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Serotonin and cholecystokinin synergistically stimulate rat vagal primary afferent neurones

dc.contributor.authorLi, Y.en_US
dc.contributor.authorWu, X. Y.en_US
dc.contributor.authorOwyang, Chungen_US
dc.date.accessioned2010-04-01T15:12:03Z
dc.date.available2010-04-01T15:12:03Z
dc.date.issued2004-09en_US
dc.identifier.citationLi, Y.; Wu, X. Y.; Owyang, C. (2004). "Serotonin and cholecystokinin synergistically stimulate rat vagal primary afferent neurones." The Journal of Physiology 559(2): 651-662. <http://hdl.handle.net/2027.42/65669>en_US
dc.identifier.issn0022-3751en_US
dc.identifier.issn1469-7793en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/65669
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15235095&dopt=citationen_US
dc.format.extent234780 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Science Ltden_US
dc.rightsThe Physiological society 2004en_US
dc.titleSerotonin and cholecystokinin synergistically stimulate rat vagal primary afferent neuronesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysiologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumGastroenterology Research Unit, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI, USAen_US
dc.identifier.pmid15235095en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/65669/1/jphysiol.2004.064816.pdf
dc.identifier.doi10.1113/jphysiol.2004.064816en_US
dc.identifier.sourceThe Journal of Physiologyen_US
dc.identifier.citedreferenceAndrews PL & Davison JS ( 1990 ). Activation of vagal afferent terminals by 5-HT is mediated by 5-HT 3 receptors in the anaesthetized ferret. J Physiol 422, 92 P.en_US
dc.identifier.citedreferenceAttoub S, Moizo L, Laignwau JP, Alchepo B, Lewin MJ & Bado A ( 1998 ). YM022, a highly potent and selective CCKB antagonist inhibiting gastric acid secretion in the rat, the cat and isolated rabbit glands. Fundam Clin Pharmacol 12, 256 – 262.en_US
dc.identifier.citedreferenceBlackshaw LA & Grundy D ( 1993 ). Effects of 5-hydroxytryptamine on discharge of vagal mucosal afferent fibres from the upper gastrointestinal tract of the ferret. J Auton Nerv Syst 45, 41 – 50.en_US
dc.identifier.citedreferenceBueno L, Fioramonti J, Delvaux M & Frexinos J ( 1997 ). Mediators and pharmacology of visceral sensitivity: from basic to clinical investigations. Gastroenterology 112, 1714 – 1743.en_US
dc.identifier.citedreferenceCox JE ( 1994 ). Duodenal sucrose and glucose infusions enhance suppression by cholecystokinin of sham feeding. Am J Physiol 266, R466 – R471.en_US
dc.identifier.citedreferenceCox JE ( 1998 ). Cholecystokinin satiety involves CCKA receptors perfused by the superior pancreaticoduodenal artery. Am J Physiol 274, R1390 – R1396.en_US
dc.identifier.citedreferenceDavison JS & Clarke GD ( 1988 ). Mechanical properties and sensitivity to CCK of vagal gastric slowly adapting mechanoreceptors. Am J Physiol 255, G55 – G61.en_US
dc.identifier.citedreferenceDe Ponti F & Tonini M ( 2001 ). Irritable bowel syndrome: new agents targeting serotonin receptor subtypes. Drugs 61, 317 – 332.en_US
dc.identifier.citedreferenceEmeran AE & Gebhart GF ( 1994 ). Basic and clinical aspects of visceral hyperalgesia. Gastroenterology 107, 271 – 293.en_US
dc.identifier.citedreferenceGrider JR, Foxx-Orenstein AE & Jin JG ( 1998 ). 5-Hydroxytryptamine 4 receptor agonists initiate the peristaltic reflex in human, rat, and guinea pig intestine. Gastroenterology 115, 370 – 380.en_US
dc.identifier.citedreferenceHebel R & Stromberg RW ( 1976 ). Anatomy of Laboratory Rat. Williams & Wilkins, Baltimore.en_US
dc.identifier.citedreferenceHillsley K & Grundy D ( 1998 ). Serotonin and cholecystokinin activate different populations of rat mesenteric vagal afferents. Neurosci Lett 225, 63 – 66.en_US
dc.identifier.citedreferenceJulian GM & Lawrence CB ( 1992 ). Selectivity of cholecystokinin (CCK) receptor antagonists, MK-329 and L-365,260, for axonally-transported CCK binding sites on the rat vagus nerve. Neurosci Lett 137, 229 – 231.en_US
dc.identifier.citedreferenceLankisch TO, Tsunoda Y, Lu Y & Owyang C ( 2002 ). Characterization of CCK A receptor affinity states and Ca 2+ signal transduction in vagal nodose ganglia. Am J Physiol Gastrointest Liver Physiol 282, G1002 – G1008.en_US
dc.identifier.citedreferenceLi Y, Hao Y & Owyang C ( 1997 ). High-affinity CCK-A receptors on the vagus nerve mediate CCK-stimulated pancreatic secretion in rats. Am J Physiol 273, G679 – G685.en_US
dc.identifier.citedreferenceLi Y, Hao YB, Zhu JX & Owyang C ( 2000 ). Serotonin released from intestinal enterochromaffin cells mediates luminal non-CCK-stimulated pancreatic secretion in rats. Gastroenterology 118, 1197 – 1207.en_US
dc.identifier.citedreferenceLi Y & Owyang C ( 1993 ). Vagal afferent pathways mediate physiological action of cholecystokinin on pancreatic secretion. J Clin Invest 92, 418 – 424.en_US
