Abstract
Dysbiosis, an imbalance in the gut microbiota, is implicated in a wide array of diseases, including gastrointestinal disorders (e.g., IBD, IBS), metabolic conditions (e.g., obesity, type 2 diabetes), neurological issues (e.g., mood disorders, neurodegeneration), and immune-related ailments (e.g., autoimmune diseases, cancer). This review explores the mechanisms, efficacy, and therapeutic potential of herbal plants in managing dysbiosis, highlighting their advantages over conventional treatments like antibiotics, which often cause prolonged microbial perturbations. The gut microbiota, dominated by Firmicutes and Bacteroidetes, supports digestion, immune regulation, and pathogen defense. Dysbiosis arises from factors such as diet, stress, and medications, leading to reduced microbial diversity, pathogen overgrowth, and impaired barrier function. Herbal plants offer multimodal actions: prebiotic effects (e.g., polysaccharides promoting SCFAs), selective antimicrobial activity (e.g., berberine inhibiting pathogens while sparing commensals), gut barrier enhancement (e.g., curcumin upregulating tight-junction proteins), and immunomodulation (e.g., polyphenols reducing inflammation). Specific herbs like Panax ginseng, Allium sativum, Zingiber officinale, and others demonstrate anti-dysbiotic properties in preclinical and clinical studies, improving microbiota profiles and symptoms in conditions like IBS and colitis. Polyherbal formulations, such as Triphala (Ayurveda) and Gegen Qinlian Decoction (TCM), leverage synergies for enhanced efficacy, reduced resistance, and dose-sparing. However, challenges include safety risks (e.g., herb-drug interactions, toxicity), standardization issues, and regulatory inconsistencies. Current evidence from in vitro, animal, and early human trials shows promise, but gaps in large-scale RCTs and microbiome standardization persist. Future directions emphasize integration into functional foods, personalized therapies, and rigorous research for evidence-based use in gut health management.
Keywords
Dysbiosis, Gut microbiota, Herbal plants, Prebiotic effects, antimicrobial selectivity, Polyherbal formulations, Safety challenges, Therapeutic potential
Introduction
Over the past ten years, there has been a significant increase in the interest in human microbiota, particularly in gut microbiota. Even if there are many studies showing that changes in the microbiota makeup are linked to a variety of illnesses, the notion of a "healthy gut microbiota" is still ambiguous [1]. One of the largest interfaces (250–400 mm) between the host, environmental variables, and antigens in the human body is represented by the human gastrointestinal (GI) tract [2]. The term Gut Microbiota refers to all microbes that reside in the digestive system, including viruses, archaea, protists, fungi, and bacteria. Among the many advantages that the microbiota provides to the host are metabolism of nutrients and digestion, synthesis of vitamins, control of the immune system, defense against pathogens, maintenance of gut health and integrity, and metabolic functions. Cancer and chronic illnesses, weight and metabolism, brain and mental health, and systemic health [3]. The over 100 bacterial phyla that have been identified are the subject of this study. The adult human gut microbiota is primarily composed of the Bacteroidetes and Firmicutes phyla, with lesser amounts of Proteobacteria, Verrucomicrobia, Actinobacteria, Fusobacteria, and Cyanobacteria [1]. Dysbiosis is a sign of an unbalanced microbial ecosystem in which the "good" bacteria are unable to effectively control the "bad" ones, and a list of related illnesses. These illnesses are often complicated in terms of both pathogenesis and consequences, and the intestinal microbiota increases daily. The Dysbiosis of Gut Microbiota (DOGMA) was recently discovered to be responsible for all three aspects of the syndrome, which includes hyper-androgenism (acne, hirsutism), anovulation/menstrual irregularity, and hyper-androgenism. the formation of several tiny cysts in the ovaries [4]. It is known that a change in the gut microbiota away from a healthy or normal state (i.e., eubiosis) causes disruption. Dysbiosis [5] is a term for it. Its clinical significance is due to its connection to a wide variety of illnesses and its impact on the course of health and disease. The human microbiome, sometimes known as a "virtual organ," is essential to preserving general health by assisting with digestion, vitamin production, and modulation. Dysbiosis is caused by a variety of factors, including genetic abnormalities, stress, diet, alcohol intake, and infection [3]. The immune system is responsible for defending the body against pathogens. and drugs, among other things [6]. The effects of antimicrobials on dysbiosis have been discussed in a number of studies, and the length of time that microbiota disturbances last seems to vary between antimicrobials for, Some medications (e.g., tetracyclines, macrolides, and sulfonamides) have a shorter disturbance duration [7], while others last for months (e.g., cephalosporins) or years (e.g., fluoroquinolones, clindamycin). Dysbiosis upsets the equilibrium between beneficial and harmful gut bacteria, which can result in neurological, metabolic, and gastrointestinal problems. The direct effects of dysbiosis are on gut health because the microbiota is crucial for digestion, barrier integrity, and immune regulation [8]. Dysbiosis has a direct impact on gut health because the microbiota is essential for these processes. for immunity regulation, barrier integrity, and digestion. The gut microbiota communicates with the brain via neural, immune, and metabolic pathways [9]. The usual course of action for treating dysbiosis is to use conventional methods. although it includes antibiotics, probiotics, and dietary changes, these are severely constrained in comparison to the possible applications of medicinal herbs [10]. Medicinal herbs have demonstrated maybe because of its potential to change the gut flora by encouraging beneficial bacteria (a prebiotic effect). Giving phytochemicals and polyphenols that block pathogens without killing beneficial microbes. Anti-inflammatory and boosting the gut barrier function and providing antioxidant effects. Examples:
1) Berberine (from Berberis spp.) - has gut-modulating and antibacterial effects.
