill running at 50, 65, 80% VO2peak (VO2, HR, etc.), 1500 m time-trial performance, plasma [NO3].Plasma NO3
submax VO2
HR ↔
1500 m TT time ↔
Carriker et al. [118]M, high fit (n =6) and low Fit (n =5),
(n =11)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.2 mmol) (150 min before)/4 daysBeet it (James White Drinks, Ltd., Ipswich, UK)Submaximal treadmill bouts at 45%, 60%, 70%, 80%, 85% of VO2max
(VO2, HR, RER, RPE)
VO2
VO2
HR ↔
RER ↔
RPE ↔
Pinna et al. [119]M, master swimmers
(n = 14)
EC1: BRJ,
EC2: PLA
EC1: BRJ 500 mL/day (5.5 mmol) (a set time each day)/6 daysReed Beet Juice, (Aureli, Ortucchio, Italy)Control Swimming Test (VO2, VCO2, VE, Aerobic exergy expenditure)Aerobic energy expenditure ↓
VO2
VCO2
VE ↔
Rasica et al. [103]M (n = 2) and
W (n = 8)
obese adolescents
(n = 10)
EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (10 mmol) (a set time each day)/6 daysBeet It (James White Drinks, Ipswich, UK)Moderate-intensity endurance (6 min × 2), Severe-intensity endurance (to exhaustion) (MRT, primary VO2, VO2 gain, VO2 slow component, End-exercise VO2, HR, lactate, TTE)MRT ↓
VO2
VO2 gain ↔
VO2 slow component ↓
End-exercise VO2
HR ↔
Lactate ↔
TTE ↑
Tan et al. [102]M, recreationally active (n = 12)EC1: BRJ + BRJ
EC2: BRJ + PLA
EC3: PLA + PLA
EC1: BRJ 2 × 70 mL/day (12.8 mmol) (150 min before, 60 min after)/3 days
EC2: BRJ 2 × 70 mL (12.8 mmol NO3) (150 min before)/3 days
Beet it (James White Drinks, Ipswich, UK)Moderate-intensity endurance Cycling (2 × 15 min) (VO2, VO2 drift, O2 cost, HR, RPE, Lactate, Plasma NO2)(EC1) VO2 drift ↓
O2 cost ↓
Mean VO2
HR ↔
RPE ↔
Lactate ↔
Muscle glycogen ↔
(EC1, EC2) Muscle ATP ↓
(EC1, EC2) Plasma NO2
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 9. Acute effects of beetroot juice supplementation on sprint and power performance.
Table 9. Acute effects of beetroot juice supplementation on sprint and power performance.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Cuenca et al. [108]M, healthy resistance-trained (n = 15)EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (180 min before)/1 dayBeet-It-Pro Elite Shot (Beet IT; James White Drinks Ltd., Ipswich, UK)30 s Wingate sprint (Peak power, Mean power, Time-to-peak, fatigue index, CMJ, EMG, Lactate, HR, RPE)Peak power ↑
Mean power ↑
Time-to-peak ↓
Fatigue index ↔
CMJ ↔
EMG fatigue ↔ Lactate/HR/RPE ↔
Demirli et al. [111]M, recreational adolescent judokas
(n = 35)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (120 min before)/1 dayBeet It Sport (James White Drinks Ltd., Suffolk, England, UK)4 min randori + Sargent jump + Back strength + Handgrip + SJFT (throws, index, 1 min HR)Jump height ↑
Back strength ↑
Handgrip strength
SJFT throws ↑
1 min post-SJFT HR ↓
SJFT index ↓
Immediate post HR ↔ RPE ↔
Esen et al. [120]M, trained rugby players (n = 12)EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (120 min before)/1 day
EC1: BRJ 140 mL/day (0.08 mmol) (180 min before)/1 day
Beet It (James White Drinks Ltd., Ipswich, UK)YYIR1 (distance, HR, RPE, lactate, CMJ, IMTP, blood pressure)Distance ↔
HR ↔
Lactate ↔
RPE ↔,
CMJ ↔
IMTP ↔
BP ↔
Jurado-Castro et al. [110]W, physically active athletes
(n = 14)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (120 min before)/1 dayBeet It Sport (James White Drinks Ltd., Suffolk, England, UK)Isometric mid-thigh pull test, CMJ, back-squat velocity test, NIRS (IMTP peak force, IMTP RFD, CMJ height, CMJ peak power, CMJ peak velocity, squat mean propulsive velocity, squat peak velocity)IMTP peak force ↑
