Changes in intestinal motility and gut microbiota composition in a rat stress model

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

Sudo, N., Chida, Y., Aiba, Y., Sonoda, J., Oyama, N., Yu, X., Kubo, C., & Koga, Y. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.063388 · Cited by 2,735 · see citing works

Early life stress alters behavior, immunity, and microbiota in rats: implications for irritable bowel syndrome and psychiatric illnesses

O'Mahony, S. M., Marchesi, J. R., Scully, P., Codling, C., Ceolho, A.-M., Quigley, E. M. M., Cryan, J. F., & Dinan, T. G. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.06.026 · Cited by 1,069 · see citing works

Neonatal maternal separation alters stress-induced responses to viscerosomatic nociceptive stimuli in rat

Coutinho, S. V., Plotsky, P. M., Sablad, M., Miller, J. C., Zhou, H., Bayati, A. I., McRoberts, J. A., & Mayer, E. A. (2002) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00240.2001 · Cited by 456 · see citing works

Maternal separation as a model of brain-gut axis dysfunction

O’Mahony, S. M., Hyland, N. P., Dinan, T. G., & Cryan, J. F. (2011) · Psychopharmacology · doi:10.1007/s00213-010-2010-9 · Cited by 415 · see citing works

Central Nervous System Effects of the Neurohypophyseal Hormones and Related Peptides

de Wied, D., Diamant, M., & Fodor, M. (1993) · Frontiers in Neuroendocrinology · doi:10.1006/frne.1993.1009 · Cited by 327 · see citing works

Corticotropin-releasing factor directly mediates colonic responses to stress

Williams, C. L., Peterson, J. M., Villar, R. G., & Burks, T. F. (1987) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1987.253.4.g582 · Cited by 244 · see citing works

N-3 Polyunsaturated Fatty Acids (PUFAs) Reverse the Impact of Early-Life Stress on the Gut Microbiota

Pusceddu, M. M., El Aidy, S., Crispie, F., O’Sullivan, O., Cotter, P., Stanton, C., Kelly, P., Cryan, J. F., & Dinan, T. G. (2015) · PLOS ONE · doi:10.1371/journal.pone.0139721 · Cited by 214 · see citing works

Health-related quality of life, work productivity, and health care resource utilization of subjects with irritable bowel syndrome: Baseline results from logic (longitudinal outcomes study of gastrointestinal symptoms in Canada), a naturalistic study

Paré, P., Gray, J. R., Lam, S., Balshaw, R. F., Khorasheh, S., Barbeau, M., Kelly, S., & McBurney, C. R. (2006) · Clinical Therapeutics · doi:10.1016/j.clinthera.2006.10.010 · Cited by 199 · see citing works

Conditioned emotional response in rats enhances colonic motility through the central release of corticotropin-releasing factor

Gué, M., Junien, J., & Bueno, L. P. (1991) · Gastroenterology · doi:10.1016/0016-5085(91)90270-u · Cited by 144 · see citing works

CRF in the paraventricular nucleus mediates gastric and colonic motor response to restraint stress

Mönnikes, H., Schmidt, B. G., Raybould, H. E., & Taché, Y. (1992) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1992.262.1.g137 · Cited by 144 · see citing works

The microbiota link to irritable bowel syndrome

Jeffery, I. B., Quigley, E. M. M., Öhman, L., Simrén, M., & O’Toole, P. W. (2012) · Gut Microbes · doi:10.4161/gmic.21772 · Cited by 111 · see citing works

Protective effect of agaro-oligosaccharides on gut dysbiosis and colon tumorigenesis in high-fat diet-fed mice

Higashimura, Y., Naito, Y., Takagi, T., Uchiyama, K., Mizushima, K., Ushiroda, C., Ohnogi, H., Kudo, Y., Yasui, M., Inui, S., et al. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00324.2015 · Cited by 97 · see citing works

Involvement of the 5-HT3receptor in CRH-induced defecation in rats

Miyata, K., Ito, H., & Fukudo, S. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.5.g827 · Cited by 72 · see citing works

Intracisternal injection of CRF antagonist blocks surgical stress-induced inhibition of gastric secretion in the rat