2) Curcumin (from turmeric) – promotes microbiome diversity and has anti-inflammatory properties.
3) Polyphenols in green tea encourage the growth of Bifidobacterium and Lactobacillus [11].
2. Gut Microbiota and Dysbiosis
The gut microbiota, also known as the gut flora or gut microbiome, is a complicated and ever-changing community made up of trillions of microorganisms. that are mainly found in the gastrointestinal (GI) system. Viruses (which make up more than 99% of the microbes), archaea, fungi, bacteria (which predominate), and viruses are all members of this community. protozoa, and bacteriophages) are examples of the microbiota. Its disturbance (dysbiosis) is associated with illnesses such as, and it interacts symbiotically with the host, affecting overall health. Inflammatory bowel illness, diabetes, obesity, and even neurological disorders. The microbiota is formed at birth and changes with time, becoming adult-like by the age of around Age 2–3. It has a high degree of functional redundancy, which means that various microbial communities can carry out similar functions, but individual profiles are unique and frequently vary more between individuals. than over time in a single individual [12, 13] Gut microbiota: The gut has the most diverse and concentrated microbiota, which is made up of bacteria that are mostly from the Firmicutes, Bacteroidetes, actinobacteria, and proteobacteria phyla. For immunological control, metabolism, and digestion, this society is crucial. Age, health, and diet all have an impact on the composition, which varies significantly from one individual to the next (Table no. 1 provides all the information).
Dysbiosis
Significant human illnesses, such as inflammatory bowel disease, obesity, allergies, and autoimmune and auto inflammatory diseases, have been associated with dysbiosis. All three elements of the syndrome of hyper-androgenism (acne, hirsutism), anovulation/ menstrual irregularity, and the Dysbiosis of Gut Microbiota (DOGMA) have been shown to be caused by it. the formation of several little cysts on the ovaries [4]. Lifestyle also appears to have a significant impact, and even patients with type 2 diabetes showed a moderate amount of gut microbial dysbiosis. The diet in Western nations, which is characterized by increased intake of red meat, animal fat, and excessive sugar, is a contributing factor to the chronic illnesses that affect over 50% of the adult population. Furthermore, foods low in fiber might be crucial in influencing the microbiota of the human gut. Additionally, studies have indicated that the Western diet causes dysbiosis and promotes endotoxemia, probably as a result of intestinal permeability and barrier function degradation [14, 15].
Dysbiosis mechanism
The intricate link between gut microbiota dysbiosis and the onset of cardiovascular illnesses (CVDs) is demonstrated by the dysbiosis mechanism. Negative effects of dysbiosis include elevated vascular inflammation, gut barrier dysfunction, and systemic inflammation brought about by decreased microbial diversity and an increase in pro-inflammatory bacteria. Changes in important microbial metabolites, such as increased trimethylamine-N-oxide (TMAO) and decreased short-chain fatty acids (SCFAs), which are both heavily linked to cardiovascular pathophysiology, mediate these conditions. Through processes like endothelial malfunction, plaque development, and disease progression, such imbalances increase the risk of cardiovascular diseases, which are manifested as heart failure, hypertension, myocardial infarction, and atherosclerosis. Importantly, the therapeutic potential of natural compounds, including flavonoids, omega-3 fatty acids, resveratrol, curcumin, and marine-derived bioactive, which can help in targeting gut dysbiosis by restoring microbiota balance and enhancing therapeutic efficacy. Thus, modulating gut microbiota through natural bioactive emerges as a promising strategy for reducing cardiovascular disease burden [16].
Table 1. The major bacterial phyla, their approximate proportions in healthy adults, key genera, and example species
|
Phylum (Alternative Name)
|
Approximate Proportion
|
Key General
|
Example Species
|
Notes
|
|
1) Firmicutes (Bacillota)
|
40-60%
|
Clostridium, Faecalibacterium, Ruminococcus, Eubacterium, Lactobacillus, Pepto coccus, Pepto streptococcus
|
Faecalibacterium parasitize (most common in adults), Ruminococcus bromic (resistant starch degrader), Clostridium sporogeneses (tryptophan metabolizer), Lactobacillus plantarum
|
Dominant in fermentation; increases in elderly; anti-inflammatory roles.
|
|
2) Bacteroidetes (Bacteroidota)
|
30-50%
|
Bacteroides, Prevotella
|
Bacteroides thetaiotaomicron (polysaccharide degrader), Bacteroides fragilis
|
Major in colon; aids fiber digestion; higher in high-fiber diets (e.g., rural African populations).
|
|
3) Actinobacteria (Actinomycetal)
|
5-10%
|
Bifidobacterium
|
Bifidobacterium adolescent’s, Bifidobacterium longum
|
Vitamin producers (e.g., folate, B12); higher in breast-fed infants.
|
|
4) Actinobacteria (Actinomycetal)
|
1-5%
|
Escherichia
|
Escherichia coli
|
Includes some facultative anaerobes; can increase in dysbiosis.
|
|
5) Verrucomicrobia
|
<1%
|
Ackerman Nia
|
Akarnania municipia
|
Mucin degrader; linked to metabolic health and reduced inflammation.
|
Types of Dysbiosis
Dysbiosis refers to an imbalance in the microbial communities (microbiome) within the body, most commonly in the gut but also in other areas like the skin, mouth, or vagina.