IMTP RFD ↑
CMJ peak power ↑
CMJ height/peak velocity/peak force ↔
50% 1RM_Squat velocity ↑ 75% 1RM_Squat velocity ↔
Lopez-Samanes et al. [91]M, young basketball players (n = 10)EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (180 min before)/1 dayBeet It Sport (James White Drinks Ltd., Suffolk, England, UK)Simulated 5-on-5 match + battery test (CMJ, 10 m sprint, 20 m sprint, handgrip test, agility T-test)CMJ ↔
10 m sprint time ↔
20 m sprint time ↔
Handgrip strength ↔
Agility time ↔
Lopez-Samanes et al. [73]M, well-trained tennis players
(n = 13)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (180 min before)/1 dayBeetroot juice (Beet IT; James White Drinks Ltd., Ipswich, UK)CMJ, Handgrip, 5–0–5 agility, 10 m sprint, Tennis serve test (CMJ height, CMJ, handgrip strength, agility time, 10-m sprint time, serve velocity, HR, RPE)CMJ ↔
Handgrip ↔
Agility time ↔
10 m sprint ↔
Serve velocity ↔
HR/RPE ↔
Lopez-Samanes et al. [75]W, semi-pro rugby players
(n = 14)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.8 mmol) (150 min before)/1 day
EC2: PLA 140 mL/day (0.08 mmol) (150 min before)/1 day
Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UKCMJ, handgrip strength, 10 m sprint, 30 m sprint, modified agility T-test, Bronco test (CMJ, handgrip strength, 10-m sprint time, 30-m sprint time, agility time, Bronco time)CMJ↑
Handgrip strength ↔
10 m sprint time ↔
30 m sprint time ↔
Agility time ↔
Bronco time ↔
López-Samanes et al. [74]W, elite female field hockey players (n =11)EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (150 min before)/1 day
EC2: BRJ 70 mL/day (0 mmol) (150 min before)/1 day
Beet-It-Pro Elite Shot, James White Drinks Ltd., Ipswich, UKCMJ, isometric handgrip strength, 20 m sprint, repeated sprint ability test, simulated match play
(CMJ height, handgrip strength, 20-m sprint time, repeated sprint ability mean time, total distance, high-intensity distance)
CMJ height ↔
Handgrip strength ↔
20 m sprint time ↔
Repeated sprint ability mean time ↔
Total distance ↔
High-intensity distance ↔
Montalvo-Alonso et al. [121]M, resistance-trained (n = 13)EC1: CAF
EC2: BRJ
EC3: CAF + BRJ
EC4: PLA
EC2: BRJ 70 mL/day (6.5 mmol) (180 min before)/1 day
EC4: BRJ 70 mL/day (0.04 mmol) (150 min before)/1 day
Beet IT (James White Drinks Ltd., Ipswich, UK)Back squat & bench press strength/power test + endurance at 65% 1RM (Back-squat & bench-press 25/50/75/90/100%1RM mean & peak velocity/power; endurance reps, mean velocity, mean power; plus, load)(EC1, EC2, EC3) Back squat mean velocity & mean power ↑
Bench press ↔
(EC1, EC2, EC3) Endurance (65% 1RM back squat) ↑
Endurance (bench press) ↔
Rimer et al. [109]M, trained athletes
(n = 13)
EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (11.2 mmol) (150 min before)/1 dayBEET It Sport (James White Drinks Ltd., Ipswich, UK)3–4 s maximal sprint, 30 s maximal isokinetic cycling test
(Maximal power, Optimal cadence, 30-s peak power, total work, fatigue index)
Maximal power ↑
Optimal cadence ↑
30 s peak power ↔
Total work ↔
Fatigue index ↔
Shannon et al. [99]M, runners or triathletes
(n = 8)
EC1: BRJ + 1500 m TT
EC2: PLA + 1500 m TT
EC3: BRJ + 10,000 m TT
