Vagal afferent responses to fatty acids of different chain length in the rat

Bioassay of plasma cholecystokinin in rats: Effects of food, trypsin inhibitor, and alcohol

Liddle, R. A., Goldfine, I. D., & Williams, J. A. (1984) · Gastroenterology · doi:10.1016/0016-5085(84)90524-9 · Cited by 410

International Union of Pharmacology. XXI. Structure, Distribution, and Functions of Cholecystokinin Receptors

Noble, F., Wank, S. A., Crawley, J. N., Bradwejn, J., Seroogy, K. B., Hamon, M., & Roques, B. P. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01427-3 · Cited by 385

A relation between the chain length of fatty acids and the slowing of gastric emptying

Hunt, J. N., & Knox, M. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008411 · Cited by 301

Fatty acid chain length determines cholecystokinin secretion and effect on human gastric motility

McLaughlin, J. T., Lucà, M. G., Jones, M. N., D’Amato, M., Dockray, G. J., & Thompson, D. G. (1999) · Gastroenterology · doi:10.1016/s0016-5085(99)70227-1 · Cited by 262

Effects of cholecystokinin (CCK-8) on two classes of gastroduodenal vagal afferent fibre

Blackshaw, L. A., & Grundy, D. (1990) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(90)90185-l · Cited by 221

Vagal sensors in the rat duodenal mucosa: distribution and structure as revealed by in vivo DiI-tracing

Berthoud, H., Kressel, M., Raybould, H., & Neuhuber, W. (1995) · Anatomy and Embryology · doi:10.1007/bf00187819 · Cited by 216

Analysis of the responses of myenteric neurons in the small intestine to chemical stimulation of the mucosa

Bertrand, P. P., Kunze, W., Bornstein, J. C., Furness, J. B., & Smith, M. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.273.2.g422 · Cited by 208

Cholecystokinin and Pancreozymin, one single Hormone?

Jorpes, E., & Mutt, V. (1966) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1966.tb03185.x · Cited by 196

Mechanism(s) of butyrate transport in Caco-2 cells: role of monocarboxylate transporter 1

Hadjiagapiou, C., Schmidt, L. N., Dudeja, P. K., Layden, T. J., & Ramaswamy, K. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.4.g775 · Cited by 182

I. CCK receptors: an exemplary family

Wank, S. A. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.4.g607 · Cited by 180

Disorders in the gut and liver are involved in depression contagion between isosexual post-stroke depression mice and the healthy cohabitors

Wang, H., Wang, B., Pan, M.-B., Jiang, S.-T., Wang, Y.-C., Zhu, Y., Zhang, Q., & Dong, Y. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114246 · Cited by 15

Cholecystokinin and hypothalamic corticotrophin-releasing factor participate in endotoxin-induced hypophagia

Rorato, R. C., Reis, W. L., Antunes‐Rodrigues, J., & Elias, L. L. K. (2011) · Experimental Physiology · doi:10.1113/expphysiol.2010.056465 · Cited by 12

Cannabinoid CB1 receptor restrains accentuated activity of hypothalamic corticotropin-releasing factor and brainstem tyrosine hydroxylase neurons in endotoxemia-induced hypophagia in rats

Rorato, R. C., Reis, W. L., Borges, B. C., Antunes‐Rodrigues, J., & Elias, L. L. K. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.009 · Cited by 12

Gut nutrient sensing by the abdominal vagus

Uneyama, H., Tanaka, T., & Torii, K. (2004) · Folia Pharmacologica Japonica · doi:10.1254/fpj.124.210 · Cited by 12

The endogenous CCK mediation of electroacupuncture stimulation-induced satiety in rats

Kim, S. K., Bae, H., Lee, G., Jeong, H., Woo, H., Han, J.-B., Kim, Y., Lee, H., Shin, M., Hong, M., et al. (2008) · Peptides · doi:10.1016/j.peptides.2008.01.002 · Cited by 12

Enteric neuropathy and the vagus nerve: Therapeutic implications

Bonaz, B. L. (2024) · Neurogastroenterology & Motility · doi:10.1111/nmo.14842 · Cited by 12

Neutrophils in the Focus: Impact on Neuroimmune Dynamics and the Gut–Brain Axis

Kršek, A., & Batičić, L. (2024) · Gastrointestinal Disorders · doi:10.3390/gidisord6030039 · Cited by 13

