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Review

Protective Potential of Satureja montana-Derived Polyphenols in Stress-Related Central Nervous System Disorders, Including Dementia

1
Department of Pharmacology, Toxicology and Pharmacotherapy, Faculty of Pharmacy, Medical University, 9002 Varna, Bulgaria
2
Institute of Neurobiology, Bulgarian Academy of Sciences, 23 Academician Georgi Bonchev St, 1113 Sofia, Bulgaria
3
Department of Medical Physics and Biophysics, Faculty of Medicine, Medical University of Sofia, 15 Academician Ivan Evstratiev Geshov Blvd., 1431 Sofia, Bulgaria
4
Clinic of Endocrinology, Military Medical Academy, 3 Sveti Georgi Sofiyski St, 1606 Sofia, Bulgaria
5
Department of Pharmaceutical Botany, Faculty of Pharmacy, Iuliu Hațieganu University of Medicine and Pharmacy, 400337 Cluj-Napoca, Romania
6
Faculty of Medicine, University Prof. Assen Zlatarov, 1 Prof. Yakimov St., 8010 Burgas, Bulgaria
7
Department of Neurosurgery, Military Medical Academy, 3 Sveti Georgi Sofiyski St, 1606 Sofia, Bulgaria
8
Department of Healthcare, Faculty of Public Health, Healthcare and Sport, South-West University, 66 Ivan Mihailov St, 2700 Blagoevgrad, Bulgaria
*
Authors to whom correspondence should be addressed.
Curr. Issues Mol. Biol. 2025, 47(7), 556; https://doi.org/10.3390/cimb47070556
Submission received: 20 June 2025 / Revised: 11 July 2025 / Accepted: 15 July 2025 / Published: 17 July 2025

Abstract

Satureja montana (SM) is acknowledged as a highly pharmacologically important species within the vast Lamiaceae family, indigenous to the Balkan area. Traditionally, this plant has been employed as a culinary spice, especially in Bulgarian gastronomy. Additionally, it is widely recognized that mental health is affected by the nature and quality of dietary consumption. Results: Ethnopharmacological research underscores the potential of SM in influencing various chronic ailments, including depression and anxiety. This plant is distinguished by a rich variety of secondary metabolites that display a broad spectrum of biological activities, such as antioxidant, antidiabetic, anti-inflammatory, analgesic, antibacterial, antiviral, and antifungal effects. Particularly, two of its active phenolic compounds, rosmarinic acid and carvacrol, reveal notable anxiolytic and antidepressive properties. This review aims to explore the capacity of SM to improve mental health through its plentiful phenolic components. Recent studies indicate their efficacy in addressing Alzheimer’s-type dementia. A notable correlation exists among depression, anxiety, and cognitive decline, which includes dementia. Considering that Alzheimer’s disease (AD) is a multifaceted condition, it requires multi-targeted therapeutic strategies for both prevention and management. Conclusions: Satureja montana is recognized as potential candidate for both the prevention and management of various mental health disorders, including dementia.

Graphical Abstract

1. Introduction

Historically, medicinal and herbal plants have been utilized to treat a wide range of ailments and to alleviate symptoms of diseases. Despite significant progress in pharmaceutical production, it is estimated that 80–90% of the global population still relies on traditional medicine for treatment [1]. According to the World Health Organization, 80% of people worldwide use herbal remedies, with the market valued at approximately USD 83 billion in 2019 and projected to grow to USD 550 billion by 2030 [2]. Nevertheless, even with the increasing interest from the pharmaceutical industry in naturally sourced compounds [3], only a limited number of the therapeutic properties and biological activities of medicinal plants have been extensively studied [4,5,6]. The exploration of a medicinal plant’s potential as a therapeutic agent is inherently intricate, necessitating thorough investigations that cover its application, cultivation, extraction, identification of active compounds, efficacy, safety, and clinical evaluation [7,8,9]. While various parts of medicinal plants, including roots, seeds, leaves, and fruits, have been historically acknowledged as sources of bioactive compounds and natural products (such as salicylates, digitalis, and quinine), the transition from natural sources to drug development continues to be a demanding and labor-intensive endeavor.
Plants rich in polyphenols hold significant relevance in ethnopharmacology due to their diverse biological activities and health advantages. Various cultures integrate these plants into their traditional healing methods [10,11,12]. Polyphenols are especially noted for their strong antioxidant properties, which help neutralize free radicals and protect cells from oxidative harm. These attributes are crucial in preventing chronic diseases such as cardiovascular issues, cancer, and neurodegenerative disorders [13,14]. Moreover, polyphenols exhibit considerable anti-inflammatory effects, beneficial for managing conditions like arthritis and other inflammatory diseases. For instance, extracts from Rhamnus prinoides have shown substantial anti-inflammatory properties [15]. Additionally, polyphenols possess antimicrobial capabilities, making them effective against a range of pathogens, including bacteria, fungi, and viruses. This quality is particularly advantageous in traditional medicine for treating infections [16,17,18]. The Lamiaceae family comprises more than 230 genera and over 7000 species [19], which include thyme, mint, lemon balm, oregano, basil, rosemary, sage, and Balkan savory [20,21,22,23,24,25]. Satureja montana (Figure 1), commonly referred to as Balkan savory, is recognized as one of the most pharmacologically significant members of the extensive Lamiaceae family [26]. Balkan savory originates from the Mediterranean area. Although the present distribution of Satureja montana has expanded beyond its native Mediterranean habitat, it is not regarded as invasive in any ecosystems.
Satureja montana is widely distributed across the Balkan Peninsula and is considered an endemic species in Bulgaria [23,24,25]. Research indicates that extracts from SM are rich in total polyphenols and flavonoids, which play a significant role in its diverse biological functions [27]. Notable phenolic compounds such as rosmarinic acid, caffeic acid, and luteolin have been identified in substantial amounts within various extracts [28,29,30]. These phenolic constituents are responsible for the extensive range of biological activities exhibited by SM, including its antimicrobial and antioxidant effects.
For centuries, the plant has been recognized as a flavorful spice, particularly in traditional Bulgarian cuisine. This plant is not only versatile but also holds considerable significance in ethnopharmacology. The ethnobotanicity index quantifies the level of traditional knowledge and utilization of plants within a community. Balkan savory exhibits a high ethnobotanicity index in areas where it is customarily employed for medicinal purposes [31,32]. Additionally, the fidelity level index reflects the proportion of informants who report using a specific plant for the same primary purpose. Balkan savory demonstrates elevated fidelity level values in the treatment of digestive and respiratory ailments. In traditional medicine, it is utilized for various health conditions. Satureja montana is characterized by a diverse array of secondary metabolites that exhibit a wide range of biological activities, including antioxidant [28,30,33,34], antidiabetic [22,35], anti-inflammatory [33,36], neuroprotective [37,38,39,40], analgesic, antibacterial, antiviral, and antifungal properties [31,41,42,43,44].
The objective of the current review is to explore the potential of SM, both as a medicinal herb and a traditional spice, in promoting mental health through its rich array of phenolic compounds. It is well-established that mental health is affected by the quality and type of food consumed. Recent studies are increasingly clarifying the connection between dietary practices and mental well-being, with a multitude of research indicating a significant correlation between the two [45]. The functionality, structure, and composition of the brain are contingent upon the availability of vital amino acids, lipids, vitamins, and minerals, making cognitive performance and mental health susceptible to nutritional variations [46,47,48,49]. Evidence suggests that following a nutritious diet, characterized by a high consumption of spices, vegetables, fruits, fish, nuts, and whole grains—similar to the Mediterranean diet—can have positive effects, protect mental health, and reduce the risk of depression [50,51,52,53]. Furthermore, research into the effects of poor dietary choices on mental health and cognitive functions highlights the importance of sustaining a healthy diet [54,55,56,57,58]. Additionally, factors such as neurotransmitters, neuropeptides, endogenous gut hormones, and gut microbiota can also be influenced by changes in dietary composition [59,60,61,62,63].

2. Materials and Methods

To accomplish the established goal, we gathered and thoroughly examined the most recent scientific literature regarding the neuroprotective properties of Satureja montana extracts and their primary polyphenolic constituents. A comprehensive literature review was conducted utilizing the Web of Science, Scopus, PubMed, and ResearchGate databases, from which we selected a number of articles, predominantly published within the last decade. The research employed a variety of keywords and their combinations, including SM, polyphenols, rosmarinic acid, ellagic acid, chlorogenic acid, antioxidant, neuroprotection, neurotransmitter, oxidative stress, inflammation, apoptosis, anti-cholinesterase, and signaling pathways. The selection process entailed the removal of duplicate entries, screening of titles and abstracts, and a detailed full-text assessment of potentially pertinent articles. Both original research and review articles published in English were incorporated into the manuscript.
The inclusion criteria are articles published in peer-reviewed journals; studies published in English; original research and review articles that concentrate on the neuroprotective, antioxidant, anti-inflammatory, or cholinesterase-inhibiting properties of Satureja montana extracts or their individual polyphenols; and studies that include in vitro, in vivo, or clinical data.
Conversely, the criteria for exclusion are non-English publications; articles lacking sufficient or relevant data concerning neuroprotective activity; publications that consist solely of abstracts, conference proceedings, or editorials; and studies that exclusively examine other species without a specific mention of Satureja montana or its pertinent constituents.
The screening strategy included the elimination of duplicate entries using reference management software. The remaining records underwent a two-step screening procedure: (1) an initial review of titles and abstracts for relevance, followed by (2) a full-text assessment of the articles that remained. Two authors conducted the screening independently, and any discrepancies were addressed through discussion.
To evaluate the quality of the studies included, we took into account factors such as the clarity of the study design, the suitability of experimental models, the robustness of statistical analysis, and the relevance to neuroprotective mechanisms. For both in vivo and in vitro studies, we assessed parameters like sample size, the inclusion of control groups, and the reproducibility of results. Review articles were evaluated based on their thoroughness and the citation of primary literature.

3. Results

3.1. Bioactive Compounds of Satureja montana

The main compounds derived from Satureja montana can be categorized into several classes based on their chemical nature. From the group of monoterpenes, carvacrol, p-cymene, γ-terpinene, and thymol are found [64,65]. Oxygenated monoterpenes are represented by carvacrol methyl ether, borneol, and linalool [66]. Of the sesquiterpenes, β-Caryophyllene is present in concentrations ranging from 2.74% to 4.71%, and Spathulenol is found in smaller amounts [67]. The main phenolic acid components isolated from savory are rosmarinic and ellagic acids [28]. In addition, an investigation examining the composition of two varietal forms of Satureja montana observed that the phenolic compounds’ carvacrol:thymol ratio was significantly elevated in the subsp. montana (exceeding 300) in comparison to the subsp. variegate [65].
The primary constituents of the essential oil include carvacrol, p-cymene, γ-terpinene, and thymol. Carvacrol is the most abundant phenolic monoterpene, with concentrations ranging from 44.5% to 45.7% [68,69]. P-cymene accounts for approximately 12.6% to 16.9%, while γ-terpinene is present in amounts between 8.1% and 8.7% [68,69]. Thymol is also present in considerable quantities, reaching 81.79% in certain studies [26]. In terms of phenolic compounds, rosmarinic acid is recognized as a significant phenolic component in the dry extract of Satureja montana [29]. Additional phenolic acids identified in SM include caffeic acid, chlorogenic acid, and ellagic acid [26,28,70]. The triterpenes compounds are represented by ursolic and oleanolic acids [70].
Table 1 presents a summary of the constituents isolated from Balkan savory.
Satureja montana possesses a high concentration of phenolic compounds, which makes the plant an important resource for both medicinal applications and preservation purposes.
Two SM active phenolic compounds—rosmarinic acid and carvacrol—possess strong anxiolytic and antidepressive effects [71,72]. Each of these two phenolic compounds also exhibits antiviral, antibacterial, antioxidant, antimutagenic, anti-inflammatory, and anxiolytic effects [73,74,75,76,77,78].
A summary of the available data is presented in Table 2.
A comprehensive study on Satureja montana was recently conducted in Bulgaria [79]. The dry methanol–water extract of SM was standardized based on its rosmarinic acid and carvacrol content. The findings indicated that the total phenolic content of the dry extract of SM was greater than that reported in the previous literature.

