Microbiota–neuroepithelial signalling across the gut–brain axis

The gut microbiota as an environmental factor that regulates fat storage

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Short Chain Fatty Acids (SCFAs)-Mediated Gut Epithelial and Immune Regulation and Its Relevance for Inflammatory Bowel Diseases

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The Human Intestinal Microbiome in Health and Disease

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Gut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson's disease

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Indigenous bacteria from the gut microbiota regulate host serotonin biosynthesis

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The role of short-chain fatty acids in microbiota–gut–brain communication

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Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders

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Pathogen Recognition and Inflammatory Signaling in Innate Immune Defenses

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Microglia Function in the Central Nervous System During Health and Neurodegeneration

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Postnatal microbial colonization programs the hypothalamic–pituitary–adrenal system for stress response in mice

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The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism

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The Intestinal Microbiota Affect Central Levels of Brain-Derived Neurotropic Factor and Behavior in Mice

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Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases

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Nociceptors: the sensors of the pain pathway

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Transneuronal Propagation of Pathologic α-Synuclein from the Gut to the Brain Models Parkinson’s Disease

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Gut microbes promote colonic serotonin production through an effect of short-chain fatty acids on enterochromaffin cells

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Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function

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The brain-gut-microbiome axis

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Bile acids and the gut microbiota: metabolic interactions and impacts on disease

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Vagus Nerve as Modulator of the Brain–Gut Axis in Psychiatric and Inflammatory Disorders

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Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice

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Microbial Regulation of Host Physiology by Short-chain Fatty Acids

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A gut-brain neural circuit for nutrient sensory transduction

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The sensory-efferent function of capsaicin-sensitive sensory neurons

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Enterochromaffin cells are gut chemosensors that couple to sensory neural pathways

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Mechanisms underlying microbial-mediated changes in social behavior in mouse models of autism spectrum disorder

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The enteric nervous system and gastrointestinal innervation: integrated local and central control

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Distinguishing features of long COVID identified through immune profiling

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The gut-brain axis

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Inter-kingdom signalling: Communication between bacteria and their hosts

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Long-term benefit of microbiota transfer therapy on autism symptoms and gut microbiota

Kang, D.-W., Adams, J. B., Coleman, D. M., Pollard, E. L., Maldonado, J., McDonough-Means, S., Caporaso, J. G., & Krajmalnik-Brown, R. (2019) · Scientific Reports · doi:10.1038/s41598-019-42183-0 · Cited by 749 · see citing works

A Neural Circuit for Gut-Induced Reward

Han, W., Téllez, L. A., Perkins, M. H., Pérez-Martínez, I. O., Qu, T., Ferreira, J. G. P., Ferreira, T. L., Quinn, D., Liu, Z.-W., Gao, X., et al. (2018) · Cell · doi:10.1016/j.cell.2018.08.049 · Cited by 739 · see citing works

A systematic literature review on obesity: Understanding the causes & consequences of obesity and reviewing various machine learning approaches used to predict obesity

Safaei, M., Sundararajan, E. A., Driss, M., Boulila, W., & Shapi'i, A. (2021) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2021.104754 · Cited by 720 · see citing works

Bile acid receptors as targets for drug development

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Function and mechanisms of enteroendocrine cells and gut hormones in metabolism

Gribble, F. M., & Reimann, F. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0168-8 · Cited by 670 · see citing works

Critical role of gut microbiota in the production of biologically active, free catecholamines in the gut lumen of mice

Asano, Y., Hiramoto, T., Nishino, R., Aiba, Y., Kimura, T., Yoshihara, K., Koga, Y., & Sudo, N. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00341.2012 · Cited by 659 · see citing works

Sensory neurons that detect stretch and nutrients in the digestive system

Williams, E. K., Chang, R. B., Strochlic, D. E., Umans, B. D., Lowell, B. B., & Liberles, S. D. (2016) · Cell · doi:10.1016/j.cell.2016.05.011 · Cited by 645 · see citing works

Identification of an Intestinal Microbiota Signature Associated With Severity of Irritable Bowel Syndrome

Tap, J., Derrien, M., Törnblom, H., Brazeilles, R., Cools-Portier, S., Doré, J., Störsrud, S., Le Nevé, B., Öhman, L., & Simrén, M. (2017) · Gastroenterology · doi:10.1053/j.gastro.2016.09.049 · Cited by 642 · see citing works

