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[氯丙嗪对小鼠肠道运动的抑制作用及其拮抗剂]

[Inhibitory action of chlorpromazine on intestinal movement in mice and its antagonistic agents].

作者信息

Xiong Y Q, Li B H

机构信息

Department of Pharmacology, Jiangxi Medical College, Nanchang, China.

出版信息

Zhongguo Yao Li Xue Bao. 1994 May;15(3):235-9.

PMID:7976378
Abstract

Adynamic ileus is a toxic effect produced by chlorpromazine (Chl). The present study is to analyze the inhibitory action of Chl on the intestinal movement of mice and to search its antagonistic remedies. Inhibition was evaluated by 2 tests: the loss of defecation reflex and the inhibited transport of phenol red in the intestinal tract. Chl (1-2 mg.kg-1 i.p. or 1 microgram per mouse i.c.v.) inhibited the intestinal movement powerfully. Scopolamine (Sco 4 mg.kg-1 i.p. or 4-8 micrograms per mouse i.c.v.) produced the same effect. The i.v. ED50 (L95) of Chl and Sco for inhibition of the defecation reflex were 0.85 (0.79-0.93) and 3.49 (3.24-3.78) mg.kg-1, respectively. Haloperidol (1-4 mg.kg-1 i.p.), sulpiride (10 mg.kg-1 i.p.), and phentolamine (2-4 mg.kg-1 i.p. or 4 micrograms per mouse i.c.v.) did not affect the defecation reflex. In the isolated guinea pig ileum the pA2 value of Chl against carbachol (Car) was 4.5 and that of Sco was 9.1. In addition, the inhibitory effect caused by Sco was antagonized by physostigmine (Phy 0.08 mg.kg-1 sc), but not by pilocarpine (Pil 100-200 micrograms per mouse i.c.v.) and 4-aminopyridine (4-AP 1 microgr per mouse i.c.v.), whereas that caused by Chl was antagonized by Pil (100 micrograms per mouse i.c.v.) and 4-AP (1 microgram per mouse i.c.v.), but not by Phy. Neostigmine (Neo 0.05 mg.kg-1 sc) or Car (0.05 mg.kg-1 sc) combined with 4-AP (2 mg.kg-1 sc) exhibited a synergetic effect against Chl-induced inhibition.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

动力性肠梗阻是氯丙嗪(Chl)产生的一种毒性作用。本研究旨在分析氯丙嗪对小鼠肠道运动的抑制作用,并寻找其拮抗补救措施。通过两项试验评估抑制作用:排便反射丧失和肠道中酚红转运受抑制。氯丙嗪(腹腔注射1 - 2毫克/千克或每只小鼠脑室内注射1微克)强烈抑制肠道运动。东莨菪碱(腹腔注射4毫克/千克或每只小鼠脑室内注射4 - 8微克)产生相同效果。氯丙嗪和东莨菪碱抑制排便反射的静脉注射半数有效量(L95)分别为0.85(0.79 - 0.93)和3.49(3.24 - 3.78)毫克/千克。氟哌啶醇(腹腔注射1 - 4毫克/千克)、舒必利(腹腔注射10毫克/千克)和酚妥拉明(腹腔注射2 - 4毫克/千克或每只小鼠脑室内注射4微克)不影响排便反射。在离体豚鼠回肠中,氯丙嗪对卡巴胆碱(Car)的pA2值为4.5,东莨菪碱的为9.1。此外,东莨菪碱引起的抑制作用可被毒扁豆碱(皮下注射0.08毫克/千克)拮抗,但不能被毛果芸香碱(每只小鼠脑室内注射100 - 200微克)和4 - 氨基吡啶(每只小鼠脑室内注射1微克)拮抗,而氯丙嗪引起的抑制作用可被毛果芸香碱(每只小鼠脑室内注射100微克)和4 - 氨基吡啶(每只小鼠脑室内注射1微克)拮抗,但不能被毒扁豆碱拮抗。新斯的明(皮下注射0.05毫克/千克)或卡巴胆碱(皮下注射0.05毫克/千克)与4 - 氨基吡啶(皮下注射2毫克/千克)联合使用对氯丙嗪诱导的抑制作用表现出协同效应。(摘要截选至250字)

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