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急性给予丁酰苯类药物后的进食和饮水相互作用。

Feeding and drinking interactions after acute butyrophenone administration.

作者信息

Rowland N, Engle D J

出版信息

Pharmacol Biochem Behav. 1977 Oct;7(4):295-301. doi: 10.1016/0091-3057(77)90223-4.

Abstract

The effects on feeding and drinking of various doses of droperidol, haloperidol and spiroperidol were studied in a number of paradigms. All three buryrophenones produced generally similar effects. After food deprivation, feeding was slightly increased at low doses but was decreased at the higher doses; the concomitant postprandial drinking was attenuated at all doses. Desalivate rats showed a marked attenuation of feeding (and prandial drinking) at low doses, but when wet mash was given instead of pellets and water a normal dose-response relationship was obtained. After water deprivation drinking was attenuated at all doses, and when food was also available during the drinking test the food intake was decreased in proportion to the drinking. Drinking was blocked more when food was present than in its absence. Insulin and 2-deoxyglucose induced feeding in sated rats was attenuated but not abolished by haloperidol. The findings are discussed relative to the role of activation and brain catecholamines in feeding and drinking.

摘要

在多种实验范式中研究了不同剂量的氟哌利多、氟哌啶醇和螺哌隆对摄食和饮水的影响。所有这三种丁酰苯类药物产生的总体效果相似。禁食后,低剂量时摄食略有增加,但高剂量时摄食减少;所有剂量下餐后饮水均减弱。唾液分泌减少的大鼠在低剂量时摄食(和餐后饮水)明显减弱,但当给予湿软食而非颗粒饲料和水时,可获得正常的剂量反应关系。禁水后所有剂量下饮水均减弱,且在饮水测试期间同时提供食物时,食物摄入量与饮水量成比例减少。与无食物时相比,有食物时饮水受到的抑制更强。氟哌啶醇可减弱但不能消除胰岛素和2-脱氧葡萄糖诱导的饱食大鼠的摄食。结合激活作用和脑儿茶酚胺在摄食和饮水中的作用对这些发现进行了讨论。

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