3.2. Relation of Stress to the Pathogenesis of Certain Mental Disorders

Stress, as a variable significantly shaped by lifestyle choices, in addition to being a physiological defense response of the body, is considered a major risk factor associated with mental disorders, as shown in Figure 2.
Stress induces the activation of the sympathetic–adrenal–medullary and hypothalamic–pituitary–adrenal (HPA) systems, wherein the hypothalamus initiates the ‘fight or flight’ response. This response results in elevated heart rate, blood pressure, and glucose levels, suggesting a potential link between stress and mental health disorders due to the dysfunction of the HPA axis, which may lead to cellular changes [80,81,82,83,84].
There are several mechanisms through which stress is thought to influence mental status (Figure 3).
Stress can lead to the activation of brain immune cells, resulting in the release of pro-inflammatory mediators. This process may enhance the expression of inflammatory genes and promote lipid peroxidation, ultimately jeopardizing both the structure and function of neurons [85]. Chronic stress may affect brain pathology through with crucial mechanism such as tau hyperphosphorylation and synapse missorting [86]. Another possible link is oxidative stress, in large due to the production of reactive oxygen species (ROS) causing an inefficient mitochondrial function [87]. Furthermore, stress may cause an impairment of neuronal functions and structures such as the signaling pathway Fyn kinase and the NR2B-containing N-methyl-D-aspartate (NMDA) receptors, causing a reduction in GABA-ergic neurons and a decrease in Reelin protein expression [88,89].
As a natural response of the body when presented with adverse, demanding, or challenging conditions, stress causes a strain on both physical and mental functions. While the body induces adaptive responses designed to combat this strain, prolonged or excessive stress can lead to depression, anxiety, and cognitive dysfunction and may even increase the risk of development of mental and physical disease [83,90,91].
Chronic stress is known to lead to cognitive impairment. This is most likely due to elevated levels of glucocorticoids and corticotropin-releasing hormone causing neurotransmitter alterations, atrophy in the hippocampus and cortex, and shortening of the dendritic branches [92,93,94,95,96,97,98,99,100].
Stress is frequently involved in development of anxiety and depression. Affecting approximately 300 million people worldwide, anxiety and depression are one of the most prevalent and debilitating mental disorders [101,102,103]. Persistent systemic inflammation indicators, such as elevated pro-inflammatory cytokines, myelopoiesis and lymphopoiesis irregularities, and gut–epithelium and blood–brain barrier disturbances, can be found in individuals with stress-induced pathological conditions [104,105,106,107,108].
There is a significant interrelationship among depression, anxiety, and cognitive impairments, as well as cognitive decline. Anxiety has been linked to an elevated risk of both the onset and progression of somatic diseases [109,110]. Furthermore, a correlation has been identified between this psychiatric condition and complications arising from cardiovascular diseases [110]. Individuals suffering from insulin resistance who also experience anxiety are at a heightened risk of developing type 2 diabetes, with the coexistence of these two conditions further increasing the probability of adverse outcomes [111,112]. Each of the aforementioned disorders is linked to a greater likelihood of developing additional mental health issues [109,113]. Specifically, anxiety is associated with a higher risk of developing coexisting anxiety disorders or depression [109]. Depression itself is further connected to neurotic, somatoform, and personality disorders, as well as substance abuse and behavioral syndromes. The prevalence of comorbidity tends to escalate with the severity of depressive symptoms [113,114,115,116,117]. Moreover, depression and anxiety are closely associated with cognitive impairments and dementia. Although AD mainly influences cognitive abilities and memory, neuropsychiatric symptoms often emerge during the progression of the disease. The anxiety prevalence ranges from 9.4% during the preclinical phase to as high as 39% in cases of mild to severe cognitive decline, whereas the depression prevalence varies between 14.8% and 40% in mild to moderate stages of Alzheimer’s disease [118,119,120,121,122,123,124].
Mild cognitive impairment (MCI) is a significant transitional stage between typical aging and the onset of dementia. The prevalence of MCI among the elderly population is estimated to range from 5.0% to 36.7%, with approximately 11% to 13% of individuals with MCI progressing to dementia within a two-year period [125,126,127,128]. Psychological symptoms frequently associated with MCI include depression and anxiety, both of which can adversely affect cognitive functioning and contribute to the progression toward dementia [129,130]. Notably, cognitive deficits are more pronounced in individuals experiencing both depression and anxiety [131,132]. Depression is recognized as a major risk factor contributing to the progression of cognitive decline and the onset of dementia, whereas anxiety may affect this progression in both direct and indirect ways [133,134,135,136].
Among individuals with MCI, the prevalence of depression is approximately 32%. The use of antidepressants does not appear to provide a protective effect against the onset of dementia, and those with MCI are at an increased risk of developing severe cognitive impairment [137,138,139]. The conversion rate from MCI to dementia is notably higher in those with depression, ranging from 25% to 28%, with a significant conversion rate of 31% to AD in depressed patients compared to 13.5% in those without depression [140]. While anxiety has not been researched as thoroughly as depression, its connection to cognitive function is intricate, with prevalence rates ranging from 9.9% to 52% among individuals with MCI, especially affecting executive functions [134,141,142,143,144]. Dementia and anxiety can serve as significant clinical indicators; specifically, anxiety may act as a predictor of cognitive deterioration, whereas depression can help identify individuals with MCI who are at an increased risk of progressing to Alzheimer’s disease [140,144].

3.3. CNS-Activity of Satureja montana

According to data presented by the World Health Organization, roughly 4% of the worldwide population experienced anxiety disorders as of 2019 [145]. Moreover, it is important to acknowledge that a considerable number of anxiety disorders frequently remain undiagnosed [146]. Various obstacles are linked to the treatment of depression and anxiety, including variables such as age, polypharmacy or polypragmasy, an escalation in adverse drug reactions, comorbid conditions, a decline in quality of life, and increasing treatment expenditures. The COVID-19 pandemic and the associated restrictions have resulted in an over 25% rise in the incidence of these psychiatric disorders [147]. All pharmacological agents prescribed for the management of depressive disorders and anxiety are associated with possible adverse effects, including addiction, headaches, seizures, sexual dysfunction, suicidal ideation, and dependence [148]. Given the potential for adverse effects and delayed therapeutic outcomes, numerous patients exhibit hesitance regarding the prescription of psychotropic medications, which may lead to non-adherence to the suggested treatment [149,150]. The constraints associated with the utilization of these medications highlight the imperative for research into novel therapeutic alternatives for these conditions [148,151].
Ethnopharmacology reports the potential of SM to affect some stress-related chronic mental diseases, including anxiety, depression, mild cognitive impairments, and dementia. In a rat model designed to assess acute stress, the dry extract of SM significantly enhanced locomotor activity and extended the social interaction duration while concurrently diminishing anxiety-related behaviors [79]. Acute cold stress substantially reduced the duration of novel-object-recognition time in laboratory rats, indicating a significant anxiolytic effect associated with SM. The implications of neurotransmitters, specifically 5-hydroxytryptamine and gamma-aminobutyric acid (GABA), were examined [152]. The bioactive constituents in Satureja montana, including rosmarinic acid and carvacrol, exhibited moderate anxiolytic effects [79]. In a rat model subjected to chronic stress, the dry extract of SM revealed anxiolytic properties. The spontaneous locomotor activity of the experimental rats was also altered [153,154], reinforcing certain behavioral assessments aimed at evaluating both anxiolytic and antidepressant effects [152,155]. Research has established that rosmarinic acid affects T-type calcium ion channels within the central nervous system, in addition to influencing GABA-ergic and cholinergic pathways [71]. A study from 2022 proposed that the anxiolytic mechanism may primarily involve the modulation of ion channels within the central nervous system and cholinergic mediation, along with various other mechanisms contributing to the anxiolytic properties of the dry extract of SM [79]. Furthermore, the investigation carried out by Melo et al. (2010) suggests that carvacrol interacts with a range of neurotransmitters, including GABA, noradrenaline, and serotonin [156]. In addition to the findings by Vilmosh et al. (2022) [79], our comprehensive literature review did not reveal any studies that specifically examine the effects of the dry extract of SM on anxiety. It was concluded that the dry extract may exhibit a more pronounced anxiolytic effect in comparison to the individual active compounds when utilized in isolation. This observation supports the hypothesis of a synergistic interaction between the principal components, rosmarinic acid and carvacrol [79].
Chronic low-grade inflammation and oxidative stress are implicated in the etiology of anxiety, which correlates with elevated plasma levels of corticosterone, a byproduct of stress responses [157,158,159]. Consequently, when evaluating the anxiolytic properties of rosmarinic acid and carvacrol, it is essential to consider their antioxidant and anti-inflammatory effects [72,160,161].
Epidemiological studies indicate that the prevalence of depression aligns closely with that of anxiety disorders. The presence of depressive disorder significantly diminishes an individual’s quality of life [162]. This condition typically manifests in an episodic manner; however, it remains unpredictable regarding the frequency and duration of episodes, as well as the efficacy of various treatment options. The recovery process is often extended, accompanied by a considerable risk of relapse [163]. Similar to anxiety, depression acts as a distinct risk factor for various health complications, encompassing diabetes, cardiovascular ailments, chronic respiratory diseases, and arthritis, in addition to cognitive deficits and neurodegenerative conditions like AD.
An examination of the effects of Satureja montana and its principal constituents, specifically rosmarinic acid and carvacrol, on recognition memory, social interaction, and depressive behaviors was conducted in experimental models [79]. The dry extract of SM demonstrated notable enhancements in the exploration duration of novel objects and the length of social interactions, particularly at dosages of 250 mg/kg and 500 mg/kg body weight. The higher dosage significantly influenced the discrimination index (DI), indicating an improvement in recognition memory. In contrast, while rosmarinic acid exhibited some anxiolytic properties, it did not exert a significant effect on social interaction or recognition memory; similarly, carvacrol did not demonstrate any meaningful effects on these parameters. The extract of Satureja montana displayed more pronounced anxiolytic and antidepressant effects compared to its individual components, likely owing to synergistic interactions among its constituents. The findings regarding rosmarinic acid are consistent with the existing literature, which underscores the anxiolytic properties of this phenolic compound [164,165,166]. In a manner analogous to rosmarinic acid, carvacrol has also been reported to enhance cognitive function in rodent models [167,168], which contrasts with the findings presented by Vilmosh et al. (2022) [79]. These discrepancies may be elucidated by the variations in the memory impairment models utilized and the differing treatment durations with the phenolic compounds.
The study revealed that the dry extract of Satureja montana significantly augmented the exploration time of a novel object in recognition memory assessments, with the higher dosage of 500 mg/kg body weight. Rosmarinic acid also manifested a significant impact on recognition memory, whereas carvacrol did not exhibit any notable influence. Nevertheless, the existing literature presents contradictory findings regarding the effects of rosmarinic acid on recognition memory [164,165].
The dry extract of Satureja montana exhibited robust anxiolytic and antidepressant effects, surpassing both rosmarinic acid and carvacrol when administered separately [79]. In social interaction assessments, the dry extract of SM improved the duration of interactions in rats subjected to chronic stress, whereas rosmarinic acid did not produce similar outcomes. The findings imply that the synergistic effects of the compounds within the dry extract may contribute to its enhanced cognitive and emotional benefits compared to the individual components. According to two separate studies conducted in 2021, rosmarinic acid has been documented to yield a significant antidepressant effect by decreasing the duration of immobility in the forced swim test [169,170]. Conversely, Vilmosh et al. (2022) noted that rosmarinic acid influenced depressive-like behavior solely within the framework of a chronic stress model [79]. This discrepancy may stem from the prolonged treatment duration and the distinct physiological mechanisms activated in the two stress models employed. Chronic stress is associated with a decline in the activity of dopaminergic neurons in the ventral tegmental area, while rosmarinic acid is recognized for its ability to elevate dopamine levels, thereby clarifying its observed antidepressant effects [171,172].
In contrast to the findings related to rosmarinic acid, the investigation conducted by Vilmosh et al. (2022) revealed that carvacrol did not exhibit any antidepressant properties [79], thus calling into question the interpretations established within the existing literature [173,174]. This divergence may stem from differences in the dosages administered and the methodologies utilized to induce depressive states. Although carvacrol is recognized for its effects on dopamine and serotonin neurotransmission [134], it is conceivable that these pathways are inadequate to mitigate the stress-induced disruptions within the central nervous system.

