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长期给予氟哌啶醇诱导大鼠中枢神经系统超敏反应的动力学分析。I. pA2的测定。

Kinetic analysis of central nervous system supersensitivity induced in rats by long-term haloperidol administration. I. pA2 determination.

作者信息

Palermo-Neto J, Bernardi M M, Saban R

出版信息

Pharmacology. 1984;28(4):203-10. doi: 10.1159/000137963.

Abstract

A kinetic analysis of central dopamine receptors in control and in experimental rats, withdrawn from long-term haloperidol treatment was made in vivo. Using the stereotyped behavior induced by apomorphine administration as the response, the relative affinity of metoclopramide as reflected by pA2 values, was examined in normal and supersensitive rats. Metoclopramide antagonized apomorphine stereotypy in a dose-dependent and competitive manner. At each dose tested, metoclopramide produced a larger rightward shift of the apomorphine dose-response curve in the control rats than in withdrawn rats. The Schild plot resulted in a straight line, the slopes being -1.2 +/- 0.3 and -0.8 +/- 0.2 for control and experimental rats, respectively. These findings suggest a decrease in receptor affinity after long-term haloperidol treatment, a concept not demonstrated in binding studies in vitro.

摘要

对长期接受氟哌啶醇治疗后停药的对照大鼠和实验大鼠的中枢多巴胺受体进行了体内动力学分析。以阿扑吗啡给药诱导的刻板行为作为反应,在正常和超敏大鼠中检测了甲氧氯普胺由pA2值反映的相对亲和力。甲氧氯普胺以剂量依赖性和竞争性方式拮抗阿扑吗啡刻板行为。在每个测试剂量下,甲氧氯普胺使对照大鼠的阿扑吗啡剂量-反应曲线向右移动的幅度大于停药大鼠。施尔德图呈直线,对照大鼠和实验大鼠的斜率分别为-1.2±0.3和-0.8±0.2。这些发现表明长期氟哌啶醇治疗后受体亲和力降低,这一概念在体外结合研究中未得到证实。

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