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κ-阿片受体激动剂和吗啡对饥饿及未饥饿大鼠食物摄入量和尿量的影响。

Effects of kappa-opioid receptor agonists and morphine on food intake and urinary output in food-deprived and nondeprived rats.

作者信息

Ramarao P, Bhargava H N

机构信息

Department of Pharmacodynamics, University of Illinois, Chicago 60612.

出版信息

Pharmacol Biochem Behav. 1989 Jun;33(2):375-80. doi: 10.1016/0091-3057(89)90517-0.

Abstract

The effects of kappa-opioid receptor agonists, bremazocine, U-50, 488H and tifluadom and of a mu-opioid receptor agonist, morphine, on food intake and urinary output in food-deprived and nondeprived Sprague-Dawley rats was determined. In food-deprived animals, intraperitoneal administration of bremazocine at 0.1 mg/kg increased food intake but at 1.0 and 10.0 mg/kg doses decreased it. Tifluadom (0.1-10.0 mg/kg) had no effect on food intake. U-50,488H at 1.0 mg/kg increased food intake, whereas 10.0 mg/kg dose decreased the food consumption. In nondeprived rats, the kappa-opioid receptor agonists failed to produce any effect on food consumption. In food-deprived rats, all the three kappa-opioid receptor agonists increased the urinary output at the highest dose (10 mg/kg). In nondeprived rats similar effects as in food-deprived rats were observed except bremazocine increased urinary output at all the doses used. These results with kappa-opioid agonists may be related to either the existence of more than one population of kappa-opioid receptors or their differential actions at the opioid receptor types.

摘要

研究了κ-阿片受体激动剂布瑞马唑辛、U-50,488H和替氟朵,以及μ-阿片受体激动剂吗啡对饥饿和未饥饿的Sprague-Dawley大鼠食物摄入量和尿量的影响。在饥饿动物中,腹腔注射0.1mg/kg的布瑞马唑辛可增加食物摄入量,但1.0mg/kg和10.0mg/kg剂量则会减少食物摄入量。替氟朵(0.1 - 10.0mg/kg)对食物摄入量没有影响。1.0mg/kg的U-50,488H可增加食物摄入量,而10.0mg/kg剂量则会减少食物消耗量。在未饥饿的大鼠中,κ-阿片受体激动剂对食物消耗量没有任何影响。在饥饿大鼠中,所有三种κ-阿片受体激动剂在最高剂量(10mg/kg)时都会增加尿量。在未饥饿的大鼠中,观察到与饥饿大鼠类似的效果,只是布瑞马唑辛在所有使用的剂量下都会增加尿量。κ-阿片受体激动剂的这些结果可能与存在不止一种类型的κ-阿片受体或它们在阿片受体类型上的不同作用有关。

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