Hansen M B, Thørboll J E, Beubler E, Skadhauge E
Department of Anatomy and Physiology, Royal Veterinary and Agricultural University, Kosice, Frederiksberg, Denmark.
Physiol Res. 1994;43(2):83-93.
The purpose of this study was to elucidate the intestinal serotonin (5-HT) receptor subtypes involved in fluid transport in the pig jejunum in vivo. The fluid accumulating effect of intraluminally administered 5-HT, renzapride, methysergide, ketanserin, granisetron, citalopram and intravenous indomethacin, was tested in tied-off loops in vivo. 5-HT caused a dose-dependent fluid accumulation, which was reduced by indomethacin by about 30%. Renzapride, methysergide, ketanserin, granisetron and citalopram all caused fluid accumulation. Taking into account these fluid accumulating effects, renzapride, methysergide, ketanserin and granisetron reduced the fluid accumulating effect of 5-HT, giving a maximal reduction of 70, 46, 76, and 80%, respectively. These data suggest the existence of intestinal 5-HT receptor subtypes involved in fluid transport in the pig jejunum. The antagonistic effects of indomethacin, ketanserin and granisetron, suggest the involvement of prostaglandins, as well as the 5-HT2 and the 5-HT3 receptor subtypes in the fluid accumulating response of 5-HT.
本研究的目的是阐明参与猪空肠体内液体转运的肠道5-羟色胺(5-HT)受体亚型。在体内结扎肠袢中测试了腔内给予5-HT、renzapride、麦角新碱、酮色林、格拉司琼、西酞普兰以及静脉注射吲哚美辛的液体蓄积作用。5-HT引起剂量依赖性液体蓄积,吲哚美辛使其减少约30%。Renzapride、麦角新碱、酮色林、格拉司琼和西酞普兰均引起液体蓄积。考虑到这些液体蓄积作用,renzapride、麦角新碱、酮色林和格拉司琼降低了5-HT的液体蓄积作用,最大降低分别为70%、46%、76%和80%。这些数据表明存在参与猪空肠液体转运的肠道5-HT受体亚型。吲哚美辛、酮色林和格拉司琼的拮抗作用表明前列腺素以及5-HT2和5-HT3受体亚型参与了5-HT的液体蓄积反应。