Stephens, R. L., Yang, H., Rivier, J., & Taché, Y. (1988) · Peptides · doi:10.1016/0196-9781(88)90090-3 · Cited by 55 · see citing works

Early-life events. Effects on aging

Kajantie, E. (2008) · HORMONES · doi:10.1007/bf03401501 · Cited by 54 · see citing works

Le dysfonctionnement du « brain-gut »

Bonaz, B. L., & Sabaté, J. (2009) · Gastroentérologie Clinique et Biologique · doi:10.1016/s0399-8320(09)71525-8 · Cited by 33 · see citing works

The Newly Developed CRF1-Receptor Antagonists, NGD 98-2 and NGD 9002, Suppress Acute Stress-Induced Stimulation of Colonic Motor Function and Visceral Hypersensitivity in Rats

Million, M., Zhao, J.-F., Luckey, A. E., Czimmer, J., Maynard, G. D., Kehne, J. H., Hoffman, D. C., & Taché, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073749 · Cited by 29 · see citing works

Survey of Clinical Practice for Irritable Bowel Syndrome in East Asian Countries

Fukudo, S., Hahm, K., Zhu, Q., Sollano, J. D., Rani, A. A., Syam, A. F., Kachintorn, U., Suzuki, H., Kamiya, T., Joh, T., et al. (2015) · Digestion · doi:10.1159/000369078 · Cited by 19 · see citing works

Influence of the corticotropin releasing hormone (CRH) on the brain-blood barrier permeability in cerebral ischemia in rats.

Hendryk, S., Jędrzejowska–Szypułka, H., Jośko, J., Jarząb, B., & Döhler, K.-D. (2002) · PubMed · Cited by 19 · see citing works

Anxiety, depression, and the microbiome: A role for gut peptides

Lach, G., Schellekens, H., Dinan, T. G., & Cryan, J. F. (2018) · Neurotherapeutics · doi:10.1007/s13311-017-0585-0 · Cited by 573 · see citing works

The impact of the Fungus-Host-Microbiota interplay uponCandida albicansinfections: current knowledge and new perspectives

d’Enfert, C., Kaune, A.-K., Alaban, L. R., Chakraborty, S., Cole, N. L., Delavy, M., Kosmala, D., Marsaux, B., Fróis-Martins, R., Morelli, M., et al. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa060 · Cited by 351 · see citing works

The Role of Microbiome in Insomnia, Circadian Disturbance and Depression

Li, Y., Hao, Y., Fan, F., & Zhang, B. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00669 · Cited by 294 · see citing works

The Microbiota-Gut-Brain Axis in Neuropsychiatric Disorders: Pathophysiological Mechanisms and Novel Treatments

Kim, Y., & Shin, C. (2018) · Current Neuropharmacology · doi:10.2174/1570159x15666170915141036 · Cited by 273 · see citing works

Gut dysbiosis, defective autophagy and altered immune responses in neurodegenerative diseases: Tales of a vicious cycle

Chidambaram, S. B., Essa, M. M., Rathipriya, A. G., Bishir, M., Ray, B., Mahalakshmi, A. M., Tousif, A. H., Sakharkar, M. K., Kashyap, R. S., Friedland, R. P., et al. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107988 · Cited by 204 · see citing works

Antidepressive Mechanisms of Probiotics and Their Therapeutic Potential

Yong, S. J., Tong, T., Chew, J., & Lim, W. L. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01361 · Cited by 217 · see citing works

Stress and the gut microbiota-brain axis

Molina‐Torres, G., Rodríguez-Arrastia, M. J., Román, P., Sánchez‐Labraca, N., & Cardona, D. (2019) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000478 · Cited by 181 · see citing works

Microbiome and Its Role in Irritable Bowel Syndrome

Pimentel, M., & Lembo, A. J. (2020) · Digestive Diseases and Sciences · doi:10.1007/s10620-020-06109-5 · Cited by 167 · see citing works

The Microbiota-Inflammasome Hypothesis of Major Depression

Inserra, A., Rogers, G. B., Licinio, J., & Wong, M. (2018) · BioEssays · doi:10.1002/bies.201800027 · Cited by 134 · see citing works

Multi-hit early life adversity affects gut microbiota, brain and behavior in a sex-dependent manner

