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急性给予抗抑郁/抗惊恐药物苯乙肼后,大脑单胺氧化酶活性、大脑单胺和氨基酸水平随时间的变化。

Time-dependent changes in brain monoamine oxidase activity and in brain levels of monoamines and amino acids following acute administration of the antidepressant/antipanic drug phenelzine.

作者信息

Parent M B, Habib M K, Baker G B

机构信息

Department of Psychology, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Biochem Pharmacol. 2000 May 15;59(10):1253-63. doi: 10.1016/s0006-2952(00)00244-6.

DOI:10.1016/s0006-2952(00)00244-6
PMID:10736426
Abstract

Phenelzine (PLZ) is a non-selective monoamine oxidase (MAO) inhibitor commonly used to treat depression and panic disorder. Acute administration of PLZ produces several neurochemical changes, including an increase in brain levels of the catecholamines norepinephrine (NE) and dopamine (DA), of 5-hydroxytryptamine (5-HT), and of the amino acids alanine and gamma-aminobutyric acid (GABA). The goal of the present series of experiments was to characterize the time course of these PLZ-induced changes. Male Sprague-Dawley rats were sacrificed 6, 24, 48, 96, 168, or 336 hr after acute PLZ administration (15 or 30 mg/kg, i.p., based on free base weight). Whole brain levels of monoamines and amino acids were determined using HPLC, and MAO A and B activities were determined using a radiochemical procedure. The results indicated that PLZ changed amino acid levels 6 and 24 hr after injection, but not 48 hr later. In contrast, the effects of PLZ on MAO activity and monoamines were longer-lasting. For example, PLZ-induced increases in dopamine and 5-HT were observed 1 week after injection, and PLZ-induced inhibition of MAO activity persisted for 2 weeks. Thus, in addition to demonstrating that the effects of PLZ on MAO activity and monoamines were long-lasting, these results indicate that the effects of PLZ on MAO activity and on brain levels of monoamines and amino acids are temporally dissociated. These findings regarding the long-term effects of PLZ on neurochemistry will have considerable critical implications for the design and interpretation of behavioral studies of the acute effects of PLZ.

摘要

苯乙肼(PLZ)是一种非选择性单胺氧化酶(MAO)抑制剂,常用于治疗抑郁症和恐慌症。急性给予PLZ会产生多种神经化学变化,包括大脑中儿茶酚胺去甲肾上腺素(NE)、多巴胺(DA)、5-羟色胺(5-HT)以及氨基酸丙氨酸和γ-氨基丁酸(GABA)水平的升高。本系列实验的目的是描述这些PLZ诱导变化的时间进程。雄性Sprague-Dawley大鼠在急性给予PLZ(15或30mg/kg,腹腔注射,基于游离碱重量)后6、24、48、96、168或336小时被处死。使用高效液相色谱法测定全脑单胺和氨基酸水平,使用放射化学程序测定MAO A和B的活性。结果表明,PLZ在注射后6和24小时改变了氨基酸水平,但48小时后没有。相比之下,PLZ对MAO活性和单胺的影响持续时间更长。例如,注射后1周观察到PLZ诱导的多巴胺和5-HT增加,PLZ诱导的MAO活性抑制持续2周。因此,除了证明PLZ对MAO活性和单胺的影响是持久的之外,这些结果还表明PLZ对MAO活性以及单胺和氨基酸脑水平的影响在时间上是分离的。这些关于PLZ对神经化学长期影响的发现将对PLZ急性效应的行为研究的设计和解释产生相当重要的影响。

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