T Brannan, A Prikhojan, M D Yahr
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引用次数: 1

摘要

急性给药Ro 41-1049 (1-50 mg/kg IP)导致多巴胺代谢产物3,4-二羟基苯乙酸(DOPAC)和同型香草酸(HVA)基础水平呈剂量依赖性降低,多巴胺基础水平升高。在Ro 41-1049 (20 mg/kg IP)处理的大鼠中,左旋多巴(100 mg/kg IP)使纹状体多巴胺水平比对照组增加更多,而DOPAC和HVA的形成则减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of a selective MAO-A inhibitor (Ro 41-1049) on striatal L-dopa and dopamine metabolism: an in vivo study.

We administered Ro 41-1049, an inhibitor of the enzyme monoamine oxidase type A (MAO-A) to rats and monitored extracellular catecholamine levels in the corpus striatum before and after the intraperitoneal (IP) administration of a bolus of L-dopa. Acute administration of Ro 41-1049 (1-50 mg/kg IP) produced a dose-dependent decrease in basal levels of the dopamine metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) and an increase in basal levels of dopamine. In rats treated with Ro 41-1049 (20 mg/kg IP), L-dopa administration (100 mg/kg IP) produced a greater increase in striatal levels of dopamine than it did in controls, while DOPAC and HVA formation was attenuated. We conclude that inhibition of central MAO-A activity promotes synaptic accumulation of dopamine following administration of pharmacological doses of L-dopa.

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