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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Cholecystokinin-A receptors modulate gastric sensory and motor responses to gastric distension and duodenal lipid

Feinle, C., D’Amato, M., & Read, N. W. (1996) · Gastroenterology · doi:10.1053/gast.1996.v110.pm8613041 · Cited by 164 · see citing works

Capsaicin attenuates suppression of sham feeding induced by intestinal nutrients

Yox, D. P., & Ritter, R. C. (1988) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1988.255.4.r569 · Cited by 160 · see citing works

Direct and indirect actions of 5‐hydroxytryptamine on the discharge of mesenteric afferent fibres innervating the rat jejunum

Hillsley, K., Kirkup, A. J., & Grundy, D. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.551bw.x · Cited by 150 · see citing works

Fatty acids stimulate cholecystokinin secretion via an acyl chain length‐specific, Ca2+‐dependent mechanism in the enteroendocrine cell line STC‐1

McLaughlin, J. T., Lomax, R. B., Hall, L., Dockray, G. J., Thompson, D. G., & Warhurst, G. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.011by.x · Cited by 142 · see citing works

Characterization of cholecystokininA and cholecystokininB receptors expressed by vagal afferent neurons

Moriarty, P., Dimaline, R., Thompson, D. G., & Dockray, G. J. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00675-6 · Cited by 131 · see citing works

Intestinal lipid inhibits gastric emptying via CCK and a vagal capsaicin-sensitive afferent pathway in rats

Holzer, H. H., Turkelson, C. M., Solomon, T. E., & Raybould, H. E. (1994) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1994.267.4.g625 · Cited by 127 · see citing works

Anatomical Relationship between Vagal Afferent Fibers and CCK-Immunoreactive Entero-Endocrine Cells in the Rat Small Intestinal Mucosa

Berthoud, H. R., & Patterson, L. M. (1996) · Cells Tissues Organs · doi:10.1159/000147837 · Cited by 125 · see citing works

Role of Cholecystokinin in the Regulation of Gastrointestinal Motility

Grider, J. R. (1994) · Journal of Nutrition · doi:10.1093/jn/124.suppl_8.1334s · Cited by 121 · see citing works

Sensitivity of vagal mucosal afferents to cholecystokinin and its role in afferent signal transduction in the rat.

Richards, W., Hillsley, K., Eastwood, C., & Grundy, D. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021781 · Cited by 117 · see citing works

Vagal receptors sensitive to lipids in the small intestine of the cat

Melone, J. (1986) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(86)90060-3 · Cited by 106 · see citing works

Satiety effects of cholecystokinin in humans

Lieverse, R. J., Jansen, J. B. �. �., Masclee, A., & Lamers, C. B. H. W. (1994) · Gastroenterology · doi:10.1016/0016-5085(94)90397-2 · Cited by 98 · see citing works

I. Sensing of lipid by the intestinal mucosa

Raybould, H. E. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.277.4.g751 · Cited by 97 · see citing works

Responses of celiac and cervical vagal afferents to infusions of lipids in the jejunum or ileum of the rat

Randich, A., Tyler, W. J., Cox, J. E., Meller, S. T., Kelm, G. R., & Bharaj, S. S. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.1.r34 · Cited by 89 · see citing works

Inhibition of gastric emptying in response to intestinal lipid is dependent on chylomicron formation

Raybould, H. E., Meyer, J. H., Tabrizi, Y., Liddle, R. A., & Tso, P. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.6.r1834 · Cited by 89 · see citing works

Expression of cholecystokinin a receptors in neurons innervating the rat stomach and intestine

Sternini, C., Wong, H. C., Pham, T., GIORGIO, R. D., Miller, L. J., Kuntz, S. M., Reeve, J. R., Walsh, J. H., & Raybould, H. E. (1999) · Gastroenterology · doi:10.1016/s0016-5085(99)70399-9 · Cited by 85 · see citing works

Excitatory effect of P2X receptor activation on mesenteric afferent nerves in the anaesthetised rat

Kirkup, A. J., Booth, C. E., Chessell, I. P., Humphrey, P. P. A., & Grundy, D. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00551.x · Cited by 84 · see citing works

Suppression of meal size by intestinal nutrients is eliminated by celiac vagal deafferentation