Rincel, M., Aubert, P., Chevalier, J., Grohard, P. ‐., Basso, L., de Oliveira, C. M., Helbling, J., Lévy, É., Chevalier, G., Leboyer, M., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.03.006 · Cited by 132 · see citing works

Gut–Brain Axis and Mood Disorder

Liu, L., & Zhu, G. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00223 · Cited by 119 · see citing works

Metabolic Labeling of Peptidoglycan with NIR‐II Dye Enables In Vivo Imaging of Gut Microbiota

Wang, W., Yang, Q., Du, Y., Zhou, X., Du, X., Wu, Q., Lin, L., Song, Y., Li, F., Yang, C. J., et al. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201910555 · Cited by 113 · see citing works

Facilitation of kindling epileptogenesis by chronic stress may be mediated by intestinal microbiome

Medel‐Matus, J., Shin, D. H., Dorfman, E., Sankar, R., & Mazarati, A. M. (2018) · Epilepsia Open · doi:10.1002/epi4.12114 · Cited by 107 · see citing works

DHA-phospholipids (DHA-PL) and EPA-phospholipids (EPA-PL) prevent intestinal dysfunction induced by chronic stress

Cao, W., Wang, C., Chin, Y., Chen, X., Gao, Y., Yuan, S., Xue, C., Wang, Y., & Tang, Q. (2018) · Food & Function · doi:10.1039/c8fo01404c · Cited by 104 · see citing works

Shedding light on biological sex differences and microbiota–gut–brain axis: a comprehensive review of its roles in neuropsychiatric disorders

Shobeiri, P., Kalantari, A., Teixeira, A. L., & Rezaei, N. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00422-6 · Cited by 105 · see citing works

Intestinal Barrier Dysfunction and Microbiota–Gut–Brain Axis: Possible Implications in the Pathogenesis and Treatment of Autism Spectrum Disorder

Dargenio, V. N., Dargenio, C., Castellaneta, S., De Giacomo, A., Laguardia, M., Schettini, F., Francavilla, R., & Cristofori, F. (2023) · Nutrients · doi:10.3390/nu15071620 · Cited by 98 · see citing works

Neuropeptides in gut-brain axis and their influence on host immunity and stress

Wei, P., Keller, C., & Li, L. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.02.018 · Cited by 94 · see citing works

Uncovering the pathophysiology of irritable bowel syndrome by exploring the gut-brain axis: a narrative review

Tang, H.-Y., Jiang, A., Wang, X., Wang, H., Guan, Y., Li, F., & Shen, G.-M. (2021) · Annals of Translational Medicine · doi:10.21037/atm-21-2779 · Cited by 87 · see citing works

Intestinal autophagy links psychosocial stress with gut microbiota to promote inflammatory bowel disease

Wang, S., Shao, B., Zhao, S., Chang, X., Wang, P., Miao, C., Li, Z., & Bai, Y. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1634-x · Cited by 86 · see citing works

Chronic Unpredictable Mild Stress in Rats Induces Colonic Inflammation

Wei, L., Li, Y., Tang, W., Sun, Q., Chen, L., Wang, X., Liu, Q., Yu, S., Yu, S., Liu, C., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01228 · Cited by 83 · see citing works

Social Stress Affects Colonic Inflammation, the Gut Microbiome, and Short‐chain Fatty Acid Levels and Receptors

Maltz, R. M., Keirsey, J. K., Kim, S. C., Mackos, A. R., Gharaibeh, R. Z., Moore, C. C., Xu, J., Somogyi, Á., & Bailey, M. T. (2018) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0000000000002226 · Cited by 78 · see citing works

Possibilities and limits for using the gut microbiome to improve captive animal health

Diaz, J., & Reese, A. T. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00155-8 · Cited by 77 · see citing works

The Microbiota–Gut–Brain Axis and Epilepsy

Yue, Q., Cai, M., Xiao, B., Zhan, Q., & Zeng, C. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01130-2 · Cited by 75 · see citing works

The microbiota-gut-brain axis: An emerging role for the epigenome

Louwies, T., Johnson, A. C., Orock, A. M., Yuan, T., & Meerveld, B. G. (2019) · Experimental Biology and Medicine · doi:10.1177/1535370219891690 · Cited by 66 · see citing works