Impaired aryl hydrocarbon receptor ligand production by the gut microbiota is a key factor in metabolic syndrome

Natividad, J. M., Agus, A., Planchais, J., Lamas, B., Jarry, A. C., Martin, R., Michel, M.-L., Chong-Nguyen, C., Roussel, R., Straube, M., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.07.001 · Cited by 642 · see citing works

Enteric nervous system: sensory transduction, neural circuits and gastrointestinal motility

Spencer, N. J., & Hu, H. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0271-2 · Cited by 607 · see citing works

A metabolic pathway for bile acid dehydroxylation by the gut microbiome

Funabashi, M., Grove, T. L., Wang, M., Varma, Y., McFadden, M. E., Brown, L. C., Guo, C., Higginbottom, S., Almo, S. C., & Fischbach, M. A. (2020) · Nature · doi:10.1038/s41586-020-2396-4 · Cited by 590 · see citing works

Absence of the gut microbiota enhances anxiety-like behavior and neuroendocrine response to acute stress in rats

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GPR41/FFAR3 and GPR43/FFAR2 as Cosensors for Short-Chain Fatty Acids in Enteroendocrine Cells vs FFAR3 in Enteric Neurons and FFAR2 in Enteric Leukocytes

Nøhr, M. K., Pedersen, M. H., Gille, A., Egerod, K. L., Engelstoft, M. S., Husted, A. S., Sichlau, R. M., Grunddal, K. V., Poulsen, S. S., Han, S., et al. (2013) · Endocrinology · doi:10.1210/en.2013-1142 · Cited by 575 · see citing works

The maternal microbiome modulates fetal neurodevelopment in mice

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The gut as a sensory organ

Furness, J. B., Rivera, L. R., Cho, H., Bravo, D. M., & Callaghan, B. P. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.180 · Cited by 549 · see citing works

Bacterial metabolite indole modulates incretin secretion from intestinal enteroendocrine L cells

Chimerel, C., Emery, E., Summers, D. K., Keyser, U., Gribble, F. M., & Reimann, F. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.10.032 · Cited by 548 · cited 1× · see citing works

Gut microbiota dynamics in a prospective cohort of patients with post-acute COVID-19 syndrome

Liu, Q., Mak, J. W. Y., Su, Q., Yeoh, Y. K., Lui, G. C.-Y., Ng, S. S., Zhang, F., Li, A. Y. L., Lu, W., Hui, D. S. C., et al. (2022) · Gut · doi:10.1136/gutjnl-2021-325989 · Cited by 540 · see citing works

Effects of Psychological, Environmental and Physical Stressors on the Gut Microbiota

Karl, J. P., Hatch‐McChesney, A., Arcidiacono, S. M., Pearce, S., Pantoja-Feliciano, I. G., Doherty, L. A., & Soares, J. W. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02013 · Cited by 535 · see citing works

Long-term neurologic outcomes of COVID-19

Xu, E., Xie, Y., & Al-Aly, Z. (2022) · Nature Medicine · doi:10.1038/s41591-022-02001-z · Cited by 530 · see citing works

Genetic identification of vagal sensory neurons that control feeding

Bai, L., Mesgarzadeh, S., Ramesh, K. S., Huey, E. L., Liu, Y., Gray, L. A., Aitken, T. J., Chen, Y., Beutler, L. R., Ahn, J. S., et al. (2019) · Cell · doi:10.1016/j.cell.2019.10.031 · Cited by 494 · see citing works

A gut-derived metabolite alters brain activity and anxiety behaviour in mice

Needham, B. D., Funabashi, M., Adame, M. D., Wang, Z., Boktor, J. C., Haney, J., Wu, W.-L., Rabut, C., Ladinsky, M. S., Hwang, S.-J., et al. (2022) · Nature · doi:10.1038/s41586-022-04396-8 · Cited by 489 · see citing works

Neuroepithelial circuit formed by innervation of sensory enteroendocrine cells

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Intestinal serotonin and fluoxetine exposure modulate bacterial colonization in the gut

Fung, T. C., Vuong, H. E., Luna, C. G. G., Pronovost, G. N., Aleksandrova, A. A., Riley, N. G., Vavilina, A., McGinn, J., Rendon, T. K., Forrest, L. R., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0540-4 · Cited by 481 · see citing works