Walls, E. K., Phillips, R. J., Wang, F., Holst, M., & Powley, T. L. (1995) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1995.269.6.r1410 · Cited by 84 · see citing works

Vagotomy attenuates suppression of sham feeding induced by intestinal nutrients

Yox, D. P., Stokesberry, H., & Ritter, R. C. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.260.3.r503 · Cited by 79 · see citing works

Differential effects of calcium channel antagonists (?-conotoxin GVIA, nifedipine, verapamil) on the electrically-evoked release of [3H]acetylcholine from the myenteric plexus, phrenic nerve and neocortex of rats

Wessler, I. K., Dooley, D. J., Werhand, J., & Schlemmer, F. (1990) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00180653 · Cited by 75 · see citing works

Intraduodenal Free Fatty Acids Rather than Triglycerides Are Responsible for the Release of CCK in Humans

Guimbaud, R., Moreau, J., Bouisson, M., Durand, S., Escourrou, J. R., Vaysse, N., & Frexinos, J. (1997) · Pancreas · doi:10.1097/00006676-199701000-00012 · Cited by 73 · see citing works

Role of cholecystokinin as a regulator of solid and liquid gastric emptying in humans

Borovicka, J., Kreiss, C. M., Asal, K., Remy, B., Mettraux, C., Wells, A. S., Read, N. W., Jansen, J. B. �. �., D'Amato, M., Delaloye, A. B., et al. (1996) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1996.271.3.g448 · Cited by 56 · see citing works

Peptone stimulates CCK-releasing peptide secretion by activating intestinal submucosal cholinergic neurons.

Li, Y., & Owyang, C. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118568 · Cited by 54 · see citing works

Regional and cellular heterogeneity of cholecystokinin receptors mediating muscle contraction in the gut

Grider, J. R., & Makhlouf, G. M. (1987) · Gastroenterology · doi:10.1016/0016-5085(87)90855-9 · Cited by 54 · see citing works

Duodenal lipid inhibits gastric acid secretion by vagal, capsaicin-sensitive afferent pathways in rats

Lloyd, K. C. K., Holzer, H. H., Zittel, T. T., & Raybould, H. E. (1993) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1993.264.4.g659 · Cited by 48 · see citing works

L-type calcium channels in enterochromaffin cells from guinea pig and human duodenal crypts: An in situ study

Lomax, R. B., Gallego, S., Novalbos, J., Garcı́a, A. G., & Warhurst, G. (1999) · Gastroenterology · doi:10.1016/s0016-5085(99)70286-6 · Cited by 41 · see citing works

Somatostatin is released in response to cholecystokinin by activation of type A CCK receptors

Lloyd, K. C. K., Maxwell, V., Chuang, C. N., Wong, H. C., Soll, A. H., & Walsh, J. H. (1994) · Peptides · doi:10.1016/0196-9781(94)90006-x · Cited by 36 · see citing works

Role of neuropeptide-sensitive L-type Ca2+channels in histamine release in gastric enterochromaffin-like cells

Zeng, N., Athmann, C., Kang, T., Walsh, J. H., & Sachs, G. M. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.277.6.g1268 · Cited by 30 · see citing works

Effect of cholecystokinin-A receptor blockade on lipid-induced gastric relaxation in humans

Mesquita, M. A., Thompson, D. G., Troncon, L. E. D. A., D’Amato, M., Rovati, L. C., & Barlow, J. D. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.273.1.g118 · Cited by 30 · see citing works

Cholecystokinin receptors

Boden, P., Hall, M. D., & Hughes, J. M. (1995) · Cellular and Molecular Neurobiology · doi:10.1007/bf02071316 · Cited by 30 · see citing works

Intestinal effects of the products of lipid digestion on gastric electrical activity in the cat

Melone, J., & Mei, N. (1991) · Gastroenterology · doi:10.1016/0016-5085(91)90206-z · Cited by 26 · see citing works

Effects of calcium channel blockade on intestinal fluid secretion: sites of action

Peregrin, A. T., Ahlman, H. K., Jodal, M., & Lundgren, O. (1997) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1997.00173.x · Cited by 21 · see citing works

Presynaptic calcium channels mediating synaptic transmission in submucosal neurones of the guinea‐pig caecum

Cunningham, S. M. C., Mihara, S., & Higashi, H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.425bn.x · Cited by 16 · see citing works

Acetate absorption in the normal and secreting rat jejunum.

