Plant-Derived Bioactive Compounds: One Health Perspective
Abstract
1. Introduction
2. Plant-Derived Bioactive Compounds: An Overview
3. Mechanisms of Action of Plant-Derived Bioactive Compounds
3.1. Conserved Molecular and Cellular Pathways
3.2. Structure–Mechanism Relationships in Plant-Derived Bioactive Compounds
3.3. From Molecular Mechanisms to One Health Effects
4. One Health Relevance of Bioactive Compounds
4.1. Plant-Derived Bioactive Compounds and Human Health
4.1.1. Impact of Plant-Derived Bioactive Compounds on Human Health
4.1.2. Cardiovascular and Metabolic Health
4.1.3. Obesity and Low-Grade Inflammation
4.1.4. Cancer Prevention and Cellular Protection
4.1.5. Ageing, Cognitive Function, and Skin Health
4.2. Plant-Derived Bioactive Compounds and Animal Health
4.2.1. Plant-Derived Bioactive Compounds as Alternatives to Antibiotics
4.2.2. Modulation of Gut Health, Microbiota, and Immune Function
4.2.3. Implications for Zoonotic Risk and Antimicrobial Resistance
4.3. Environmental Health and Ecosystem Sustainability
4.3.1. Role of Plant-Derived Bioactive Compounds in Ecological Interactions
4.3.2. Applications in Biopesticides, Biofertilisers, and Sustainable Agriculture
4.3.3. Reduction in Environmental Impact and Contribution to One Health
5. Applicability of Selected Plant-Derived Bioactive Compounds: Evidence-Based Case Examples Within One Health
5.1. Human Health
5.2. Animal Health
5.3. Environmental Health
| Compound | Conformation | Pathway | Experimental Models | Human Health | Animal Health | Environmental Relevance | References |
|---|---|---|---|---|---|---|---|
| Quercetin | Flavonol (C15H10O7) with five hydroxyls at positions 3, 5, 7, 3′, 4′. | Inhibition of IκBα phosphorylation and NF-κB activation. | Humans; Broiler chickens; Swine; Ruminants. | In coronary artery disease, oral supplementation (120 mg/day) reduced circulating IL-1β and TNF-α and downregulated IκBα expression. | In broiler chickens, dietary quercetin supplementation at 200–400 ppm for 35 days increased the European production efficiency factor (EPEF), decreased total coliforms and Clostridium perfringens, increased Lactobacillus counts, and improved antioxidant status, meat quality and overall productive performance. | Reduced need for AGPs; lower drug residues in products and effluents. | [119,120,121,123,128,129,130,131] |
| Resveratrol | Stilbene (3,5,4′-trihydroxystilbene) with two phenolic rings linked by an ethylenic bond. | Activation of SIRT1/AMPK; inhibition of PI3K/Akt/mTOR; modulation of ERK/JNK/p38 and Bcl-2/Bax-dependent apoptosis. | Humans; Broiler chickens; Swine; Ruminants; Fish. | In T2D (1 g/day for 45 days), improved insulin sensitivity and reduced fasting glucose. | In weaned piglets, dietary resveratrol at 300 mg/kg feed for 42 days improved growth, antioxidant status, intestinal morphology and barrier function and lowered inflammatory markers; in growing–finishing pigs, 300–600 mg/kg for 49 days enhanced meat quality and reduced carcass fat; in fish species such as tilapia, turbot and rainbow trout, inclusion of 0.05–0.3% of the diet for 9 weeks increased antioxidant capacity, disease resistance and flesh quality, although the highest doses could attenuate growth. | Substitution for AGPs reduces antibiotic discharge into ecosystems and mitigates AMR spread; lower methane improves environmental footprint. | [102,122,125,132,133,134,135,136] |
| Curcumin | Curcuminoid (diferuloylmethane) with two phenolic rings linked by a conjugated β-diketone chain bearing hydroxyl and methoxy groups. | Modulation of NF-κB, AMPK and COX-2; induction in SOD, CAT, and GPx; inhibition of IκB kinase; regulation of p38/JNK in inflammation and apoptosis. | Humans; Broiler chickens; Swine. | In T2D and ulcerative colitis, oral supplementation (80 mg/day for 3 months) reduced HbA1c, fasting glucose and clinical disease activity. | In poultry, dietary curcumin supplementation at about 0.25–0.5% of the diet for 8 weeks reduced oocyst shedding (Eimeria), improved egg quality, decreased abdominal fat and enhanced immunity and oxidative stability of meat. | Supports replacement of pharmaceutical additives; applicable to biosensors and active packaging, reducing chemical burden in ecosystems. | [60,62,126,127,137,138,139,140,141,142,143] |