EC4: PLA + 10,000 m TT
EC1, EC3: BRJ 140 mL/day (12.5 mmol) (180 min before)/1 day
EC2, EC4: PLA 140 mL/day (0.01 mmol) (180 min before)/1 day
Beet It (James White Ltd., Ipswich, UK)1500 m TT, 10,000 m TT (time-to-complete, post-exercise blood lactate)(EC1) 1500 m TT time ↓, Lactate ↑
(EC3) 10,000 m TT time ↔
Lactate ↔
Wang et al. [122]M, college bodybuilders
(n = 16)
EC1: BRJ
EC2: PLA
EC1: BRJ 250 mL/day (12.48 mmol) (150 min before)/1 day
EC2: BRJ 250 mL/day (0.0005 mmol) (150 min before)/1 day
beetroot powder (Felicific Inc., New York, NY, USA)Isometric circuit endurance test targeting elbow flexors, core muscles, forearm muscles, knee extensors (MVIC × 70% until fatigue) (MVIC peak torque, serum NO3, NO2, endurance, HR, RPE, lactate, RMS EMG)Serum NO3
Serum NO2
MVIC peak torque ↔
Endurance ↑
HR ↔
RPE ↔
Lactate ↔
RMS EMG ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 10. Chronic effects of beetroot juice supplementation on sprint and power performance.
Table 10. Chronic effects of beetroot juice supplementation on sprint and power performance.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Hemmatinafar et al. [123]W, semi-professional volleyball players (n = 12)EC1: BRJ
EC2: PLA
EC1: BRJ 400 mL/day (4.1 mmol) (120 min–38 h after)/2 daysBeetroot juice (red beet, Zarghan Lepoi Farms, Shiraz, Iran)Wall-sit endurance, V-Sit reach flexibility test, Vertical jump height, PPT, Thigh swelling testWall-sit endurance ↑
V-Sit reach flexibility ↑
Vertical jump height ↔
PPT ↑
Thigh swelling ↓
Jonvik et al. [124]M, recreational cyclists (n = 20), national talent speed-skaters (n = 22), Olympic track cyclists (n =10)
(n = 52)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (morning)/6 days
EC2: BRJ 140 mL/day (0.008 mmol) (morning)/6 days
Beet it (James White Drinks Ltd., Ipswich, UK)3 × 30 s Wingate tests (cycle ergometer)
(peak power, mean power, time to peak power, plasma NO3, plasma NO2)
Peak power ↔
Mean power ↔
Time to peak power ↓
Plasma NO3
Plasma NO2
Nyakayiru et al. [125]M, trained amateur league soccer players
(n = 32)
EC1: BRJ
EC2: PLA
EC1: BRJ 140 mL/day (12.9 mmol) (evening)/6 days
EC2: BRJ 140 mL/day (0 mmol) (evening)/6 days
Beet It (James White Drinks Ltd., Ipswich, UK)Yo-Yo IR1
(total distance, peak HR, mean HR, post-test blood lactate, RPE, plasma NO3/NO2, saliva NO3/NO2)
Total distance ↑
Peak HR ↔
Mean HR ↔
Blood lactate ↔
RPE ↔
Plasma & saliva nitrate/nitrite ↑
Thompson et al. [126]M (n = 18) and
W (n = 12)
Recreationally active adults
(n = 30)
EC1: SIT
EC2: SIT + BRJ
EC3: SIT + potassium NO3; KNO3
EC2: BRJ 2 × 70 mL/day (12.8 mmol) (morning, evening)/4 weeksBeet it, James White Drinks, Ipswich, UK4-week SIT: 3 sessions/week × 4 weeks (VO2peak, time-to-task failure, muscle lactate (3 min), plasma NO3 response during severe exercise, phosphocreatine recovery time constant)(EC2) VO2peak ↑
Time-to-task failure ↑
Muscle lactate↓
Plasma NO3 fall during severe exercise ↓
PCr recovery time constant ↔
Yang et al. [127]M, college athletes
(n = 21)
EC1: BFR
EC2: BFR + BRJ
EC2: BRJ 80 mL/day (8 mmol) (a set time each day)/4 weeksBeetroot juice (M-ACTION, Shanghai, China)Isokinetic BFR knee-extensor training: 5 sets (1 × 30 + 4 × 15 reps), 30% peak torque, 120°/s angular velocity, 40% limb occlusion
(peak torque, peak power, average power, fatigue index, torque/power decline rate, 30 s anaerobic power)