Watson, A. J. M., Elliott, E. J., Rolston, D. D. K., Borodo, M. M., Farthing, M. J. G., & Fairclough, P. D. (1990) · Gut · doi:10.1136/gut.31.2.170 · Cited by 13 · see citing works

The effects of nifedipine and verapamil on high K+ induced contractions of the rat intestinal tract in vivo.

Maggi, C. A., Grimaldi, G., & Meli, A. (1983) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.33.335 · Cited by 11 · see citing works

Characterization of CCK A Receptor Mediated Pepsinogen Secretion in Porcine Chief Cells

Meyer, G., Beinborn, M., & Sewing, K. (2008) · Pharmacology · doi:10.1159/000139414 · Cited by 5 · see citing works

Untitled work

Ciliax (1999) · doi:10.1002/(sici)1096-9861(19990621)409:1

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

Dalile, B., Van Oudenhove, L., Vervliet, B., & Verbeke, K. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0157-3 · Cited by 3,357 · see citing works

The vagus nerve at the interface of the microbiota-gut-brain axis

Bonaz, B., Bazin, T., & Pellissier, S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00049 · Cited by 1,397 · see citing works

Short-Chain Fatty-Acid-Producing Bacteria: Key Components of the Human Gut Microbiota

Fusco, W. G., Bernabeu, M., Cintoni, M., Porcari, S., Rinninella, E., Kaitsas, F., Lener, E., Mele, M. C., Gasbarrini, A., Collado, M. C., et al. (2023) · Nutrients · doi:10.3390/nu15092211 · Cited by 1,318 · see citing works

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

Breit, S., Kupferberg, A., Rogler, G., & Hasler, G. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00044 · Cited by 1,189 · see citing works

Free Fatty Acid Receptors in Health and Disease

Kimura, I., Ichimura, A., Ohue‐Kitano, R., & Igarashi, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00041.2018 · Cited by 1,032 · see citing works

The neuropharmacology of butyrate: the bread and butter of the microbiota-gut-brain axis

Stilling, R. M., van de Wouw, M., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.011 · Cited by 891 · see citing works

The gut microbiota and the brain–gut–kidney axis in hypertension and chronic kidney disease

Yang, T., Richards, E. M., Pepine, C. J., & Raizada, M. K. (2018) · Nature Reviews Nephrology · doi:10.1038/s41581-018-0018-2 · Cited by 753 · 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

Vagal pathways for microbiome-brain-gut axis communication

Forsythe, P., Bienenstock, J., & Kunze, W. A. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_5 · Cited by 576 · see citing works

Microbiome, probiotics and neurodegenerative diseases: deciphering the gut brain axis

Westfall, S., Lomis, N., Kahouli, I., Dia, S. Y., Singh, S. P., & Prakash, S. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2550-9 · Cited by 551 · see citing works

Sympathetic and sensory innervation of brown adipose tissue

Bartness, T. J., Vaughan, C. H., & Song, C. K. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.182 · Cited by 459 · see citing works

Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health

Berding, K., Vlckova, K., Marx, W., Schellekens, H., Stanton, C., Clarke, G., Jacka, F., Dinan, T. G., & Cryan, J. F. (2021) · Advances in Nutrition · doi:10.1093/advances/nmaa181 · Cited by 451 · see citing works

Gut Microbiota in Hypertension and Atherosclerosis: A Review

Verhaar, B. J. H., Prodan, A., Nieuwdorp, M., & Muller, M. (2020) · Nutrients · doi:10.3390/nu12102982 · Cited by 411 · see citing works

Neural innervation of white adipose tissue and the control of lipolysis

Bartness, T. J., Liu, Y., Shrestha, Y. B., & Ryu, V. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.04.001 · Cited by 358 · see citing works

The vagus nerve, food intake and obesity

Berthoud, H.-R. (2008) · Regulatory Peptides · doi:10.1016/j.regpep.2007.08.024 · Cited by 316 · see citing works

Role of Microbiota-Gut-Brain Axis in Regulating Dopaminergic Signaling

Hamamah, S., Aghazarian, A., Nazaryan, A., Hajnal, A. S., & Covașă, M. (2022) · Biomedicines · doi:10.3390/biomedicines10020436 · Cited by 317 · see citing works

