The DOI matches its Crossref record; 402 of the 407 references it cites were found in a registry or an index.
The Neuroendocrinology of the Microbiota-Gut-Brain Axis: A Behavioural Perspective
Open accessAbstract
The human gut harbours trillions of symbiotic bacteria that play a key role in programming different aspects of host physiology in health and disease. These intestinal microbes are also key components of the gut-brain axis, the bidirectional communication pathway between the gut and the central nervous system (CNS). In addition, the CNS is closely interconnected with the endocrine system to regulate many physiological processes. An expanding body of evidence is supporting the notion that gut microbiota modifications and/or manipulations may also play a crucial role in the manifestation of specific behavioural responses regulated by neuroendocrine pathways. In this review, we will focus on how the intestinal microorganisms interact with elements of the host neuroendocrine system to modify behaviours relevant to stress, eating behaviour, sexual behaviour, social behaviour, cognition and addiction.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This relationship, like the microbiota-gut-brain axis itself, is bidirectional -the microbiota can modulate stress-induced alterations in anxiety, memory, cognition and neuroinflammation (for reviews, see Cussotto et al., 2018;Farzi et al., 2018;Foster et al., 2017;Rea et al., 2016;Sherwin et al., 2016a).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Cussotto et al., 2018
In the citing paper
“The development of the blood-brain barrier is now well established to be contingent upon the presence of commensal gut flora (10, 11).”
From Association Between Gut Microbiota and Autism Spectrum Disorder: A Systematic Review and Meta-Analysis (2019) · cites this paper as [10]
Citations
Cites
1 retracted
Million, M., Angelakis, E., Maraninchi, M., Henry, M., Giorgi, R., Valero, R., Vialettes, B., & Raoult, D. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.20 · Cited by 362
RetractedAn obesity-associated gut microbiome with increased capacity for energy harvest
Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444 · cited 2×
“germ-free mice with an obese microbiota resulted in a significantly greater increase in total body fat than colonization with a lean microbiota (Turnbaugh et al., 2006).”
BackgroundA human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Human gut microbes associated with obesity
Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785 · cited 2×
“to obesity and this can occur in a causative way (Backhed et al., 2004; Ley et al., 2006; Ridaura et al., 2013; Turnbaugh et al., 2009b).”
BackgroundA core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics
Gibson, G. R., & Roberfroid, M. B. (1995) · Journal of Nutrition · doi:10.1093/jn/125.6.1401 · Cited by 7,659 · cited 1×
“host by selectively stimulating the growth and/or activity of one or a limited number of bacteria in the colon, thus improving host health” (Gibson and Roberfroid, 1995) but this concept has been expanded more recently (Bindels et al.”
BackgroundLinking long-term dietary patterns with gut microbial enterotypes
Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513 · cited 1×
“33 microbiota composition (Conlon and Bird, 2014; De Filippo et al., 2010; Queipo-Ortuno et al., 2013; Wu et al., 2011); however the converse might also be true.”
BackgroundThe gut microbiota as an environmental factor that regulates fat storage
Bäckhed, F., Ding, H., Wang, T., Hooper, L. V., Koh, G. Y., Nagy, A., Semenkovich, C. F., & Gordon, J. I. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407076101 · Cited by 6,245
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176 · cited 1×
“Both obese humans and mice have been shown to have a specific microbial profile that is different from lean people, with the relative proportion of Bacteroidetes decreased in obese subjects (Ley et al., 2005; Ley et al., 2006).”