1. Loss of Beneficial Microorganisms (Type 1 Dysbiosis)
This involves a reduction or depletion of keystone microbial species that play protective, anti-inflammatory, or supportive roles in maintaining ecosystem balance. Beneficial bacteria, such as certain strains of Bifidobacterium or Lactobacillus, help ferment dietary fibers into short-chain fatty acids (SCFAs) like butyrate, which nourish gut cells and regulate immune responses. This can lead to impaired barrier function (e.g., "leaky gut") and increased susceptibility to infections or autoimmune conditions [17].
2. Expansion of Potentially Harmful Microorganisms (Type 2 Dysbiosis)
there is an overgrowth or dominance of pathobionts—microbes that are normally present in low numbers but become harmful when they expand excessively. Examples include opportunistic pathogens like Clostridium difficile, Escherichia coli variants, or fungi such as Candida [18].
3. Loss of Microbial Diversity (Type 3 Dysbiosis)
This category describes a general reduction in the overall richness and evenness of the microbiome, leading to a less resilient ecosystem. Healthy microbiomes typically feature high alpha-diversity (variety within a single site), which provides functional redundancy and stability against perturbations. Causes include long-term antibiotic exposure, high-fat/low-fiber diets, or aging. loss of beneficial microbes may pave the way for pathobiont expansion. Dysbiosis can also be site-specific, such as oral dysbiosis (linked to periodontal disease) or vaginal dysbiosis (associated with bacterial vaginosis [19].
Reference
- Sekirov, I.; Russell, S.L.; Antunes, L.C.; Finlay, B.B. Gut microbiota in health and disease. Physiol. Rev. 2010, 90, 859–904.
- BEng mark, S. (1998) Ecological control of the gastrointestinal tract. The role of probiotic flora. Gut 42, 2–7 doi:10.1136/gut.42.1.2
- Baumler, A.J. and Sperandio, V. (2016) Interactions between the microbiota and pathogenic bacteria in the gut. Nature 535, 85–93 doi:10.1038/nature18849
- Tremellen, K.; Pearce, K. Dysbiosis of Gut Microbiota (DOGMA)—A novel theory for the development of polycystic ovarian syndrome. Med. Hypotheses 2012, 79, 104–112.
- Thursby E, Juge N. Introduction to the human gut microbiota. Biochem J. 2017;474(11):1823-1836. doi:10.1042/bcj20160510
- Lawley TD, Walker AW. Intestinal colonization resistance. Immunology. 2013;138(1):1-11. doi:10.1111/j.1365-2567.2012. 03616.x
- Zimmermann P, Curtis N. The effect of antibiotics on the composition of the intestinal microbiota – a systematic review. J Infect. 2019;79(6):471-489. doi: 10.1016/j.jinf.2019.10.008
- https://en.m.wikipedia.org/wiki/Dysbiosis?utm_source=chatgpt.com
- Kasar GN, Rasal PB, Upaganlawar AB, Pagar DS, Surana KR, Mahajan SK, Sonawane DD. Navigating dysbiosis: Insights into gut microbiota disruption and health outcomes, Community Acquir Infect. 2025;12. doi:10.54844/cai.2024.0778
- Sun, S., et al. (2020). Herbal medicine and gut microbiota: interactions and implications for health. Pharmacological Research, 158, 104894.
- Zhang, X., et al. (2019). Berberine promotes gut microbiota homeostasis and improves intestinal barrier function in diabetic rats. American Journal of Translational Research, 11(7), 4050–4060.
- https://en.wikipedia.org/wiki/Gut_microbiota
- https://www.bmj.com/content/361/bmj.k2179
- Huang, E.Y.; Devkota, S.; Moscoso, D.; Chang, E.B.; Leone, V.A. The role of diet in triggering human inflammatory disorders in the modern age. Microbes Infect. 2013, 15, 765–774.
- Pendyala, S.; Walker, J.M.; Holt, P.R. A high-fat diet is associated with endotoxemia that originates from the gut. Gastroenterology 2012, 142, 1100–1101.