Sensory and sympathetic nervous system control of white adipose tissue lipolysis

Bartness, T. J., Shrestha, Y. B., Vaughan, C. H., Schwartz, G. J., & Song, C. K. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.08.031 · Cited by 289 · see citing works

Extrinsic primary afferent signalling in the gut

Brookes, S. J., Spencer, N. J., Costa, M., & Zagorodnyuk, V. P. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.29 · Cited by 288 · see citing works

The G-Protein−Coupled Receptor GPR40 Directly Mediates Long-Chain Fatty Acid−Induced Secretion of Cholecystokinin

Liou, A. P., Lu, X., Sei, Y., Zhao, X., Pechhold, S. B., Carrero, R. J., Raybould, H. E., & Wank, S. A. (2010) · Gastroenterology · doi:10.1053/j.gastro.2010.10.012 · Cited by 276 · see citing works

The gut microbiome in Alzheimer’s disease: what we know and what remains to be explored

Chandra, S., Sisodia, S. S., & Vassar, R. J. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00595-7 · Cited by 278 · see citing works

The role of gut and genital microbiota and the estrobolome in endometriosis, infertility and chronic pelvic pain

Salliss, M. E., Farland, L. V., Mahnert, N. D., & Herbst‐Kralovetz, M. M. (2021) · Human Reproduction Update · doi:10.1093/humupd/dmab035 · Cited by 287 · see citing works

Role of the gut-brain axis in energy and glucose metabolism

Wachsmuth, H. R., Weninger, S. N., & Duca, F. A. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00677-w · Cited by 269 · see citing works

Vagus Nerve and Underlying Impact on the Gut Microbiota-Brain Axis in Behavior and Neurodegenerative Diseases

Han, Y., Wang, B., Gao, H., He, C., Hua, R., Liang, C., Zhang, S., Wang, Y., Xin, S., & Xu, J. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s384949 · Cited by 265 · see citing works

Gastrointestinal mechanisms of satiation for food

Ritter, R. C. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.012 · Cited by 263 · see citing works

Brain–gut–microbiome interactions in obesity and food addiction

Gupta, A., Osadchiy, V., & Mayer, E. A. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-020-0341-5 · Cited by 268 · see citing works

Communication of gut microbiota and brain via immune and neuroendocrine signaling

Kasarełło, K., Cudnoch‐Jędrzejewska, A., & Czarzasta, K. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1118529 · Cited by 270 · see citing works

Role of the vagus nerve in the development and treatment of diet‐induced obesity

de Lartigue, G. (2016) · The Journal of Physiology · doi:10.1113/jp271538 · Cited by 238 · see citing works

Neuropod Cells: The Emerging Biology of Gut-Brain Sensory Transduction

Kaelberer, M. M., Rupprecht, L. E., Liu, W. W., Weng, P., & Bohórquez, D. V. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-091619-022657 · Cited by 236 · see citing works

Butyrate, a metabolite of intestinal bacteria, enhances sleep

Szentirmai, É., Millican, N. S., Massie, A. R., & Kapás, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-43502-1 · Cited by 216 · see citing works

Gut Microbiota and Cardiovascular Disease: Evidence on the Metabolic and Inflammatory Background of a Complex Relationship

Nesci, A., Carnuccio, C., Ruggieri, V., D’Alessandro, A., Giorgio, A. D., Santoro, L., Gasbarrini, A., Santoliquido, A., & Ponziani, F. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24109087 · Cited by 227 · see citing works

Jejunal nutrient sensing is required for duodenal-jejunal bypass surgery to rapidly lower glucose concentrations in uncontrolled diabetes

Breen, D. M., Rasmussen, B. A., Kokorovic, A., Wang, R., Cheung, G. W. C., & Lam, T. K. T. (2012) · Nature Medicine · doi:10.1038/nm.2745 · Cited by 209 · see citing works

Thematic review series: Adipocyte Biology. Sympathetic and sensory innervation of white adipose tissue

Bartness, T. J., & Song, C. K. (2007) · Journal of Lipid Research · doi:10.1194/jlr.r700006-jlr200 · Cited by 209 · see citing works

Role of Gut Microbiota in Neuroendocrine Regulation of Carbohydrate and Lipid Metabolism via the Microbiota-Gut-Brain-Liver Axis