Changes in gut-brain axis parameters in adult rats of both sexes with different feeding pattern that were early nicotine-exposed

Rodrigues, V. S. T., de Moura, E. G., Peixoto, T. C., Soares, P. N., Lopes, B. P., Oliveira, E., Manhães, A. C., Atella, G. C., Kluck, G. E. G., Cabral, S. S., et al. (2021) · Food and Chemical Toxicology · doi:10.1016/j.fct.2021.112656 · Cited by 11

Functional dyspepsia patients have lower mucosal cholecystokinin concentrations in response to duodenal lipid

van Boxel, O. S., Linde, J. J. M. T., Oors, J., Otto, B., Weusten, B. L. A. M., Feinle‐Bisset, C., Smout, A. J. P. M., & Siersema, P. D. (2013) · European Journal of Gastroenterology & Hepatology · doi:10.1097/meg.0000000000000001 · Cited by 11

Relationship between peptide YY, cholecystokinin and fermentation products in fasted, re-fed and ad libitum fed broiler chickens

Melo‐Durán, D., González‐Ortiz, G., Solà‐Oriol, D., Martínez-Mora, M., Pérez, J. F., & Bedford, M. R. (2018) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2018.11.007 · Cited by 11

Butyrate in broiler diets : impact of butyrate presence in distinct gastrointestinal tract segments on digestive function, microbiota composition and immune responses

Moquet, P. C. A. (2018) · doi:10.18174/449961 · Cited by 11

The brain pathobiome in Alzheimer's disease

Shanmugam, N. K. N., Eimer, W. A., Kumar, D. K. V., & Tanzi, R. E. (2024) · Neurotherapeutics · doi:10.1016/j.neurot.2024.e00475 · Cited by 11

[Macronutrients, food intake and body weight; the role of fat].

Carrillo, J. A.-B., Torregrosa, M. D., Almendros, M. M., López‐Millán, B., Burgos, M. A., & Muñoz, E. M. D. V. (2014) · PubMed · doi:10.3305/nh.2015.31.1.8439 · Cited by 10

Making Sense of Gut Contents

Dockray, G. J. (2003) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520310000799 · Cited by 10

Gamma-delta T cells suppress microbial metabolites that activate striatal neurons and induce repetitive/compulsive behavior in mice

Cox, L. M., Tatematsu, B. K., Guo, L., LeServe, D. S., Mayrink, J., Oliveira, M. G., Donnelly, D. J., Fonseca, R. C., Lemos, L., Lanser, T. B., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.01.214 · Cited by 10

Modulation of anxiety-like behavior in galactooligosaccharide-fed mice: A potential role for bacterial tryptophan metabolites and reduced microglial reactivity

Spencer, K. D., Bline, H., Chen, H. J., Verosky, B. G., Hilt, M. E., Jaggers, R. M., Gur, T., Mathé, E. A., & Bailey, M. T. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.024 · Cited by 9

From Gut to Brain: The Impact of Short-Chain Fatty Acids on Brain Cancer

Saadh, M. J., Allela, O. Q. B., Kareem, R. A., Sanghvi, G. V., Menon, S. V., Sharma, P., Tomar, B. S., Sharma, A., Sameer, H. N., Hamad, A. K., et al. (2025) · NeuroMolecular Medicine · doi:10.1007/s12017-025-08830-8 · Cited by 9

Gut-brain-liver axis in growth hormone deficiency: role of microbiota-derived short-chain fatty acids in ethnic variability and therapeutic development

Meng, D., Kong, W., Cheng, S., Liu, H., & Huang, C. (2025) · Frontiers in Public Health · doi:10.3389/fpubh.2025.1541654 · Cited by 9

Inflammation Spreading: Negative Spiral Linking Systemic Inflammatory Disorders and Alzheimer’s Disease

Ni, J., & Wu, Z. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.638686 · Cited by 9

Enterocyte–afferent nerve interactions in dietary fat sensing

Mansouri, A., & Langhans, W. (2014) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12339 · Cited by 9

Rats acquire stronger preference for flavors consumed towards the end of a high-fat meal

Myers, K. P. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.01.004 · Cited by 9