- Wang, Z., & Zhao, Y. (2018). Gut microbiota derived metabolites in cardiovascular health and disease. Protein & Cell, 9(5), 416–431. https://doi.org/10.1007/s13238-018-0549-0
- DeGruttola, A. K., Low, D., Mizoguchi, A., & Mizoguchi, E. (2016). Current Understanding of Dysbiosis in Disease in Human and Animal Models. Inflammatory Bowel Diseases, 22(5), 1137–1150. doi:10.1097/MIB.0000000000000750
- Levy, M., Kolodziejczyk, A. A., Thaiss, C. A., & Elinav, E. (2017). Dysbiosis and the immune system. Nature Reviews Immunology, 17(4), 219–232. doi:10.1038/nri.2017.7
- Mosca, A., Leclerc, M., & Hugot, J. P. (2016). Gut Microbiota Diversity and Human Diseases: Should We Reintroduce Key Predators in Our Ecosystem? Frontiers in Microbiology, 7, 455. doi:10.3389/fmicb.2016.00455
- DeGruttola, A. K., Low, D., Mizoguchi, A., & Mizoguchi, E. (2016). Current Understanding of Dysbiosis in Disease in Human and Animal Models. Inflammatory Bowel Diseases, 22(5), 1137–1150. doi:10.1097/MIB.0000000000000750
- Cani, P. D., Amar, J., Iglesias, M. A., Poggi, M., Knauf, C., Bastelica, D., ... & Burcelin, R. (2007). Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes, 56(7), 1761–1772. doi:10.2337/db06-1491
- Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., ... & Dinan, T. G. (2019). The Microbiota-Gut-Brain Axis. Physiological Reviews, 99(4), 1877–2013. doi:10.1152/physrev.00018.2018
- Levy, M., Kolodziejczyk, A. A., Thaiss, C. A., & Elinav, E. (2017). Dysbiosis and the immune system. Nature Reviews Immunology, 17(4), 219–232. doi:10.1038/nri.2017.7
- Peterson, C. T., Vaughn, A. R., Sharma, V., Chopra, D., & Mills, P. J. (2018). Effects of Turmeric and Curcumin on the Gut Microbiota and Host Physiology: A Review of Mechanisms and Clinical Implications. Frontiers in Nutrition, 5, 116. doi:10.3389/fnut.2018.00116
- Corrêa, T. A. F., Rogero, M. M., Hassimotto, N. M. A., & Lajolo, F. M. (2019). The two-way polyphenols-microbiota interactions and their effects on obesity and related metabolic diseases. Frontiers in Nutrition, 6, 188. doi:10.3389/fnut.2019.00188
- Catalkaya, G., Venema, K., Lucini, L., Rocchetti, G., Cappelli, G., & Capanoglu, E. (2020). Interaction of dietary polyphenols with gut microbiota and their impact on host health. Current Opinion in Food Science, 32, 149–156. doi: 10.1016/j.cofs.2020.08.006
- Slavin, J. (2013). Fiber and prebiotics: Mechanisms and health benefits. Nutrients, 5(4), 1417–1435. doi:10.3390/nu5041417
- Zhang, Y., Gu, Y., Ren, H., Wang, S., Zhong, H., Zhao, X., ... & Zhang, X. (2020). Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study). Nature Communications, 11(1), 5015. doi:10.1038/s41467-020-18414-8
- Wang, J., Ghosh, S. S., & Ghosh, S. (2017). Curcumin improves intestinal barrier function: Modulation of tight junction proteins and associated signaling pathways. Frontiers in Physiology, 8, 234. doi:10.3389/fphys.2017.00234
- Shapiro, H., Singer, P., Halpern, Z., & Bruck, R. (2007). Polyphenols in the treatment of inflammatory bowel disease and acute pancreatitis. Gut, 56(3), 426–435. doi:10.1136/gut.2006.094599
- Wu, H. J., & Wu, E. (2012). The role of gut microbiota in immune homeostasis and autoimmunity. Gut Microbes, 3(1), 4–14. doi:10.4161/gmic.19320
- Kim, J. H., & Yi, Y. S. (2020). Ginsenosides: Potential therapeutic agents for gastrointestinal diseases. Journal of Ginseng Research, 44(4), 562–572. https://doi.org/10.1016/j.jgr.2019.11.002
- Cortés-Rojas, D. F., de Souza, C. R. F., & Oliveira, W. P. (2014). Clove (Syzygium aromaticum): A precious spice. Asian Pacific Journal of Tropical Biomedicine, 4(2), 90–96. https://doi.org/10.1016/S2221-1691(14)60215-X
- Batiha, G. E.-S., et al. (2020). Syzygium aromaticum L. (Clove) essential oil and its active compound, eugenol, exhibit potent antihyperglycemic and antihyperlipidemic activities in diabetic rats. Journal of Traditional and Complementary Medicine, 11(2), 117–124. https://doi.org/10.1016/j.jtcme.2020.03.001
- Bayati, M., & Lotfi, A. (2020). Garlic (Allium sativum): A review of its potential use as an antimicrobial and prebiotic agent in gastrointestinal disorders. Journal of Herbal Medicine, 22, 100346. https://doi.org/10.1016/j.hermed.2020.100346
- Pérez-Rubio, M., et al. (2017). Garlic (Allium sativum) and its antimicrobial activity in food preservation and gut health. Food Chemistry, 235, 247–255. https://doi.org/10.1016/j.foodchem.2017.05.057
- Kumar, N. V., & Srinivasa, H. (2021). Ginger (Zingiber officinale): A potential therapeutic agent for gastrointestinal disorders. Phytotherapy Research, 35(5), 2412–2423. https://doi.org/10.1002/ptr.6982
- Bode, A. M., & Dong, Z. (2011). The amazing and mighty ginger. In: Benzie, I. F. F., & Wachtel-Galor, S. (Eds.), Herbal Medicine: Biomolecular and Clinical Aspects (2nd ed.). CRC Press/Taylor & Francis. https://www.ncbi.nlm.nih.gov/books/NBK92775/