Wang, S., Yu, Y., & Adeli, K. (2020) · Microorganisms · doi:10.3390/microorganisms8040527 · Cited by 214 · see citing works

Gastric satiation is volumetric, intestinal satiation is nutritive

Powley, T. L., & Phillips, R. J. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.04.037 · Cited by 205 · see citing works

Increased colonic propionate reduces anticipatory reward responses in the human striatum to high-energy foods

Byrne, C. S., Chambers, E. S., Alhabeeb, H., Chhina, N., Morrison, D. J., Preston, T., Tedford, C., Fitzpatrick, J., Irani, C., Busza, A., et al. (2016) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.126706 · Cited by 201 · see citing works

The role of gut microbiota in pathogenesis of Alzheimer's disease

Bostancıklıoğlu, M. (2019) · Journal of Applied Microbiology · doi:10.1111/jam.14264 · Cited by 200 · see citing works

Luminal amino acid sensing in the rat gastric mucosa

Uneyama, H., Niijima, A., Gabriel, A. S., & Torii, K. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00587.2005 · Cited by 199 · see citing works

Profiling of G protein-coupled receptors in vagal afferents reveals novel gut-to-brain sensing mechanisms

Egerod, K. L., Petersen, N., Timshel, P. N., Rekling, J. C., Wang, Y., Liu, Q., Schwartz, T. W., & Gautron, L. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.03.016 · Cited by 191 · see citing works

Impaired intestinal afferent nerve satiety signalling and vagal afferent excitability in diet induced obesity in the mouse

Daly, D., Park, S. J., Valinsky, W. C., & Beyak, M. J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.204594 · Cited by 188 · see citing works

Emerging role of gut microbiota dysbiosis in neuroinflammation and neurodegeneration

Solanki, R., Karande, A. A., & Ranganathan, P. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1149618 · Cited by 192 · see citing works

Signalling from the periphery to the brain that regulates energy homeostasis

Kim, K., Seeley, R. J., & Sandoval, D. A. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2018.8 · Cited by 181 · see citing works

Bacteroides fragilis polysaccharide A is necessary and sufficient for acute activation of intestinal sensory neurons

Mao, Y.-K., Kasper, D. L., Wang, B., Forsythe, P., Bienenstock, J., & Kunze, W. A. (2013) · Nature Communications · doi:10.1038/ncomms2478 · Cited by 178 · see citing works

Probiotics: Potential novel therapeutics for microbiota-gut-brain axis dysfunction across gender and lifespan

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 171 · see citing works

Abdominal vagal afferent neurones: an important target for the treatment of gastrointestinal dysfunction

Andrews, P. L. R. (2002) · Current Opinion in Pharmacology · doi:10.1016/s1471-4892(02)00227-8 · Cited by 157 · see citing works

Role of Fat Hydrolysis in Regulating Glucagon-Like Peptide-1 Secretion

Beglinger, S., Drewe, J., Schirra, J. J., Göke, B., D’Amato, M., & Beglinger, C. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-1062 · Cited by 146 · see citing works

A potential role for the gut microbiome in substance use disorders

Meckel, K. R., & Kiraly, D. D. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05232-0 · Cited by 141 · see citing works

Anterograde transneuronal viral tract tracing reveals central sensory circuits from white adipose tissue

Song, C. K., Schwartz, G. J., & Bartness, T. J. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90786.2008 · Cited by 141 · see citing works

Short chain fatty acids: the messengers from down below

Mansuy‐Aubert, V., & Ravussin, Y. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1197759 · Cited by 133 · see citing works

Neural Systems Controlling the Drive to Eat: Mind Versus Metabolism

Zheng, H., & Berthoud, H.-R. (2008) · Physiology · doi:10.1152/physiol.00047.2007 · Cited by 131 · see citing works

Gut microbiota-derived short-chain fatty acids and hypertension: Mechanism and treatment

Yang, F., Chen, H., Gao, Y., An, N., Li, X., Pan, X., Yang, X., Tian, L., Sun, J., Xiong, X., et al. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110503 · Cited by 131 · see citing works

Abdominal vagal mediation of the satiety effects of CCK in rats

Reidelberger, R. D., Hernandez, J., Fritzsch, B., & Hulce, M. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00646.2003 · Cited by 125 · see citing works

Microbiota in obesity: interactions with enteroendocrine, immune and central nervous systems