Chronic Stress, Inflammation, and Colon Cancer: A CRH System-Driven Molecular Crosstalk

Baritaki, S., de Bree, E., Chatzaki, Ε., & Pothoulakis, C. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101669 · Cited by 67 · see citing works

Dairy Propionibacterium freudenreichii ameliorates acute colitis by stimulating MUC2 expression in intestinal goblet cell in a DSS-induced colitis rat model

Ma, S., Yeom, J., & Lim, Y. (2020) · Scientific Reports · doi:10.1038/s41598-020-62497-8 · Cited by 59 · see citing works

Involvement of Corticotropin-Releasing Factor and Receptors in Immune Cells in Irritable Bowel Syndrome

Chatoo, M., Li, Y., Ma, Z., Coote, J. H., Du, J.-Z., & Chen, X. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00021 · Cited by 50 · see citing works

Maternal separation in rodents: a journey from gut to brain and nutritional perspectives

Rincel, M., & Darnaudéry, M. (2019) · Proceedings of The Nutrition Society · doi:10.1017/s0029665119000958 · Cited by 50 · see citing works

The Complex Molecular Picture of Gut and Oral Microbiota–Brain-Depression System: What We Know and What We Need to Know

Scassellati, C., Marizzoni, M., Cattane, N., Lopizzo, N., Mombelli, E., Riva, M. A., & Cattaneo, A. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.722335 · Cited by 40 · see citing works

Metabolome and microbiome profiling of a stress-sensitive rat model of gut-brain axis dysfunction

Bassett, S. A., Young, W., Fraser, K., Dalziel, J. E., Webster, J., Ryan, L., Fitzgerald, P., Stanton, C., Dinan, T. G., Cryan, J. F., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-50593-3 · Cited by 35 · see citing works

The Local Defender and Functional Mediator: Gut Microbiome

Yang, H., & Duan, Z. (2018) · Digestion · doi:10.1159/000484687 · Cited by 34 · see citing works

Pharmacological restoration of gut barrier function in stressed neonates partially reverses long-term alterations associated with maternal separation

Rincel, M., Olier, M., Minni, A., de Oliveira, C. M., Matime, Y., Gaultier, E., Grit, I., Helbling, J., Costa, A., Lépinay, A. L., et al. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05252-w · Cited by 33 · see citing works

IUPHAR review: Microbiota-gut-brain axis and its role in neuropsychiatric disorders

Lee, S.-H., Han, C., & Shin, C. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107749 · Cited by 36 · see citing works

Effects of psychological stress on inflammatory bowel disease via affecting the microbiota–gut–brain axis

Chen, Y., Chen, X., Lin, S., Huang, S., Li, L., Hong, M., Li­, ­., Ma, L., & Ma, J. (2025) · Chinese Medical Journal · doi:10.1097/cm9.0000000000003389 · Cited by 29 · see citing works

Irritable Bowel Syndrome-Like Symptoms in Ulcerative Colitis Patients in Clinical Remission: Association with Residual Colonic Inflammation

Ishihara, S., Kawashima, K., Fukuba, N., Tada, Y., Kotani, S., Mishima, Y., Oshima, N., & Kinoshita, Y. (2018) · Digestion · doi:10.1159/000494412 · Cited by 26 · see citing works

Social isolation in adolescence and long-term changes in the gut microbiota composition and in the hippocampal inflammation: Implications for psychiatric disorders – Dirk Hellhammer Award Paper 2021

Lopizzo, N., Marizzoni, M., Begni, V., Mazzelli, M., Provasi, S., Borruso, L., Riva, M. A., & Cattaneo, A. (2021) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2021.105416 · Cited by 24 · see citing works

Early Life Adversity, Microbiome, and Inflammatory Responses

Beurel, E., & Nemeroff, C. B. (2024) · Biomolecules · doi:10.3390/biom14070802 · Cited by 22 · see citing works

The effect of neonatal maternal separation on short-chain fatty acids and airway inflammation in adult asthma mice

