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单胺氧化酶“B型”的选择性抑制

Selective inhibition of the "B form" of monoamine oxidase.

作者信息

Magyar K, Knoll J

出版信息

Pol J Pharmacol Pharm. 1977 May-Jun;29(3):233-46.

PMID:887501
Abstract

Deprenyl (phenyl-isopropyl-methyl-propinylamine) is a potent inhibitor of monoamine oxidase (MAO) and like the acetylenic type of inhibitors it induces irreversible inhibition of the enzyme. Its levorotatory isomer is a more potent inhibitor than the dextrorotatory one. Deprenyl elevates the concentration of 3H-noradrenaline (3H-NA) in the synaptosomal fraction of rat heart homogenate while pargyline, probably due to its releasing effect, decreases 3H-NA content in the same fraction. Deprenyl is a selective inhibitor of the "B form" of MAO, which preferentially oxidizes beta-phenylethylamine as substrate.

摘要

司来吉兰(苯基异丙基甲基炔丙胺)是一种强效单胺氧化酶(MAO)抑制剂,与炔类抑制剂一样,它能诱导该酶的不可逆抑制。其左旋异构体比右旋异构体的抑制作用更强。司来吉兰可提高大鼠心脏匀浆突触体部分中3H-去甲肾上腺素(3H-NA)的浓度,而帕吉林可能由于其释放作用,会降低同一部分中的3H-NA含量。司来吉兰是MAO“B型”的选择性抑制剂,它优先氧化β-苯乙胺作为底物。

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