The effect of various chlorpromazine derivatives on the apomorphine-elicited inhibition of synaptosomal tyrosine hydroxylase activity.

Psychopharmacology communications Pub Date : 1975-01-01
R L Bronaugh, M Goldstein
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Abstract

The effects of chlorpromazine and of some metabolites of chlorpromazine on the apomorphine-elicited inhibition of synaptosomal tyrosine hydroxylase activity were investigated. Chlorpromazine, nor1-chlorpromazine and 7-hydroxychlorpromazine reverse the apomorphine-elicited inhibition of tyrosine hydroxylase activity while nor1-chlorpromazine sulfoxide and nor2-chlorpromazine sulfoxide have no effect on this inhibition. 6-Hydroxychlorpromazine and promethazine also reverse the enzyme inhibition by apomorphine but are less potent than chlorpromazine or 7-hydroxychlorpromazine. These results show that chlorpromazine and its metabolites with antipsychotic activity are more effective in reversing the apomorphine-elicited inhibition of tyrosine hydroxylase than those metabolites which are devoid of antipsychotic activity.

各种氯丙嗪衍生物对阿吗啡诱导的突触体酪氨酸羟化酶活性抑制的影响。
研究了氯丙嗪及其代谢物对阿波啡诱导的突触体酪氨酸羟化酶活性的抑制作用。氯丙嗪、诺1-氯丙嗪和7-羟氯丙嗪可逆转阿吗啡引起的酪氨酸羟化酶活性抑制,而诺1-氯丙嗪亚砜和诺2-氯丙嗪亚砜对这种抑制作用无影响。6-羟氯丙嗪和异丙嗪也能逆转阿扑吗啡对酶的抑制作用,但效果不如氯丙嗪或7-羟氯丙嗪。这些结果表明,氯丙嗪及其代谢物具有抗精神病活性,比不具有抗精神病活性的代谢物更能有效地逆转阿吗啡引起的酪氨酸羟化酶抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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