BackgroundDe Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579
Research works printed but not linked: 2
- Chrousos, 1995, The hypothalamic–pituitary–adrenal axis and immune-mediated inflammation, N. Engl. J. Med., 332, 1351, 10.1056/NEJM199505183322008 · DOI · Paper page
- Tsigos, 2002, Hypothalamic–pituitary–adrenal axis, neuroendocrine factors and stress, J. Psychosom. Res., 53, 865, 10.1016/S0022-3999(02)00429-4 · DOI · Paper page
Cited by
Sorted by citations
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286
Global Impacts of Western Diet and Its Effects on Metabolism and Health: A Narrative Review
Clemente‐Suárez, V. J., Beltrán-Velasco, A. I., Redondo-Flórez, L., Martín-Rodríguez, A., & Tornero-Aguilera, J. F. (2023) · Nutrients · doi:10.3390/nu15122749 · Cited by 933
Impact of microbiota on central nervous system and neurological diseases: the gut-brain axis
Ma, Q., Xing, C., Long, W., Wang, H. Y., Liu, Q., & Wang, R. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1434-3 · Cited by 767
“A notable role of human digestive system in brain development has been proposed [15, 50].”
BackgroundGut Microbiota and Energy Homeostasis in Fish
Butt, R. L., & Volkoff, H. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00009 · Cited by 637
McGuinness, A. J., Davis, J. A., Dawson, S. L., Loughman, A., Collier, F., O’Hely, M., Simpson, C. A., Green, J., Marx, W., Hair, C., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01456-3 · Cited by 502
“They influence many aspects of physiology via neural, hormonal and immunological pathways [1, 2], so much so that some describe the gut microbiome as a ‘virtual organ’ [3, 4].”
BackgroundThe microbiota–gut–brain axis and neurodevelopmental disorders
Wang, Q., Yang, Q., & Liu, X. (2023) · Protein & Cell · doi:10.1093/procel/pwad026 · Cited by 429
The HPA axis dysregulation in severe mental illness: Can we shift the blame to gut microbiota?
Misiak, B., Łoniewski, I., Marlicz, W., Frydecka, D., Szulc, A., Rudzki, L., & Samochowiec, J. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.109951 · Cited by 343
Zhu, F., Guo, R., Wang, W., Ju, Y., Wang, Q., Ma, Q., Sun, Q., Fan, Y., Xie, Y., Yang, Z., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0475-4 · Cited by 323
The gut microbiota-immune-brain axis: therapeutic implications
O’Riordan, K. J., Moloney, G. M., Keane, L., Clarke, G., & Cryan, J. F. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.101982 · Cited by 333
“32 Immune-HPA interactions, demonstrated through microbial translocation and inflam-matory cytokine activation, underscore the gut microbiota’s role in HPA signaling.”
Xu, M., Xu, X., Li, J., & Li, F. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00473 · Cited by 309
The Gut Microbiome Influences Host Endocrine Functions
Rastelli, M., Cani, P. D., & Knauf, C. (2019) · Endocrine Reviews · doi:10.1210/er.2018-00280 · Cited by 331
Gut-Brain Psychology: Rethinking Psychology From the Microbiota–Gut–Brain Axis
Liang, S., Wu, X., & Jin, F. (2018) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2018.00033 · Cited by 279
Obesity and gut–microbiota–brain axis: A narrative review
Asadi, A., Mehr, N. S., Mohamadi, M. H., Shokri, F., Heidary, M., Sadeghifard, N., & Khoshnood, S. (2022) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.24420 · Cited by 266
Gut Microbiota and Their Neuroinflammatory Implications in Alzheimer’s Disease
Giau, V. V., Wu, S., Jamerlan, A., An, S. S. A., Kim, S., & Hulme, J. (2018) · Nutrients · doi:10.3390/nu10111765 · Cited by 239
“Accumulating evidence suggests that the composition of the gut microbiota may also have a role in several other metabolic conditions involving the CNS [42,43].”