Non-Coding RNAs and Gut Microbiota in the Pathogenesis of Cardiac Arrhythmias: The Latest Update

Suga, N., Ikeda, Y., Yoshikawa, S., Taniguchi, K., Sawamura, H., & Matsuda, S. (2023) · Genes · doi:10.3390/genes14091736 · Cited by 7

The Enteric Nervous System as a Mediator of Microbiota‐Gut‐Brain Interactions in Parkinson's Disease

Valdetaro, L., Ricciardi, M. C., Almeida, P. G., Stockler‐Pinto, M. B., & Gomes, A. L. T. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70339 · Cited by 8

Existence of NO-triggered vagal afferent activation in the rat gastric mucosa

Uneyama, H., Niijima, A., Kitamura, A., & Torii, K. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.10.009 · Cited by 8

Specialized, Pro-Resolving Mediators as Potential Therapeutic Agents for Alleviating Fibromyalgia Symptomatology

Livshits, G., & Kalinkovich, A. (2021) · Pain Medicine · doi:10.1093/pm/pnab060 · Cited by 8

Research progress on intestinal microbiota regulating cognitive function through the gut-brain axis

Lin, K., Peng, F., He, K., Qian, Z., Mei, X., Su, Z., Wujimaiti, Y., Xia, X., & Zhang, T. (2024) · Neurological Sciences · doi:10.1007/s10072-024-07525-5 · Cited by 8

Duodenal lipid‐induced symptom generation in gastroesophageal reflux disease: role of apolipoprotein A‐IV and cholecystokinin

van Boxel, O. S., Linde, J. J. M. T., Oors, J., Otto, B., Feinle‐Bisset, C., Smout, A. J. P. M., & Siersema, P. D. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01880.x · Cited by 7

How the gut sends signals in response to food

Dockray, G. J. (2009) · International Dairy Journal · doi:10.1016/j.idairyj.2009.11.013 · Cited by 7

Phage-Microbiota Crosstalk: Implications for Central Nervous System Disorders

Salari, V., Parrella, E., Mengoni, F., Cintra, L., Bertini, G., & Fabene, P. F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136183 · Cited by 6

Diet–Microbiome–Brain Axis and Mental Health: Biological Mechanisms and Nutritional Implications

Uţu, D., Nodiți-Cuc, A.-R., Kiș, A. M., Popovici, R. A., Pitic, D. E., Trusculescu, L.-M., Marian, D., Nan, A. G., Matin, A. S., Cîmpian, D. M., et al. (2026) · Nutrients · doi:10.3390/nu18091412 · Cited by 6

New Insights on the Role of Bioactive Food Derivatives in Neurodegeneration and Neuroprotection

Fisette, A., Sergi, D., Breton-Morin, A., Descôteaux, S., & Martinoli, M. (2022) · Current Pharmaceutical Design · doi:10.2174/1381612828666220919085742 · Cited by 5

Vagal Afferents Innervating the Gastrointestinal Tract

Grundy, D., & Beyak, M. J. (2005) · Frontiers in neuroscience · doi:10.1201/9780203492314.ch12 · Cited by 6

Reduced mechanosensitivity of duodenal vagal afferent neurons after an acute switch from milk-based to plant-based diets in anaesthetized pigs.

Bligny, D., Blat, S., Chauvin, A., Guérin, S., & Ch, M. (2005) · PubMed · Cited by 6

Gut Feeding the Brain:DrosophilaGut an Animal Model for Medicine to Understand Mechanisms Mediating Food Preferences

Sadaqat, Z., Kaushik, S., & Kain, P. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.96503 · Cited by 11

The emerging role of the microbial-gastrointestinal-neural axis

McLean, P. G., Calver, A. R., Alpers, D., Collins, S. M., Shanahan, F., & Lee, K. (2009) · Gastroenterology Insights · doi:10.4081/gi.2009.e3 · Cited by 6

Antibiotics in elderly Chinese population and their relations with hypertension and pulse pressure

Li, Z., Liu, K., Zhao, J., Yang, L., Chen, G., Liu, A., Wang, Q., Wang, S., Li, X., Cao, H., et al. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-022-20613-3 · Cited by 5

Which Microbes Like My Diet and What Does It Mean for My Heart?