Qian, L.-L., Lu, L., Huang, L., Wen, Q., Xie, J., Jin, W., Li, H., & Jiang, L. (2018) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2018.05.004 · Cited by 19 · see citing works

Individual Nutrition Is Associated with Altered Gut Microbiome Composition for Adults with Food Insecurity

Bixby, M., Gennings, C., Malecki, K. M. C., Sethi, A. K., Safdar, N., Peppard, P. E., & Eggers, S. I. (2022) · Nutrients · doi:10.3390/nu14163407 · Cited by 18 · see citing works

The Effects of Short-Chain Fatty Acids on Rat Colonic Hypermotility Induced by Water Avoidance Stress

Yuan, F., Tan, W., Ren, H., Yan, L., Wang, Y., & Luo, H. (2020) · Drug Design Development and Therapy · doi:10.2147/dddt.s246619 · Cited by 18 · see citing works

A Probiotic Mixture Induces Anxiolytic- and Antidepressive-Like Effects in Fischer and Maternally Deprived Long Evans Rats

Daugé, V., Philippe, C., Mariadassou, M., Rué, O., Martin, J., Rossignol, M., Dourmap, N., Svilar, L., Tourniaire, F., Monnoye, M., et al. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.581296 · Cited by 15 · see citing works

Lactobacillus reuteri effects on maternal separation stress in newborn mice

Park, E. S., Freeborn, J., Venna, V. R., Roos, S., Rhoads, J. M., & Liu, Y. (2021) · Pediatric Research · doi:10.1038/s41390-021-01374-0 · Cited by 15 · see citing works

Gut microbiome in neuropsychiatric disorders

Granados, D. M. M., Villasana‐Salazar, B., Coan, A. C., Rizzi, L., Balthazar, M. L. F., Godoi, A. B., do Canto, A. M., da Rosa, D. C., Silva, L. S., Tacla, R., et al. (2022) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x-anp-2021-0052 · Cited by 17 · see citing works

Metabolic Labeling of Peptidoglycan with NIR‐II Dye Enables In Vivo Imaging of Gut Microbiota

Wang, W., Yang, Q., Du, Y., Zhou, X., Du, X., Wu, Q., Lin, L., Song, Y., Li, F., Yang, C. J., et al. (2019) · Angewandte Chemie · doi:10.1002/ange.201910555 · Cited by 13 · see citing works

Preventive effect of peptides derived from fermented milk on chronic stress-induced brain damage and intestinal dysfunction in mice

Joung, J. Y., Song, J. G., Lee, B., Kim, H. W., & Oh, N. S. (2023) · Journal of Dairy Science · doi:10.3168/jds.2023-23320 · Cited by 12 · see citing works

Involvement of toll-like receptor 5 on mouse model of colonic hypersensitivity induced by neonatal maternal separation

Mallaret, G., Lashermes, A., Méleine, M., Boudieu, L., Barbier, J., Aissouni, Y., Gelot, A., Chassaing, B., Gewirtz, A. T., Ardid, D., et al. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i29.3903 · Cited by 13 · see citing works

Chronic Kidney Disease Elicits an Intestinal Inflammation Resulting in Intestinal Dysmotility Associated with the Activation of Inducible Nitric Oxide Synthesis in Rat

Yu, C., Tan, S., Wang, Z., Deng, B., Li, J., Wang, Q., Zhou, C., Kang, X., Yu, Z., & Zhuang, S. (2018) · Digestion · doi:10.1159/000481618 · Cited by 12 · see citing works

Dynamics of Spatial Organization of Bacterial Communities in a Tunable Flow Gut Microbiome‐on‐a‐Chip

Lee, J., Menon, N., Truong, H. D., & Lim, C. (2025) · Small · doi:10.1002/smll.202410258 · Cited by 12 · see citing works

New perspectives on microbiome-dependent gut-brain pathways for the treatment of depression with gastrointestinal symptoms: from bench to bedside

Liu, M., Fan, G., Meng, L., Yang, K., & Liu, H. (2024) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300343 · Cited by 10 · see citing works

Stress and corticotropin releasing factor (CRF) promote necrotizing enterocolitis in a formula-fed neonatal rat model

Bell, R. L., Withers, G. S., Kuypers, F. A., Stehr, W., & Bhargava, A. (2021) · PLoS ONE · doi:10.1371/journal.pone.0246412 · Cited by 7 · see citing works

