Effects of metformin on intestinal 5-hydroxytryptamine (5-HT) release and on 5-HT3 receptors

被引:0
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作者
L.X. Cubeddu
H. Bönisch
M. Göthert
G. Molderings
K. Racké
G. Ramadori
K.J. Miller
H. Schwörer
机构
[1] Department of Pharmacology,
[2] School of Pharmacy,undefined
[3] Central University of Venezuela,undefined
[4] Venezuela,undefined
[5] NOVA Southeastern University,undefined
[6] 3200 S University Dr.,undefined
[7] HPD,undefined
[8] College of Pharmacy,undefined
[9] Ft. Lauderdale,undefined
[10] FL 33328,undefined
[11] USA,undefined
[12] Institute of Pharmacology and Toxicology,undefined
[13] University of Bonn,undefined
[14] 53113 Bonn,undefined
[15] Germany,undefined
[16] Department of Internal Medicine,undefined
[17] Division of Gastroenterology and Endocrinology,undefined
[18] University of Göttingen,undefined
[19] Robert-Koch-Strasse 40,undefined
[20] 37075 Göttingen,undefined
[21] Germany,undefined
关键词
Metformin 5-HT receptors 5-HT release 5-HT3 receptors Enterochromaffin cells;
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摘要
Nearly 30% of patients treated with metformin experience gastrointestinal side effects. Since release of 5-hydroxytryptamine (5-HT) from the intestine is associated with nausea, vomiting, and diarrhea, we examined whether metformin induces 5-HT release from the intestinal mucosa. In 40% of tissue biopsy specimens of human duodenal mucosa, metformin (1, 10, and 30 µM) caused an increase in 5-HT outflow by 35, 70, and 98%, respectively. Peak increases in 5-HT outflow were observed after 10–15 min exposure to metformin, returning to baseline levels after 25 min. Tetrodotoxin (1 µM) reduced by about 50% the metformin-evoked increase in 5-HT outflow (P<0.05). Metformin-evoked release was not affected by scopolamine + hexamethonium, propranolol, the 5-HT3 receptor antagonist dolasetron, naloxone, or the NK1 receptor antagonist L703606. In the presence of tetrodotoxin (1 µM), somatostatin (1 µM) further reduced metformin-induced 5-HT release by 15–20%.
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页码:85 / 91
页数:6
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