Sawicka, E., Moniuszko-Malinowska, A. M., & Kamiński, K. A. (2021) · Nutrients · doi:10.3390/nu13114146 · Cited by 5

Role of microbiota in pain: From bench to bedside

Ren, H., Cao, B., Xu, Q., Zhao, R., Li, H., & Wei, B. (2025) · iMetaOmics. · doi:10.1002/imo2.58 · Cited by 7

Tuberculosis-related Mood Disorders: Probiotics as a Next-Generation Strategy

Bhardwaj, A., & Gupta, R. (2023) · Current Probiotics · doi:10.2174/0126666499221169231123062539 · Cited by 4

Effects of gastric distension and infusion of umami and bitter taste stimuli on vagal afferent activity

Horn, C. C., Murat, C., Rosazza, M. R., & Still, L. (2011) · Brain Research · doi:10.1016/j.brainres.2011.08.057 · Cited by 4

IV. Visceral afferents: an update

Raybould, H. E. (2003) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00123.2003 · Cited by 4

Gut–brain interactions

Kano, M., & Fukudo, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00036-x · Cited by 6

The Gut Microbiota and the Nerve-Bone Axis: Insights from a Mendelian Randomization and Mediation Analysis

Qiao, X., Lou, Y., Chen, H., Zhang, H., Cao, J., Xu, F., Guo, L., & Pan, Q. (2025) · Journal of Multidisciplinary Healthcare · doi:10.2147/jmdh.s524720 · Cited by 3

Sex-dependent locus coeruleus vulnerability in Alzheimer’s disease: gut dysbiosis as a driver and probiotic intervention as rescue

Stapleton, H. M., Borges, D. D. S., Trindade, E. B. S. D. M., & Yuan, Q. (2026) · Biology of Sex Differences · doi:10.1186/s13293-026-00834-8 · Cited by 3

Short-Chain Fatty Acids Regulate Poultry Feed Intake via the Hypothalamus: Receptor-Mediated and Epigenetic Mechanisms

Wang, Y., Xiao, X., Zheng, B., Bai, D., Zhang, Y., Zhen, W., Zhang, B., & Ma, Y. (2026) · Animals · doi:10.3390/ani16060954 · Cited by 3

Autonomic nervous system dysfunction in irritable bowel syndrome: pathophysiology and therapeutic implications

Bai, Y., Yu, M., Weng, C., Xu, J., Zheng, M., & Lv, B. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1832540 · Cited by 4

The gut microbiome as a factor in the development of Parkinson's disease

Арамайисовна, Б. Л., Poluektova, E. A., & Poluektov, M. G. (2023) · Neurology neuropsychiatry Psychosomatics · doi:10.14412/2074-2711-2023-1-90-96 · Cited by 3

Gut Microbiota Moderates Multimodal Brain Structure-Function Integration and Behavioral Cognition in Growth Hormone Deficient Children

Wang, K., Fu, Y., Li, L., Zhang, L., Huang, M., Yan, W., Shan, X., Yan, Z., & Lü, Y. (2024) · Neuroendocrinology · doi:10.1159/000539097 · Cited by 4

Vagal Afferent Neurons and Pain

Jänig, W. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00406-0 · Cited by 3

Dapagliflozin, a Sodium-Glucose Co-transporter-2 Inhibitor, Acutely Reduces Energy Expenditure in Brown Adipose Tissue via Neural Signals in Mice

Chiba, Y., Yamada, T., & Katagiri, H. (2018) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.17-00223-3 · Cited by 3

Combinational Approaches Targeting Various Aspects Involved in Intestinal Barrier Dysfunction-Induced Anxiety

Kale, P. P., & Pallar, A. (2022) · Current Drug Targets · doi:10.2174/1389450123666220428093419 · Cited by 4

Role of microbiota-gut-brain axis in neurodegenerative diseases and the potential of microbiome-targeted dietary strategies: a review of current evidence and future perspective

Zhang, S., Chen, W., Ma, C., Luo, Y., Dong, L., Hu, X., Chen, F., & Li, D. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250215 · Cited by 2

Acetate concentration correlates with MSNA in patients with resistant hypertension

Carnagarin, R., Sesa‐Ashton, G., Ward, N. C., Nolde, J. M., Joyson, A., Chan, J., Jose, A., & Schlaich, M. P. (2025) · Clinical Autonomic Research · doi:10.1007/s10286-025-01144-6 · Cited by 2