The gut microbiome modulates the susceptibility to traumatic stress in a sex‐dependent manner

Shen, D., Chang, L., Su, F., Huang, S., Xu, H., Si, Y., Wang, F., & Xue, Y.-X. (2024) · Journal of Neuroscience Research · doi:10.1002/jnr.25315 · Cited by 6 · see citing works

Animal models with characteristics of irritable bowel syndrome with diarrhea: current applications and future perspectives

Chen, J., Zhang, T., Liu, Y., Dong, X., & Liu, J. (2024) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00060.2024 · Cited by 6 · see citing works

Stress co‐opts the gut to affect epileptogenesis. Commentary on “Facilitation of kindling epileptogenesis by chronic stress may be mediated by intestinal microbiome”

Pittman, Q. J. (2019) · Epilepsia Open · doi:10.1002/epi4.12326 · Cited by 6 · see citing works

Mechanistic insights into the antidepressant potential of plant-derived flavonoids: A preclinical review

Cui, Y., Ursuliak, Z., & Rupasinghe, H. P. V. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111567 · Cited by 5 · see citing works

Structural Alteration of Gut Microbiota During the Amelioration of Chronic Psychological Stress-Aggravated Diabetes-Associated Cognitive Decline by a Traditional Chinese Herbal Formula, ZiBu PiYin Recipe

Zhou, W., Zhan, L., Xu, H., & Zhang, L. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220692 · Cited by 5 · see citing works

Gut microbiome as a therapeutic target in the treatment of depression and anxiety

Ab, K. (2021) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro2021121111129 · Cited by 5 · see citing works

Neonatal intestinal injury induced by maternal separation: pathogenesis and pharmacological targets

Li, B., Yu, F. Z., Minich, A., Hock, A., Lee, C. M., & Pierro, A. (2018) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2018-0370 · Cited by 5 · see citing works

A Future Avenue of Treatment Ulcerative Colitis Targeting Macrophage Polarization: A Phytochemical Application

Saurabh, N. K., Khan, M. M., & Kirabo, A. (2024) · Crohn s & Colitis 360 · doi:10.1093/crocol/otae070 · Cited by 4 · see citing works

The Impact of Psychotrauma and Emotional Stress Vulnerability on Physical and Mental Functioning of Patients with Inflammatory Bowel Disease

Nass, B. Y. S., Dibbets, P., & Markus, C. R. (2023) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph20216976 · Cited by 4 · see citing works

Differences in gut microbial patterns associated with salivary biomarkers in young Japanese adults

Seura, T., & Fukuwatari, T. (2020) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2019-034 · Cited by 4 · see citing works

Metagenomic gut microbiome analysis of Japanese patients with multiple chemical sensitivity/idiopathic environmental intolerance

Watai, K., Suda, W., Kurokawa, R., Sekiya, K., Hayashi, H., Iwata, M., Nagayama, K., Nakamura, Y., Hamada, Y., Kamide, Y., et al. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03239-y · Cited by 4 · see citing works

Updates in interaction of gastroesophageal reflux disease and extragastroesophageal digestive diseases

Li, Y., & Duan, Z. (2022) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2022.2056018 · Cited by 3 · see citing works

Gut Dysbiosis in Insomnia and Diurnal Cycle

Kumar, R. (2022) · Springer eBooks · doi:10.1007/978-981-16-6760-2_8 · Cited by 2 · see citing works

Dynamics of Virulence of Commensals: Preventive Phenotypical Mutability

Chepur, S. V., Nn, P., Sayganov, S. A., Chubar, O. V., Сергеевна, Б. Л., & Litvinenko, I. (2023) · Biology Bulletin Reviews · doi:10.1134/s207908642306004x · Cited by 2 · see citing works

[A Review of Chronic Stress and the Initiation and Evolution of Cancer].