| Thymol | Monoterpenoid phenol (2-isopropyl-5-methylphenol) with an isopropyl and a para-hydroxyl group on the aromatic ring. | Modulation of NF-κB and COX-2 signalling. | Humans; Broiler chickens; Swine; Ruminants; Fish. | Antimicrobial against S. aureus, E. coli, Candida spp, anti-inflammatory effect (NF-κB, COX-2), antioxidant, potential in inflammatory disorders and cancer. | ↑ Growth, ↓ Clostridium spp., improved meat/egg quality. ↑Lactobacillus, ↓ E. coli, better digestibility, ↑ survival, immunity, resistance to infections. | Reduced antibiotic residues in manure; ↓ coliforms, ammonia, methane and odour in livestock units. | [58,59,60,63,64,144] |
| Carvacrol | Monoterpenoid phenol, positional isomer of thymol (5-isopropyl-2-methylphenol) with an ortho-hydroxyl group. | Modulation of NF-κB and MAPKs. | Humans; Broiler chickens; Swine; Ruminants; fish. | Anti-inflammatory (↓ TNF-α, IL-6, IL-1β), antimicrobial against Gram± bacteria and Candida biofilms; neuroprotective and metabolically beneficial. In a phase I clinical study, healthy adults supplemented orally with 1–2 mg/kg/day of carvacrol for 30 days showed good safety and tolerability, with only mild laboratory changes remaining within normal reference ranges. | Dietary incorporation of carvacrol resulted in clear zootechnical and health benefits across species. In broilers, 200–500 mg/kg feed for 28–42 days increased growth and feed efficiency and reduced Clostridium perfringens and Salmonella spp; in weaned piglets, 100 mg/kg for 14 days reduced post-weaning diarrhoea; in laying hens, 300 mg/kg for ~50 weeks improved egg quality and antioxidant status; in fish, 1–3 g/kg in feed increased survival. | ↓ Antibiotic reliance; ↓ pathogen shedding in litter and manure; ↓ odour and ammonia emissions; ↓ methane from ruminants; lower environmental pharmaceutical load. | [65,124,145,146] |
| Rosmarinic acid | Polyphenolic ester of caffeic acid and 3,4-dihydroxyphenyllactic acid, with two catechol moieties. | Modulation of NF-κB and MAPKs (ERK, JNK, p38); regulation of PI3K/Akt. | Humans; Broiler chickens; Rodents; Fish. | Anti-inflammatory and antioxidant; neuroprotective (Alzheimer’sParkinson’s); improves glucose metabolism; hepatoprotective and anticancer. In patients with seasonal allergic rhinoconjunctivitis, oral rosmarinic acid at 50 or 200 mg/day for 21 days reduced nasal symptoms and neutrophil/eosinophil infiltration. | In rodent models, oral rosmarinic acid at 1–50 mg/kg/day for 12 days protected kidney, liver, heart and brain from toxic, ischaemic or diabetic injury by reducing oxidative stress, inflammation and apoptosis; in poultry and fish, diets enriched with rosmarinic-acid-rich extracts administered for several weeks improved antioxidant status, immune responses and survival under infectious challenge. | Used in green nanomaterials for pollutant removal; enables partial replacement of synthetic additives and reduces pharmaceutical residues in ecosystems. | [147,148,149] |
6. Challenges and Future Perspectives
7. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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| Class of Plant-Derived Bioactive Compounds | Representative Molecules | Main Mechanisms of Action | References |
|---|---|---|---|
| Polyphenols | Quercetin, resveratrol, catechins, olive oil, and wine polyphenols | Scavenging of reactive oxygen species; modulation of NF-κB, MAPK, and Nrf2 pathways; improvement of endothelial function and mitochondrial activity | [24,25,48,51] |