- Cernáková, M., & Kostálová, D. (2002). Antimicrobial activity of berberine—A constituent of Hydrastis canadensis L. Folia Microbiologica, 47(4), 375–378. https://doi.org/10.1007/BF02818693
- Badgujar, S. B., Patel, V. V., & Bandivdekar, A. H. (2014). Foeniculum vulgare Mill: A review of its botany, phytochemistry, pharmacology, and contemporary applications. BioMed Research International, 2014, 842674. https://doi.org/10.1155/2014/842674
- Portincasa, P., et al. (2016). Curcumin and fennel essential oil improve symptoms and quality of life in patients with irritable bowel syndrome. Journal of Gastrointestinal and Liver Diseases, 25(2), 151–157. https://doi.org/10.15403/jgld.2014.1121.252.ccm
- Manohar, V., et al. (2001). Antifungal activities of origanum oil against Candida albicans. Molecular and Cellular Biochemistry, 228(1-2), 111–117. https://doi.org/10.1023/A:1013311632207
- Chedid, V., et al. (2014). Herbal therapy is equivalent to rifaximin for the treatment of small intestinal bacterial overgrowth. Global Advances in Health and Medicine, 3(3), 16–24. https://doi.org/10.7453/gahmj.2014.019
- Force, M., Sparks, W. S., & Ronzio, R. A. (2000). Inhibition of enteric parasites by emulsified oil of oregano in vivo. Phytotherapy Research, 14(3), 213–214. https://doi.org/10.1002/(SICI)1099-1573(200005)14:33.0.CO;2-U
- Chumpitazi, B. P., Kearns, G. L., & Shulman, R. J. (2018). "Review article: The physiologic effects and safety of peppermint oil and its efficacy in irritable bowel syndrome and other functional disorders." Alimentary Pharmacology & Therapeutics, 47(6), 738–752. https://doi.org/10.1111/apt.14519
- Khanna, R., MacDonald, J. K., & Levesque, B. G. (2014). "Peppermint oil for the treatment of irritable bowel syndrome: A systematic review and meta-analysis." Journal of Clinical Gastroenterology, 48(6), 505–512. https://doi.org/10.1097/MCG.0b013e3182a88357
- Prajapati, R. P., Kalaria, M. V., & Karkar, B. (2020). "Therapeutic potential of fenugreek in the management of gastrointestinal disorders: A review." Journal of Ethnopharmacology, 262, 113098. https://doi.org/10.1016/j.jep.2020.113098
- Chevli, P., Goyal, A., & Jialal, I. (2023). "Fenugreek in the management of irritable bowel syndrome: A systematic review and meta-analysis." Phytotherapy Research, 37(2), 456–465. https://doi.org/10.1002/ptr.7634
- Hong, S. W., Chun, J., Park, S., Lee, H. J., Im, J. P., & Kim, J. S. (2018). "Aloe vera is effective and safe in short-term treatment of irritable bowel syndrome: A systematic review and meta-analysis." Journal of Neurogastroenterology and Motility, 24(4), 528–535. https://doi.org/10.5056/jnm18077
- Langmead, L., Feakins, R. M., Goldthorpe, S., Holt, H., Tsironi, E., De Silva, A., ... & Rampton, D. S. (2004). "Randomized, double-blind, placebo-controlled trial of oral aloe vera gel for active ulcerative colitis." Alimentary Pharmacology & Therapeutics, 19(7), 739–747. https://doi.org/10.1111/j.1365-2036.2004.01902.x
- Werawatganon, D., & Rakananurak, N. (2019). "Aloe vera attenuated gastric injury on indomethacin-induced gastropathy in rats." Evidence-Based Complementary and Alternative Medicine, 2019, 7690768. https://doi.org/10.1155/2019/7690768
- Subramaniyan, V., & Chakravarthi, S. (2019). "Polyherbal Formulation Concept for Synergic Action: A Review." Journal of Drug Delivery and Therapeutics, 9(1-s), 548–552. https://doi.org/10.22270/jddt.v9i1-s.2339
- Zhang, R., Zhu, X., Li, X., & Li, S. (2015). "Network pharmacology databases for traditional Chinese medicine: Review and assessment." Frontiers in Pharmacology, 10, 123. https://doi.org/10.3389/fphar.2019.00123
- Atal, C. K., Dubey, S. K., & Singh, J. (1985). "Biochemical basis of enhanced drug bioavailability by piperine: Evidence that piperine is a potent inhibitor of drug metabolism." Journal of Pharmacology and Experimental Therapeutics, 232(1), 258–262. https://pubmed.ncbi.nlm.nih.gov/3964179/
- Peterson, C. T., Denniston, K., & Chopra, D. (2017). "Therapeutic uses of Triphala in Ayurvedic medicine." Journal of Alternative and Complementary Medicine, 23(8), 607–614. https://doi.org/10.1089/acm.2017.0083
- Xu, J., Chen, H. B., & Li, S. L. (2017). "Understanding the molecular mechanisms of the interplay between herbal medicines and gut microbiota." Medicinal Research Reviews, 37(5), 1140–1185. https://doi.org/10.1002/med.21431
- Li, S., & Zhang, B. (2013). "Traditional Chinese medicine network pharmacology: Theory, methodology and application." Chinese Journal of Natural Medicines, 11(2), 110–120. https://doi.org/10.1016/S1875-5364(13)60037-0
- Parasuraman, S., Thing, G. S., & Dhanaraj, S. A. (2014). "Polyherbal formulation: Concept of Ayurveda." Pharmacognosy Reviews, 8(16), 73–80. https://doi.org/10.4103/0973-7847.134229
- Ayush, A., & Chattopadhyay, I. (2019). "Synergistic interactions of phytochemicals with antimicrobial agents: Potential strategy to counteract drug resistance." Chemico-Biological Interactions, 308, 294–303. https://doi.org/10.1016/j.cbi.2019.05.050