Liu, M., Xie, X., Li, Q., & Xu, C. S. (2021) · PubMed Central · doi:10.12182/20210160203 · Cited by 2 · see citing works

Importance of the Microbiota in Early Life and Influence on Future Health

Collins, J. M., Cryan, J. F., & O’Mahony, S. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99971-7.00017-5 · Cited by 2 · see citing works

Role of polyphenols in epilepsy: from the perspective of gut microbiota

Xu, X., Shi, J., Cai, G., Ma, C., Wang, W., Feng, R., Boczek, T., Tang, Y., He, Z., & Guo, F. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250303 · Cited by 1 · see citing works

Impact of Sex, Gonadectomy, and Repeated Restraint Stress on Gut Microbiome in Mice

Mekadim, C., Mrázek, J., Vodička, M., Ergang, P., Fliegerova, K. O., Mahayri, T. M., Chawengsaksophak, K., & Pácha, J. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05305-6 · Cited by 1 · see citing works

Contextual & physiological markers for individual distress (CP-MIND). Brain health as a comprehensive framework for Mental-health equity

Morales, J. P., Macchiavello, F., & Rojas‐Thomas, F. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.034 · Cited by 2 · see citing works

Application of a food trigger score to identify common dietary triggers among Saudi adults with irritable bowel syndrome

Ajabnoor, S. M., & Tashkandi, L. (2026) · Saudi Journal of Gastroenterology · doi:10.4103/sjg.sjg_454_25 · Cited by 1 · see citing works

Intestinal microbiota and stress: how much do we know so far

Hyder, N., & Raza, M. L. (2026) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2026.2706149 · Cited by 1 · see citing works

Evaluating Small Intestinal Motility in a Rat Model of Adolescent Irritable Bowel Syndrome

Sato, M., Kudo, T., Arai, N., Kyodo, R., HOSOI, K., Sakaguchi, K., Ikuse, T., Jimbo, K., Ohtsuka, Y., & Shimizu, T. (2022) · Juntendō Igaku/Juntendo igaku · doi:10.14789/jmj.jmj21-0050-oa · Cited by 1 · see citing works

Liens entre microbiote intestinal et comportement de type anxiodépressif chez le rongeur

Rabot, S., Naudon, L., & Daugé, V. (2018) · Phytothérapie · doi:10.3166/phyto-2018-0090 · Cited by 1 · see citing works

Gut Hormones and Neuropeptides as Mediators of Microbiome–Brain Communication

Holzer, P. D., & Farzi, A. (2020) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190931544.013.1 · Cited by 1 · see citing works

Estrogen-gut microbiota interactions and irritable bowel syndrome

Jiang, F.-R., Hang, L., Zhou, Y., Feng, Y., & Yuan, J. (2022) · World Chinese Journal of Digestology · doi:10.11569/wcjd.v30.i12.511 · Cited by 1 · see citing works

Gut symptoms in the depressed elderly: The interactions between emotion and gastrointestinal neuroendocrinology

Ting, C.-H., & Chen, C. (2021) · Journal of the Chinese Medical Association · doi:10.1097/jcma.0000000000000521 · Cited by 1 · see citing works

腸内微生物叢・代謝物ビッグデータを どのように食・食品機能性研究に応用するか？

裕二, 内. (2019) · doi:10.32153/ffr.15.0_4

[Progresses on the effects and mechanisms of stress on gut microbiota].

Song, L., Zhang, J., & Duan, L.-P. (2020) · PubMed

Evaluation of Small Intestinal Motility in a Rat Model of Irritable Bowel SyndromePreprint

Sato, M., Kudo, T., Arai, N., Kyodo, R., Hosoi, K., Sakaguchi, K., Ikuse, T., Jimbo, K., Ohtsuka, Y., & Shimizu, T. (2021) · Research Square · doi:10.21203/rs.3.rs-763246/v1

A review of the use of probiotics in the treatment of ulcerative colitis

Ghaleh, H. E. G., & Bahrami, S. (2023) · Modern Medical Laboratory Journal · doi:10.30699/mmlj17.6.1.15

Correlação entre microbiota intestinal e distúrbios neurológicos

Leite, C. D. A. E. A., dos Santos, J. P. L., Armada, L., Leite, M. A. A., Barcellos, C. T., Tavares, T. D. M., & Orsini, M. A. (2024) · Enfermagem Brasil · doi:10.33233/eb.v22i6.5570