3.4. Neuroprotective Mechanisms of Satureja montana

3.4.1. Antioxidant Activity

Satureja montana contains a wealth of phenolic compounds, including rosmarinic acid, caffeic acid, and flavonoids such as rutin. These compounds are recognized for their potent antioxidant capabilities, which can alleviate oxidative stress, a critical contributor to neurodegenerative disorders. Furthermore, the essential oils derived from SM have shown considerable radical scavenging activity, suggesting their ability to counteract free radicals and diminish oxidative harm.
The majority of the advantageous effects of Balkan savory on human health can be attributed to its notable antioxidant and anti-inflammatory properties. Research has confirmed the presence of free radical-scavenging activity through three distinct in vitro methods, leading the authors to classify the examined dry extract of SM as an effective antioxidant. Notably, SM exhibited superior antioxidant activity when compared to findings associated with other species within Satureja sp. [34]. Both in vitro and in vivo studies demonstrated SM’s ability to neutralize free radicals and to influence the endogenous antioxidant system of the human body. Simultaneously, it was determined that SM possesses a local anti-inflammatory effect that is comparable to that of diclofenac. SM demonstrates a propensity to lower serum levels of IL-6, IL-1b, and TNF in both acute and chronic stress models. The authors proposed that the inhibition of cyclooxygenase is the most probable mechanism underlying the action of SM. In addition, akin to its antioxidant properties, the anti-inflammatory effect of the extract is notably more significant when compared to the effects of rosmarinic acid and carvacrol used independently [34].
The neuroprotective antioxidant mechanisms of compounds obtained from Satureja montana encompass various biochemical pathways and functions, as illustrated in Table 3.
Direct Antioxidant Activity. Extracts of Satureja montana demonstrate considerable antioxidant properties in vitro, primarily attributed to their ability to scavenge free radicals, thereby mitigating oxidative stress. An in vitro study conducted in 2007 highlighted the potential of Satureja montana L. subsp. kitaibelii extract as a natural source of antioxidants and antimicrobial agents [175]. The research indicated that phenolic compounds present in plant extracts demonstrate considerable antioxidant activity by neutralizing free radicals and inhibiting the breakdown of hydroperoxides. The total phenolic content was assessed using the Folin–Ciocalteu method and HPLC, revealing strong correlations between total phenolic content and antioxidant activity across various assays, with r2 values ranging from 0.62 to 0.90.
Table 3. Mechanisms of antioxidant activity of Satureja montana-derived compounds.
Table 3. Mechanisms of antioxidant activity of Satureja montana-derived compounds.
MechanismDescriptionRef.
Direct Antioxidant ActivityScavenging of free radicals, reducing oxidative stress[176]
Enzyme ModulationIncreased activity of SOD, CAT, and GSR[35,177]
Reduction in Lipid PeroxidationDecreased lipid peroxidation, protecting cell membranes[33,177]
Anti-inflammatory EffectsDecreased levels of TNF-α and IL-6[176]
Hepatoprotective EffectsReduced oxidative stress enzymes and inflammatory cells in the liver[33]
Neuroprotective PathwaysActivation of Nrf2/ARE pathway, enhancing antioxidant protein expression[178,179]
Drug Delivery PotentialUse of niosomes for stable and targeted delivery of antioxidants[180]
Furthermore, the antioxidant activity of SM varietettes was assessed utilizing three methods, revealing that the essential oils exhibited remarkable radical scavenging effects against the ABTS radical, with an IC50 ranging from 30.02 to 34.5 µg/mL [65].
The antioxidant characteristics, as part of the anti-inflammatory effects of Balkan savory extract, were reported in 2024 [176]. The antioxidant properties of the dry SM extract were validated using three distinct in vitro techniques; however, the activity observed was lower than what has been documented in prior research, possibly attributable to differences in the extract compositions.
Enzyme Modulation. The SM extract has demonstrated an enhancement in the activity of essential antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT), and glutathione reductase (GSR) [33,177]. These enzymes are vital for the neutralization of ROS and the preservation of cellular redox equilibrium.
Reduction in Lipid Peroxidation. Extracts of Satureja montana diminish lipid peroxidation, a significant indicator of oxidative damage to cellular membranes. This mitigation plays a crucial role in safeguarding neuronal cells against oxidative injury [33,177].
Anti-inflammatory Effects. SM extracts demonstrate anti-inflammatory effects by reducing the concentrations of pro-inflammatory cytokines, including TNF-α and IL-6, in specific stress models [176]. This is significant because inflammation frequently occurs alongside oxidative stress in neurodegenerative disorders.
Hepatoprotective Effects through Antioxidant Activity. In studies utilizing animal models, extracts of Satureja montana have demonstrated hepatoprotective properties by diminishing oxidative stress enzymes and inflammatory cell presence in the liver, thereby indirectly bolstering the overall antioxidant defense systems [33].
Neuroprotective Pathways. While research specifically focusing on Satureja montana and its neuroprotective effects is scarce, analogous compounds derived from other botanical sources have been shown to stimulate the Nrf2/ARE signaling pathway, thereby increasing the production of antioxidant proteins and offering neuroprotective benefits [178,179]. This pathway plays a vital role in protecting cells from oxidative damage.
Potential for Drug Delivery. Novel methodologies, including the utilization of niosomes infused with Satureja extracts, have demonstrated potential in augmenting the stability and precise delivery of antioxidants to neural tissues, consequently enhancing neuroprotective effects [180].

3.4.2. Anti-Inflammatory Activity

The phenolic compounds found in Satureja montana, such as rosmarinic acid, exhibit anti-inflammatory properties. Chronic inflammation plays a significant role in neurodegeneration, and mitigating this inflammation may safeguard neuronal cells. The anti-inflammatory properties of compounds derived from SM, especially concerning neuroprotection, involve multiple biochemical pathways. The following outlines the principal mechanisms identified in the current literature:
Oxidative Stress Reduction. The dry extract of SM demonstrates considerable antioxidant properties, which play a vital role in alleviating oxidative stress, a prevalent factor in neuroinflammation and neurodegeneration. This antioxidant capability aids in neutralizing free radicals and diminishing ROS, thus safeguarding neuronal cells from oxidative harm [176].
Modulation of Pro-inflammatory Cytokines. In a model of acute stress, the dry extract of Satureja montana administered at a dosage of 250 mg/kg markedly reduced the concentrations of pro-inflammatory cytokines, including TNF-α and IL-6, when compared to other substances such as carvacrol and rosmarinic acid [176]. This decrease in cytokine levels suggests its potential role in regulating inflammatory responses within the brain.
Blood–Brain Barrier (BBB) Protection. Carvacrol, a principal constituent of SM, has demonstrated efficacy in reducing brain edema and inhibiting blood–brain barrier permeability following traumatic brain injury. This effect is mediated by its antioxidant properties, which lower levels of malondialdehyde and ROS while enhancing SOD activity and overall antioxidant capacity [181]. Preserving the integrity of the BBB is crucial for averting neuroinflammation and the resulting neuronal injury.
Matrix Metalloproteinase Inhibition. Carvacrol administration additionally inhibits the expression of matrix metalloproteinase-9 (MMP-9), an enzyme responsible for the degradation of extracellular matrix components and compromising blood–brain barrier (BBB) integrity. Through the inhibition of MMP-9, carvacrol contributes to the maintenance of the structural integrity of the BBB [181].
Neuroprotective Pathways. Natural compounds, such as those derived from Satureja montana, exhibit neuroprotective properties primarily through the activation of signaling pathways, including the phosphoinositide 3-kinase (PI3K)/Akt and mitogen-activated protein kinase (MAPK) pathways. These pathways are integral to antioxidant defense mechanisms and cellular survival, thereby enhancing neuroprotection [182].
The neuroprotective anti-inflammatory mechanisms of Satureja montana encompass various biochemical pathways and functions, as illustrated in Table 4.

3.4.3. Anti-Apoptotic Properties

The anti-apoptotic properties of Balakan savory, particularly in relation to neuroprotection, can be deduced from its observed effects in other biological systems, given the scarcity of direct studies on its neuroprotective mechanisms. Research on a rat model indicates that Satureja montana extract reduces the expression of pro-apoptotic genes such as Fas and Bax while enhancing the expression of anti-apoptotic genes like Bcl-2 in testicular tissue, thereby suggesting a potential mechanism for neuronal protection against apoptosis [183]. Furthermore, SM extract exhibits notable antioxidant activity, effectively reducing lipid peroxidation and restoring glutathione levels, which are vital for safeguarding cells from oxidative stress-related apoptosis. The extract also decreases pro-apoptotic proteins like Fas and Bax while increasing anti-apoptotic proteins such as Bcl-2, establishing a critical balance necessary for preventing cell death. Additionally, Satureja montana extract enhances the expression of peroxisome proliferator-activated receptor-gamma (PPAR-γ) and normalizes Akt1 protein levels, both of which play significant roles in cell survival pathways, promoting growth and inhibiting apoptosis. This study further demonstrated that the extract mitigates DNA fragmentation, a key indicator of apoptosis, underscoring its importance in maintaining cellular integrity, neuronal health, and function.

3.4.4. Acetylcholinesterase Inhibition

Inhibition of acetylcholinesterase (AChE) can enhance cholinergic transmission, which is beneficial in conditions like Alzheimer’s disease where cholinergic deficits are prominent. In a comparative analysis of different species within the Lamiaceae family, Satureja montana emerged as one of the plants demonstrating significant acetylcholinesterase inhibitory activity at a concentration of 1 mg/mL [37]. Additionally, essential oils from Satureja montana inhibited human serum cholinesterase activity, indicating the potential for treating neurological diseases [184]. Further, extracts from SM, obtained through supercritical fluid extraction, showed significant inhibition of butyrylcholinesterase (BChE). The nonvolatile fractions, rich in bioactive compounds including (+)-catechin, chlorogenic acid, vanillic acid, and protocatechuic acid, were particularly effective [38]. The main active compounds identified in Satureja species include carvacrol, γ-terpinene, thymol, and rosmarinic acid, which contribute to their cholinesterase inhibitory activity [185,186]. Essential oils extracted from SM also demonstrated inhibitory effects on AChE, suggesting their potential use in therapeutic applications [39,40].
Mechanisms of neuroprotective activity of Satureja montana are summarized in Figure 4.

4. Discussion

4.1. Neuroprotective and Psychotropic Potential of Satureja montana

This review emphasizes the significant neuropharmacological capabilities of Satureja montana, a plant abundant in bioactive substances like carvacrol and rosmarinic acid. The dry extract of SM exhibited enhanced anxiolytic, antidepressant, and cognitive-enhancing properties in both acute and chronic stress models when compared to its individual components. These results indicate a synergistic interaction among its phytochemicals, highlighting the therapeutic advantages of utilizing whole-plant extracts over the administration of isolated compounds.

4.2. Mechanistic Insights into CNS Activity of Satureja montana

The anxiolytic and antidepressant properties of SM are believed to arise from its modulation of central neurotransmitters, especially serotonin, dopamine, and noradrenaline. Furthermore, its engagement with GABA-ergic and cholinergic pathways, along with its effect on T-type calcium channels, enhances its neuroactive characteristics. The extract has also been shown to alleviate stress-induced behavioral impairments in experimental models, which include changes in locomotor activity, social interaction, and immobility duration in the Forced Swim test. These behavioral results align with mechanisms associated with emotional regulation and neurochemical equilibrium.
Oxidative stress and chronic inflammation play pivotal roles in the development of neurodegenerative and psychiatric disorders. SM demonstrates significant antioxidant capabilities, boosting the function of natural antioxidant enzymes such as superoxide dismutase, catalase, and glutathione reductase. It effectively diminishes lipid peroxidation and neutralizes ROS, thus safeguarding neuronal health. Simultaneously, its anti-inflammatory properties are facilitated by the downregulation of pro-inflammatory cytokines (such as TNF-α and IL-6) and the inhibition of cyclooxygenase activity, exhibiting a potency that surpasses that of its individual components.
The extract enhanced recognition memory and the ability to discriminate novel objects, particularly in animal models experiencing chronic stress. The cognitive benefits were not as pronounced when rosmarinic acid or carvacrol was used separately, suggesting that a synergistic effect is observed in the full extract. Notably, SM demonstrated considerable inhibitory activity against AChE, highlighting its potential for cholinergic enhancement, which is a crucial focus in the treatment of Alzheimer’s disease.
In addition to its antioxidant and anti-inflammatory properties, SM also affects anti-apoptotic signaling. It reduces the expression of pro-apoptotic genes such as Fas and Bax while enhancing the levels of anti-apoptotic markers like Bcl-2. Furthermore, it modulates survival pathways including Akt and PPAR-γ, which are essential for preventing neuronal death and maintaining cognitive function, especially in the context of chronic stress.

4.3. Clinical Implications and Future Directions

While the findings are encouraging, the discourse highlights significant deficiencies in the existing body of literature. There is a lack of clinical research assessing the effectiveness and safety of Satureja montana in human subjects. The majority of investigations have focused on animal studies or in vitro experiments, which, although valuable, require careful consideration prior to application in clinical settings. In vitro and animal research frequently employs concentrations and methods of administration that are challenging to replicate in human subjects. Variations in metabolism, permeability of the blood–brain barrier, and systemic bioavailability of these substances present considerable obstacles. Additionally, differences in experimental designs, treatment lengths, and dosages of compounds lead to variations in outcomes, especially when analyzing the distinct impacts of rosmarinic acid and carvacrol. The lack of standardized extract formulations and discrepancies in study design further complicate the ability to compare findings across different studies, thereby diminishing their clinical relevance. This review primarily examines the mechanistic properties of the neuroprotective effects attributed to the key components found in savory extracts. However, forthcoming clinical studies that concentrate on optimal dosing strategies, suitable pharmaceutical formulations, and specific target populations will be crucial for their implementation in therapeutic settings.

5. Conclusions

Satureja montana may represent a valuable and promising alternative in the prevention and treatment of various mental health disorders, including dementia. The main mechanisms by which it affects pathological processes in the CNS are significant anxiolytic activity, anticholinergic activity, and strong antioxidant and anti-inflammatory properties producing moderate cognitive benefits. Satureja montana exhibits several properties that could contribute to neuroprotection, including antioxidant, anti-inflammatory, and anti-apoptotic effects, modulation of neurotrophic factors, and acetylcholinesterase inhibition. These mechanisms collectively suggest that Balkan savory has the potential to protect against neurodegenerative diseases and support overall neuronal health. However, despite there being existing literature regarding the composition and biological activity of Satureja montana, further research is essential to elucidate its established pharmacological effects and their potential complex mechanisms.

Author Contributions

Conceptualization, L.T.; literature overview and literature resources, L.T., S.D., S.A., and D.S.; methodology, V.B.G., V.G., D.S., and S.T.; writing—original draft preparation, S.D., S.A., D.S., and L.T.; writing—review and editing, L.T., S.D., V.P., and R.K.; project administration, R.K.; funding acquisition, R.K. All authors have read and agreed to the published version of the manuscript.