Peak torque ↑
Peak power ↑
Average power ↑
Fatigue index ↓
Torque/power decline rate ↓
30 s anaerobic power ↑
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.
Table 11. Effects of beetroot juice supplementation on team-sport performance and recovery.
Table 11. Effects of beetroot juice supplementation on team-sport performance and recovery.
ReferenceParticipantsExperimental ConditionsSupplementation ProtocolSupplement SourceVariablesResults
Martin et al. [114]M (n = 9) and W (n = 7) moderately trained team-sport athletes (n = 16)EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (4.8 mmol) (120 min before)/1 day
EC2: PLA 70 mL/day (120 min before)/1 day
Beet It (James White Drinks Ltd., Ipswich, UK)Repeated 8 s maximal sprints, 30 s active recovery, individualized workload (200% peak ramp test), to exhaustion
(Completed sprints, total work, mean/peak power, VO2, HR, lactate, RPE)
Sprint completed ↓
Total work ↓
Mean power ↔
Peak power ↔
HR ↔
RPE ↔
Clifford et al. [112]M, team-sport players, soccer (n = 10), rugby (n = 5), basketball (n = 2) hockey (n = 2), handball (n = 1), (n = 20)EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 250 mL/day (6.2 mmol) (morning, evening)/3 daysLove Beets Super Tasty Beetroot Juice (Gs Fresh Ltd., Cambridgeshire, UK)Repeated Sprint Test, 30 s rest, forced deceleration zone 10 m, performed twice (CMJ height, Reactive Strength Index, PPT, sprint time, fatigue index)CMJ height ↑
Reactive Strength Index ↑
PPT↑
Sprint time ↔
Fatigue index ↔
Thompson et al. [113]M, recreational team-sport players (local field hockey, football and rugby) (n = 16)EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (6.4 mmol) (morning, evening)/7 days
EC2: BRJ 2 × 70 mL/day (0.04 mmol) (morning, evening)/7 days
Beet it, James White Drinks Ltd., Ipswich, UKIntermittent sprint test (peak power, mean power, fatigue index, VO, HR, RPE), choice reaction test, stroop, RVIPPeak power ↑
Mean power ↑
Total work ↑
Fatigue index ↔
VO2
HR/RPE ↔
Choice reaction time ↑
Stroop ↑
Stroop ↔
RVIP↑
Thompson et al. [13]M, team-sport players (local football, rugby and hockey teams) (n = 36)EC1: BRJ
EC2: PLA
EC1: BRJ 70 mL/day (6.4 mmol) (150 min before)/5 days
EC2: BRJ 70 mL/day (0.04 mmol) (150 min before)/5 days
Beet it (James White Drinks Ltd., Ipswich, UK)5 × 20 m maximal sprints (30 s walk recovery) + Yo-Yo IR1 (2 × 20 m shuttles, 10 s active recovery; to exhaustion) (5/10/20 m split times, reaction time, Stroop test, Yo-Yo IR1 distance, lactate, HR, RPE)5 m split ↔
10 m split ↑
20 m split ↑
Reaction time ↑
Stroop performance ↑
Yo-Yo IR1 distance ↑
Lactate/HR/RPE ↔
Wylie et al. [38]M, team-sport players (n = 10)EC1: BRJ
EC2: PLA
EC1: BRJ 2 × 70 mL/day (4.1 mmol) (morning, evening)/5 days
EC2: BRJ 2 × 70 mL/day (0.04 mmol) (morning, evening)/5 days
Beet It (James White Drinks Ltd., Ipswich, UK)24 × 6 s all-out sprints (24 s rest) + 7 × 30 s all-out (240 s rest) + 6 × 60 s self-paced (60 s rest) (mean power, total work, fatigue index, pulmonary gas exchange, blood lactate, plasma NO2)plasma NO2
Mean power ↑
7 × 30 s protocol ↔
6 × 60 s protocol ↔
VO2
Blood lactate ↔
Note. Arrows indicate statistically significant differences as reported in the original studies (↑ increase, ↓ decrease); ↔ indicates no statistically significant difference.