BackgroundFrom correlation to causality: the case of Subdoligranulum
Hul, M. V., Roy, T. L., Prifti, E., Dao, M. C., Paquot, A., Zucker, J., Delzenne, N. M., Muccioli, G. G., Clément, K., & Cani, P. D. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1849998 · Cited by 230
Bosi, A., Banfi, D., Bistoletti, M., Giaroni, C., & Baj, A. (2020) · International Journal of Tryptophan Research · doi:10.1177/1178646920928984 · Cited by 221
You’ve got male: Sex and the microbiota-gut-brain axis across the lifespan
Jaggar, M., Rea, K., Spichak, S., Dinan, T. G., & Cryan, J. F. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100815 · Cited by 200
Self-citationWhen Rhythms Meet the Blues: Circadian Interactions with the Microbiota-Gut-Brain Axis
Teichman, E. M., O’Riordan, K. J., Gahan, C. G. M., Dinan, T. G., & Cryan, J. F. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.02.008 · Cited by 199
Key role of gut microbiota in anhedonia-like phenotype in rodents with neuropathic pain
Yang, C., Fang, X., Zhan, G., Huang, N., Li, S., Bi, J., Jiang, R., Yang, L., Miao, L., Zhu, B., et al. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0379-8 · Cited by 176
Snigdha, S., Ha, K., Tsai, P., Dinan, T. G., Bartos, J. D., & Shahid, M. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107978 · Cited by 173
Gazerani, P. (2020) · Nutrients · doi:10.3390/nu12061658 · Cited by 186
“It has been proposed that cross-talk between the gut and brain may impact several neurological [58] and behavioral [59] disorders.”
BackgroundThe Gut Microbiome and Sex Hormone-Related Diseases
He, S., Li, H., Yu, Z., Zhang, F., Liang, S., Liu, H., Chen, H., & Lü, M. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.711137 · Cited by 181
Checa-Ros, A., Jeréz-Calero, A., Molina-Carballo, A., Campoy, C., & Muñoz-Hoyos, A. (2021) · Nutrients · doi:10.3390/nu13010249 · Cited by 164
“The gut microbiome directly influences the production of glucocorticoids and immune mediators, such as tumor necrosis factor-alpha (TNF-α) and interleukins-1beta and 6 (IL-1β and IL-6), which in turn stimulates the HPA axis [69].”
BackgroundSepsis‐Induced Brain Dysfunction: Pathogenesis, Diagnosis, and Treatment
Pan, S., Lv, Z., Wang, R., Shu, H., Yuan, S., Yu, Y., & Shang, Y. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1328729 · Cited by 169
“And other di ff erent kinds of hormones induced by enteroendo-crine cells also transmit peripheral in fl ammatory signals through the vagus nerve to the autonomic nervous system nucleus, neuroendocrine centers, and behavioral centers, driving corresponding changes [66, 74 – 76].”
Microbiota‐gut‐brain axis as a regulator of reward processes
García‐Cabrerizo, R., Carbia, C., O’Riordan, K. J., Schellekens, H., & Cryan, J. F. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15284 · Cited by 150
“Numerous preclinical evidence show that the intestinal microbiota can be altered under different chronic psychosocial stressors (Cussotto et al., 2018).”
BackgroundThe Relationship Between the Gut Microbiome-Immune System-Brain Axis and Major Depressive Disorder
Foster, J. A., Baker, G. B., & Dursun, S. M. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.721126 · Cited by 161
“For example, exposure to various types of stress has been reported to alter the microbiota profile, and alteration of the gut microbiota can affect responses to stress, anxiety-like behavior and, as described below, activation of the hypothalamicpituitary-adrenal (HPA) axis [reviews: (40, 44)].”
BackgroundLignans and Gut Microbiota: An Interplay Revealing Potential Health Implications
Senizza, A., Rocchetti, G., Mosele, J. I., Patrone, V., Callegari, M. L., Morelli, L., & Lucini, L. (2020) · Molecules · doi:10.3390/molecules25235709 · Cited by 132
Spichak, S., Bastiaanssen, T. F. S., Berding, K., Vlckova, K., Clarke, G., Dinan, T. G., & Cryan, J. F. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.044 · Cited by 127
Bicknell, B. T., Liebert, A. D., Borody, T. J., Herkes, G., McLachlan, C. S., & Kiat, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119577 · Cited by 135
“The gut microbiome also appears to be essential for the successful development of the HPA axis [106], with a developing microbiome stimulating inflammatory markers such as TNF-α , IL-1 β , and IL-6, which help mature the HPA axis [107]. and IL-6, which help mature the HPA axis [107].”
