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抗精神病药物对多巴胺代谢及多巴胺敏感腺苷酸环化酶活性的区域效应。

Regional effects of neuroleptics on dopamine metabolism and dopamine-sensitive adenylate cyclase activity.

作者信息

Scatton B, Bischoff S, Dedek J, Korf J

出版信息

Eur J Pharmacol. 1977 Aug 15;44(4):287-92. doi: 10.1016/0014-2999(77)90301-6.

Abstract

The effect of haloperidol, chlorpromazine, thioridazine and sulpride on the levels of DOPAC and HVA, as an index of DA turnover, and on the activity of DA-stimulated adenylate cyclase was investigated inthe striatum, the nucleus accumbens and the tuberculum olfactorium of the rat brain. Haloperidol, chlorpromazine and thioridazine caused a more marked increase in DA turnover in the striatum than in the mesolimbic areas, while the reverse was true for sulpiride. In contrast, although the relative potency of these compounds varied greatly, the Ki of each drug for the DA-sensitive adenylate cyclase was similar in three structures of rat brain. The results indicate that in the three brain structures investigated there was no correlation between the differential effects of neuroleptics on dopamine turnover in vivo and the blockade by these drug of the DA-sensitive adenylate cyclase activity in vitro.

摘要

在大鼠脑的纹状体、伏隔核和嗅结节中,研究了氟哌啶醇、氯丙嗪、硫利达嗪和舒必利对作为多巴胺(DA)周转指标的3,4-二羟基苯乙酸(DOPAC)和高香草酸(HVA)水平以及对DA刺激的腺苷酸环化酶活性的影响。氟哌啶醇、氯丙嗪和硫利达嗪使纹状体中DA周转的增加比中脑边缘区域更明显,而舒必利则相反。相反,尽管这些化合物的相对效力差异很大,但每种药物对DA敏感的腺苷酸环化酶的抑制常数(Ki)在大鼠脑的三个结构中相似。结果表明,在所研究的三个脑结构中,抗精神病药物对体内多巴胺周转的不同影响与这些药物在体外对DA敏感的腺苷酸环化酶活性的阻断之间没有相关性。

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