Microbiota and the social brain

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Microbiota-derived metabolites as drivers of gut–brain communication

Ahmed, H., Leyrolle, Q., Koistinen, V., Kärkkäinen, O., Layé, S., Delzenne, N., & Hanhineva, K. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2102878 · Cited by 462 · see citing works

Microbiota modulate sympathetic neurons via a gut–brain circuit

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Specific probiotic therapy attenuates antibiotic induced visceral hypersensitivity in mice

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An Atlas of Vagal Sensory Neurons and Their Molecular Specialization

Kupari, J., Häring, M., Agirre, E., Castelo‐Branco, G., & Ernfors, P. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.096 · Cited by 445 · see citing works

Meningeal γδ T cells regulate anxiety-like behavior via IL-17a signaling in neurons

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Prodromal Parkinson disease subtypes — key to understanding heterogeneity

Berg, D., Borghammer, P., Fereshtehnejad, S.-M., Heinzel, S., Horsager, J., Schaeffer, E., & Postuma, R. B. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-021-00486-9 · Cited by 409 · see citing works

Farnesoid X receptor inhibits glucagon-like peptide-1 production by enteroendocrine L cells

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GPR119 Is Essential for Oleoylethanolamide-Induced Glucagon-Like Peptide-1 Secretion From the Intestinal Enteroendocrine L-Cell

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TRPA1 regulates gastrointestinal motility through serotonin release from enterochromaffin cells

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Gastrointestinal and brain barriers: unlocking gates of communication across the microbiota–gut–brain axis

Aburto, M. R., & Cryan, J. F. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-023-00890-0 · Cited by 391 · see citing works

A body–brain circuit that regulates body inflammatory responses

Jin, H., Li, M., Jeong, E., Castro-Martinez, F., & Zuker, C. S. (2024) · Nature · doi:10.1038/s41586-024-07469-y · Cited by 383 · see citing works

Recirculating Intestinal IgA-Producing Cells Regulate Neuroinflammation via IL-10

Rojas, O. L., Pröbstel, A.-K., Porfilio, E. A., Wang, A. A., Charabati, M., Sun, T., Lee, D. S. W., Galicia, G., Ramaglia, V., Ward, L. A., et al. (2019) · Cell · doi:10.1016/j.cell.2018.11.035 · Cited by 382 · see citing works

Diagnosis and Treatment of Irritable Bowel Syndrome

Camilleri, M. (2021) · JAMA · doi:10.1001/jama.2020.22532 · Cited by 370 · see citing works

Gut microbiome composition may be an indicator of preclinical Alzheimer’s disease

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The receptor TGR5 mediates the prokinetic actions of intestinal bile acids and is required for normal defecation in mice

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The vagus nerve in appetite regulation, mood, and intestinal inflammation

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Serotonin reduction in post-acute sequelae of viral infection

Wong, A. C., Devason, A. S., Umana, I. C., Cox, T. O., Dohnalová, L., Litichevskiy, L., Perla, J., Lundgren, P., Etwebi, Z., Izzo, L., et al. (2023) · Cell · doi:10.1016/j.cell.2023.09.013 · Cited by 359 · see citing works

Composition of gut microbiota in children with autism spectrum disorder: a systematic review and meta-analysis

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Identification of Enteroendocrine Regulators by Real-Time Single-Cell Differentiation Mapping

Gehart, H., van Es, J. H., Hamer, K., Beumer, J., Kretzschmar, K., Dekkers, J. F., Rios, A., & Clevers, H. (2019) · Cell · doi:10.1016/j.cell.2018.12.029 · Cited by 346 · see citing works

The enteric nervous system relays psychological stress to intestinal inflammation

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Insular cortex neurons encode and retrieve specific immune responses

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Gut-licensed IFNγ+ NK cells drive LAMP1+TRAIL+ anti-inflammatory astrocytes

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Advances in Meningeal Immunity

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Enteroendocrine cells sense bacterial tryptophan catabolites to activate enteric and vagal neuronal pathways

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An Overview on Fecal Branched Short-Chain Fatty Acids Along Human Life and as Related With Body Mass Index: Associated Dietary and Anthropometric Factors

Ríos-Covián, D., González, S., Nogacka, A. M., Arboleya, S., Salazar, N., Gueimonde, M., & Reyes-Gavilán, C. G. D. L. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00973 · Cited by 320 · see citing works

