Ehrenpreis S, Kimura I, Kobayashi T, Kimura M
Life Sci. 1987 Apr 27;40(17):1695-8. doi: 10.1016/0024-3205(87)90019-1.
We have investigated the mechanism by which morphine contracts hog bile duct and sphincter of Oddi. Morphine contraction is antagonized by naloxone, competitively on the sphincter, noncompetitively on the bile duct. Diphenhydramine at low concentration (3.4 X 10(-6)M) also antagonizes both actions of morphine. Histamine has a very potent contracting action on the sphincter and bile duct and this is antagonized by diphenhydramine. Burimamide only weakly antagonizes the actions of morphine or histamine. Compound 48/80 causes a pronounced contraction of sphincter and bile duct following which morphine effects are greatly attenuated. These results suggest that morphine-induced contraction of the sphincter of Oddi and bile duct is mediated by a two step reaction involving interaction with a specific opiate receptor leading to the release of histamine which combines with an H1 receptor to produce the effect.
我们已经研究了吗啡使猪胆管和Oddi括约肌收缩的机制。纳洛酮可拮抗吗啡的收缩作用,在括约肌上为竞争性拮抗,在胆管上为非竞争性拮抗。低浓度(3.4×10⁻⁶M)的苯海拉明也可拮抗吗啡的这两种作用。组胺对括约肌和胆管有很强的收缩作用,而苯海拉明可拮抗这种作用。布立马胺只能微弱地拮抗吗啡或组胺的作用。48/80化合物可使括约肌和胆管明显收缩,随后吗啡的作用会大大减弱。这些结果表明,吗啡诱导的Oddi括约肌和胆管收缩是由一个两步反应介导的,该反应涉及与特定阿片受体相互作用导致组胺释放,组胺再与H1受体结合产生效应。