Funding

Grant KΠ-06-H73/5-05.12.2023 from the National Science Fund, Sofia, Bulgaria, funded this research.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
AChEAcetylcholinesterase 
ADAlzheimer’s disease
BBBBlood–brain barrier
BChEButyrylcholinesterase
CAT Catalase
CNSCentral nervous system
DIDiscrimination index
GABAGamma-aminobutyric acid
GSRGlutathione reductase
MAPKMitogen-activated protein kinase 
MCIMild cognitive impairment
MMP-9Matrix metalloproteinase-9
NMDAN-methyl-D-aspartate
PI3KPhosphoinositide 3-kinase 
PPAR-γPeroxisome proliferator-activated receptor-gamma
ROSReactive oxygen species
SMSatureja montana
SOD Superoxide dismutase

References

  1. Tugume, P.; Nyakoojo, C. Ethno-pharmacological survey of herbal remedies used in the treatment of paediatric diseases in Buhunga parish, Rukungiri District, Uganda. BMC Complement. Altern. Med. 2019, 19, 353. [Google Scholar] [CrossRef] [PubMed]
  2. Herbal Medicine Market. 2021. Available online: https://www.insightslice.com/herbal-medicine-market (accessed on 23 December 2024).
  3. Jakovljević, M.; Vladić, J.; Vidović, S.; Pastor, K.; Jokić, S.; Molnar, M.; Jerković, I. Application of Deep Eutectic Solvents for the Extraction of Rutin and Rosmarinic Acid from Satureja montana L. and Evaluation of the Extracts Antiradical Activity. Plants 2020, 9, 153. [Google Scholar] [CrossRef] [PubMed]
  4. Nasim, N.; Sandeep, I.S.; Mohanty, S. Plant-derived natural products for drug discovery: Current approaches and prospects. Nucleus 2022, 65, 399–411. [Google Scholar] [CrossRef] [PubMed]
  5. Sharma, P.; Manchanda, R.; Goswami, R.; Chawla, S. Biodiversity and Therapeutic Potential of Medicinal Plants. In Environmental Concerns and Sustainable Development; Shukla, V., Kumar, N., Eds.; Springer: Singapore, 2020. [Google Scholar] [CrossRef]
  6. Davis, C.C.; Choisy, P. Medicinal plants meet modern biodiversity science. Curr. Biol. 2024, 34, R158–R173. [Google Scholar] [CrossRef] [PubMed]
  7. Sun, W.; Shahrajabian, M.H. Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health. Molecules 2023, 28, 1845. [Google Scholar] [CrossRef] [PubMed]
  8. Rahman, M.H.; Bajgai, J.; Fadriquela, A.; Sharma, S.; Trinh, T.T.; Akter, R.; Jeong, Y.J.; Goh, S.H.; Kim, C.-S.; Lee, K.-J. Therapeutic Potential of Natural Products in Treating Neurodegenerative Disorders and Their Future Prospects and Challenges. Molecules 2021, 26, 5327. [Google Scholar] [CrossRef] [PubMed]
  9. Aware, C.B.; Patil, D.N.; Suryawanshi, S.S.; Mali, P.R.; Rane, M.R.; Gurav, R.G.; Jadhav, J.P. Natural bioactive products as promising therapeutics: A review of natural product-based drug development. S. Afr. J. Bot. 2022, 151, 512–528. [Google Scholar] [CrossRef]
  10. Wangensteen, H.; Diallo, D.; Paulsen, B.S. Medicinal plants from Mali: Chemistry and biology. J. Ethnopharmacol. 2017, 176, 429–437. [Google Scholar] [CrossRef] [PubMed]
  11. de Rus Jacquet, A.; Timmers, M.; Ma, S.Y.; Thieme, A.; McCabe, G.P.; Vest, J.H.C.; Lila, M.A.; Rochet, J.C. Lumbee traditional medicine: Neuroprotective activities of medicinal plants used to treat Parkinson’s disease-related symptoms. J. Ethnopharmacol. 2017, 206, 408–425. [Google Scholar] [CrossRef] [PubMed]
  12. Veeren, B.; Ghaddar, B.; Bringart, M.; Khazaal, S.; Gonthier, M.P.; Meilhac, O.; Diotel, N.; Bascands, J.L. Phenolic Profile of Herbal Infusion and Polyphenol-Rich Extract from Leaves of the Medicinal Plant Antirhea borbonica: Toxicity Assay Determination in Zebrafish Embryos and Larvae. Molecules 2020, 25, 4482. [Google Scholar] [CrossRef] [PubMed]
  13. Ciupei, D.; Colişar, A.; Leopold, L.; Stănilă, A.; Diaconeasa, Z.M. Polyphenols: From Classification to Therapeutic Potential and Bioavailability. Foods 2024, 13, 4131. [Google Scholar] [CrossRef] [PubMed]
  14. Dini, I.; Grumetto, L. Recent Advances in Natural Polyphenol Research. Molecules 2022, 27, 8777. [Google Scholar] [CrossRef] [PubMed]
  15. Chen, G.-L.; Mutie, F.M.; Xu, Y.-B.; Saleri, F.D.; Hu, G.-W.; Guo, M.-Q. Antioxidant, Anti-inflammatory Activities and Polyphenol Profile of Rhamnus prinoides. Pharmaceuticals 2020, 13, 55. [Google Scholar] [CrossRef] [PubMed]
  16. Costa, A.; Bonner, M.Y.; Arbiser, J.L. Use of Polyphenolic Compounds in Dermatologic Oncology. Am. J. Clin. Dermatol. 2016, 17, 369–385. [Google Scholar] [CrossRef] [PubMed]
  17. Rubio-Moraga, A.; Argandoña, J.; Mota, B.; Pérez, J.; Verde, A.; Fajardo, J.; Gómez-Navarro, J.; Castillo-López, R.; Ahrazem, O.; Gómez-Gómez, L. Screening for polyphenols, antioxidant and antimicrobial activities of extracts from eleven Helianthemum taxa (Cistaceae) used in folk medicine in southeastern Spain. J. Ethnopharmacol. 2013, 148, 287–296. [Google Scholar] [CrossRef] [PubMed]
  18. Benslama, A.; Harrar, A.; Gül, F.; Demirtaş, I. Phenolic compounds, antioxidant and antibacterial activities of Zizyphus lotus L. leaves extracts. Nat. Prod. J. 2017, 7, 316–322. [Google Scholar] [CrossRef]
  19. Zarshenas, M.M.; Krenn, L. Phytochemical and pharmacological aspects of Salvia mirzayanii Rech. f. & Esfand. J. Evid.-Based Complement. Altern. Med. 2015, 20, 65–72. [Google Scholar] [CrossRef]
  20. Uritu, C.M.; Mihai, C.T.; Stanciu, G.D.; Dodi, G.; Alexa-Stratulat, T.; Luca, A.; Leon-Constantin, M.M.; Stefanescu, R.; Bild, V.; Melnic, S.; et al. Medicinal plants of the family Lamiaceae in pain therapy: A review. Pain Res. Manag. 2018, 2018, 7801543. [Google Scholar] [CrossRef] [PubMed]
  21. Zawiślak, G.; Nurzyńska-Wierdak, R. Variation in winter savory (Satureja montana L.) yield and essential oil production as affected by different plant density and number of harvests. Acta Sci. Pol. Hortorum Cultus 2017, 16, 159–168. [Google Scholar] [CrossRef]
  22. Jafari, F.; Ghavidel, F.; Zarshenas, M.M. A critical overview on the pharmacological and clinical aspects of popular Satureja species. J. Acupunct. Meridian Stud. 2016, 9, 118–127. [Google Scholar] [CrossRef] [PubMed]
  23. Beshkov, S. Contributions to the knowledge of the Geometridae fauna of the Balkan Peninsula with some new species for Bulgaria, Serbia, Albania, and Macedonia. Atalanta 2017, 48, 275–290. [Google Scholar]
  24. Šilić, Č. Monografija rodova Satureja L., Calamintha Miller, Micromeria Bentham, Acinos Miller i Clinopodium L. u Flori Jugoslavije; Zemaljski muzej BiH: Sarajevo, Bosnia and Herzegovina, 1979. [Google Scholar]
  25. World Checklist of Selected Plant Families. Available online: http://ww2.bgbm.org/EuroPlusMed (accessed on 11 November 2024).
  26. Hudz, N.; Makowicz, E.; Shanaida, M.; Białoń, M.; Jasicka-Misiak, I.; Yezerska, O.; Svydenko, L.; Wieczorek, P.P. Phytochemical evaluation of tinctures and essential oil obtained from Satureja montana herb. Molecules 2020, 25, 4763. [Google Scholar] [CrossRef] [PubMed]
  27. Čutović, N.; Batinić, P.; Marković, T.; Jovanović, A.A. Optimization of the extraction process from Satureja montana L.: Physicochemical characterization of the extracts. Hem. Ind. 2023, 77, 251–263. [Google Scholar] [CrossRef]
  28. Kremer, D.; Košir, I.J.; Končić, M.Z.; Čerenak, A.; Potočnik, T.; Srečec, S.; Randić, M.; Kosalec, I. Antimicrobial and antioxidant properties of Satureja montana L. and S. subspicata Vis. (Lamiaceae). Curr. Drug Targets 2015, 16, 1623–1633. [Google Scholar] [CrossRef] [PubMed]
  29. Vilmosh, N.; Georgieva-Kotetarova, M.; Dimitrova, S.; Zgureva, M.; Atanassova, P.K.; Hrischev, P.I.; Kostadinova, I. Composition and chronic toxicity of dry methanol-aqueous extract of wild-growing Satureja montana. Folia Med. 2023, 65, 482–489. [Google Scholar] [CrossRef] [PubMed]
  30. Hassanein, H.D.; Hah, S.-A.A.; Abdelmohsen, M.M. Antioxidant polyphenolic constituents of Satureja montana L. growing in Egypt. Int. J. Pharm. Pharm. Sci. 2014, 6, 578–581. [Google Scholar]
  31. Fortini, P.; Di Marzio, P.; Guarrera, P.M.; Iorizzi, M. Ethnobotanical study on the medicinal plants in the Mainarde Mountains (central-southern Apennine, Italy). J. Ethnopharmacol. 2016, 184, 208–218. [Google Scholar] [CrossRef] [PubMed]
  32. Vitalini, S.; Puricelli, C.; Mikerezi, I.; Iriti, M. Plants, people, and traditions: Ethnobotanical survey in the Lombard Stelvio National Park and neighboring areas (Central Alps, Italy). J. Ethnopharmacol. 2015, 173, 435–458. [Google Scholar] [CrossRef] [PubMed]
  33. Milijašević, B.; Steinbach, M.; Mikov, M.; Rašković, A.; Čapo, I.; Živković, J.; Borišev, I.; Panić, J.Ć.; Teofilović, B.; Vujčić, M.; et al. Impact of winter savory extract (Satureja montana L.) on biochemical parameters in serum and oxidative status of liver with application of principal component analysis in extraction solvent selection. Eur. Rev. Med. Pharmacol. Sci. 2022, 26, 4721–4734. [Google Scholar] [CrossRef] [PubMed]
  34. Vilmosh, N. Изследване на Фармакoлoгични Ефекти на Satureja montana. Ph.D. Thesis, Plovdiv Medical University, Plovdiv, Bulgaria, 2022. Available online: https://ras.nacid.bg/api/reg/FilesStorage?key=108d0d7c-d26f-44d4-a601-c58eaad770a9&mimeType=application/pdf&fileName=%D0%90%D0%B2%D1%82%D0%BE%D1%80%D0%B5%D1%84%D0%B5%D1%80%D0%B0%D1%82_%D0%B4%D1%80%20%D0%92%D0%B8%D0%BB%D0%BC%D0%BE%D1%88.pdf&dbId=1 (accessed on 10 July 2025).
  35. Sefidkon, F.; Bistgani, Z.E. Integrative review on ethnobotany, essential oil, phytochemical, agronomy, molecular, and pharmacological properties of Satureja species. J. Essent. Oil Res. 2021, 33, 114–132. [Google Scholar] [CrossRef]
  36. Demyashkin, G.; Sataieva, T.; Shevkoplyas, L.; Kuevda, T.; Ahrameeva, M.; Parshenkov, M.; Mimuni, A.; Pimkin, G.; Atiakshin, D.; Shchekin, V.; et al. Burn wound healing activity of hydroxyethylcellulose gels with different water extracts obtained from various medicinal plants in Pseudomonas aeruginosa-infected rabbits. Int. J. Mol. Sci. 2024, 25, 8990. [Google Scholar] [CrossRef] [PubMed]
  37. Vladimir-Knežević, S.; Blažeković, B.; Kindl, M.; Vladić, J.; Lower-Nedza, A.D.; Brantner, A.H. Acetylcholinesterase inhibitory, antioxidant, and phytochemical properties of selected medicinal plants of the Lamiaceae family. Molecules 2014, 19, 767–782. [Google Scholar] [CrossRef] [PubMed]
  38. Silva, F.V.; Martins, A.; Salta, J.; Neng, N.R.; Nogueira, J.M.; Mira, D.; Gaspar, N.; Justino, J.; Grosso, C.; Urieta, J.S.; et al. Phytochemical profile and anticholinesterase and antimicrobial activities of supercritical versus conventional extracts of Satureja montana. J. Agric. Food Chem. 2009, 57, 11557–11563. [Google Scholar] [CrossRef] [PubMed]
  39. Les, F.; Galiffa, V.; Cásedas, G.; Moliner, C.; Maggi, F.; López, V.; Gómez-Rincón, C. Essential oils of two subspecies of Satureja montana L. against gastrointestinal parasite Anisakis simplex and acetylcholinesterase inhibition. Molecules 2024, 29, 4640. [Google Scholar] [CrossRef] [PubMed]
  40. Rezende, D.A.S.; Cardoso, M.; Konig, I.F.M.; Lunguinho, A.S.; Ferreira, V.R.F.; Brandão, R.M.; Gonçalves, R.R.P.; Caetano, A.R.S.; Nelson, D.L.; Remedio, R.N. Repellent effect on Rhipicephalus sanguineus and inhibition of acetylcholinesterase by volatile oils. Rev. Bras. Farmacogn. 2021, 31, 470–476. [Google Scholar] [CrossRef]
  41. Gomes, F.; Dias, M.I.; Lima, Â.; Barros, L.; Rodrigues, M.E.; Ferreira, I.C.F.R.; Henriques, M. Satureja montana L. and Origanum majorana L. decoctions: Antimicrobial activity, mode of action, and phenolic characterization. Antibiotics 2020, 9, 294. [Google Scholar] [CrossRef] [PubMed]
  42. Aćimović, M.; Šovljanski, O.; Pezo, L.; Travičić, V.; Tomić, A.; Zheljazkov, V.D.; Ćetković, G.; Švarc-Gajić, J.; Brezo-Borjan, T.; Sofrenić, I. Variability in biological activities of Satureja montana subsp. montana and subsp. variegata based on different extraction methods. Antibiotics 2022, 11, 1235. [Google Scholar] [CrossRef] [PubMed]
  43. Vitanza, L.; Maccelli, A.; Marazzato, M.; Scazzocchio, F.; Comanducci, A.; Fornarini, S.; Crestoni, M.E.; Filippi, A.; Fraschetti, C.; Rinaldi, F.; et al. Satureja montana L. essential oil and its antimicrobial activity alone or in combination with gentamicin. Microb. Pathog. 2019, 126, 323–331. [Google Scholar] [CrossRef] [PubMed]
  44. Ezaouine, A.; Nouadi, B.; Sbaoui, Y.; Bennis, F. Use of the genus Satureja as a food supplement: Possible modulation of the immune system via intestinal microbiota during SARS-CoV-2 infection. Anti-Infect. Agents 2022, 20, e221221199259. [Google Scholar] [CrossRef]
  45. Dinan, T.G.; Stanton, C.; Long-Smith, C.; Kennedy, P.; Cryan, J.F.; Cowan, C.S.M.; Cenit, M.C.; van der Kamp, J.W.; Sanz, Y. Feeding melancholic microbes: MyNewGut recommendations on diet and mood. Clin. Nutr. 2019, 38, 1995–2001. [Google Scholar] [CrossRef] [PubMed]