Pesticide exposure and the microbiota-gut-brain axis
Matsuzaki, R., Gunnigle, E., Geissen, V., Clarke, G. A., Nagpal, J. K., & Cryan, J. F. (2023) · The ISME Journal · doi:10.1038/s41396-023-01450-9 · Cited by 129
“, HPA axis), neuronal and immune pathways [46].”
BackgroundWang, S., Ishima, T., Qu, Y., Shan, J., Chang, L., Wei, Y., Zhang, J., Pu, Y., Fujita, Y., Tan, Y., et al. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.06.006 · Cited by 118
Tirelle, P., Breton, J., Riou, G., Déchelotte, P., Coëffier, M., & Ribet, D. (2020) · BMC Microbiology · doi:10.1186/s12866-020-02018-9 · Cited by 116
Li, J., Fang, B., Pang, G., Zhang, M., & Ren, F. (2019) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2019.05.018 · Cited by 107
Wang, Y., An, Y., Ma, W., Yu, H., Lu, Y., Zhang, X., Wang, Y., Liu, W., Wang, T., & Xiao, R. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01873-7 · Cited by 106
Visceral pain: gut microbiota, a new hope?
Pusceddu, M. M., & Gareau, M. G. (2018) · Journal of Biomedical Science · doi:10.1186/s12929-018-0476-7 · Cited by 102
Shobeiri, P., Kalantari, A., Teixeira, A. L., & Rezaei, N. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00422-6 · Cited by 113
“Several studies reported on the potential mechanisms of microbiome–CNS crosstalk, including endocrine [28], the vagus nerve [29, 30], immune [31, 32] and neuropeptide/neurotransmitter systems [33, 34], and signaling molecules.”
BackgroundZhang, K., Fujita, Y., Chang, L., Qu, Y., Pu, Y., Wang, S., Shirayama, Y., & Hashimoto, K. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0571-x · Cited by 99
Wang, S., Qu, Y., Chang, L., Pu, Y., Zhang, K., & Hashimoto, K. (2019) · Journal of Affective Disorders · doi:10.1016/j.jad.2019.09.064 · Cited by 95
The effects of gut microbiota on appetite regulation and the underlying mechanisms
Yu, M., Yu, B., & Chen, D. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2414796 · Cited by 100
“20,21 The gut microbiota plays a pivotal role in the regulation of appetite, as they can modulate physiological processes including insulin sensitivity, glucose homeostasis, and the balance of energy intake through the production of metabolites like short-chain fatty acids (SCFAs).”