6. Conclusions and Future Directions

Beetroot juice exerts its most consistent physiological actions through marked enhancement of nitrate–nitrite–NO bioavailability, improvements in redox balance, and microbiome-related modulation of nitrate-reduction capacity. Acute ingestion reliably increases circulating NOx and triggers short-term biochemical responses, yet these changes translate only minimally into classical metabolic markers such as glucose, insulin, lipids, or endocrine hormones. Chronic supplementation produces more sustained adaptations—including elevated fasting nitrate, enhanced oral and gut microbial nitrate reduction, and reductions in oxidative stress—although long-term effects on glycemic or lipid regulation remain inconsistent across studies. With respect to exercise performance, BRJ appears to benefit submaximal endurance tasks that depend on oxygen efficiency, whereas findings in high-intensity intermittent or strength–power exercise are variable and task-specific. Taken together, current evidence suggests that BRJ influences metabolic health primarily through NO-mediated and antioxidant pathways rather than through consistent modulation of conventional metabolic indices or uniform improvements in performance. This review should be interpreted in light of its narrative design, which does not aim to provide a systematic or exhaustive synthesis of the literature. Variations in the depth of evidence across domains reflect the current availability and maturity of human studies, underscoring the need for further research in less-studied areas. Future research should aim to clarify the sources of variability in metabolic responses to BRJ, including age-related declines in nitrate responsiveness, individual differences in oral and gut nitrate-reducing microbiota, and baseline cardiometabolic status. Multi-omics approaches integrating metabolomics, metagenomics, and mitochondrial bioenergetics are needed to delineate the mechanistic links between BRJ’s bioactive components and downstream metabolic outcomes beyond NO production alone. In the exercise domain, task-specific and responder-focused study designs are warranted to identify which individuals and exercise modalities benefit most from BRJ, particularly in high-intensity or neuromuscular contexts where current findings are inconsistent. Dose–response relationships, optimal timing strategies, chronic versus acute stacking effects, and interactions with diet, oral hygiene, and habitual nitrate intake also require systematic evaluation. Finally, translating BRJ research to clinical populations—including individuals with hypertension, endothelial dysfunction, insulin resistance, or age-related metabolic decline—remains an important avenue for determining its therapeutic potential in cardiometabolic health.

Author Contributions

Study conception and design, H.-Y.P., S.-W.K. and K.L.; Data collection, S.C., S.K., Y.Z., Y.S., J.-H.C. and S.W.; Table preparation, S.C., S.K. and Y.Z.; Figure creation, J.-H.C., Y.S. and S.W.; Writing—original draft, E.L., J.-H.C., Y.S. and S.W.; Writing—review and editing, E.L. and H.-Y.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