  46. Castro, A.I.; Gomez-Arbelaez, D.; Crujeiras, A.B.; Granero, R.; Aguera, Z.; Jimenez-Murcia, S.; Sajoux, I.; Lopez-Jaramillo, P.; Fernandez-Aranda, F.; Casanueva, F.F. Effect of a very low-calorie ketogenic diet on food and alcohol cravings, physical and sexual activity, sleep disturbances, and quality of life in obese patients. Nutrients 2018, 10, 1348. [Google Scholar] [CrossRef] [PubMed]
  47. Delpech, J.-C.; Madrigal, J.L.M.; Masto, G.; Pazos, R.; Dexter, J.; McLaughlin, B.; Sheridan, J.F.; Godbout, J.P. Microglia in neuronal plasticity: Influence of stress. Neuropharmacology 2015, 96, 19–28. [Google Scholar] [CrossRef] [PubMed]
  48. Lépinay, A.L.; Larrieu, T.; Joffre, C.; Acar, N.; Garate, I.; Castanon, N.; Layé, S. Perinatal high-fat diet increases hippocampal vulnerability to the adverse effects of subsequent high-fat feeding. Psychoneuroendocrinology 2015, 53, 82–93. [Google Scholar] [CrossRef] [PubMed]
  49. de la Torre, R.; de Sola, S.; Hernández, G.; Farré, M.; Pujol, J.; Rodríguez, J.; Espadaler, J.M.; Langohr, K.; Cuenca-Royo, A.; Principe, A.; et al. Safety and efficacy of cognitive training plus epigallocatechin-3-gallate in young adults with Down’s syndrome (TESDAD): A double-blind, randomised, placebo-controlled, phase 2 trial. Lancet Neurol. 2016, 15, 801–810. [Google Scholar] [CrossRef] [PubMed]
  50. Lai, J.S.; Hiles, S.; Bisquera, A.; Hure, A.J.; McEvoy, M.; Attia, J. A systematic review and meta-analysis of dietary patterns and depression in community-dwelling adults. Am. J. Clin. Nutr. 2014, 99, 181–197. [Google Scholar] [CrossRef] [PubMed]
  51. Psaltopoulou, T.; Sergentanis, T.N.; Panagiotakos, D.B.; Sergentanis, I.N.; Kosti, R.; Scarmeas, N. Mediterranean diet, stroke, cognitive impairment, and depression: A meta-analysis. Ann. Neurol. 2013, 74, 580–591. [Google Scholar] [CrossRef] [PubMed]
  52. Lassale, C.; Batty, G.D.; Baghdadli, A.; Jacka, F.; Sánchez-Villegas, A.; Kivimäki, M.; Akbaraly, T. Healthy dietary indices and risk of depressive outcomes: A systematic review and meta-analysis of observational studies. Mol. Psychiatry 2019, 24, 965–986. [Google Scholar] [CrossRef] [PubMed]
  53. Firth, J.; Marx, W.; Dash, S.; Carney, R.; Teasdale, S.B.; Solmi, M.; Stubbs, B.; Schuch, F.B.; Carvalho, A.F.; Jacka, F.; et al. The effects of dietary improvement on symptoms of depression and anxiety: A meta-analysis of randomized controlled trials. Psychosom. Med. 2019, 81, 265–280. [Google Scholar] [CrossRef] [PubMed]
  54. Agrawal, R.; Gomez-Pinilla, F. ‘Metabolic syndrome’ in the brain: Deficiency in omega-3 fatty acid exacerbates dysfunctions in insulin receptor signalling and cognition. J. Physiol. 2012, 590, 2485–2499. [Google Scholar] [CrossRef] [PubMed]
  55. Prenderville, J.A.; Kennedy, P.J.; Dinan, T.G.; Cryan, J.F. Adding fuel to the fire: The impact of stress on the ageing brain. Trends Neurosci. 2015, 38, 13–25. [Google Scholar] [CrossRef] [PubMed]
  56. Dallman, M.F. Stress-induced obesity and the emotional nervous system. Trends Endocrinol. Metab. 2010, 21, 159–165. [Google Scholar] [CrossRef] [PubMed]
  57. Gibson, E.L. Emotional influences on food choice: Sensory, physiological and psychological pathways. Physiol. Behav. 2006, 89, 53–61. [Google Scholar] [CrossRef] [PubMed]
  58. Oliver, G.; Wardle, J. Perceived effects of stress on food choice. Physiol. Behav. 1999, 66, 511–515. [Google Scholar] [CrossRef] [PubMed]
  59. El Aidy, S.; Dinan, T.G.; Cryan, J.F. Gut microbiota: The conductor in the orchestra of immune–neuroendocrine communication. Clin. Ther. 2015, 37, 954–967. [Google Scholar] [CrossRef] [PubMed]
  60. Sandhu, K.V.; Sherwin, E.; Schellekens, H.; Stanton, C.; Dinan, T.G.; Cryan, J.F. Feeding the microbiota-gut-brain axis: Diet, microbiome, and neuropsychiatry. Transl. Res. 2017, 179, 223–244. [Google Scholar] [CrossRef] [PubMed]
  61. Schellekens, H.; Finger, B.C.; Dinan, T.G.; Cryan, J.F. Ghrelin signalling and obesity: At the interface of stress, mood and food reward. Pharmacol. Ther. 2012, 135, 316–326. [Google Scholar] [CrossRef] [PubMed]
  62. Torres-Fuentes, C.; Schellekens, H.; Dinan, T.G.; Cryan, J.F. The microbiota–gut–brain axis in obesity. Lancet Gastroenterol. Hepatol. 2017, 2, 747–756. [Google Scholar] [CrossRef] [PubMed]
  63. de Wouw, M.V.; Schellekens, H.; Dinan, T.G.; Cryan, J.F. Microbiota-gut-brain axis: Modulator of host metabolism and appetite. J. Nutr. 2017, 147, 727–745. [Google Scholar] [CrossRef] [PubMed]
  64. Wesołowska, A.; Grzeszczuk, M.; Jadczak, D. Influence of harvest term on the content of carvacrol, p-cymene, γ-terpinene and β-caryophyllene in the essential oil of Satureja montana. Not. Bot. Horti. Agrobo. 2014, 42, 392–397. [Google Scholar] [CrossRef]
  65. Caprioli, G.; Lupidi, G.; Maggi, F. Comparison of chemical composition and antioxidant activities of two Winter savory subspecies (Satureja montana subsp. variegata and Satureja montana subsp. montana) cultivated in Northern Italy. Nat. Prod. Res. 2019, 33, 3143–3147. [Google Scholar] [CrossRef] [PubMed]
  66. Bojović, D.; Šoškić, M.; Tadic, V. Comparative study of chemical composition of the essential oils from Satureja cuneifolia Ten. and Satureja montana L., Lamiaceae collected at National park Lovćen, Montenegro. Stud. Univ. Babes-Bolyai Chem. 2018, 63, 167–180. [Google Scholar] [CrossRef]
  67. Bezić, N.; Skočibušić, M.; Dunkić, V. Phytochemical composition and antimicrobial activity of Satureja montana L. and Satureja cuneifolia Ten. essential oils. Acta Bot. Croat. 2005, 64, 313–322. [Google Scholar]
  68. Marin, M.; Novaković, M.; Tešević, V.; Marin, P.D. Antioxidative, antibacterial and antifungal activity of the essential oil of wild-growing Satureja montana L. from Dalmatia, Croatia. Flavour Fragr. J. 2012, 27, 216–223. [Google Scholar] [CrossRef]
  69. Skocibusić, M.; Bezić, N. Phytochemical analysis and in vitro antimicrobial activity of two Satureja species essential oils. Phytother. Res. 2004, 18, 967–970. [Google Scholar] [CrossRef] [PubMed]
  70. Abdelshafeek, K.A.; Osman, A.F.; Mouneir, S.M.; Elhenawy, A.A.; Abdallah, W.E. Phytochemical profile, comparative evaluation of Satureja montana alcoholic extract for antioxidants, anti-inflammatory and molecular docking studies. BMC Complement. Med. Ther. 2023, 23, 108. [Google Scholar] [CrossRef] [PubMed]
  71. Rahbardar, M.G.; Hosseinzadeh, H. Effects of rosmarinic acid on nervous system disorders: An updated review. Naunyn Schmiedebergs Arch. Pharmacol. 2020, 393, 1779–1795. [Google Scholar] [CrossRef] [PubMed]
  72. Mohammedi, Z. Carvacrol: An update of biological activities and mechanism of action. Open Access J. Chem. 2017, 1, 53–62. [Google Scholar] [CrossRef]
  73. Elufioye, T.O.; Habtemariam, S. Hepatoprotective effects of rosmarinic acid: Insight into its mechanisms of action. Biomed. Pharmacother. 2019, 112, 108600. [Google Scholar] [CrossRef] [PubMed]
  74. Burt, S.A.; Adolfse, S.J.; Ahad, D.S.; Tersteeg-Zijderveld, M.H.; Jongerius-Gortemaker, B.G.; Post, J.A.; Brüggemann, H.; Santos, R.R. Cinnamaldehyde, carvacrol and organic acids affect gene expression of selected oxidative stress and inflammation markers in IPEC-J2 cells exposed to Salmonella typhimurium. Phytother. Res. 2016, 30, 1988–2000. [Google Scholar] [CrossRef] [PubMed]
  75. Lesjak, M.; Simin, N.; Orcic, D.; Franciskovic, M.; Knezevic, P.; Beara, I.; Aleksic, V.; Svircev, E.; Buzas, K.; Mimica-Dukic, N. Binary and tertiary mixtures of Satureja hortensis and Origanum vulgare essential oils as potent antimicrobial agents against Helicobacter pylori. Phytother. Res. 2016, 30, 476–484. [Google Scholar] [CrossRef] [PubMed]
  76. Rajput, J.D.; Bagul, S.D.; Pete, U.D.; Zade, C.M.; Padhye, S.B.; Bendre, R.S. Perspectives on medicinal properties of natural phenolic monoterpenoids and their hybrids. Mol. Divers. 2018, 22, 225–245. [Google Scholar] [CrossRef] [PubMed]
  77. El-Hagrassi, A.M.; Abdallah, W.E.; Osman, A.F.; Abdelshafeek, K.A. Phytochemical study of bioactive constituents from Satureja montana L. growing in Egypt and their antimicrobial and antioxidant activities. Asian J. Pharm. Clin. Res. 2018, 11, 142–148. [Google Scholar] [CrossRef]
  78. Serrano, C.; Matos, O.; Teixeira, B.; Ramos, C.; Neng, N.; Nogueira, J.; Nunes, M.L.; Marques, A. Antioxidant and antimicrobial activity of Satureja montana L. extracts. J. Sci. Food Agric. 2011, 91, 1554–1560. [Google Scholar] [CrossRef] [PubMed]
  79. Vilmosh, N.; Delev, D.; Kostadinov, I.; Zlatanova, H.; Kotetarova, M.; Kandilarov, I.; Kostadinova, I. Anxiolytic effect of Satureja montana dry extract and its active compounds rosmarinic acid and carvacrol in acute stress experimental model. J. Integr. Neurosci. 2022, 21, 124. [Google Scholar] [CrossRef] [PubMed]
  80. Rai, D.; Bhatia, G.; Sen, P.; Palit, G. Anti-stress effects of Ginkgo biloba and Panax ginseng: A comparative study. J. Pharmacol. Sci. 2003, 93, 458–464. [Google Scholar] [CrossRef] [PubMed]
  81. Sierra-Fonseca, J.A.; Gosselink, K.L. Tauopathy and neurodegeneration: A role for stress. Neurobiol. Stress 2018, 9, 105–112. [Google Scholar] [CrossRef] [PubMed]
  82. Debora, S.; Jasmin, V.; Baba, V.; Gomathi, S. Impact of stress on health. Narayana Nurs. J. 2018, 5, 11–14. [Google Scholar]
  83. Yaribeygi, H.; Panahi, Y.; Sahraei, H.; Johnston, T.P.; Sahebkar, A. The impact of stress on body function: A review. EXCLI J. 2017, 16, 1057. [Google Scholar] [CrossRef] [PubMed]
  84. Manganyi, M.C.; Gunya, B.; Mavundza, E.J.; Sibuyi, N.R.S.; Meyer, M.; Madiehe, A.M. A chewable cure “kanna”: Biological and pharmaceutical properties of Sceletium tortuosum. Molecules 2021, 26, 2557. [Google Scholar] [CrossRef] [PubMed]
  85. Liu, Y.-Z.; Wang, Y.-X.; Jiang, C.-L. Inflammation: The common pathway of stress-related diseases. Front. Hum. Neurosci. 2017, 11, 273283. [Google Scholar] [CrossRef] [PubMed]
  86. Lopes, S.; Yu, L.; Zhang, L.; Rudenko, A.; Hahn, K.; McLeod, F.; Brotherton, D.; Maguire, J.; Bading, H.; Frenguelli, B.G.; et al. Tau protein is essential for stress-induced brain pathology. Proc. Natl. Acad. Sci. USA 2016, 113, E3755–E3763. [Google Scholar] [CrossRef] [PubMed]
  87. Federico, A.; Cardaioli, E.; Da Pozzo, P.; Formichi, P.; Gallus, G.N.; Radi, E. Mitochondria, oxidative stress and neurodegeneration. J. Neurol. Sci. 2012, 322, 254–262. [Google Scholar] [CrossRef] [PubMed]
  88. Bockmühl, Y.; Patchev, A.V.; Bauer, M.; Almeida, O.F. Methylation at the CpG island shore region upregulates Nr3c1 promoter activity after early-life stress. Epigenetics 2015, 10, 247–257. [Google Scholar] [CrossRef] [PubMed]
  89. Lin, L.-Y.; Sibille, E.; McEwen, B.S. Early-life stress leads to impaired spatial learning and memory in middle-aged ApoE4-TR mice. Mol. Neurodegener. 2016, 11, 51. [Google Scholar] [CrossRef] [PubMed]
  90. McEwen, B.S. Physiology and neurobiology of stress and adaptation: Central role of the brain. Physiol. Rev. 2007, 87, 873–904. [Google Scholar] [CrossRef] [PubMed]
  91. McEwen, B.S. Allostasis and the epigenetics of brain and body health over the life course: The brain on stress. JAMA Psychiatry 2017, 74, 551–552. [Google Scholar] [CrossRef] [PubMed]
  92. Alcubierre, D.D.; Díaz-Rodríguez, L.; Cano, M.; Ortiz, J.; González, M.; Torres, A.; García, L.; Pacheco, D.; Luna, E. Glucocorticoids and cognitive function: A walkthrough in endogenous and exogenous alterations. J. Endocrinol. Investig. 2023, 46, 1961–1982. [Google Scholar] [CrossRef] [PubMed]
  93. Henckens, M.J.A.G.; Deussing, J.M.; Chen, A. Region-specific roles of the corticotropin-releasing factor–urocortin system in stress. Nat. Rev. Neurosci. 2016, 17, 636–651. [Google Scholar] [CrossRef] [PubMed]
  94. Spannenburg, L.; Reed, H. Adverse cognitive effects of glucocorticoids: A systematic review of the literature. Steroids 2023, 2023, 109314. [Google Scholar] [CrossRef] [PubMed]
  95. Cerqueira, J.J.; Almeida, O.F.; Sousa, N. Corticosteroid status influences the volume of the rat cingulate cortex–a magnetic resonance imaging study. J. Psychiatr. Res. 2005, 39, 451–460. [Google Scholar] [CrossRef] [PubMed]
  96. Cerqueira, J.J.; Mailliet, F.; Almeida, O.F.; Jay, T.M.; Sousa, N. Morphological correlates of corticosteroid-induced changes in prefrontal cortex-dependent behaviors. J. Neurosci. 2005, 25, 7792–7800. [Google Scholar] [CrossRef] [PubMed]
  97. Liston, C.; Gan, W.-B. Glucocorticoids are critical regulators of dendritic spine development and plasticity in vivo. Proc. Natl. Acad. Sci. USA 2011, 108, 16074–16079. [Google Scholar] [CrossRef] [PubMed]
  98. Magariños, A.M.; McEwen, B.S.; Flugge, G.; Fuchs, E. Chronic psychosocial stress causes apical dendritic atrophy of hippocampal CA3 pyramidal neurons in subordinate tree shrews. J. Neurosci. 1996, 16, 3534–3540. [Google Scholar] [CrossRef] [PubMed]