The gut–brain axis mediates sugar preference

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Short-chain fatty acids modify colonic motility through nerves and polypeptide YY release in the rat

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Probiotic Bacteria in Stimulating Human Physiological Responses: Metabolic Function and Overall Health

Chong, S. Y., Raja‐Razali, R. B., Ismail, N. H., Ushidee-Radzi, M. A., Zahia-Azizan, N. A., Manickam, M., Norhisham, D. ‘., Ilham, Z., Reale, A., Nazzaro, S., et al. (2026) · Foods · doi:10.3390/foods15122079 · Cited by 2 · see citing works

A Comprehensive Review of the Gut–Microbiota–Brain Axis in Alzheimer’s Disease: From Pathophysiology to Potential Therapies

Ziaka, M. (2026) · Pathogens · doi:10.3390/pathogens15070659 · Cited by 2 · see citing works

Microbiota in cholestatic diseases: crosstalk among bile composition, the biliary microbiome, and host immunity

Yang, Y., Ren, L., Zhang, Y., Wang, X., Shang, J., & Zhang, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1884030 · Cited by 2 · see citing works

Gut-on-a-Chip: From Biomimetic Design to Precision Biomedical Applications

Lin, Q., Zhou, F., Hao, W., Zhang, P., Xiao, R., & Cha, R. (2026) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6c10688 · Cited by 2 · see citing works

Investigating the Mechanism and Strategy of Treating Premature Ejaculation with TCM through the Gut-Brain Axis-Mediated Trp/Tph2/5-HT Pathway

Sun, D., Zhao, F., Wang, H., Du, G., Yan, B., & Yu, W. (2025) · Integrative Medicine in Nephrology and Andrology · doi:10.1097/imna-d-24-00065 · Cited by 1 · see citing works

Potential Benefits of Behaviors and Lifestyle for Human Health and Well-Being

Stachera, Ł., Góras, K., Janowska, K., Muszkat-Pośpiech, E., Wojciechowska, A., Świderska-Kołacz, G., Zmorzyński, S., & Czerwik-Marcinkowska, J. (2025) · Nutrients · doi:10.3390/nu17203253 · Cited by 3 · see citing works

Efficacy and Safety of Auricular Acupressure for Insomnia in Patients With Functional Dyspepsia: A Randomized Controlled Trial

Shen, M., Li, Z.-J., Zhou, R., Lou, Q.-Y., Ying, Z.-K., Liu, S., Feng, D.-D., Yang, D., Jiang, L.-X., Wang, X., et al. (2025) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000003880 · Cited by 1 · see citing works

Short-term high-altitude exposure protects working memory by balancing intestinal microbiota

Zhang, X., Sun, N., Yang, J., Wang, H., Zhao, S., Chen, Y. Z., Duan, L., Gan, B., Cai, J., Su, R., et al. (2026) · BMC Microbiology · doi:10.1186/s12866-025-04535-x · Cited by 1 · see citing works

Alternations along gut-brain axis in response to hypo- and hyper-osmotic stress in yellowfin seabream (Acanthopagrus latus)

Zhang, J., Lin, G., Xie, N., Ye, Y., Zhao, H., & Lü, J. (2026) · Aquaculture Reports · doi:10.1016/j.aqrep.2026.103533 · Cited by 1 · see citing works

A Combined Colon Organoid‐Sensory Neuron Model Reveals Epithelial Contribution to Moringin Efficacy Against Painful Inflammatory Bowel Disease

Margiotta, F., Lucarini, E., Toti, A., Cataldi, M. G., Ciampi, C., Nicola, G. R. D., Mannelli, L. D. C., & Ghelardini, C. (2026) · Phytotherapy Research · doi:10.1002/ptr.70303 · Cited by 1 · see citing works

Gene regulatory and biomolecular networks and their multifaceted biotechnological applications

Kar, S., Barua, M., Chot, E., Azad, R. K., & Shukla, P. (2026) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-026-04891-4 · Cited by 1 · see citing works

Microbiota-Driven microglia reprogramming reverses depressive-like behaviors through Peripheral-to-Central immune crosstalk

Wu, J., Zhou, X., Luo, T., Wang, X., Zuo, H., Yang, R., Tian, R., Wu, Y., Wu, Y. F., Jiang, W., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03545-z · Cited by 1 · see citing works