BackgroundComplementary Feeding Methods—A Review of the Benefits and Risks
Boswell, N. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18137165 · Cited by 93
Wang, J., Yang, Y., Shi, Y., Wei, L., Gao, L., & Liu, M. (2024) · Environment International · doi:10.1016/j.envint.2024.108523 · Cited by 102
The microbiota-gut-brain axis: Focus on the fundamental communication pathways
Bistoletti, M., Bosi, A., Banfi, D., Giaroni, C., & Baj, A. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.08.012 · Cited by 91
Pavlovian Conditioning of Immunological and Neuroendocrine Functions
Hadamitzky, M., Lückemann, L., Pacheco‐López, G., & Schedlowski, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00033.2018 · Cited by 89
Xiao, S., Jiang, S., Qian, D., & Duan, J. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10312-4 · Cited by 89
Baldi, S., Mundula, T., Nannini, G., & Amedei, A. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i39.6715 · Cited by 90
Pu, Y., Chang, L., Qu, Y., Wang, S., Zhang, K., & Hashimoto, K. (2019) · Aging · doi:10.18632/aging.102221 · Cited by 80
A biological framework for emotional dysregulation in alcohol misuse: from gut to brain
Carbia, C., Lannoy, S., Maurage, P., López‐Caneda, E., O’Riordan, K. J., Dinan, T. G., & Cryan, J. F. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00970-6 · Cited by 82
Ağagündüz, D., Bingöl, F. G., Çelik, E., Cemali, Ö., Özenir, Ç., Özoğul, F., & Capasso, R. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03609-y · Cited by 80
Regulation of endocrine systems by the microbiome: Perspectives from comparative animal models
Williams, C. L., García‐Reyero, N., Martyniuk, C. J., Tubbs, C. W., & Bisesi, J. H. (2020) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2020.113437 · Cited by 75
Inulin ameliorates schizophrenia via modulation of the gut microbiota and anti-inflammation in mice
Guo, L., Xiao, P., Zhang, X., Yang, Y., Yang, M., Wang, T., Lu, H., Tian, H., Wang, H., & Liu, J. (2021) · Food & Function · doi:10.1039/d0fo02778b · Cited by 74
Precocious puberty and microbiota: The role of the sex hormone–gut microbiome axis
Calcaterra, V., Rossi, V., Massini, G., Regalbuto, C., Hruby, C., Panelli, S., Bandi, C., & Zuccotti, G. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1000919 · Cited by 83
“More studies on humans are needed to better understand the underlying mechanisms of this axis (4, 75).”
BackgroundAcne and Stress: Impact of Catecholamines on Cutibacterium acnes
Borrel, V., THOMAS, P. A., Catovic, C., Racine, P., Konto‐Ghiorghi, Y., Lefeuvre, L., Poc, C. D., Zouboulis, C. C., & Feuilloley, M. G. J. (2019) · Frontiers in Medicine · doi:10.3389/fmed.2019.00155 · Cited by 72
Curcumin Alleviates DSS‐Induced Anxiety‐Like Behaviors via the Microbial‐Brain‐Gut Axis
Zhang, F., Zhou, Y., Chen, H., Jiang, H., Zhou, F., Lü, B., & Xu, M. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6244757 · Cited by 69
“Therefore, some scholars suggest the MGB axis, which involves bidirectional communication between the microbiota and brain [12].”
BackgroundWu, Y., Wang, Y., Hu, A., Shu, X., Huang, W., Liu, J., Wang, B., Zhang, R., Yue, M., & Yang, C. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.946096 · Cited by 78
The role of the gut microbiome in opioid use
Ren, M., & Lotfipour, S. (2019) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000538 · Cited by 69
“An abundance of evidence in both humans and animals supports an essential role of gut microbiota in regulating brain function, mood, stress, and behavioral responses to rewards, including food and drugs of abuse (Collins and Bercik, 2009; Diaz Heijtz et al., 2011; Clarke et al., 2013; Selkrig et al., 2014; Cussotto et…”
BackgroundSun, Y., Zeng, X., Liu, Y., Zhan, S., Wu, Z., Zheng, X., & Zhang, X. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.07.090 · Cited by 69
Neuroinflammation, Microbiota-Gut-Brain Axis, and Depression: The Vicious Circle
Reyes-Martínez, S., Segura-Real, L., Gómez-García, A. P., Tesoro-Cruz, E., Constantino-Jonapa, L. A., Amedei, A., & Aguirre‐García, M. M. (2023) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2203065 · Cited by 78
Traina, G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00345 · Cited by 69
Flux, M. C., & Lowry, C. A. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104578 · Cited by 70
Zyoud, S. H., Smale, S., Waring, W. S., Sweileh, W. M., & Al‐Jabi, S. W. (2019) · BMC Gastroenterology · doi:10.1186/s12876-019-1076-z · Cited by 70
The Role of the Gut-Brain Axis in Attention-Deficit/Hyperactivity Disorder
Dam, S. A., Mostert, J. C., Szopinska-Tokov, J., Bloemendaal, M., Amato, M. P., & Vásquez, A. A. (2019) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2019.05.001 · Cited by 66
Tomizawa, Y., Kurokawa, S., Ishii, D., Miyaho, K., Ishii, C., Sanada, K., Fukuda, S., Mimura, M., & Kishimoto, T. (2020) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyaa070 · Cited by 64
“A previous animal study reported a significant difference in specific species composition between rats treated with escitalopram and those receiving vehicle, while the beta diversity in principal coordinate analysis did not differ significantly (Cussotto et al., 2018).”