| Flavonoids | Apigenin, luteolin, hesperidin, anthocyanins | Antioxidant and anti-inflammatory activity; regulation of cytokine production; modulation of immune and metabolic signalling | [49,50,54,59] |
| Phenolic acids | Apigenin, luteolin, hesperidin, anthocyanins | Antioxidant and anti-inflammatory activity; regulation of cytokine production; modulation of immune and metabolic signalling | [49,52,70,71] |
| Terpenoids and essential oil constituents | Caffeic, chlorogenic, and rosmarinic acids | Reduction in oxidative stress and inflammation; modulation of insulin resistance and glucose metabolism | [72,73,74] |
| Carotenoids | Caffeic, chlorogenic, and rosmarinic acids | Reduction in oxidative stress and inflammation; modulation of insulin resistance and glucose metabolism | [75,76,77] |
| Health Domain | Main Bioactive Compounds Involved | Key Biological Mechanisms | Reported Health Outcomes | References |
|---|---|---|---|---|
| Cardiovascular health | Polyphenols, flavonoids | Reduction in oxidative stress; improvement of endothelial function; inhibition of vascular inflammation and platelet aggregation | Lower blood pressure; improved lipid profile; reduced cardiovascular risk | [51,76,82,93,94] |
| Type 2 diabetes and glycaemic control | Polyphenols, phenolic acids, flavonoids | Enhancement of insulin sensitivity; modulation of glucose metabolism; regulation of AGE–RAGE axis; microbiota-mediated effects | Improved glycaemic control and metabolic balance | [52,71,84,95] |
| Obesity and metabolic inflammation | Polyphenols, prebiotic fibres | Regulation of adipogenesis and lipid metabolism; modulation of gut microbiota; increased SCFA production | Reduced low-grade inflammation; support of weight management | [54,60,85,86,87] |
| Cancer prevention | Flavonoids, stilbenes, phenolic acids | Modulation of apoptosis, angiogenesis and inflammatory signalling; antioxidant protection | Chemopreventive effects; improved cellular homeostasis | [88,89,90,96] |
| Ageing, cognitive function and skin health | Polyphenols, carotenoids, anthocyanins | Regulation of oxidative stress, mitochondrial function and autophagy; activation of SIRT1 and AMPK pathways | Slowed functional decline; improved cognitive performance; enhanced skin integrity | [50,77,81,91,92,97,98] |
| Plant-Derived Bioactive Compounds | Animal Model (In Vivo) | Main Observed Effects | Relevance Within the One Health Framework | References |
|---|---|---|---|---|
| Essential oil constituents (thymol, carvacrol, eugenol) | Poultry, swine | Reduced intestinal colonisation by pathogenic bacteria; improved feed conversion ratio; modulation of gut microbiota | Reduced use of antibiotic growth promoters; lower selective pressure for AMR | [67,68] |
| Plant polyphenols (e.g., quercetin, resveratrol) | Poultry, piglets, fish | Improved antioxidant status; enhanced gut integrity; modulation of immune responses | Improved animal resilience reduces therapeutic antibiotic interventions | [68,111] |
| Tannin-rich plant extracts | Ruminants, poultry | Reduced enteric pathogens; improved nitrogen utilisation; modulation of rumen microbiota | Lower environmental contamination and reduced antimicrobial inputs | [68,111] |
| Plant-derived prebiotics (dietary fibres, polysaccharides) | Poultry, swine | Increased beneficial gut bacteria; enhanced short-chain fatty acid production; improved intestinal barrier function | Improved gut health contributes to reduced zoonotic risk | [99,106] |
| Phytogenic blends (plant extracts; essential oils) | Poultry, swine | Improved growth performance; reduced intestinal inflammation; enhanced immune competence | Supports antibiotic-free production systems | [67,69] |
| Plant-derived bioactives combined with probiotics or antimicrobial peptides | Poultry, piglets | Synergistic improvement of gut microbiota stability and immune balance | Integrated strategies reduce AMR dissemination along the food chain | [106,112] |