MEKK3 bridges gut-brain communication and cerebral cavernous malformation pathogenesis

Chen, P., Han, H., Huang, Y., Shen, Y., Jiang, X., Song, X., Qian, C., Chen, L., & Zhao, Y. (2026) · Cell Death Discovery · doi:10.1038/s41420-026-03062-6 · Cited by 1 · see citing works

Stress accelerates hepatocellular carcinoma progression via a gut microbial-metabolite axis

Hu, Z., Yue, P., Yuan, M., Zhang, Z., Li, Q., Yang, T., Li, Y., Ding, B., Fan, Z., Yang, B., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1790214 · Cited by 2 · see citing works

Inflammatory bowel disease and psoriasis as causal drivers of psychiatric disorders: A two-stage Mendelian randomization study grounded in the gut-brain-skin axis

Li, H., Guo, Y., Zhang, Z., Yang, J., Li, Y., Fu, X., & Yang, S. (2026) · Journal of Affective Disorders · doi:10.1016/j.jad.2026.121978 · Cited by 1 · see citing works

Gut-brain axis research in schizophrenia: Historical evolution, emerging computational models, and translational challenges – A narrative review

Sangeeta, S., Sawant, B. S., Vedavathi, S., Sreenithya, M., Chikkanna, U., Sreeraj, V. S., Kumar, V., Holla, B., Shivakumar, V., & Kishore Kumar, R. (2026) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2026.105037 · Cited by 1 · see citing works

A multi-organ metabolomics atlas reveals molecular dysregulations in Alzheimer’s disease mouse models

Zuffa, S., Allaband, C., Charron‐Lamoureux, V., Caraballo‐Rodríguez, A. M., Patan, A., Mohanty, I., Agongo, J., Bostick, J. W., Connerly, T. J., Thron, T., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117499 · Cited by 1 · see citing works

3-O-p-coumaroylquinic acid and 4-O-p-coumaroylquinic acid from Hemerocallis citrina Baroni exert antidepressant effects via CA/Dopa/DA/NE and PKA/CREB/BDNF signaling pathways

Jiang, F., Qiu, Z., Zhong, J., Tian, Y., Liu, J., Zhu, Y., Zhao, L., Chen, S., Chen, H. L., Wang, H., et al. (2026) · npj Science of Food · doi:10.1038/s41538-026-00934-0 · Cited by 1 · see citing works

Oral probiotic delivery-based therapeutic strategies for inflammatory bowel disease

Li, S., Deng, H., Fu, S., Li, J., Luo, X., Chen, Z., Wang, P., Feng, X., Chen, Y., Fu, C., et al. (2026) · Asian Journal of Pharmaceutical Sciences · doi:10.1016/j.ajps.2026.101187 · Cited by 1 · see citing works

The sixth sense of the brain: interoception in organoid study

Li, J., Wang, F., Gao, Q., Chen, X., Bai, L., & Su, J. (2026) · Bone Research · doi:10.1038/s41413-026-00569-7 · Cited by 1 · see citing works

Decoding the power of the microbiome in human health

Kumar, M., Almohannadi, N., & Khodor, S. A. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1877371 · Cited by 1 · see citing works

The Gut–Immune–Brain Axis in Aging: Integrating Immunosenescence, Inflammaging, and Neuroinflammation for Precision Medicine

Bajić, D., Vučković, J., Pupovac, N., Slavić, D., Stojsic, M., Hodoba, N., Todorović, N., Plazačić, M., & Milosevic, N. P. (2026) · Medical Sciences · doi:10.3390/medsci14050536 · Cited by 1 · see citing works

Oral health and behavioral problems in children living with and without HIV in South Africa

Barrios-Tascon, A., Wang, T., Strehlau, R., Tobin, N. H., Violari, A., Li, F., Patel, F., Liberty, A., Shiau, S., Wadhwa, S., et al. (2025) · AIDS Care · doi:10.1080/09540121.2025.2536720

The pathogenic theory of homeostasis threshold deviation (HTD) in wide-range oscillatory physiological parameters: novel perspectives for hypertension and metabolic disease treatment

Sun, W. Y., Sun, J.-Y., & Kong, X. (2025) · Life Metabolism · doi:10.1093/lifemeta/loaf029