ResultGut microbiota and neuropsychiatric disorders: Implications for neuroendocrine-immune regulation
Ge, T., Yao, X., Zhao, H., Yang, W., Zou, X., Peng, F., Li, B., & Cui, R. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105909 · Cited by 62
Mood‐related central and peripheral clocks
Ketchesin, K. D., Becker‐Krail, D. D., & McClung, C. A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14253 · Cited by 67
“Short- chain fatty acids, such as butyrate, acetate, and propionate, are common metabolic byproducts released by gut microbiota and have been shown to alter host immune responses, metabolism, and neurotransmitter synthesis (Cussotto et al., 2018; Rogers et al., 2016).”
BackgroundInfluentialThe contribution of age-related changes in the gut-brain axis to neurological disorders
Khan, R., Gesù, C. M. D., Lee, J., & McCullough, L. D. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2302801 · Cited by 62
Bioque, M., González-Rodríguez, A., García‐Rizo, C., Cobo, J., Monreal, J. A., Usall, J., Soria, V., & Labad, J. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110130 · Cited by 58
Chemogenetics defines a short-chain fatty acid receptor gut–brain axis
Barki, N., Bolognini, D., Börjesson, U., Jenkins, L., Riddell, J. S., Hughes, D. I., Ulven, T., Hudson, B. D., Ulven, E. R., Dekker, N., et al. (2022) · eLife · doi:10.7554/elife.73777 · Cited by 58
Meng, G., Zhou, X., Wang, M., Zhou, L., Wang, Z., Wang, M., Deng, J., Wang, Y., Zhou, Z., Zhang, Y., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.03.066 · Cited by 54
“Gut microbes can bidirectionally interact with the brain through autonomic neurotransmitters and metabolites; thus, the concept of the “microbiota-gut-brain” axis has been widely accepted in recent years [13].”
BackgroundChiu, L., & Gilbert, S. F. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817996-3.00015-3 · Cited by 55
The gut–brain axis in vertebrates: implications for food intake regulation
Blanco, A. M., Calo, J., & Soengas, J. L. (2021) · Journal of Experimental Biology · doi:10.1242/jeb.231571 · Cited by 60
Wang, J., Qin, Y., Wu, Q., Zeng, D., Gao, X., Wang, Q., Li, Z., Ni, Y., Li, H., Zhang, P., et al. (2025) · Nature Medicine · doi:10.1038/s41591-025-03724-5 · Cited by 56
The gut microbiome, immune modulation, and cognitive decline: insights on the gut-brain axis
Zhang, R., Ding, N., Feng, X., & Liao, W. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1529958 · Cited by 61
Leung, R., & Covașă, M. (2021) · Nutrients · doi:10.3390/nu13082581 · Cited by 55
“Increasing evidence suggests that these gut microbes affect endocrine functions through two pathways: directly through the production of bioactive metabolites like SCFAs, and indirectly, as modulators of inflammatory responses, immune responses and hormonal secretion [85].”