Depresión, ansiedad y microbiota intestinal: mecanismos neurobiológicos

Kransel, M. S. S., Zafra, J. J. J., Diago, I. O., & Becerra-Hernández, L. V. (2024) · Acta neurológica colombiana · doi:10.22379/anc.v40i3.1341 · Cited by 3

Metabolic Signals in the Control of Food Intake

Woods, S. C. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-48643-1_10 · Cited by 3

Recent advances in understanding depressive disorder: Possible relevance to brain stimulation therapies

Kunugi, H., & Tikhonova, M. A. (2022) · Progress in brain research · doi:10.1016/bs.pbr.2022.01.023 · Cited by 2

Does the vagus nerve mediate the effects of polyunsaturated fatty acid treatment on behavioral, neuroendocrine and cytokine changes elicited by exogenous interleukin-1β challenge?

Mravec, B. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.11.011 · Cited by 2

Role of Microbiota-Derived Exosomes in Gut–Brain Communication for the Treatment of Brain Disorders

Agnihotri, T. G., Gomte, S. S., Peddinti, V., Rout, B., Shewale, R. S., Janjal, P., & Jain, A. (2024) · Springer eBooks · doi:10.1007/978-981-99-8373-5_9 · Cited by 1

The Enigmatic Gut-Brain-Immune Trio in Brain and Behavior Disorders

Mythri, R. B. (2025) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/979-8-3693-7432-0.ch019 · Cited by 1

Intestinal short-chain fatty acid turnover is not associated with resting state functional connectivity in mesolimbic dopaminergic network in healthy adults

Wijdeveld, M., Schrantee, A., Azor, J. T., van Baarzel, F., van Duinkerken, E., Nieuwdorp, M., & IJzerman, R. G. (2025) · Neuroimage Reports · doi:10.1016/j.ynirp.2025.100285 · Cited by 1

Expression patterns of T1R3 in duodenal epithelial cells with some gastrointestinal hormone

Oda, M., Seta, Y., Kataoka, S., Toyono, T., Toyoshima, K., & Morimoto, Y. (2011) · Archivum histologicum japonicum · doi:10.1679/aohc.73.177 · Cited by 2

"Recognizing Hunger" - A Training to Abate Insulin Resistance, Associated Subclinical Inflammation and Cardiovascular Risks

Ciampolini, M. (2012) · InTech eBooks · doi:10.5772/32354

Internal tracheal sensory neuron wiring and function in Drosophila larvae

Qian, C. S. (2018) · doi:10.7916/d8fj40qh · Cited by 1

Role of the Gut Microbiome and Its Modulation in Neurodegenerative Diseases

Prabhakar, P., & Punnaveetil, S. (2022) · Springer eBooks · doi:10.1007/978-981-16-6703-9_5 · Cited by 1

Cholecystokinin and the exocrine pancreas

Williams, J. A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-23720-1.00010-1 · Cited by 1

Fermented dairy products intake and stroke risk: analyses of NHANES 2007–2018 data

Ma, S., Miao, Y., & Wu, X. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1593174 · Cited by 1

Beyond the Microbiome: The Gut’s Role in Hypertension

Deng, W., Zhu, M., Lloyd, I., Nedunuri, M., Zhou, C., Liu, W., Li, Y., Li, Q., Wang, X., Zhang, Q., et al. (2025) · Function · doi:10.1093/function/zqaf037 · Cited by 2

The Gut and Type 2 Diabetes Mellitus

Boyce, S. (2020) · Springer eBooks · doi:10.1007/978-3-030-28803-7_42 · Cited by 1

Molecular Signaling in the Gut–Brain Axis in Stress

Page, A. J., & Li, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813156-5.00012-1 · Cited by 1

Much to do about gas

Camilleri, M., & Delgado-Aros, S. (2002) · Gastroenterology · doi:10.1053/gast.2002.35772 · Cited by 1

Upper gastrointestinal disorders: symptom generation and proton pump inhibitor use

van Boxel, O. S. (2010) · Utrecht University Repository (Utrecht University)