| Plant-derived bioactives in aquaculture feeds | Fish | Enhanced innate immunity; reduced disease-related mortality; improved redox balance | Reduced antimicrobial use in aquatic environments | [111] |
| Compound/Source | Main Ecological Function | Botanical Biopesticide | One Health Relevance | References |
|---|---|---|---|---|
| Azadirachtin (Azadirachta indica) | Insect growth regulation | Botanical biopesticide | Reduced reliance on synthetic pesticides; protection of non-target species | [69,99,103,111,112,114] |
| Pyrethrins (Chrysanthemum spp.) | Neurotoxic to insect pests | Biopesticide in integrated pest management | Lower environmental persistence and toxicity | [69,103,111,114] |
| Phenolic acids (root exudates) | Plant defence and microbial signalling | Rhizosphere modulation | Enhanced soil microbial balance | [67,68,69,99,103,104,106,107,108,109,110,111,112,115] |
| Humic and fulvic acids | Soil conditioning and nutrient cycling | Biofertilisers and soil amendments | Improved soil health and crop resilience | [69,99,103,104,106,107,108,110,111,112,113,114,115,116,117,118] |
| Seaweed-derived polysaccharides | Biostimulation | Improved root growth and nutrient uptake | Sustainable crop productivity | [114] |
| Aspect | Plant-Derived Bioactive Compounds | Conventional Synthetic Inputs | One Health Implications | References |
|---|---|---|---|---|
| Environmental persistence | Generally biodegradable with shorter environmental half-life | Often persistent and bioaccumulative | Reduced long-term soil and water contamination | [103,116] |
| Ecotoxicity to non-target organisms | Lower toxicity when properly applied; reduced impact on pollinators and aquatic life | High toxicity reported for pollinators, soil fauna and aquatic organisms | Protection of ecosystem services and biodiversity | [103,111] |
| Resistance development | Multitarget modes of action reduce resistance pressure | Single-target mechanisms favour resistance emergence | Lower risk of resistance spread across ecosystems | [112,116] |
| Impact on soil microbiota | Supports microbial diversity and functional resilience | Disrupts soil microbial communities | Enhanced soil health and nutrient cycling | [111,115] |
| Contribution to AMR dissemination | Indirect reduction through lower chemical and antimicrobial pressure | Promotes co-selection of resistance traits | Reduced environmental AMR reservoirs | [108,113,117] |
| Alignment with sustainability frameworks | Compatible with circular economy and integrated pest management | Often incompatible with long-term sustainability goals | Supports One Health and Sustainable Development Goals | [112,116] |
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Gonçalves, A.C.; Pinto, A.R.; Cima, A.; Olo-Fontinha, E.; Martins, J.C.L.; Garcia, J.; Lemos, A.; Saavedra, M.J.; Pintado, M.M.; Alves, M.J. Plant-Derived Bioactive Compounds: One Health Perspective. Appl. Sci. 2026, 16, 327. https://doi.org/10.3390/app16010327
Gonçalves AC, Pinto AR, Cima A, Olo-Fontinha E, Martins JCL, Garcia J, Lemos A, Saavedra MJ, Pintado MM, Alves MJ. Plant-Derived Bioactive Compounds: One Health Perspective. Applied Sciences. 2026; 16(1):327. https://doi.org/10.3390/app16010327
Chicago/Turabian StyleGonçalves, Ana C., Ana R. Pinto, André Cima, Eva Olo-Fontinha, Joana C. L. Martins, Juliana Garcia, André Lemos, Maria José Saavedra, Maria Manuela Pintado, and Maria José Alves. 2026. "Plant-Derived Bioactive Compounds: One Health Perspective" Applied Sciences 16, no. 1: 327. https://doi.org/10.3390/app16010327
APA StyleGonçalves, A. C., Pinto, A. R., Cima, A., Olo-Fontinha, E., Martins, J. C. L., Garcia, J., Lemos, A., Saavedra, M. J., Pintado, M. M., & Alves, M. J. (2026). Plant-Derived Bioactive Compounds: One Health Perspective. Applied Sciences, 16(1), 327. https://doi.org/10.3390/app16010327