Mulders, R. J., de Git, K. C. G., Schéle, E., Dickson, S. L., Sanz, Y., & Adan, R. A. H. (2018) · Obesity Reviews · doi:10.1111/obr.12661 · Cited by 118 · see citing works

The interplay between sleep and gut microbiota

Han, M., Yuan, S., & Zhang, J. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.12.016 · Cited by 120 · 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

Depression and lifestyle: Focusing on nutrition, exercise, and their possible relevance to molecular mechanisms

Kunugi, H. (2023) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13551 · Cited by 112 · see citing works

The Role of Short-Chain Fatty Acids of Gut Microbiota Origin in Hypertension

Wu, Y., Xu, H., Tu, X., & Gao, Z. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.730809 · Cited by 108 · see citing works

Activation of the α7 nicotinic receptor promotes lipopolysaccharide-induced conversion of M1 microglia to M2.

Zhang, Q., Lu, Y., Bian, H., Guo, L., & Zhu, H. (2017) · PubMed Central · Cited by 106 · see citing works

Localization of orexin-1 receptors to vagal afferent neurons in the rat and humans

Burdyga, G., Lal, S., Spiller, D. G., Jiang, W. Y., Thompson, D. G., Attwood, S. E., Saeed, S. R., Grundy, D., Varró, A., Dimaline, R., et al. (2003) · Gastroenterology · doi:10.1053/gast.2003.50020 · Cited by 107 · see citing works

Neurodegenerative disorders and gut-brain interactions

Singh, A., Dawson, T. M., & Kulkarni, S. (2021) · Journal of Clinical Investigation · doi:10.1172/jci143775 · Cited by 102 · see citing works

The gut microbiome in Parkinson's disease: A culprit or a bystander?

Keshavarzian, A., Engen, P. A., Bonvegna, S., & Cilia, R. (2020) · Progress in brain research · doi:10.1016/bs.pbr.2020.01.004 · Cited by 104 · see citing works

The central and biodynamic role of gut microbiota in critically ill patients

Wozniak, H., Beckmann, T. S., Fröhlich, L., Soccorsi, T., Terrier, C. L., de Watteville, A., Schrenzel, J., & Heidegger, C. (2022) · Critical Care · doi:10.1186/s13054-022-04127-5 · Cited by 100 · see citing works

Effect of CCK-1 receptor blockade on ghrelin and PYY secretion in men

Degen, L. P., Drewe, J., Piccoli, F., Gräni, K., Oesch, S., Bunea, R., D’Amato, M., & Beglinger, C. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00734.2006 · Cited by 100 · see citing works

I. Morphology and topography of vagal afferents innervating the GI tract

Powley, T. L., & Phillips, R. J. (2002) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00249.2002 · Cited by 99 · see citing works

Intestinal Sensing of Nutrients

Tolhurst, G., Reimann, F. M., & Gribble, F. M. (2011) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-24716-3_14 · Cited by 97 · see citing works

Epigenetics in depression and gut-brain axis: A molecular crosstalk

Begum, N., Mandhare, A., Tryphena, K. P., Srivastava, S., Shaikh, M. F., Singh, S. B., & Khatri, D. K. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1048333 · Cited by 99 · see citing works

Malnutrition in systemic sclerosis.

Harrison, E., Herrick, A., Mclaughlin, J., & Lal, S. (2012) · Rheumatology · doi:10.1093/rheumatology/kes160 · Cited by 83 · see citing works

Are gut dysbiosis, barrier disruption, and endotoxemia related to adipose tissue dysfunction in metabolic disorders? Overview of the mechanisms involved

Silva, D., Viana, S., Carvalho, E., Reis, F., & Matafome, P. N. (2023) · Internal and Emergency Medicine · doi:10.1007/s11739-023-03262-3 · Cited by 95 · see citing works

Cholecystokinin pathways modulate sensations induced by gastric distension in humans

Lal, S., McLaughlin, J. T., Barlow, J. D., D’Amato, M., Giacovelli, G., Varró, A., Dockray, G. J., & Thompson, D. G. (2004) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00351.2003 · Cited by 93 · see citing works

The gut-brain axis rewired: adding a functional vagal nicotinic “sensory synapse”