Editorial: Dietary modulation of gut microbiota-X axis

Li, B., Bottacini, F., & Yang, Y. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1693629

Microbiote néonatal et comportement alimentaire chez l’adulte

Parnet, P., Dréan, G. L., Naour, M., Grit, I., Heberden, C., Chatelier, E. L., & Michel, C. (2025) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2025.07.005

An “electric” microbial cue to control food intake behavior

Li, H., & Mucida, D. (2025) · Cell Metabolism · doi:10.1016/j.cmet.2025.09.007

Research Progress on the Mechanism of Acupuncture Treatment for Perimenopausal Insomnia

叶, 升. (2025) · Traditional Chinese Medicine · doi:10.12677/tcm.2025.1410608

Gut Microbiota–Leptin crosstalk in obesity and metabolic dysregulation

Singh, L. S., & Sharma, L. A. (2025) · Obesity Medicine · doi:10.1016/j.obmed.2025.100671

Lactobacillus helveticus-derived whey alleviates scopolamine-induced cognitive impairment in mice via the gut-brain axis

Sun, Y., Gao, S., Jiang, Y., Liu, Z., Xia, A., Lee, Y. K., Yang, B., Liu, X., Zhou, P., Zhao, J., et al. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.108073

Nasal, Oral, and Gut Microbiome Influences on Perception of Sensory Qualities of Food

Menghi, L., & Cattaneo, C. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-29139-5.00039-2

Is Manganese the Root Cause of Human Mental Disorders?Preprint

Bai, Y., Wang, X., Wang, Y., & Xue, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.06.698023

TEMPORAL SUCCESSION, KEYSTONE MICROBIOTA IDENTIFICATION, AND CORRELATION ANALYSIS BETWEEN THE INTESTINAL MICROBIOTA OF JUVENILE NIBEA ALBIFLORA AND THE BACTERIAL COMMUNITY IN CULTURE WATER

Shuai, Y., Xu, D., Yu-Yan, L. U. O., Rui-Yi, C. H. E. N., Wei-Hua, H. U., Wang, L.-G., & Li, H. (2026) · Acta Hydrobiologica Sinica · doi:10.3724/1000-3207.2025.2025.0276

Bidirectional interactions along the microbiota–gut–brain axis in radiation-induced brain injury: mechanisms and therapeutic insights

Yuan, Y., Wang, N., Ning, K., & Dang, X. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1774021

Role of CB1 receptors in the gastrointestinal tract after microbiota depletion and natural recolonization

Beraldi, E. J., Habibyan, Y. B., Keenan, C. M., Wallace, L. E., & Sharkey, K. A. (2026) · Scientific Reports · doi:10.21203/rs.3.rs-8854797/v1

Prenatal exposure to low-dose ciprofloxacin antibiotic increased male offspring’s defensive aggressive behaviors via a gut–phosphatidylcholine–α7 nAChR axis

Cao, A., Liu, Y., Qi, D., Li, Z., Du, Y., Xu, Q., Yue, J., Zheng, L., Wang, Y., Cui, J., et al. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.106572

Microbial metabolites: Bridging the gut-brain divide in ischemic stroke

Dang, W., Li, W., Dong, F., Huang, Y., He, S., & Zhu, Y. (2026) · Microbiological Research · doi:10.1016/j.micres.2026.128510

Glucagon‐Like Peptide‐2 Receptor: A Master Integrator of Gut‐Brain‐Liver Communication in Metabolic and Cognitive Health

Jiang, Y., Han, G., Zhang, Z., Hu, S., & Mu, M. (2026) · Comprehensive physiology · doi:10.1002/cph4.70144

Pre-treatment with baicalein alleviates the diquat-induced microglial pyroptosis through gut microbiota–derived indole-3-propionic acid and DDX3X/G3BP1 pathway

Li, T., Feng, M., Wang, P., Jiang, M., Cui, J., Jin, M., Song, C., Li, L., & Lu, Y. (2026) · Cell Biology and Toxicology · doi:10.1007/s10565-026-10189-w

Dysbiosis of gut microbiota synergizes with the activation of enteric glial cells to promote Alzheimer's disease

Sun, Q., Li, Y., Wang, Y., Tao, S.-S., Huan, X., Li, Y.-Q., & Zhang, H. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261441247

