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D-和L-苯丙胺及哌醋甲酯对大鼠纹状体多巴胺生物合成的不同影响。

Differential effects of D- and L-amphetamine and methylphenidate on rat striatal dopamine biosynthesis.

作者信息

Kuczenski R, Segal D S

出版信息

Eur J Pharmacol. 1975 Feb;30(2):244-51. doi: 10.1016/0014-2999(75)90106-5.

Abstract

Methylphenidate and the optical isomers of amphetamine have differential effects, in vivo and in vitro on rat striatal synaptosomal dopamine (DA) biosynthesis. Whereas the systemic administration of D- or L-amphetamine produces a dose-dependent decrease in synaptosomal DA synthesis, with ED50's of 1.1 and 3.5 mg/kg, respectively, methylphenidate, at doses which produce comparable degrees of stereotypes behavior, has no effect on this measure of DA biosynthesis. In vitro, D- and L-amphetamine exhibit a three-fold difference in ED50's (1 times 10-minus 6 M and 3 times 10-minus 6 M, respectively) with respect to both activation of striatal synpatosomal DA synthesis, and to reversal of reserpine-induced inhibition of DA synthesis. In contrast, although in vitro methylphenidate can partially activate DA synthesis, it does not overcome the reserpeine-induced inhibition. The data are discussed in terms of the possible differential mechanisms by which these two types of stimulants may exert their effects on sterotypy.

摘要

哌甲酯和苯丙胺的光学异构体在体内和体外对大鼠纹状体突触体多巴胺(DA)生物合成具有不同的作用。D-或L-苯丙胺全身给药会使突触体DA合成呈剂量依赖性降低,其半数有效剂量(ED50)分别为1.1和3.5mg/kg,而哌甲酯在产生相当程度刻板行为的剂量下,对这种DA生物合成指标没有影响。在体外,D-和L-苯丙胺在激活纹状体突触体DA合成以及逆转利血平诱导的DA合成抑制方面,半数有效剂量存在三倍差异(分别为1×10⁻⁶M和3×10⁻⁶M)。相比之下,尽管体外哌甲酯可部分激活DA合成,但它不能克服利血平诱导的抑制作用。根据这两种类型兴奋剂可能对刻板行为产生作用的不同机制对数据进行了讨论。

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