Perez‐Burgos, A., Mao, Y., Bienenstock, J., & Kunze, W. A. (2014) · The FASEB Journal · doi:10.1096/fj.13-245282 · Cited by 91 · see citing works

The Role of Bacteria and Its Derived Metabolites in Chronic Pain and Depression: Recent Findings and Research Progress

Li, S., Hua, D., Wang, Q., Yang, L., Wang, X., Luo, A., & Yang, C. (2019) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyz061 · Cited by 91 · see citing works

Dissecting the Role of Subtypes of Gastrointestinal Vagal Afferents

Wang, Y. B., de Lartigue, G., & Page, A. J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00643 · Cited by 92 · see citing works

Gut-Brain Axis in the Early Postnatal Years of Life: A Developmental Perspective

Jena, A., Montoya, C. A., Mullaney, J. A., Dilger, R. N., Young, W., McNabb, W. C., & Roy, N. C. (2020) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2020.00044 · Cited by 92 · see citing works

Microbiota and Microglia Interactions in ASD

Davoli-Ferreira, M., Thomson, C. A., & McCoy, K. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.676255 · Cited by 90 · see citing works

Brain modulation by the gut microbiota: From disease to therapy

Mitra, S., Dash, R., Nishan, A. A., Habiba, S. U., & Moon, I. S. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2022.12.001 · Cited by 87 · see citing works

The Role of Short-Chain Fatty Acids in Microbiota–Gut–Brain Cross-Talk with a Focus on Amyotrophic Lateral Sclerosis: A Systematic Review

Moțățăianu, A., Şerban, G. M., & Andone, S. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015094 · Cited by 90 · see citing works

Luminal sensing in the gut: an overview.

Dockray, G. (2003) · PubMed · Cited by 86 · see citing works

Neuroimmune and epithelial interactions in intestinal inflammation

Sharkey, K. A. (2002) · Current Opinion in Pharmacology · doi:10.1016/s1471-4892(02)00215-1 · Cited by 85 · see citing works

Signalling the state of the digestive tract

Grundy, D. (2006) · Autonomic Neuroscience · doi:10.1016/j.autneu.2006.01.009 · Cited by 81 · see citing works

Relationship Between Short-chain Fatty Acids and Parkinson’s Disease: A Review from Pathology to Clinic

Duan, W.-X., Wang, F., Liu, J., & Liu, C. (2023) · Neuroscience Bulletin · doi:10.1007/s12264-023-01123-9 · Cited by 78 · see citing works

Review article: the role of the autonomic nervous system in the pathogenesis and therapy of IBD

Mogilevski, T., Burgell, R., Aziz, Q., & Gibson, P. R. (2019) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15433 · Cited by 75 · see citing works

Acetate, a Short-Chain Fatty Acid, Acutely Lowers Heart Rate and Cardiac Contractility Along with Blood Pressure

Poll, B. G., Xu, J., Jun, S., Sanchez, J., Zaidman, N. A., He, X., Lester, L., Berkowitz, D. E., Paolocci, N., Gao, W. D., et al. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.000187 · Cited by 75 · see citing works

White adipose tissue sensory nerve denervation mimics lipectomy-induced compensatory increases in adiposity

Shi, H., & Bartness, T. J. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00036.2005 · Cited by 75 · see citing works

Gut–Brain Axis in Regulation of Blood Pressure

Yang, T., & Zubcevic, J. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00845 · Cited by 74 · see citing works

Gut microbiome-mediated epigenetic regulation of brain disorder and application of machine learning for multi-omics data analysis

Kaur, H., Singh, Y., Singh, S., & Singh, R. B. (2020) · Genome · doi:10.1139/gen-2020-0136 · Cited by 72 · see citing works

Neuroinflammatory remodeling of the anterior cingulate cortex as a key driver of mood disorders in gastrointestinal disease and disorders

Matisz, C. E., & Gruber, A. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.12.020 · Cited by 70 · see citing works

The versatility of the vagus

Dockray, G. J. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.01.009 · Cited by 72 · see citing works

The role of the vagus nerve in appetite control: Implications for the pathogenesis of obesity

Cork, S. C. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12643 · Cited by 73 · see citing works

Microbiota‐microglia connections in age‐related cognition decline

Zhou, R., Qian, S., Cho, W. C. S., Zhou, J., Jin, C., Zhong, Y., Wang, J., Zhang, X., Xu, Z., Tian, M., et al. (2022) · Aging Cell · doi:10.1111/acel.13599 · Cited by 71 · see citing works