- Stermitz, F. R., Lorenz, P., Tawara, J. N., Zenewicz, L. A., & Lewis, K. (2000). "Synergy in a medicinal plant: Antimicrobial action of berberine potentiated by 5′-methoxyhydnocarpin, a multidrug pump inhibitor." Proceedings of the National Academy of Sciences, 97(4), 1433–1437. https://doi.org/10.1073/pnas.97.4.1433
- Seukep, J. A., Kuiate, J. R., & Yimdjo, M. C. (2020). "Efflux pump inhibitors from natural origins as potential therapeutics for multidrug-resistant bacterial infections." Frontiers in Microbiology, 11, 593070. https://doi.org/10.3389/fmicb.2020.593070
- Atal, C. K., Dubey, S. K., & Singh, J. (1985). "Biochemical basis of enhanced drug bioavailability by piperine: Evidence that piperine is a potent inhibitor of drug metabolism." Journal of Pharmacology and Experimental Therapeutics, 232(1), 258–262. https://pubmed.ncbi.nlm.nih.gov/3964179/
- Subramanian, U., Poongavana, S., & Vanisree, A. J. (2016). "Polyherbal formulations for antimicrobial therapy: A review." International Journal of Pharma and Bio Sciences, 7(4), 659–666. https://doi.org/10.22376/ijpbs.2016.7.4.b659-666
- World Health Organization (WHO). (2004). WHO guidelines on safety monitoring of herbal medicines in pharmacovigilance systems. https://www.who.int/publications/i/item/9241592214
- Fu, P. P., Xia, Q., Guo, L., Yu, H., & Chan, P. C. (2004). Toxicity of pyrrolizidine alkaloids—a short review. Chemical Research in Toxicology, 17(9), 1131–1141. https://doi.org/10.1021/tx049941r
- Saper, R. B., Phillips, R. S., Sehgal, A., Khouri, N., Davis, R. B., Paquin, J., ... & Kales, S. N. (2008). Lead, mercury, and arsenic in US- and Indian-manufactured Ayurvedic medicines sold via the Internet. JAMA, 300(8), 915–923. https://doi.org/10.1001/jama.300.8.915
- Ernst, E. (2002). Adulteration of Chinese herbal medicines with synthetic drugs: A systematic review. Journal of Internal Medicine, 252(2), 107–113. https://doi.org/10.1046/j.1365-2796.2002.00999.x
- Chalasani, N. P., Maddur, H., Russo, M. W., Hoofnagle, J. H., & Szabo, G. (2021). ACG Clinical Guideline: Diagnosis and management of idiosyncratic drug-induced liver injury. American Journal of Gastroenterology, 116(5), 878–898. https://doi.org/10.14309/ajg.0000000000001259
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). (2020). Green Tea. In LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. https://www.ncbi.nlm.nih.gov/books/NBK547925/
- National Center for Complementary and Integrative Health (NCCIH). (2020). Herbs at a Glance: St. John’s Wort. https://www.nccih.nih.gov/health/st-johns-wort
- Asher, G. N., Corbett, A. H., & Hawke, R. L. (2017). "Common herbal dietary supplement–drug interactions." American Family Physician, 96(2), 101–107. https://www.aafp.org/afp/2017/0715/afp20170715p101.pdf
- Borrelli, F., Capasso, R., & Izzo, A. A. (2007). "Garlic (Allium sativum L.): Adverse effects and drug interactions in humans." Molecular Nutrition & Food Research, 51(11), 1386–1397. https://doi.org/10.1002/mnfr.200700072
- Ang-Lee, M. K., Moss, J., & Yuan, C. S. (2001). "Herbal medicines and perioperative care." JAMA, 286(2), 208–216. https://doi.org/10.1001/jama.286.2.208
- Zhang, W., Tan, T. M. C., & Lim, L. Y. (2007). "Impact of curcumin-induced changes in P-glycoprotein and CYP3A expression on the pharmacokinetics of peroral celiprolol and midazolam in rats." Drug Metabolism and Disposition, 35(1), 110–115. https://doi.org/10.1124/dmd.106.011072
- Appiah-Opong, R., Commandeur, J. N. M., van Vugt-Lussenburg, B., & Vermeulen, N. P. E. (2007). "Inhibition of human recombinant cytochrome P450s and ABC transporters by curcumin." Xenobiotica, 37(5), 548–560. https://doi.org/10.1080/00498250701339166
- Bhardwaj, R. K., Glaeser, H., Becquemont, L., Klotz, U., Gupta, S. K., & Fromm, M. F. (2002). "Piperine, a major constituent of black pepper, inhibits human P-glycoprotein and CYP3A4." Journal of Pharmacology and Experimental Therapeutics, 302(2), 645–650. https://doi.org/10.1124/jpet.102.034412
- World Health Organization (WHO). (2003). WHO Guidelines on Good Agricultural and Collection Practices (GACP) for Medicinal Plants. https://www.who.int/publications/i/item/9241546271
- European Medicines Agency (EMA), Committee on Herbal Medicinal Products (HMPC). (2011). Guideline on quality of herbal medicinal products/traditional herbal medicinal products. https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-quality-herbal-medicinal-products-traditional-herbal-medicinal-products-revision-1_en.pdf
- Newmaster, S. G., Grguric, M., Shanmughanandhan, D., Ramalingam, S., & Ragupathy, S. (2013). "DNA barcoding detects contamination and substitution in North American herbal products." BMC Medicine, 11, 222. https://doi.org/10.1186/1741-7015-11-222 (Note: This study was later retracted; see retraction notice in BMC Medicine, 2017, 15, 204, https://doi.org/10.1186/s12916-017-0969-5).