  99. Radley, J.J.; Rocher, A.B.; Martinez, A.; Vasquez, S.; Williams, S.; Bloom, F.E.; Hof, P.R.; Morrison, J.H. Repeated stress induces dendritic spine loss in the rat medial prefrontal cortex. Cereb. Cortex 2006, 16, 313–320. [Google Scholar] [CrossRef] [PubMed]
  100. Wellman, C.L. Dendritic reorganization in pyramidal neurons in medial prefrontal cortex after chronic corticosterone administration. J. Neurobiol. 2001, 49, 245–253. [Google Scholar] [CrossRef] [PubMed]
  101. Ferrara, M.; Langiano, E.; Brango, T.D.; Vito, E.D.; Cioccio, L.D.; Bauco, C. Prevalence of stress, anxiety and depression in Alzheimer caregivers. Health Qual. Life Outcomes 2008, 6, 93. [Google Scholar] [CrossRef] [PubMed]
  102. Quick, J.C.; Henderson, D.F. Occupational stress: Preventing suffering, enhancing wellbeing. Int. J. Environ. Res. Public Health 2016, 13, 459. [Google Scholar] [CrossRef] [PubMed]
  103. Jope, R.S.; Cheng, Y.; Lowell, J.A.; Worthen, R.J.; Sitbon, Y.H.; Beurel, E. Stressed and inflamed, can GSK3 be blamed? Trends Biochem. Sci. 2017, 42, 180–192. [Google Scholar] [CrossRef] [PubMed]
  104. Dantzer, R.; O’Connor, J.C.; Freund, G.G.; Johnson, R.W.; Kelley, K.W. From inflammation to sickness and depression: When the immune system subjugates the brain. Nat. Rev. Neurosci. 2008, 9, 46–56. [Google Scholar] [CrossRef] [PubMed]
  105. Dantzer, R. Neuroimmune interactions: From the brain to the immune system and vice versa. Physiol. Rev. 2018, 98, 477–504. [Google Scholar] [CrossRef] [PubMed]
  106. Hodes, G.E.; Kana, V.; Menard, C.; Merad, M.; Russo, S.J. Neuroimmune mechanisms of depression. Nat. Neurosci. 2015, 18, 1386–1393. [Google Scholar] [CrossRef] [PubMed]
  107. Menard, C.; Pfau, M.L.; Hodes, G.E.; Kana, V.; Wang, V.X.; Bouchard, S.; Takahashi, A.; Flanigan, M.E.; Aleyasin, H.; LeClair, K.B.; et al. Social stress induces neurovascular pathology promoting depression. Nat. Neurosci. 2017, 20, 1752–1760. [Google Scholar] [CrossRef] [PubMed]
  108. Øines, E.; Murison, R.; Mrdalj, J.; Grønli, J.; Milde, A.M. Neonatal maternal separation in male rats increases intestinal permeability and affects behavior after chronic social stress. Physiol. Behav. 2012, 105, 1058–1066. [Google Scholar] [CrossRef] [PubMed]
  109. Ströhle, A.; Schüle, C.; Breuer, A.; Kluge, M.; Müller, M.B. The Diagnosis and Treatment of Anxiety Disorders. Dtsch. Arztebl. Int. 2018, 155, 611–620. [Google Scholar] [CrossRef] [PubMed]
  110. Connor, J.P.; Haber, P.S.; Hall, W.D. Alcohol use disorders. Lancet 2016, 387, 988–998. [Google Scholar] [CrossRef] [PubMed]
  111. Jiang, L.; Atasoy, S.; Johar, H.; Herder, C.; Peters, A.; Kruse, J.; Ladwig, K.-H. Anxiety boosts progression of prediabetes to type 2 diabetes: Findings from the prospective Cooperative Health Research in the Region of Augsburg F4 and FF4 studies. Diabet. Med. 2020, 37, 1737–1741. [Google Scholar] [CrossRef] [PubMed]
  112. Naicker, K.; Johnson, J.A.; Skogen, J.C.; Manuel, D.; Øverland, S.; Sivertsen, B.; Colman, I. Type 2 Diabetes and comorbid symptoms of depression and anxiety: Longitudinal associations with mortality risk. Diabetes Care 2017, 40, 352–358. [Google Scholar] [CrossRef] [PubMed]
  113. Steffen, A.; Nübel, J.; Jacobi, F.; Bätzing, J.; Holstiege, J. Mental and somatic comorbidity of depression: A comprehensive cross-sectional analysis of 202 diagnosis groups using German nationwide ambulatory claims data. BMC Psychiatry 2020, 20, 142. [Google Scholar] [CrossRef] [PubMed]
  114. Greenberg, P.E.; Fournier, A.A.; Sisitsky, T.; Pike, C.T.; Kessler, R.C. The economic burden of adults with major depressive disorder in the United States (2005 and 2010). J. Clin. Psychiatry 2015, 76, 155–162. [Google Scholar] [CrossRef] [PubMed]
  115. Josephson, C.B.; Jette, N. Psychiatric comorbidities in epilepsy. Int. Rev. Psychiatry 2017, 29, 409–424. [Google Scholar] [CrossRef] [PubMed]
  116. Sartorius, N. Depression and diabetes. Dialogues Clin. Neurosci. 2018, 20, 47–52. [Google Scholar] [CrossRef] [PubMed]
  117. Martini, L.; Hoffmann, F. Comorbidity of chronic back pain and depression in Germany: Results from the GEDA study, 2009 and 2010. Z. Evid. Fortbild. Qual. Gesundhwes. 2018, 137–138, 62–68. [Google Scholar] [CrossRef] [PubMed]
  118. Dubois, B.; Feldman, H.H.; Jacova, C.; Hampel, H.; Molinuevo, J.L.; Blennow, K.; DeKosky, S.T.; Gauthier, S.; Selkoe, D.; Bateman, R.; et al. Advancing research diagnostic criteria for Alzheimer’s disease: The IWG-2 criteria. Lancet Neurol. 2014, 13, 614–629. [Google Scholar] [CrossRef] [PubMed]
  119. Suárez-González, A.; Crutch, S.J.; Franco-Macías, E.; Gil-Néciga, E. Neuropsychiatric symptoms in posterior cortical atrophy and Alzheimer disease. J. Geriatr. Psychiatry Neurol. 2016, 29, 65–71. [Google Scholar] [CrossRef] [PubMed]
  120. Connors, M.H.; Seeher, K.M.; Crawford, J.; Ames, D.; Woodward, M.; Brodaty, H. The stability of neuropsychiatric subsyndromes in Alzheimer’s disease. Alzheimers Dement. 2018, 14, 880–888. [Google Scholar] [CrossRef] [PubMed]
  121. Becker, E.; Lahmann, C.O.R.; Rücker, G.; Bauer, J.; Boeker, M. Anxiety as a risk factor of Alzheimer’s disease and vascular dementia. Br. J. Psychiatry 2018, 213, 654–660. [Google Scholar] [CrossRef] [PubMed]
  122. Zhao, Q.F.; Tan, L.; Wang, H.F.; Jiang, T.; Tan, M.S.; Tan, L.; Xu, W.; Li, J.Q.; Wang, J.; Lai, T.J.; et al. The prevalence of neuropsychiatric symptoms in Alzheimer’s disease: Systematic review and meta-analysis. J. Affect Disord. 2016, 190, 264–271. [Google Scholar] [CrossRef] [PubMed]
  123. Asmer, M.S.; Kirkham, J.; Newton, H.; Ismail, Z.; Elbayoumi, H.; Leung, R.H.; Seitz, D.P. Meta-analysis of the prevalence of major depressive disorder among older adults with dementia. J. Clin. Psychiatry 2018, 70, 5. [Google Scholar] [CrossRef] [PubMed]
  124. Chen, P.; Guarino, P.D.; Dysken, M.W.; Pallaki, M.; Asthana, S.; Llorente, M.D.; Sano, M. Neuropsychiatric symptoms and caregiver burden in individuals with Alzheimer’s disease: The TEAM-AD VA cooperative study. J. Geriatr. Psychiatry Neurol. 2018, 31, 177–185. [Google Scholar] [CrossRef] [PubMed]
  125. Sanford, A.M. Mild cognitive impairment. Clin. Geriatr. Med. 2017, 33, 325–337. [Google Scholar] [CrossRef] [PubMed]
  126. Sachdev, P.S.; Lipnicki, D.M.; Kochan, N.A.; Crawford, J.D.; Thalamuthu, A.; Andrews, G.; Brayne, C.; Matthews, F.E.; Stephan, B.C.; Lipton, R.B.; et al. The prevalence of mild cognitive impairment in diverse geographical and ethnocultural regions: The COSMIC collaboration. PLoS ONE 2015, 10, e0142388. [Google Scholar] [CrossRef] [PubMed]
  127. Luis, C.A.; Loewenstein, D.A.; Acevedo, A.; Barker, W.W.; Duara, R. Mild cognitive impairment: Directions for future research. Neurology 2003, 61, 438–444. [Google Scholar] [CrossRef] [PubMed]
  128. Bruscoli, M.; Lovestone, S. Is MCI really just early dementia? A systematic review of conversion studies. Int. Psychogeriatr. 2004, 16, 129–140. [Google Scholar] [CrossRef] [PubMed]
  129. Palmer, K.; Iulio, F.D.; Varsi, A.E.; Gianni, W.; Sancesario, G.; Caltagirone, C.; Spalletta, G. Neuropsychiatric predictors of progression from amnestic-mild cognitive impairment to Alzheimer’s disease: The role of depression and apathy. J. Alzheimers Dis. 2010, 20, 175–183. [Google Scholar] [CrossRef] [PubMed]
  130. Delrieu, J.; Desmidt, T.; Camus, V.; Sourdet, S.; Boutoleau-Bretonnière, C.; Mullin, E.; Vellas, B.; Payoux, P.; Lebouvier, T.; Alzheimer’s Disease Neuroimaging Initiative. Apathy as a feature of prodromal Alzheimer’s disease: An FDG-PET ADNI study. Int. J. Geriatr. Psychiatry 2015, 30, 470–477. [Google Scholar] [CrossRef] [PubMed]
  131. Moon, B.; Kim, S.; Park, Y.H.; Lim, J.S.; Youn, Y.C.; Kim, S.; Jang, J.W.; Alzheimer’s Disease Neuroimaging Initiative. Depressive symptoms are associated with progression to dementia in patients with amyloid-positive mild cognitive impairment. J. Alzheimers Dis. 2017, 58, 1255–1264. [Google Scholar] [CrossRef] [PubMed]
  132. Sugarman, M.A.; Alosco, M.L.; Tripodis, Y.; Steinberg, E.G.; Stern, R.A. Neuropsychiatric symptoms and the diagnostic stability of mild cognitive impairment. J. Alzheimers Dis. 2018, 62, 1841–1855. [Google Scholar] [CrossRef] [PubMed]
  133. Basso, M.R.; Lowery, N.; Ghormley, C.; Combs, D.; Purdie, R.; Neel, J.; Davis, M.; Bornstein, R. Comorbid anxiety corresponds with neuropsychological dysfunction in unipolar depression. Cogn. Neuropsychiatry 2007, 12, 437–456. [Google Scholar] [CrossRef] [PubMed]
  134. Rosenberg, P.B.; Mielke, M.M.; Appleby, B.; Oh, E.; Leoutsakos, J.M.; Lyketsos, C.G. Neuropsychiatric symptoms in MCI subtypes: The importance of executive dysfunction. Int. J. Geriatr. Psychiatry 2011, 26, 364–372. [Google Scholar] [CrossRef] [PubMed]
  135. Palmer, K.; Berger, A.K.; Monastero, R.; Winblad, B.; Bäckman, L.; Fratiglioni, L. Predictors of progression from mild cognitive impairment to Alzheimer disease. Neurology 2007, 68, 1596–1602. [Google Scholar] [CrossRef] [PubMed]
  136. Potvin, O.; Forget, H.; Grenier, S.; Préville, M.; Hudon, C. Anxiety, depression, and 1-year incident cognitive impairment in community-dwelling older adults. J. Am. Geriatr. Soc. 2011, 59, 1421–1428. [Google Scholar] [CrossRef] [PubMed]
  137. Ismail, Z.; Elbayoumi, H.; Fischer, C.E.; Hogan, D.B.; Millikin, C.P.; Schweizer, T.; Mortby, M.E.; Smith, E.E.; Patten, S.B.; Fiest, K.M. Prevalence of depression in patients with mild cognitive impairment: A systematic review and meta-analysis. JAMA Psychiatry 2017, 74, 58–67. [Google Scholar] [CrossRef] [PubMed]
  138. Chan, J.Y.C.; Yiu, K.K.L.; Kwok, T.C.Y.; Wong, S.Y.S.; Tsoi, K.K.F. Depression and antidepressants as potential risk factors in dementia: A systematic review and meta-analysis of 18 longitudinal studies. J. Am. Med. Dir. Assoc. 2019, 20, 279–286. [Google Scholar] [CrossRef] [PubMed]
  139. Mitchell, A.J.; Shiri-Feshki, M. Rate of progression of mild cognitive impairment to dementia–meta-analysis of 41 robust inception cohort studies. Acta Psychiatr. Scand. 2009, 119, 252–265. [Google Scholar] [CrossRef] [PubMed]
  140. Lee, G.J.; Lu, P.H.; Hua, X.; Lee, S.; Wu, S.; Nguyen, K.; Teng, E.; Leow, A.D.; Jack, C.R., Jr.; Toga, A.W.; et al. Depressive symptoms in mild cognitive impairment predict greater atrophy in Alzheimer’s disease-related regions. Biol. Psychiatry 2012, 71, 814–821. [Google Scholar] [CrossRef] [PubMed]
  141. Lyketsos, C.G.; Lopez, O.; Jones, B.; Fitzpatrick, A.L.; Breitner, J.; DeKosky, S. Prevalence of neuropsychiatric symptoms in dementia and mild cognitive impairment: Results from the cardiovascular health study. JAMA 2002, 288, 1475–1483. [Google Scholar] [CrossRef] [PubMed]
  142. Chan, W.C.; Lam, L.C.; Tam, C.W.; Lui, V.W.; Leung, G.T.; Lee, A.T.; Chan, S.S.; Fung, A.W.; Chiu, H.F.; Chan, W.M. Neuropsychiatric symptoms are associated with increased risks of progression to dementia: A 2-year prospective study of 321 Chinese older persons with mild cognitive impairment. Age Aging 2011, 40, 30–35. [Google Scholar] [CrossRef] [PubMed]
  143. Gallagher, D.; Coen, R.; Kilroy, D.; Belinski, K.; Bruce, I.; Coakley, D.; Walsh, B.; Cunningham, C.; Lawlor, B.A. Anxiety and behavioural disturbance as markers of prodromal Alzheimer’s disease in patients with mild cognitive impairment. Int. J. Geriatr. Psychiatry 2011, 26, 166–172. [Google Scholar] [CrossRef] [PubMed]
  144. Rozzini, L.; Chilovi, B.V.; Peli, M.; Conti, M.; Rozzini, R.; Trabucchi, M.; Padovani, A. Anxiety symptoms in mild cognitive impairment. Int. J. Geriatr. Psychiatry 2009, 24, 300–305. [Google Scholar] [CrossRef] [PubMed]
  145. World Health Organization. The WHO Special Initiative for Mental Health (2019-2023): Universal Health Coverage for Mental Health. WHO. Available online: https://www.who.int/publications/i/item/special-initiative-for-mental-health-(2019-2023) (accessed on 5 December 2024).
  146. Pitman, A.; Suleman, S.; Hyde, N.; Hodgkiss, A. Depression and anxiety in patients with cancer. BMJ 2018, 361, k1415. [Google Scholar] [CrossRef] [PubMed]
  147. Taquet, M.; Holmes, E.A.; Harrison, P.J. Depression and anxiety disorders during the COVID-19 pandemic: Knowns and unknowns. Lancet 2021, 398, 1665–1666. [Google Scholar] [CrossRef] [PubMed]
  148. Fedotova, J.; Kubatka, P.; Büsselberg, D.; Shleikin, A.G.; Caprnda, M.; Dragasek, J.; Pohanka, M.; Kruzliak, P. Therapeutical strategies for anxiety and anxiety-like disorders using plant-derived natural compounds and plant extracts. Biomed. Pharmacother. 2017, 95, 437–446. [Google Scholar] [CrossRef] [PubMed]
  149. Kenda, M.; Seliškar, A.; Kreft, S.; Janeš, D.; Štrukelj, B.; Bogataj, B.; Ograjšek, A. Medicinal plants used for anxiety, depression, or stress treatment: An update. Molecules 2022, 27, 6021. [Google Scholar] [CrossRef] [PubMed]
