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rdf:type | |
lifeskim:mentions |
umls-concept:C0016293,
umls-concept:C0021853,
umls-concept:C0026056,
umls-concept:C0183683,
umls-concept:C0205296,
umls-concept:C0205923,
umls-concept:C0231491,
umls-concept:C0243192,
umls-concept:C0344211,
umls-concept:C0427574,
umls-concept:C0439852,
umls-concept:C0439861,
umls-concept:C0999699,
umls-concept:C1171411,
umls-concept:C1280500,
umls-concept:C1317973,
umls-concept:C1521721,
umls-concept:C1533691
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pubmed:issue |
1-2
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pubmed:dateCreated |
1990-4-26
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pubmed:abstractText |
Isolated segments of the guinea-pig small intestine and the guinea-pig stomach were vascularly perfused and the release of 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid into the portal venous effluent determined by high pressure liquid chromatography with electrochemical detection. Test substances were applied intraarterially. The benzodiazepine receptor agonist, midazolam, concentration-dependently increased (by 58%, at 1 nmol/l) and decreased (by 32%, at 100 nmol/l) the release of 5-HT from small intestine preparations. Both effects were blocked by the benzodiazepine receptor antagonist flumazenil (10 nmol/l) The stimulatory effect of midazolam was also abolished in the presence of tetrodotoxin (1 mumol/l) or scopolamine (100 nmol/l). In the absence of tetrodotoxin, flumazenil (10 nmol/l) alone decreased the release of 5-HT from the small intestine by 41%, but it increased the release of 5-HT by 50% in the presence of tetrodotoxin. Both effects of flumazenil were abolished in the presence of bicuculline (50 mumol/l). In the absence of tetrodotoxin, flumazenil (10 nmol/l) decreased also the release of 5-HT and its metabolite from the perfused stomach by about 40%, whereas midazolam (1 nmol/l) caused an increase by about 60%. In conclusion, benzodiazepine receptors modulate the previously described intrinsic GABAergic regulation of 5-HT release from enterochromaffin cells in the guinea-pig intestine. It is suggested that an endogenous benzodiazepine-like substance of non-neuronal origin is present in the small intestine and stomach of the guinea-pig.
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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/Flumazenil,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxyindoleacetic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Midazolam,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, GABA-A,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrodotoxin
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pubmed:status |
MEDLINE
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pubmed:issn |
0028-1298
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
341
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1690357-Animals,
pubmed-meshheading:1690357-Chromaffin System,
pubmed-meshheading:1690357-Chromatography, High Pressure Liquid,
pubmed-meshheading:1690357-Electrochemistry,
pubmed-meshheading:1690357-Female,
pubmed-meshheading:1690357-Flumazenil,
pubmed-meshheading:1690357-Guinea Pigs,
pubmed-meshheading:1690357-Hydroxyindoleacetic Acid,
pubmed-meshheading:1690357-Intestine, Small,
pubmed-meshheading:1690357-Male,
pubmed-meshheading:1690357-Midazolam,
pubmed-meshheading:1690357-Perfusion,
pubmed-meshheading:1690357-Receptors, GABA-A,
pubmed-meshheading:1690357-Serotonin,
pubmed-meshheading:1690357-Stomach,
pubmed-meshheading:1690357-Tetrodotoxin
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pubmed:articleTitle |
Effects of the benzodiazepine receptor agonist midazolam and antagonist flumazenil on 5-hydroxytryptamine release from guinea-pig intestine in vitro. Indirect support for a "natural" benzodiazepine-like substance in the intestine.
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pubmed:affiliation |
Department of Pharmacology, University of Mainz, Federal Republic of Germany.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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