BackgroundA brief period of sleep deprivation leads to subtle changes in mouse gut microbiota
Aidy, S. E., Bolsius, Y. G., Raven, F., & Havekes, R. (2019) · Journal of Sleep Research · doi:10.1111/jsr.12920 · Cited by 50
Qu, Y., Zhang, K., Pu, Y., Chang, L., Wang, S., Tan, Y., Wang, X., Zhang, J., Ohnishi, T., Yoshikawa, T., et al. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.03.095 · Cited by 50
Zhao, Q., Chen, J., Wu, M., Yin, X., Jiang, Q., Gao, H., & Zheng, H. (2023) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2023.110638 · Cited by 49
The human microbiome in sickness and in health
Requena, T., & Velasco, M. (2020) · Revista Clínica Española (English Edition) · doi:10.1016/j.rceng.2019.07.018 · Cited by 55
Human Gut Microbiota for Diagnosis and Treatment of Depression
Averina, O. V., Poluektova, E. U., Zorkina, Y., Kovtun, A. S., & Даниленко, В. Н. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115782 · Cited by 54
“The HPA axis is one of the main axes of the endocrine system [75], which regulates the effectiveness and release of monoamine neurotransmitters, changes the content of the brain-derived neurotrophic factor (BDNF) and activates immune responses and systemic inflammation.”
BackgroundKumar, A., Mehan, S., Tiwari, A., Khan, Z., Gupta, G. D., Narula, A. S., & Samant, R. (2024) · Current Pharmaceutical Design · doi:10.2174/0113816128321466240816075041 · Cited by 55
Microglia and gut microbiota: A double-edged sword in Alzheimer's disease
Bano, N., Khan, S., Ahamad, S., Kanshana, J. S., Dar, N. J., Khan, S. J., Nazir, A., & Bhat, S. A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102515 · Cited by 50
Birth signalling hormones and the developmental consequences of caesarean delivery
Kenkel, W. M. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12912 · Cited by 47
MacKay, M., Yang, B. H., Dursun, S. M., & Baker, G. B. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230222092029 · Cited by 52
“Much still remains to be known about how metabolites formed by the gut microbiota that do not cross the BBB affect the brain, although studies on interactions with the vagus nerve are providing important information [20, 34, 107].”
BackgroundLee, K., Kim, J.-K., & Kim, D. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.564271 · Cited by 44
Thomann, A., Mak, J. W. Y., Zhang, J., Wüstenberg, T., Ebert, M. P., Sung, J. J. �., Bernstein, C. N., Reindl, W., & Ng, S. C. (2020) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15787 · Cited by 44
Microbioma humano en la salud y la enfermedad
Requena, T., & Velasco, M. (2019) · Revista Clínica Española · doi:10.1016/j.rce.2019.07.004 · Cited by 49
Short Bowel Syndrome: A Paradigm for Intestinal Adaptation to Nutrition?
Beyec, J. L., Billiauws, L., Bado, A., Joly, F., & Gall, M. L. (2020) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-011720-122203 · Cited by 42
Biyong, E. F., Alfos, S., Dumetz, F., Helbling, J., Aubert, A., Brossaud, J., Foury, A., Moisan, M., Layé, S., Richard, E., et al. (2020) · International Journal of Obesity · doi:10.1038/s41366-020-00723-z · Cited by 42
A Biopsychosocial Overview of the Opioid Crisis: Considering Nutrition and Gastrointestinal Health
Wiss, D. A. (2019) · Frontiers in Public Health · doi:10.3389/fpubh.2019.00193 · Cited by 41
“The question is: how is the microbiome linked to AUD or SUD? This emerging topic considers neuroendocrine pathways that are involved in addiction, where gut microbiota may play a causal role (139).”
BackgroundKeady, M., Prado, N. A., Lim, H. C., Brown, J. L., Paris, S., & Muletz‐Wolz, C. R. (2021) · Animal Microbiome · doi:10.1186/s42523-021-00146-9 · Cited by 43
Scheepers, I. M., Cryan, J. F., Bastiaanssen, T. F. S., Rea, K., Clarke, G. A., Jaspan, H. B., Harvey, B. H., Hemmings, S. M. J., Santana, L., van der Sluis, R., et al. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14610 · Cited by 42
Inflammation in Mental Disorders: Is the Microbiota the Missing Link?