Dynamics of Commensals Virulence: Preventive Phenotypical Mutability

Chepur, S. V., Nn, P., Sayganov, S. A., Chubar, O. V., Сергеевна, Б. Л., & Litvinenko, I. (2023) · Успехи современной биологии · doi:10.31857/s0042132423030043

Gut microbiota changes and enteric therapies in critically ill patients: a narrative review

Ojima, M., Shimizu, K., & Ogura, H. (2024) · Journal of the Japanese Society of Intensive Care Medicine · doi:10.3918/jsicm.31_566

Combat Stress: Formation Mechanisms and Targets of Directed Pharmacological Effects

Chepur, S. V. (2024) · Human Physiology · doi:10.31857/s0131164624060116

Combat Stress: Formation Mechanisms and Targets of Directed Pharmacological Effects

Chepur, S. V. (2024) · Human Physiology · doi:10.1134/s0362119724701123

Additional file 1 of Metagenomic gut microbiome analysis of Japanese patients with multiple chemical sensitivity/idiopathic environmental intolerance

Watai, K., Suda, W., Kurokawa, R., Sekiya, K., Hayashi, H., Iwata, M., Nagayama, K., Nakamura, Y., Hamada, Y., Kamide, Y., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25389503

A dual pathway intervention of tES and FMT enhances emotion regulation in stressed military personnel

Cheng, C., Li, Y., Lv, W., Zhao, J., Yan, Z., & Lü, H. (2026) · Discover Mental Health · doi:10.1007/s44192-026-00375-x

Modulation de l'apport qualitatif post-natal en lipides sur le fonctionnement cérébral du nouveau-né

Aïdoud, N. (2018) · theses.fr (ABES) · doi:10.70675/6e8c9142za1bcz4dbcza6bfzebbdbfbac84a

Role of the gut-brain axis in early stress-induced emotional vulnerability

Rincel, M. (2017) · theses.fr (ABES) · doi:10.70675/5e8a972cz9ad1z42aezb89cze6474124ef90

The Microbiota–Gut–Brain Axis: From Early Life to Aging and Mental Health

Naito, Y. (2026) · Springer eBooks · doi:10.1007/978-981-95-7068-3_55

Galanin signaling in stress-induced brain–gut axis dysregulation: Receptor-specific mechanisms and context-dependent pharmacology

Zhang, E., Wang, Z., Xu, H., Wu, J., Xu, Z.-Q. D., & Liang, Y. (2026) · Peptides · doi:10.1016/j.peptides.2026.171518

Central neuroendocrine governance as a unifying framework for host–tumor interaction: From afferent sensing to therapeutic modulation

Wang, Y., Zhang, M.-L., & Jin, W. (2026) · Cancer Letters · doi:10.1016/j.canlet.2026.218906

Modulation of intestinal motility in an adolescent rat model of irritable bowel syndrome

京戸玲子, & Kyoudo, R. (2021) · Institutional Repositories DataBase (IRDB)

Integrative analysis of the gut microbiome and metabolome in a rat model with stress induced irritable bowel syndrome

Hu, Y., Chen, F., Ye, H., & Lü, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-97083-z · Cited by 17 · see citing works

Su2045 Mast Cell CRF1 Mediates Mast Cell Degranulation and Intestinal Permeability in Response to Psychological and Immunological Stress

Ayyadurai, S., Gibson, A. J., Sommerville, L. J., D’Costa, S., Edwards, L., Lennon, E. M., Pohl, C. S., Medland, J. E., Bagley, K., Winston, J. A., et al. (2015) · Gastroenterology · doi:10.1016/s0016-5085(15)31974-0

Su1943 Alterations in Intestinal Motility and Gut Microbiota Composition by Maternal Separation Stress in Rats

Murakami, T., Kamada, K., Mizushima, K., Suzuki, K., Higashimura, Y., Katada, K., Uchiyama, K., Takagi, T., Handa, O., Naito, Y., et al. (2016) · Gastroenterology · doi:10.1016/s0016-5085(16)32042-x

Effects of neonatal maternal separation on the colonic motility and enteric nervous system of adult rats

Li, B., Cheung, C., Rudd, J. A., Wu, J., & Chan, W. Y. (2017) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2017.08.2577