The authors thank the researchers whose work was included in this review and all colleagues who provided valuable feedback during the preparation of this manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
1RMOne-repetition maximum
6MWTSix-minute walk test
ADAlzheimer’s disease
AFTAfternoon
ATPAdenosine triphosphate
AUClastArea under the concentration-time curve to the last measurable concentration
AUGArea under the glucose curve
baPWVBrachial-ankle pulse wave velocity
BFRBlood flow restriction
BPBlood pressure
BRJBeetroot juice
Ca2+Calcium ion
CAIxCerebral augmentation index
cBRSCardiovagal baroreflex sensitivity
CD11bCluster of differentiation 11b
cGMPCyclic guanosine monophosphate
CAFCaffeine-supplemented group
CRPC-reactive protein
CKCreatine kinase
CMJCountermovement jump
COCardiac output
CO2Carbon dioxide
CONControlled
CRCaloric restriction
CSACross-section area
DBPDiastolic blood pressure
DCADynamic cerebral autoregulation
Deoxy-HbDeoxygenated hemoglobin
Deoxy-MbDeoxygenated myoglobin
DOMSDelayed onset muscle soreness
EMGElectromyography
EPMEarly postmenopausal
EVEEvening
EXEExercise
FBFForearm blood-flow
FMDFlow-mediated dilation
GLP-1Glucagon-like peptide-1
GPSGlobal positioning system
GSHReduced glutathione
GSSGOxidized glutathione
GTPGuanosine triphosphate
HbHemoglobin
HDHemodialysis
HFHigh-frequency
HFpEFHeart failure and preserved ejection fraction
HHbDeoxyhemoglobin
HOMA-IRHomeostatic model assessment-insulin resistance
HRHeart rate
HRVHeart rate variability
IHSIsometric handgrip strength
IMTPIsometric mid-thigh pull
IL-6Interleukin-6
IPAQInternational physical activity questionnaire
LBNPLower-body negative pressure
LFLow frequency
LPMLate postmenopausal
MMale participants
MAPMean arterial pressure
MIVCMaximal isometric voluntary contraction
MORNMorning
MPTMitochondrial permeability transition
MUFRMotor unit firing rate
MUPMotor unit potential
MVCMaximal voluntary contraction
MVICMaximal voluntary isometric contraction
NF jiggleNeuromuscular firing instability
NIRSNear-infrared spectroscopy
NITNitrate-supplemented group
NONitric oxide
NOSNitric oxide synthase
NO2-Nitrite
NO3-Nitrate
NOxNitric oxide metabolites
NRNot reported
O2Oxygen
OGTTOral glucose tolerance test
OLDOlder group
oxLDLOxidized low-density lipoprotein
PCrPhosphocreatine
PETCO2Partial pressure of end-tidal carbon dioxide
PFCPrefrontal Cortex
pHPower of Hydrogen
PIxPulsatility indices
PKGProtein kinase G
PLAPlacebo
PPOPeak power output
PPTPain pressure threshold
PSTTProgressive specific taekwondo test
PWVPulse wave variable
qNIRSQuantitative near-infrared spectroscopy
Qtw,potPotentiated quadriceps twitch force
QUICKIQuantitative insulin sensitivity check index
RBCRed blood cell
REEResting energy expenditure
RERRespiratory exchange ratio
RFDRate of force development
RIxResistivity indices
RMSRoot Mean Square
RoRRetinoic acid-related orphan receptor
ROSReactive oxygen species
RPERating of perceived exertion
RTDRate of torque development
RVIPRapid visual information processing
RyRRyanodine receptor
SBPSystolic blood pressure
SCFAsShort-chain fatty acids
SERCASarco/endoplasmic reticulum Ca2+-ATPase
sGCSoluble guanylate cyclase
SITSprint interval training
SJSquat jump
SJFTSargent jump fatigue test
SpO2Peripheral oxygen saturation
StO2Tissue oxygen saturation
SVRSystemic vascular resistance
T2DType 2 diabetes
TPRTotal peripheral resistance
TQRTotal quality recovery
TTTime-trial
TTETime to exhaustion
VEMinute ventilation
VEGVegetable-supplemented group
VE/VCO2Ventilatory equivalent for carbon dioxide
VE/VO2Ventilatory equivalent for oxygen
VLFVery-low-frequency
VO2Oxygen consumption
VO2peakPeak oxygen consumption
WFemale participant
XORXanthine oxidoreductase
YYIR1Yo-Yo Intermittent Recovery Test Level 1
YNYounger group