Marin, S., Hé, Y., Butler, K., & Tsuang, M. T. (2020) · Neuroscience Bulletin · doi:10.1007/s12264-020-00535-1 · Cited by 44
The role of mast cells in the gut and brain
Traina, G. (2021) · Journal of Integrative Neuroscience · doi:10.31083/j.jin.2021.01.313 · Cited by 48
“The intestinal microbiota influences behaviors and neural functions [19].”
BackgroundGut Microbiota Profiles in Children and Adolescents with Psychiatric Disorders
Šoltýsová, M., Tomova, A., & Ostatníková, D. (2022) · Microorganisms · doi:10.3390/microorganisms10102009 · Cited by 44
“Gut bacteria can also produce NTs or can stimulate their production in the host organism, as summarized by several authors [1,15,16].”
BackgroundPatel, J. K., Chaudhary, H., Rajput, K. N., Parekh, B., & Joshi, R. G. (2023) · Scientific Reports · doi:10.1038/s41598-023-39168-5 · Cited by 39
Kumar, N., Sahoo, N. K., Mehan, S., & verma, B. (2023) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2023.104547 · Cited by 41
Amorim, N. M. L., McGovern, E., Raposo, A. E., Khatiwada, S., Shen, S., Koentgen, S., Hold, G. L., Behary, J., El-Omar, E. M., & Zekry, A. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.770017 · Cited by 39
Avolio, E., Olivito, I., Rosina, E., Romano, L., Angelone, T., Bartolo, A. D., Scimeca, M., Bellizzi, D., D’Aquila, P., Passarino, G., et al. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.038 · Cited by 41
Gut microbiota and its roles in the pathogenesis and therapy of endocrine system diseases
Wu, Z., Tian, E., Chen, Y., Dong, Z., & Peng, Q. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127291 · Cited by 40
The critical role of gut-brain axis microbiome in mental disorders
Basiji, K., Sendani, A. A., Ghavami, S. B., Farmani, M., Kazemifard, N., Sadeghi, A., Lotfali, E., & Aghdaei, H. A. (2023) · Metabolic Brain Disease · doi:10.1007/s11011-023-01248-w · Cited by 37
“HPA is one of the main endocrine system axis (Cussotto et al. 2018 ), that regulates the effi - cacy and release of monoamine neurotransmitters, modifies the abundance of BDNF, and activates immune responses and systemic inflammation.”
BackgroundGut microbiota in obesity and related complications: Unveiling the complex interplay
Islam, M. M., Islam, M. M., Rahman, M. A., Ripon, M. A. R., & Hossain, M. S. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122211 · Cited by 37
Metadata
- Authors
- Cussotto, S., Sandhu, K. V., Dinan, T. G., & Cryan, J. F.
- Affiliations
- University College Cork (IE)
- Corresponding author
- Cryan, John F.
- Venue
- Frontiers in Neuroendocrinology
- Publisher
- Elsevier BV
- Published
- 2018-10
- Volume
- 51
- Pages
- 80-101
- ISSN
- 0091-3022 (ISSN-L)
- OpenAlex
- W2804326576
- Cited by
- 326
- References
- 407
- Citations by year
- 2026: 17 · 2025: 43 · 2024: 53 · 2023: 43 · 2022: 54 · 2021: 36 · 2020: 43 · 2019: 32 · 2018: 5
- FWCI
- 2.84
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- Locations
- Frontiers in Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Arrow@dit (Dublin Institute of Technology) (submittedVersion, cc-by-nc-nd)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- gut microbiota, gut-brain axis, neuroendocrine system, behavioral responses, stress, eating behaviour, sexual behavior, social behavior, cognition, addiction, host-microbe interactions
- MeSH terms
- Gastrointestinal Microbiome, Animals, Brain, Feeding Behavior, Humans, Learning, Neurosecretory Systems, Sexual Behavior, Social Behavior, Stress, Psychological, Behavior, Addictive
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review