Source:http://linkedlifedata.com/resource/pubmed/id/21291881
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2011-3-4
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pubmed:abstractText |
We have demonstrated that the activation of 5-hydroxytryptamine (5-HT) receptor 3 in the submucosal plexus suppresses 5-HT-induced colonic ion secretion by increasing submucosal somatostatin release. A number of psychological and physical stresses have impacts on the intestinal mucosal functions, including secretion and the epithelial barrier. Whether the 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway in the rat distal colon is involved in the stress process is still unknown. The present study aims to investigate the effect of the water-immersion restraint stress on this inhibitory pathway and its underlying mechanisms. Mucosa/submucosa preparations from the rat distal colon were mounted in the Ussing chambers for the measurement of short-circuit current (I(SC)). Real-time PCR and western blot were performed to study the expression of the 5-HT(3) receptor, 5-HT(4) receptor, and somatostatin receptor 2. Radioimmunoassay was used to measure somatostatin release. After 2h of water-immersion restraint stress, the membrane resistance (Rte) of rat mucosa/submucosa preparations was significantly decreased, but the baseline I(SC) and 5-HT-induced I(SC) responses were significantly increased. The protein expression of the submucosal 5-HT(3) receptors and mucosal somatostatin receptor 2 were down-regulated, and the 5-HT-induced somatostatin release from the mucosa/submucosa preparations was significantly reduced in the stress group. Taken together, these results suggest that the 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway is suppressed in the water-immersion restraint stressed rats, which may contribute to the acute stress-induced increase in colonic secretion.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin, 5-HT3,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin, 5-HT4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin 5-HT3 Receptor Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin,
http://linkedlifedata.com/resource/pubmed/chemical/Tropanes,
http://linkedlifedata.com/resource/pubmed/chemical/Water,
http://linkedlifedata.com/resource/pubmed/chemical/bemesetron
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1879-0712
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
10
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pubmed:volume |
656
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
94-100
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pubmed:meshHeading |
pubmed-meshheading:21291881-Animals,
pubmed-meshheading:21291881-Colon,
pubmed-meshheading:21291881-Electric Conductivity,
pubmed-meshheading:21291881-Electrophysiological Processes,
pubmed-meshheading:21291881-Gene Expression Regulation,
pubmed-meshheading:21291881-Immersion,
pubmed-meshheading:21291881-Intestinal Mucosa,
pubmed-meshheading:21291881-Male,
pubmed-meshheading:21291881-Rats,
pubmed-meshheading:21291881-Rats, Sprague-Dawley,
pubmed-meshheading:21291881-Receptors, Serotonin, 5-HT3,
pubmed-meshheading:21291881-Receptors, Serotonin, 5-HT4,
pubmed-meshheading:21291881-Receptors, Somatostatin,
pubmed-meshheading:21291881-Restraint, Physical,
pubmed-meshheading:21291881-Serotonin,
pubmed-meshheading:21291881-Serotonin 5-HT3 Receptor Antagonists,
pubmed-meshheading:21291881-Somatostatin,
pubmed-meshheading:21291881-Stress, Psychological,
pubmed-meshheading:21291881-Tropanes,
pubmed-meshheading:21291881-Water
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pubmed:year |
2011
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pubmed:articleTitle |
Colonic submucosal 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway is suppressed in water-immersion restraint stressed rats.
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pubmed:affiliation |
Department of Physiology, School of Basic Medical Sciences, Capital Medical University, Beijing (100069), PR China.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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