- Parveen, I., Gafner, S., Techen, N., Murch, S. J., & Khan, I. A. (2016). "DNA barcoding for the identification of botanicals in herbal medicine and dietary supplements: Strengths and limitations." Planta Medica, 82(14), 1225–1235. https://doi.org/10.1055/s-0042-111208
- United States Pharmacopeia (USP). (2023). Herbal Medicines Compendium. https://hmc.usp.org/
- Govindaraghavan, S., & Sucher, N. J. (2015). "Quality assessment of medicinal herbs and their extracts: Criteria and prerequisites for consistent safety and efficacy." Epilepsy & Behavior, 52(Pt B), 363–371. https://doi.org/10.1016/j.yebeh.2015.08.039
- U.S. Food and Drug Administration (FDA). (2019). Dietary Supplements: New Dietary Ingredient Notifications and Related Issues: Guidance for Industry. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/dietary-supplements-new-dietary-ingredient-notifications-and-related-issues-guidance-industry
- Wu, C., & Schiff, P. L. (2017). "Regulatory oversight of herbal medicines in the United States: A review." Journal of Dietary Supplements, 14(5), 566–578. https://doi.org/10.1080/19390211.2016.1267063
- European Medicines Agency (EMA), Committee on Herbal Medicinal Products (HMPC). (2022). Guideline on quality of herbal medicinal products/traditional herbal medicinal products (Revision 3). https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-quality-herbal-medicinal-products-traditional-herbal-medicinal-products-revision-3_en.pdf
- Pescetti, G., & Vettor, S. (2015). "Regulation of herbal medicines in the European Union: An overview." Fitoterapia, 104, 83–89. https://doi.org/10.1016/j.fitote.2015.06.014
- Jordan, S. A., Cunningham, D. G., & Marles, R. J. (2010). "Assessment of herbal medicinal products: Challenges, and opportunities to increase the knowledge base for safety assessment." Toxicology and Applied Pharmacology, 243(2), 198–216. https://doi.org/10.1016/j.taap.2009.12.005
- Shaw, D., Graeme, L., Pierre, S., Elizabeth, W., & Kelvin, C. (2012). "Pharmacovigilance of herbal medicine." Journal of Ethnopharmacology, 140(3), 513–518. https://doi.org/10.1016/j.jep.2012.01.051
- Gagnier, J. J., Boon, H., Rochon, P., Moher, D., Barnes, J., & Bombardier, C. (2006). "Recommendations for reporting randomized controlled trials of herbal interventions: Explanation and elaboration." Journal of Clinical Epidemiology, 59(11), 1134–1149. https://doi.org/10.1016/j.jclinepi.2005.12.020
- Peterson, C. T., Vaughn, A. R., Sharma, V., Chopra, D., & Mills, P. J. (2018). "Effects of turmeric and curcumin on the gut microbiota: A review of preclinical studies." BioMed Research International, 2018, 3797523. https://doi.org/10.1155/2018/3797523
- Feng, W., Ao, H., Peng, C., & Yan, D. (2019). "Gut microbiota, a new frontier to understand traditional Chinese medicines." Pharmacological Research, 142, 115–126. https://doi.org/10.1016/j.phrs.2019.02.024
- Xu, J., Lian, F., Zhao, L., Zhao, Y., Chen, X., Zhang, X., ... & Tong, X. (2015). "Structural modulation of gut microbiota by berberine and its formula Gegen Qinlian Decoction in type 2 diabetes." Scientific Reports, 5, 12867. https://doi.org/10.1038/srep12867
- An, X., Bao, Q., Di, S., Zhao, Y., Zhao, S., Zhang, H., ... & Zhang, B. (2019). "The interaction between the gut microbiota and herbal medicines." Biomedicine & Pharmacotherapy, 118, 109252. https://doi.org/10.1016/j.biopha.2019.109252
- Ried, K., Travica, N., & Sali, A. (2018). "Herbal medicines in the treatment of cardiometabolic diseases: A systematic review and meta-analysis." Frontiers in Pharmacology, 9, 1119. https://doi.org/10.3389/fphar.2018.01119
- Feng, W., Ao, H., Peng, C., & Yan, D. (2019). "Gut microbiota, a new frontier to understand traditional Chinese medicines." Pharmacological Research, 142, 115–126. https://doi.org/10.1016/j.phrs.2019.02.024
- Pferschy-Wenzig, E. M., & Bauer, R. (2015). "The relevance of pharmacognosy in the context of gut microbiota research." Phytochemistry Reviews, 14(6), 935–951. https://doi.org/10.1007/s11101-015-9429-9