  150. Bandelow, B.; Michaelis, S.; Wedekind, D. Treatment of anxiety disorders. Dialogues Clin. Neurosci. 2017, 19, 93–107. [Google Scholar] [CrossRef] [PubMed]
  151. Craske, M.G.; Stein, M.B.; Eley, T.C.; Milad, M.R.; Holmes, A.; Rapee, R.M.; Wittchen, H.-U. Anxiety disorders. Nat. Rev. Dis. Primers 2017, 3, 17024. [Google Scholar] [CrossRef] [PubMed]
  152. File, S.E.; Seth, P. A review of 25 years of the social interaction test. Eur. J. Pharmacol. 2003, 463, 35–53. [Google Scholar] [CrossRef] [PubMed]
  153. La-Vu, M.; Tobias, B.C.; Schuette, P.J.; Adhikari, A. To approach or avoid: An introductory overview of the study of anxiety using rodent assays. Front. Behav. Neurosci. 2020, 14, 145. [Google Scholar] [CrossRef] [PubMed]
  154. Tucker, L.B.; McCabe, J.T. Measuring anxiety-like behaviors in rodent models of traumatic brain injury. Front. Behav. Neurosci. 2021, 15, 682935. [Google Scholar] [CrossRef] [PubMed]
  155. Slattery, D.A.; Cryan, J.F. Using the rat forced swim test to assess antidepressant-like activity in rodents. Nat. Protoc. 2012, 7, 1009–1014. [Google Scholar] [CrossRef] [PubMed]
  156. Melo, F.H.; Venâncio, E.T.; de Sousa, D.P.; de França Fonteles, M.M.; de Vasconcelos, S.M.; Viana, G.S.; Sousa, F.C.F.D. Anxiolytic-like effect of Carvacrol (5-isopropyl-2-methylphenol) in mice: Involvement with GABAergic transmission. Fundam. Clin. Pharmacol. 2010, 24, 437–443. [Google Scholar] [CrossRef] [PubMed]
  157. Costello, H.; Gould, R.L.; Abrol, E.; Howard, R. Systematic review and meta-analysis of the association between peripheral inflammatory cytokines and generalized anxiety disorder. BMJ Open 2019, 9, e027925. [Google Scholar] [CrossRef] [PubMed]
  158. Salim, S. Oxidative stress and the central nervous system. J. Pharmacol. Exp. Ther. 2017, 360, 201–205. [Google Scholar] [CrossRef] [PubMed]
  159. Carnevali, L.; Montano, N.; Tobaldini, E.; Thayer, J.F.; Sgoifo, A. The contagion of social defeat stress: Insights from rodent studies. Neurosci. Biobehav. Rev. 2020, 111, 12–18. [Google Scholar] [CrossRef] [PubMed]
  160. Nadeem, M.; Imran, M.; Gondal, T.A.; Imran, A.; Shahbaz, M.; Amir, R.M.; Sajid, M.W.; Qaisrani, T.B.; Atif, M.; Hussain, G.; et al. Therapeutic potential of Rosmarinic acid: A comprehensive review. Appl. Sci. 2019, 9, 3139. [Google Scholar] [CrossRef]
  161. Luo, C.; Zou, L.; Sun, H.; Peng, J.; Gao, C.; Bao, L.; Ji, R.; Jin, Y.; Sun, S. A review of the anti-inflammatory effects of rosmarinic acid on inflammatory diseases. Front. Pharmacol. 2020, 11, 153. [Google Scholar] [CrossRef] [PubMed]
  162. Malhi, G.S.; Man, J.J. Depression. Lancet 2018, 392, 2299–2312. [Google Scholar] [CrossRef] [PubMed]
  163. Slattery, D.A.; Cryan, J.F. The ups and downs of modelling mood disorders in rodents. ILAR J. 2014, 55, 297–309. [Google Scholar] [CrossRef] [PubMed]
  164. Mirza, F.J.; Amber, S.; Sumera, H.; Hassan, D.; Ahmed, T.; Zahid, S. Rosmarinic acid and ursolic acid alleviate deficits in cognition, synaptic regulation, and adult hippocampal neurogenesis in an Aβ1-42-induced mouse model of Alzheimer’s disease. Phytomedicine 2021, 83, 153490. [Google Scholar] [CrossRef] [PubMed]
  165. Fonteles, A.A.; de Souza, C.M.; de Sousa Neves, J.C.; Menezes, A.P.; do Carmo, M.R.S.; Fernandes, F.D.; de Araújo, P.R.; de Andrade, G.M. Rosmarinic acid prevents against memory deficits in ischemic mice. Behav. Brain Res. 2016, 297, 91–103. [Google Scholar] [CrossRef] [PubMed]
  166. Nie, H.; Peng, Z.; Lao, N.; Wang, H.; Chen, Y.; Fang, Z.; Hou, W.; Gao, F.; Li, X.; Xiong, L.; et al. Rosmarinic acid ameliorates PTSD-like symptoms in a rat model and promotes cell proliferation in the hippocampus. Prog. Neuropsychopharmacol. Biol. Psychiatry 2014, 51, 16–22. [Google Scholar] [CrossRef] [PubMed]
  167. Elhady, M.A.; Khalaf, A.A.A.; Kamel, M.M.; Noshy, P.A. Carvacrol ameliorates behavioral disturbances and DNA damage in the brain of rats exposed to propiconazole. Neurotoxicology 2019, 70, 19–25. [Google Scholar] [CrossRef] [PubMed]
  168. Lee, B.; Yeom, M.; Shim, I.; Lee, H.; Hahm, D.H. Inhibitory effect of carvacrol on lipopolysaccharide-induced memory impairment in rats. Korean J. Physiol. Pharmacol. 2020, 24, 27–37. [Google Scholar] [CrossRef] [PubMed]
  169. Lataliza, A.A.B.; de Assis, P.M.; da Rocha Laurindo, L.; Gonçalves, E.C.D.; Raposo, N.R.B.; Dutra, R.C. Antidepressant-like effect of rosmarinic acid during LPS-induced neuroinflammatory model: The potential role of cannabinoid receptors/PPAR-γ signaling pathway. Phytother. Res. 2021, 35, 6974–6989. [Google Scholar] [CrossRef] [PubMed]
  170. Wang, J.; Wang, S.; Guo, H.; Li, Y.; Jiang, Z.; Gu, T.; Su, B.; Hou, W.; Zhong, H.; Cheng, D.; et al. Rosmarinic acid protects rats against post-stroke depression after transient focal cerebral ischemic injury through enhancing antioxidant response. Brain Res. 2021, 1757, 147336. [Google Scholar] [CrossRef] [PubMed]
  171. Fox, M.E.; Lobo, M.K. The molecular and cellular mechanisms of depression: A focus on reward circuitry. Mol. Psychiatry 2019, 24, 1798–1815. [Google Scholar] [CrossRef] [PubMed]
  172. Kondo, S.; El Omri, A.; Han, J.; Isoda, H. Antidepressant-like effects of rosmarinic acid through mitogen-activated protein kinase phosphatase-1 and brain-derived neurotrophic factor modulation. J. Funct. Foods 2015, 14, 758–766. [Google Scholar] [CrossRef]
  173. Polli, F.S.; Gomes, J.N.; Ferreira, H.S.; Santana, R.C.; Fregoneze, J.B. Inhibition of salt appetite in sodium-depleted rats by carvacrol: Involvement of noradrenergic and serotonergic pathways. Eur. J. Pharmacol. 2019, 854, 119–127. [Google Scholar] [CrossRef] [PubMed]
  174. Noshy, P.A.; Elhady, M.A.; Khalaf, A.A.A.; Kamel, M.M.; Hassanen, E.I. Ameliorative effect of carvacrol against propiconazole-induced neurobehavioral toxicity in rats. Neurotoxicology 2018, 67, 141–149. [Google Scholar] [CrossRef] [PubMed]
  175. Ćetković, G.S.; Čanadanović-Brunet, J.M.; Djilas, S.M.; Tumbas, V.T.; Markov, S.L.; Cvetković, D.D. Antioxidant Potential, Lipid Peroxidation Inhibition and Antimicrobial Activities of Satureja montana L. subsp. kitaibelii Extracts. Int. J. Mol. Sci. 2007, 8, 1013–1027. [Google Scholar] [CrossRef]
  176. Vilmosh, N.; Georgieva-Kotetarova, M.; Kandilarov, I.; Zlatanova-Tenisheva, H.; Murdjeva, M.; Kirina, V.; Dimitrova, S.; Katsarova, M.; Denev, P.; Kostadinova, I. Anti-inflammatory and in vitro antioxidant activities of Satureja montana dry extract. Folia Med. 2024, 66, 114–122. [Google Scholar] [CrossRef] [PubMed]
  177. Šućur, J.; Popović, A.; Petrović, M.; Anačkov, G.T.; Bursic, V.; Kiprovski, B.; Prvulović, D. Alleloppathic effects and insecticidal activity of the aqueous extract of Satureja montana L. J. Serbian Chem. Soc. 2015, 80, 475–484. [Google Scholar] [CrossRef]
  178. Kelsey, N.A.; Wilkins, H.M.; Linseman, D.A. Nutraceutical antioxidants as novel neuroprotective agents. Molecules 2010, 15, 7792–7814. [Google Scholar] [CrossRef] [PubMed]
  179. Gupta, R.C.; Costa, L.G. Chapter 1—Nutraceuticals in Central Nervous System Diseases: Potential Mechanisms of Neuroprotection, 2nd ed.; Gupta, R.C., Lall, R., Srivastava, A., Eds.; Nutraceuticals; Academic Press: Cambridge, MA, USA, 2021; pp. 3–15. ISBN 9780128210383. [Google Scholar] [CrossRef]
  180. Sadeghian, Z.; Bigdeli, M.R.; Moghadam, F.M.; Jahanfar, M.; Samavat, S. Niosome: A Stable Antioxidant Drug Delivery System and Improvement Effect on Neurological Defects in Animal Model of Stroke. BioNanoSci. 2025, 15, 117. [Google Scholar] [CrossRef]
  181. Abbasloo, E.; Khaksari, M.; Sanjari, M.; Kobeissy, F.; Thomas, T.C. Carvacrol decreases blood-brain barrier permeability post-diffuse traumatic brain injury in rats. Sci. Rep. 2023, 13, 14546. [Google Scholar] [CrossRef] [PubMed]
  182. Tadijan, A.; Vlašić, I.; Vlainić, J.; Đikić, D.; Oršolić, N.; Jembrek, M.J. Intracellular Molecular Targets and Signaling Pathways Involved in Antioxidative and Neuroprotective Effects of Cannabinoids in Neurodegenerative Conditions. Antioxidants 2022, 11, 2049. [Google Scholar] [CrossRef] [PubMed]
  183. Tawab, A.M.A.E.; Shahin, N.N.; AbdelMohsen, M.M. Protective effect of Satureja montana extract on cyclophosphamide-induced testicular injury in rats. Chem. Biol. Interact. 2014, 224, 196–205. [Google Scholar] [CrossRef] [PubMed]
  184. Mihajilov-Krstev, T.; Radnović, D.; Kitić, D.; Jovanović, V.S.; Mitić, V.; Stojanović-Radić, Z.; Zlatković, B. Chemical composition, antimicrobial, antioxidative and anticholinesterase activity of Satureja montana L. ssp. montana essential oil. Cent. Eur. J. Biol. 2014, 9, 668–677. [Google Scholar] [CrossRef]
  185. Öztürk, M. Anticholinesterase and antioxidant activities of Savoury (Satureja thymbra L.) with identified major terpenes of the essential oil. Food Chem. 2012, 134, 48–54. [Google Scholar] [CrossRef]
  186. Kiziltas, H. Determination of LC-HRMS profiling, antioxidant activity, cytotoxic effect and enzyme inhibitory properties of Satureja avromanica using in vitro and in silico methods. Process Biochem. 2022, 116, 157–172. [Google Scholar] [CrossRef]
Figure 1. Satureja montana from Jacob Sturm, public domain, via Wikimedia Commons (https://commons.wikimedia.org/wiki/File:Satureja_montana_-_Deutschlands_flora_in_abbildungen_nach_der_natur_-_vol._20_-_t._17.jpg, accessed on 10 July 2025).
Figure 1. Satureja montana from Jacob Sturm, public domain, via Wikimedia Commons (https://commons.wikimedia.org/wiki/File:Satureja_montana_-_Deutschlands_flora_in_abbildungen_nach_der_natur_-_vol._20_-_t._17.jpg, accessed on 10 July 2025).
Cimb 47 00556 g001
Figure 2. The dual role of stress.
Figure 2. The dual role of stress.
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Figure 3. Molecular mechanisms linking stress to mental diseases.
Figure 3. Molecular mechanisms linking stress to mental diseases.
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Figure 4. Summary of the neuroprotective mechanisms of Satureja montana.
Figure 4. Summary of the neuroprotective mechanisms of Satureja montana.
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Table 1. Main phenolic components of Satureja montana extracts.
Table 1. Main phenolic components of Satureja montana extracts.
ComponentClassNotesRef.
Carvacrol Phenolic componentPhenolic monoterpene[68,69]
ThymolPhenolic componentPhenolic monoterpene[26,64,65]
Rosmarinic acidPhenolic componentPhenolic acid[28,29,41]
Caffeic acidPhenolic componentPhenolic acid[26,28,70]
Chlorogenic acidPhenolic componentPhenolic acid[26,28,70]
Ellagic acidPhenolic componentPhenolic acid[26,28,70]
QuercetinFlavonoidFlavonol[41]
Quercetin-3-O-α-L-rhamnopyranosideFlavonoidQuercetin glycoside[41]
Quercetin-7-O-glucopyranosideFlavonoidQuercetin glycoside[41]
Luteolin-7-rhamnoside-4′-O-β-glucopyranosideFlavonoidLuteolin derivative[41]
Luteolin-7-O-glucopyranosideFlavonoidLuteolin derivative[41]
RutinFlavonoidQuercetin glycoside[28]
Table 2. Content and biological properties of major phenolic components of Satureja montana extracts.
Table 2. Content and biological properties of major phenolic components of Satureja montana extracts.
ComponentPercentage/PresenceActivityRef.
Carvacrol44.5–45.7%Antimicrobial, Antioxidant[64,65]
Anxiolytic, Antidepressant[71,72]
p-Cymene12.6–16.9%Antimicrobial[64,65]
γ-Terpinene8.1–8.7%Antioxidant[64,65]
ThymolUp to 81.79%Antimicrobial, Antioxidant[64,65]
Rosmarinic AcidMajor phenolic compoundAntioxidant, Anti-inflammatory[28,29,41,71]
Anxiolytic, Antidepressant[71,72,78]
Caffeic AcidPresentAntioxidant[28,70]
Chlorogenic AcidPresentAntioxidant[28,70]
Ellagic AcidPresentAntioxidant, Anti-inflammatory[28,70]
QuercetinPresentAntioxidant, Antimicrobial[41]
LuteolinPresentAntioxidant[41]
RutinPresentAntioxidant[26,28]
Table 4. Mechanisms of anti-inflammatory activity of Satureja montana.
Table 4. Mechanisms of anti-inflammatory activity of Satureja montana.
MechanismDescriptionRef.
Antioxidant ActivityScavenges free radicals and reduces ROS[42,181]
Cytokine ModulationDecreases pro-inflammatory cytokines (TNF-α, IL-6)[42]
BBB ProtectionReduces brain edema and prevents BBB permeability[181]
MMP-9 InhibitionSuppresses MMP-9 expression, preserving BBB integrity[181]
Signaling PathwaysActivates PI3K/Akt and MAPK pathways for cell survival[182]
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Dragomanova, S.; Tancheva, L.; Abarova, S.; Grigorova, V.B.; Gavazova, V.; Stanciu, D.; Tzonev, S.; Prandjev, V.; Kalfin, R. Protective Potential of Satureja montana-Derived Polyphenols in Stress-Related Central Nervous System Disorders, Including Dementia. Curr. Issues Mol. Biol. 2025, 47, 556. https://doi.org/10.3390/cimb47070556

