Northway M G, Burks T F
Eur J Pharmacol. 1979 Nov 16;59(3-4):237-43. doi: 10.1016/0014-2999(79)90286-3.
The effects of bolus intra-arterial doses of heroin and other stimulant drugs were studied in vascularly perfused isolated segments of dog small intestine. Heroin caused dose-related increases in intraluminal pressure similar in appearance to those caused by morphine. Perfusion with Krebs bicarbonate solution containing naloxone selectively abolished intestinal responses to heroin. Perfusion with cinanserin, a 5-hydroxytryptamine (5-HT) antagonist, decreased intestinal responses to 5-HT and heroin without affecting responses to dimethylphenylpiperazinium (DMPP) or bethanechol (BeCh). Tetrodotoxin reduced responses to heroin, 5-HT and DMPP but not responses to BeCh. Atropine antagonized contractile responses to all 4 stimulatory agents. These data indicate that heroin interacts with a conventional opiate receptor in the intestine and that the intestinal stimulatory effect of heroin is mediated by the release of endogenous 5-HT which activates intramural cholinergic neurons.
在犬小肠的血管灌注离体节段中研究了大剂量动脉内注射海洛因及其他兴奋剂的作用。海洛因导致肠腔内压力呈剂量相关增加,其表现与吗啡所致者相似。用含纳洛酮的碳酸氢盐林格液灌注可选择性消除肠道对海洛因的反应。用5-羟色胺(5-HT)拮抗剂辛那色林灌注可降低肠道对5-HT和海洛因的反应,但不影响对二甲基苯基哌嗪(DMPP)或氨甲酰甲胆碱(BeCh)的反应。河豚毒素可降低对海洛因、5-HT和DMPP的反应,但不影响对BeCh的反应。阿托品可拮抗对所有4种刺激剂的收缩反应。这些数据表明,海洛因与肠道中的传统阿片受体相互作用,海洛因的肠道刺激作用是由内源性5-HT的释放介导的,后者激活壁内胆碱能神经元。