The spinal cord-gut-immune axis as a master regulator of health and neurological function after spinal cord injury

Kigerl, K. A., Zane, K., Adams, K., Sullivan, M. B., & Popovich, P. G. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113085 · Cited by 70 · see citing works

Chylomicron components activate duodenal vagal afferents via a cholecystokinin A receptor‐mediated pathway to inhibit gastric motor function in the rat

Glatzle, J., Wang, Y., Adelson, D. W., Kalogeris, T. J., Zittel, T. T., Tso, P., Wei, J., & Raybould, H. E. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.041673 · Cited by 68 · see citing works

Standardization of methods to record Vagus nerve activity in mice

Silverman, H. A., Stiegler, A., Tsaava, T., Newman, J. E., Steinberg, B. E., Battinelli, E., Robbiati, S. F., Bouton, C. E., Huerta, P. T., Chavan, S. S., et al. (2018) · Bioelectronic Medicine · doi:10.1186/s42234-018-0002-y · Cited by 67 · see citing works

Alterations in microbiome composition and metabolic byproducts drive behavioral and transcriptional responses to morphine

Hofford, R. S., Mervosh, N. L., Euston, T. J., Meckel, K. R., Orr, A. T., & Kiraly, D. D. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01043-0 · Cited by 64 · see citing works

Nutrient-Sensing Mechanisms in the Gut as Therapeutic Targets for Diabetes

Breen, D. M., Rasmussen, B. A., Côté, C. D., Jackson, V. M., & Lam, T. K. T. (2013) · Diabetes · doi:10.2337/db13-0523 · Cited by 64 · see citing works

The Role of Short Chain Fatty Acids in Irritable Bowel Syndrome

Jiang, W., Wu, J., Zhu, S., Xin, L., Yu, C., & Shen, Z. (2022) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm22093 · Cited by 66 · see citing works

Gut Microbiota and Short Chain Fatty Acids: Influence on the Autonomic Nervous System

Bruning, J. R., Chapp, A. D., Kaurala, G. A., Wang, R., Techtmann, S. M., & Chen, Q. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00410-8 · Cited by 63 · see citing works

The role of gastrointestinal vagal afferent fibres in obesity

Kentish, S. J., & Page, A. J. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.278226 · Cited by 63 · see citing works

PPARγ in Vagal Neurons Regulates High-Fat Diet Induced Thermogenesis

Liu, C., Bookout, A. L., Lee, S., Sun, K., Jia, L., Lee, C., Udit, S., Deng, Y., Scherer, P. E., Mangelsdorf, D. J., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.01.021 · Cited by 61 · see citing works

Gut endocrine secretions and their relevance to satiety

Dockray, G. J. (2004) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2004.05.005 · Cited by 61 · see citing works

Deficits in gastrointestinal responses controlling food intake and body weight

Covașă, M. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00126.2010 · Cited by 58 · see citing works

Importance of release location on the mode of action of butyrate derivatives in the avian gastrointestinal tract

Moquet, P. C. A., Onrust, L., Immerseel, F. V., Ducatelle, R., Hendriks, W. H., & Kwakkel, R. P. (2016) · World s Poultry Science Journal · doi:10.1017/s004393391500269x · Cited by 60 · see citing works

GI Tract

(2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.tb00324.x

The long chain fatty acid oleate activates mouse intestinal afferent nerves in vitro

Webster, W. A., & Beyak, M. J. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2012-0138 · Cited by 12 · see citing works

The vagal afferent pathway does not play a major role in the induction of satiety by intestinal fatty acid in rats

Ogawa, N., Yamaguchi, H., Shimbara, T., Toshinai, K., Kakutani, M., Yonemori, F., & Nakazato, M. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2007.12.036 · Cited by 13 · see citing works

Differential effects of intestinal short- and long-chain fatty acid infusions on ingestive behavior in rats

Ji, S. (2011) · Purdue e-Pubs (Purdue University System)

Suppression of food intake by GI fatty acid infusions: roles of celiac vagal afferents and cholecystokinin

Cox, J. E., Kelm, G. R., Meller, S. T., & Randich, A. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.04.022 · Cited by 37 · see citing works