- Mirzayi, C., Renson, A., Zohra, F., Elsafoury, S., Geistlinger, L., Kasselman, L. J., ... & Waldron, L. (2021). "Reporting guidelines for human microbiome research: The STORMS checklist." Nature Medicine, 27(11), 1885–1892. https://doi.org/10.1038/s41591-021-01552-x
- An, X., Bao, Q., Di, S., Zhao, Y., Zhao, S., Zhang, H., ... & Zhang, B. (2019). "The interaction between the gut microbiota and herbal medicines." Biomedicine & Pharmacotherapy, 118, 109252. https://doi.org/10.1016/j.biopha.2019.109252
- Selma, M. V., Espín, J. C., & Tomás-Barberán, F. A. (2009). "Interaction between phenolics and gut microbiota: Role in human health." Journal of Agricultural and Food Chemistry, 57(15), 6485–6501. https://doi.org/10.1021/jf902107d
- Jordan, S. A., Cunningham, D. G., & Marles, R. J. (2010). "Assessment of herbal medicinal products: Challenges, and opportunities to increase the knowledge base for safety assessment." Toxicology and Applied Pharmacology, 243(2), 198–216. https://doi.org/10.1016/j.taap.2009.12.005
- Asher, G. N., Corbett, A. H., & Hawke, R. L. (2017). "Common herbal dietary supplement–drug interactions." American Family Physician, 96(2), 101–107. https://www.aafp.org/afp/2017/0715/afp20170715p101.pdf
- U.S. Food and Drug Administration (FDA). (2023). Label Claims for Conventional Foods and Dietary Supplements. https://www.fda.gov/food/nutrition-food-labeling-and-critical-foods/label-claims-conventional-foods-and-dietary-supplements
- Thakkar, S., Anklam, E., Xu, A., Ulberth, F., Li, J., Li, B., ... & Belcher, G. (2020). "Regulatory landscape of dietary supplements and herbal medicines from a global perspective." Regulatory Toxicology and Pharmacology, 114, 104733. https://doi.org/10.1016/j.yrtph.2020.104733
- European Food Safety Authority (EFSA), Panel on Nutrition, Novel Foods and Food Allergens (NDA). (2021). "Safety of pasteurised Akkermansia muciniphila as a novel food pursuant to Regulation (EU) 2015/2283." EFSA Journal, 19(9), e06780. https://doi.org/10.2903/j.efsa.2021.6780
- Commission Implementing Regulation (EU) 2022/168. (2022). "Authorising the placing on the market of pasteurised Akkermansia muciniphila as a novel food under Regulation (EU) 2015/2283." Official Journal of the European Union, L 33, 9–11. https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32022R0168
- Shoba, G., Joy, D., Joseph, T., Majeed, M., Rajendran, R., & Sridhar, P. R. (1998). "Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers." Planta Medica, 64(4), 353–356. https://doi.org/10.1055/s-2006-957450
- Atal, C. K., Dubey, S. K., & Singh, J. (1985). "Biochemical basis of enhanced drug bioavailability by piperine: Evidence that piperine is a potent inhibitor of drug metabolism." Journal of Pharmacology and Experimental Therapeutics, 232(1), 258–262. https://pubmed.ncbi.nlm.nih.gov/3964179/
- World Health Organization (WHO). (2019). WHO Global Report on Traditional and Complementary Medicine 2019. https://www.who.int/publications/i/item/9789241515436
- Govindaraghavan, S., & Sucher, N. J. (2015). "Quality assessment of medicinal herbs and their extracts: Criteria and prerequisites for consistent safety and efficacy." Epilepsy & Behavior, 52(Pt B), 363–371. https://doi.org/10.1016/j.yebeh.2015.08.039.
Sohail Shaikh
Corresponding author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Pooja Rasal
Co-author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Huzaifa Patel
Co-author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Parth Khandelwal
Co-author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Sanabil Shaikh
Co-author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Saniya Shaikh
Co-author
SND College of Pharmacy, Babhulgaon, Yeola -423401
Sohail Shaikh*, Pooja Rasal, Huzaifa Patel, Parth Khandelwal, Sanabil Shaikh, Saniya Shaikh, Herbal Plants in the Management of Dysbiosis: A Review of Mechanisms, Efficacy, and Therapeutic Potential, Int. J. Sci. R. Tech., 2025, 2 (11), 410-431. https://doi.org/10.5281/zenodo.17627134