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Figure 1. Overview of the physiological mechanisms through which beetroot juice (BRJ) influences nitric oxide availability, vascular function, and skeletal muscle energetics. (a) Entero-salivary nitrate reduction and hypoxic/acidic conversion of NO3 → NO2 → NO, involving deoxygenated Hb/Mb, XOR, and mitochondrial pathways. (b) Endothelial NO signaling through the sGC–cGMP–PKG pathway promotes vasodilation, blood flow regulation, and improved vascular function. (c) NO effects on skeletal muscle energetics, including enhanced mitochondrial efficiency, faster PCr resynthesis, lower ATP cost, and modulation of Ca2+ handling via RyR and SERCA. ↑ and ↓ indicate increases and decreases, respectively. The red cross denotes NO-mediated inhibition or competition of oxygen binding at cytochrome c oxidase (Complex IV).
Figure 1. Overview of the physiological mechanisms through which beetroot juice (BRJ) influences nitric oxide availability, vascular function, and skeletal muscle energetics. (a) Entero-salivary nitrate reduction and hypoxic/acidic conversion of NO3 → NO2 → NO, involving deoxygenated Hb/Mb, XOR, and mitochondrial pathways. (b) Endothelial NO signaling through the sGC–cGMP–PKG pathway promotes vasodilation, blood flow regulation, and improved vascular function. (c) NO effects on skeletal muscle energetics, including enhanced mitochondrial efficiency, faster PCr resynthesis, lower ATP cost, and modulation of Ca2+ handling via RyR and SERCA. ↑ and ↓ indicate increases and decreases, respectively. The red cross denotes NO-mediated inhibition or competition of oxygen binding at cytochrome c oxidase (Complex IV).
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Figure 2. Overview of acute and chronic health-related outcomes of beetroot juice supplementation across physiological systems. ↑ and ↓ indicate increases and decreases, respectively, while ↔ denotes no apparent change.
Figure 2. Overview of acute and chronic health-related outcomes of beetroot juice supplementation across physiological systems. ↑ and ↓ indicate increases and decreases, respectively, while ↔ denotes no apparent change.
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Figure 3. Nitrate-derived NO enhances vasodilation, mitochondrial efficiency, and Ca2+ handling, supporting improved endurance, sprint, and power performance. ↑ and ↓ indicate increases and decreases, respectively.
Figure 3. Nitrate-derived NO enhances vasodilation, mitochondrial efficiency, and Ca2+ handling, supporting improved endurance, sprint, and power performance. ↑ and ↓ indicate increases and decreases, respectively.
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MDPI and ACS Style

Lee, E.; Park, H.-Y.; Sun, Y.; Choi, J.-H.; Woo, S.; Cho, S.; Kim, S.; Zheng, Y.; Kim, S.-W.; Lim, K. Beetroot Juice and Exercise for Clinical Health and Athletic Performance: A Narrative Review. Nutrients 2026, 18, 151. https://doi.org/10.3390/nu18010151

AMA Style

Lee E, Park H-Y, Sun Y, Choi J-H, Woo S, Cho S, Kim S, Zheng Y, Kim S-W, Lim K. Beetroot Juice and Exercise for Clinical Health and Athletic Performance: A Narrative Review. Nutrients. 2026; 18(1):151. https://doi.org/10.3390/nu18010151

Chicago/Turabian Style

Lee, Eunjoo, Hun-Young Park, Yerin Sun, Jae-Ho Choi, Seungyeon Woo, Sohyang Cho, Suyoung Kim, Yuanning Zheng, Sung-Woo Kim, and Kiwon Lim. 2026. "Beetroot Juice and Exercise for Clinical Health and Athletic Performance: A Narrative Review" Nutrients 18, no. 1: 151. https://doi.org/10.3390/nu18010151

APA Style

Lee, E., Park, H.-Y., Sun, Y., Choi, J.-H., Woo, S., Cho, S., Kim, S., Zheng, Y., Kim, S.-W., & Lim, K. (2026). Beetroot Juice and Exercise for Clinical Health and Athletic Performance: A Narrative Review. Nutrients, 18(1), 151. https://doi.org/10.3390/nu18010151

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