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环二烯类杀虫剂引起大鼠体内氯丙嗪中枢抑制作用的变化。

Cyclodiene insecticides-induced changes in the central depressive effect of chlorpromazine in rats.

作者信息

Balasubramaniam E, Paul V, Kazi M

机构信息

Department of Pharmacology & Environmental Toxicology, Dr. A.L.M. Postgraduate Institute of Basic Medical Sciences, University of Madras, Taramani.

出版信息

Indian J Physiol Pharmacol. 1995 Jul;39(3):231-6.

PMID:8550115
Abstract

Spontaneous motor activity (SMA), conditioned avoidance response (CAR), muscle coordination (MC) and pentobarbital sleep were tested in rats treated orally for 90 days with tolerated doses of the cyclodiene insecticides, aldrin (1 mg/kg) and endosulfan (2 mg/kg). The same tests were repeated in similarly treated animals after injecting chlorpromazine (4 mg/kg, i.p.). Both the insecticides shortened pentobarbital sleeping time indicating their microsomal enzyme inducing property. Aldrin suppressed SMA, CAR and MC, whereas endosulfan stimulated SMA, inhibited CAR and unaltered MC. However, their concurrent action with CPZ did not result in change in the central depressive effects of the latter, but its potency during the course of its action was altered. Its potency 15 min after injection was greater and 60-180 min later was lesser in these animals than that observed in control animals. This finding was interpreted to suggest that aldrin and endosulfan has quickened the biotransformation of CPZ and thereby shortened its duration of action. A temporary promotion of its potency was accounted to its active metabolites, since prior to inactivation, CPZ is known to be metabolized by the microsomal enzymes to active compounds.

摘要

用环二烯类杀虫剂艾氏剂(1毫克/千克)和硫丹(2毫克/千克)的耐受剂量对大鼠进行90天口服给药,然后测试其自发运动活动(SMA)、条件性回避反应(CAR)、肌肉协调性(MC)和戊巴比妥诱导的睡眠。在对同样处理的动物注射氯丙嗪(4毫克/千克,腹腔注射)后,重复相同的测试。两种杀虫剂均缩短了戊巴比妥睡眠时间,表明它们具有微粒体酶诱导特性。艾氏剂抑制SMA、CAR和MC,而硫丹刺激SMA、抑制CAR且对MC无影响。然而,它们与氯丙嗪的共同作用并未导致氯丙嗪的中枢抑制作用发生变化,但在其作用过程中其效力发生了改变。在这些动物中,注射后15分钟时氯丙嗪的效力比对照动物中观察到的更强,而在60 - 180分钟后则较弱。这一发现被解释为表明艾氏剂和硫丹加快了氯丙嗪的生物转化,从而缩短了其作用持续时间。其效力的暂时增强归因于其活性代谢产物,因为在失活之前,已知氯丙嗪被微粒体酶代谢为活性化合物。

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