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司来吉兰通过类似苯丙胺的作用改变行为和尾状核多巴胺。

Deprenyl alters behavior and caudate dopamine through an amphetamine-like action.

作者信息

Okuda C, Segal D S, Kuczenski R

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla 92093-0603.

出版信息

Pharmacol Biochem Behav. 1992 Dec;43(4):1075-80. doi: 10.1016/0091-3057(92)90484-w.

Abstract

In vivo microdialysis was used to concurrently measure the behavioral and caudate dopamine (DA) responses to the alleged irreversible type B monoamine oxidase inhibitor deprenyl. The effects were contrasted to those of the type A monoamine oxidase inhibitor, clorgyline. Consistent with its effects as an irreversible monoamine oxidase inhibitor, clorgyline produced an increase in DA concentration that remained elevated for at least 6 h. In contrast, the deprenyl-induced elevation in DA concentration occurred more rapidly, achieved a higher peak response, and then returned to baseline within 2 h following drug administration. The two drugs also produced distinctive changes in DA metabolite levels. Whereas the pattern of clorgyline-induced effects were consistent with irreversible monoamine oxidase inhibition, deprenyl produced an amphetamine-like response profile. Further, deprenyl but not clorgyline significantly increased locomotor activity. These results suggest that deprenyl does not augment caudate DA levels through monoamine oxidase inhibition. Rather, the pattern of its effects on caudate DA dynamics and behavior supports previous evidence that deprenyl produces its effects through its metabolism to amphetamine-like substances.

摘要

采用体内微透析技术同时测量对所谓不可逆的B型单胺氧化酶抑制剂丙炔苯丙胺的行为反应和尾状核多巴胺(DA)反应。将这些效应与A型单胺氧化酶抑制剂氯吉兰的效应进行对比。与作为不可逆单胺氧化酶抑制剂的作用一致,氯吉兰使DA浓度升高,且至少6小时内保持升高状态。相比之下,丙炔苯丙胺引起的DA浓度升高出现得更快,达到更高的峰值反应,然后在给药后2小时内恢复到基线水平。这两种药物还使DA代谢物水平产生了明显变化。氯吉兰引起的效应模式与不可逆单胺氧化酶抑制作用一致,而丙炔苯丙胺产生了类似苯丙胺的反应模式。此外,丙炔苯丙胺而非氯吉兰显著增加了运动活性。这些结果表明,丙炔苯丙胺并非通过抑制单胺氧化酶来提高尾状核DA水平。相反,其对尾状核DA动态和行为的影响模式支持了先前的证据,即丙炔苯丙胺通过代谢为类似苯丙胺的物质而产生作用。

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