Neural pathways and cellular mechanisms of mercaptoacetate

Darling, R. A. (2010) · doi:10.7273/000006078

AN IN VITRO MURINE MODEL TO STUDY INTESTINAL MESENTERIC AFFERENT ACTIVITY IN RESPONSE TO LUMINAL FATTY ACID STIMULI

Webster, W. A. (2010) · QSpace (Queen's University Library)

EVIDENCE FOR INVOLVEMENT OF THE CYSTEINYL LEUKOTRIENE TYPE 2 RECEPTOR (CysLT2R) IN THE REGULATION OF FOOD INTAKE AND BODY WEIGHT AND POSSIBLE ROLE FOR VAGAL AFFERENTS

Al-Helaili, A. (2011) · QSpace (Queen's University Library)

AFFERENT NEURONS AFTER AN ACUTE SWITCH FROM MILK

Bligny, D., Blat, S., Chauvin, A., & Gu, S. (2005)

Nutraceutical Regulation of the Neuroimmunoendocrine Super-system

Forsythe, P. (2014) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-319-06151-1_21

LUMINAL CCK AND ITS NEURONAL ACTION ON EXOCRINE

Zabielski, R., & Secretion, P. (2003)

Modulation of neuropeptide W on gastric vagal afferents.

Li, H. (2014) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

Postprandial metabolism of infant formulas containing different fat sources : digestion, absorption, and metabolic responses

Hageman, J. H. J. (2019) · doi:10.18174/496799

Gut Dysbiosis and Neurological Disorders—An Eclectic Perspective

Bostancıklıoğlu, M., & Demir, T. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00041-3 · Cited by 1

L’axe intestin–cerveau : les pistes actuelles

Piguet, P. (2021) · Douleur et Analgésie · doi:10.3166/dea-2021-0167

Gut microbiota and hypertension, diabetes, and other cardiovascular risk factors

Duttaroy, A. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822405-2.00018-9

Further Reading

(2004) · Elsevier eBooks · doi:10.1016/b978-012553149-8/50049-1

Faculty Opinions recommendation of Apolipoprotein A-IV is involved in detection of lipid in the rat intestine.

Barrett, K. E. (2005) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5018.462506

Further Reading

(2018) · Elsevier eBooks · doi:10.1016/b978-0-12-802629-8.16001-2

Vagal Afferent Neurons and Pain

Jänig, W. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-805408-6.00406-1

Characterization of Gut Microbiota in Newly Diagnosed Patients with Depression: Does the Depressed Gut Exist?

Knudsen, J. K. (2021) · VBN Forskningsportal (Aalborg Universitet) · doi:10.54337/aau455013245

Probiotics and gut-brain axis modulation

de Oliveira, M. E. G. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89908-6.00018-2

Effects of a diverse prebiotic fibre blend on inflammation, the gut microbiota, and affective symptoms: A pilot open label randomised controlled trialPreprint

Hall, C. V., Hepsomali, P., Dalile, B., Scapozza, L., & Gurry, T. (2024) · medRxiv · doi:10.1101/2024.02.12.24302681

Gut–brain communication through microbes

Green, M., & Foster, J. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-90144-4.00002-1

Prebiotics, Probiotics, Symbiotics and Postbiotics. Nutrition and Microbiota

Ruíz-Tóvar, J., & Llavero, C. (2024) · Springer eBooks · doi:10.1007/978-3-031-65650-7_2

Incidence of Delirium Tremens in Acute Poisoning by Psychopharmacological Drugs or Corrosive Substances and Its Prevention Using Intestinal Lavage: on the Pathogenesis of Delirium Tremens

Маткевич, В. А., Potskhveriya, М. М., Vorobyeva, A. G., & Shukshin, V. S. (2025) · Russian Sklifosovsky Journal Emergency Medical Care · doi:10.23934/2223-9022-2025-14-1-112-122

Obesity and the Gut Microbiome

Chattopadhyay, S., Hazra, R., Mallick, A., Gayen, S., & Roy, S. (2025) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815324549125010006

Exploring the unknown territory of gut–brain axis in type 2 diabetes mellitus patients

Rahim, S., & Karim, M. M. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-33355-2.00007-4

Severity of Depressive Symptoms by Perceived Stress and Gut Microbiota Composition: A Sex‐Stratified Bayesian Approach in a Non‐Clinical Sample

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