AMA Style

Dragomanova S, Tancheva L, Abarova S, Grigorova VB, Gavazova V, Stanciu D, Tzonev S, Prandjev V, Kalfin R. Protective Potential of Satureja montana-Derived Polyphenols in Stress-Related Central Nervous System Disorders, Including Dementia. Current Issues in Molecular Biology. 2025; 47(7):556. https://doi.org/10.3390/cimb47070556

Chicago/Turabian Style

Dragomanova, Stela, Lyubka Tancheva, Silviya Abarova, Valya B. Grigorova, Valentina Gavazova, Dana Stanciu, Svetlin Tzonev, Vladimir Prandjev, and Reni Kalfin. 2025. "Protective Potential of Satureja montana-Derived Polyphenols in Stress-Related Central Nervous System Disorders, Including Dementia" Current Issues in Molecular Biology 47, no. 7: 556. https://doi.org/10.3390/cimb47070556

APA Style

Dragomanova, S., Tancheva, L., Abarova, S., Grigorova, V. B., Gavazova, V., Stanciu, D., Tzonev, S., Prandjev, V., & Kalfin, R. (2025). Protective Potential of Satureja montana-Derived Polyphenols in Stress-Related Central Nervous System Disorders, Including Dementia. Current Issues in Molecular Biology, 47(7), 556. https://doi.org/10.3390/cimb47070556

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