dc.identifier.citedreferenceLi Y & Owyang C ( 1996 ). Pancreatic secretion evoked by cholecystokinin and non-cholecystokinin-dependent duodenal stimuli via vagal afferent fibres in the rat. J Physiol 494, 773 – 782.en_US
dc.identifier.citedreferenceLi Y, Wu XY & Owyang C ( 2001 ). Intestinal serotonin acts as a paracrine substance to mediate pancreatic secretion stimulated by non-CCK-dependent luminal factors. Am J Physiol Gastrointest Liver Physiol 281, G916 – G923.en_US
dc.identifier.citedreferenceLi Y, Zhu J & Owyang C ( 1999 ). Electrical physiological evidence for high- and low-affinity CCK-A receptors. Am J Physiol 277, G469 – G477.en_US
dc.identifier.citedreferenceMei N & Garnier L ( 1986 ). Osmosensitive vagal receptors in the small intestine of the cat. J Auton Nerv Syst 16, 159 – 170.en_US
dc.identifier.citedreferenceNess TJ & Gebhart GF ( 1988 ). Colorectal distension as a noxious visceral stimulus: physiologic and pharmacologic characterization of pseudaffective reflexes in the rat. Brain Res 450, 153 – 169.en_US
dc.identifier.citedreferenceNiederau M, Niederau C, Strohmeyer G & Grendell JH ( 1989 ). Comparative effects of CCK receptor antagonists on rat pancreatic secretion in vivo. Am J Physiol 256, G150 – G157.en_US
dc.identifier.citedreferenceOzcelbi F & Miller LJ ( 1995 ). Phosphopeptide mapping of cholecystokinin receptors on agonist-stimulated native pancreatic acinar cells. J Biol Chem 270, 3435 – 3441.en_US
dc.identifier.citedreferenceRaybould HE & HÖlzer HH ( 1992 ). Dual capsaicin-sensitive afferent pathways mediate inhibition of gastric emptying in rat induced by carbohydrate. Neurosci Lett 141, 236 – 238.en_US
dc.identifier.citedreferenceRenehan WE, Zhang X, Beierwaltes WH & Fogel R ( 1995 ). Neurons in the dorsal motor nucleus of the vagus may integrate vagal and spinal information from the GI tract. Am J Physiol 268, G780 – G790.en_US
dc.identifier.citedreferenceRichards W, Hillsley K, Eastwood C & Grundy D ( 1996 ). Sensitivity of vagal mucosal afferents to cholecystokinin and its role in afferent signal transduction in the rat. J Physiol 497, 473 – 481.en_US
dc.identifier.citedreferenceRitter RC, Brenner L & Yox DP ( 1992 ). Participation of vagal sensory neurons in putative satiety signals from upper gastrointestinal tract. In Neuroanatomy and Physiology of Abdominal Vagal Afferents. ed. Ritter S, Ritter RC & Barnes CD, pp. 221 – 248. CRC Press, Boca Raton, Ann Arbor, Boston.en_US
dc.identifier.citedreferenceRoberts-Thomson IC, Fettman MJ, Jonsson JR & Frewin DB ( 1992 ). Responses to cholecystokinin octapeptide in patients with functional abdominal pain syndromes. J Gastroenterol Hepatol 7, 293 – 297.en_US
dc.identifier.citedreferenceSato S, Stark HA, Martines J, Beaven MA, Jensen RT & Gardner JD ( 1989 ). Receptor occupation, calcium mobilization and amylase release in pancreatic acini: effect of CCK-JMV-180. Am J Physiol 257, G202 – G209.en_US
dc.identifier.citedreferenceSchwartz GJ, McHugh PR & Moran TH ( 1991 ). Integration of vagal afferent responses to gastric loads and cholecystokinin in rats. Am J Physiol 261, R64 – R69.en_US
dc.identifier.citedreferenceSchwartz GJ & Moran TH ( 1998 ). Duodenal nutrient exposure elicits nutrient-specific gut motility and vagal afferent signals in rat. Am J Physiol 274, R1236 – R1242.en_US
dc.identifier.citedreferenceSchwartz GJ, Tougas G & Moran TH ( 1995 ). Integration of vagal afferent responses to duodenal loads and exogenous CCK in rats. Peptides 16, 707 – 711.en_US
dc.identifier.citedreferenceSmith G, Jerome C, Bushin BJ, Eterno R & Simansky KJ ( 1981 ). Abdominal vagotomy blocks the satiety effects of cholecystokinin in the rat. Science 213, 1036 – 1037.en_US
dc.identifier.citedreferenceStark HA, Sharp CM, Sutliff VE, Martinez J, Jensen RT & Gardner JD ( 1989 ). CCK-JMV-180: a protein that distinguishes high-affinity cholecystokinin receptors from low-affinity cholecystokinin receptors. Biochim Biophys Acta 1010, 145 – 150.en_US
dc.identifier.citedreferenceTalley NJ ( 2003 ). Pharmacologic therapy for the irritable bowel syndrome. Am J Gastroenterol 98, 750.en_US
dc.identifier.citedreferenceTsunoda Y & Owyang C ( 1995 ). High-affinity CCK receptors are coupled to phospholipase A2 pathways to mediate pancreatic amylase secretion. Am J Physiol 269, G435 – G444.en_US
dc.identifier.citedreferenceWeatherford SC, Laughton WB, Salabarria J, Danho W, Tilley JW, Netterville LA, Schwartz GJ & Moran TH ( 1993 ). CCK satiety is differentially mediated by high- and low-affinity CCK receptors in mice and rats. Am J Physiol 264, R244 – R249.en_US
dc.identifier.citedreferenceZhu JX, Wu XY, Owyang C & Ying L ( 2001 ). Intestinal serotonin acts as a paracrine substance to mediate vagal transmission evoked by luminal factors in the rat. J Physiol 530, 431 – 442.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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