Building bioelectronics that stick around

Wang, S., & Ma, W. (2026) · Nature Electronics · doi:10.1038/s41928-026-01619-y

Microbial-derived mediators of the gut–brain axis: Implications for neurological disorders

Abady, M. M., Shawky, A. M., & Mohammed, D. M. (2026) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2026.110394

Altered Intestinal Neurotransmission in Autism Spectrum Disorder: Expanding the Molecular Landscape of the Gut–Brain Axis

Turpin, V., & Aburto, M. R. (2026) · Digestive Diseases and Sciences · doi:10.1007/s10620-026-09911-9

Vagally Mediated Pathways: How Gut Signals Affect the Nervous System

Sengottuvel, T., Aysha, M. A., & Sneha, V. K. (2026) · Springer eBooks · doi:10.1007/978-981-95-7494-0_3

Targeting the gut-brain axis by prebiotics and probiotics: Integrating emerging strategies in IBD management

Gupta, D., Gupta, M. K., Parveen, F., & Agarwal, A. (2026) · Human Nutrition & Metabolism · doi:10.1016/j.hnm.2026.200369

The microbiota-gut–brain axis in epilepsy: Mechanistic insights and emerging probiotic-based therapeutics

Matta, T., Bishnoi, M., Chopra, K., & Kondepudi, K. K. (2026) · International review of neurobiology · doi:10.1016/bs.irn.2026.05.007

AI-Driven Delivery of Psychobiotics: Enhancing Targeted Treatments of the Gut-Brain Axis and Prospects for Personalized Applications

Huang, D., Gao, Y., Hao, K., Hu, C., Zhang, S., Gong, W., Qin, X., Du, G., Li, H., & Zhou, Y. (2026) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2026.101674

Polygonatum kingianum polysaccharides ameliorate cognitive impairments in alcohol-exposed obese mice in a sex-specific manner by regulating the gut microbiome and metabolome

Lv, J., Qu, Y., Yan, Q., Cheng, K., Wu, Q., Zhang, J., Duan, X., Han, S., Tian, H., & Shi, L. (2026) · Food Research International · doi:10.1016/j.foodres.2026.119827

Irritable Bowel Syndrome

Nazar, F. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-26472-6.00100-5

Hive mind: Microbial communities and the making of memory

Katona, L., & Cryan, J. F. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2616703123

Effects of Metabolites of Lactic Acid Bacteria on Nerve Cells of the Microbiota–Gut–Brain Axis

Kv, S. (2026) · Biochemistry (Moscow) · doi:10.1134/s0006297926600377

Integrating serum pharmacology, network pharmacology, and molecular biology analysis to reveal the mechanisms of Baihe Dihuang decoction in treating Alzheimer’s disease

Liang, X., Ning, T., Wang, Y., & Zhan, L. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1765044

Rewiring the Brain Through the Gut: Insights into Microbiota–Nervous System Interactions

Săvulescu-Fiedler, I., Benea, S. N., Căruntu, C., Nancoff, A.-S., Homentcovschi, C., & Bucurica, S. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47070489 · Cited by 45 · see citing works

Microbiota-gut-brain axis: enteroendocrine cells and the enteric nervous system form an interface between the microbiota and the central nervous system

KUWAHARA, A., MATSUDA, K., KUWAHARA, Y., ASANO, S., INUI, T., & MARUNAKA, Y. (2020) · Biomedical Research · doi:10.2220/biomedres.41.199 · Cited by 112 · see citing works

Microbiota–Gut–Brain Axis: An Integrative Overview of Communication Pathways

Martínez‐Porchas, M., Medina‐Félix, D., Olivas-Bernal, C. A., Guirado-Flores, J. S. O., Vargas‐Albores, F., Porchas‐Quijada, M., & Garibay-Valdéz, E. (2026) · Advanced Gut & Microbiome Research · doi:10.1155/agm3/8142006 · Cited by 1 · see citing works

Microbiota of the Gut–Brain Axis

Muppasani, A., & Thomas, S. (2026) · CRC Press eBooks · doi:10.1201/9781003635772-8

Role of Gut Microbiota in the Regulation of Gut-Brain Neuroendocrine Pathways: An Immunological Perspective

Ekka, R., Ahirwar, B., & Poleboina, S. (2024) · Book Publisher International (a part of SCIENCEDOMAIN International) · doi:10.9734/bpi/acmms/v7/3386