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间接作用拟交感胺的作用机制。

Mechanism of action of indirectly acting sympathomimetic amines.

作者信息

Trendelenburg U, Langeloh A, Bönisch H

出版信息

Blood Vessels. 1987;24(5):261-70. doi: 10.1159/000158702.

Abstract

The mode of action of indirectly acting sympathomimetic amines was analysed in the rat vas deferens (preloaded with 3H-(-)-noradrenaline). When monoamine oxidase (MAO), catechol-O-methyltransferase and vesicular uptake were inhibited (i.e., when the concentration of 3H-noradrenaline in the axoplasm was high), all substrates of neuronal uptake induced a carrier-mediated outward transport of 3H-noradrenaline, in strict dependence on the Km for neuronal uptake of the substrate. However, when MAO and vesicular uptake were not inhibited, some of the substrates of neuronal uptake were better releasers of 3H-noradrenaline than others; obviously, when the axoplasmic 3H-noradrenaline concentration is very low (intact vesicular uptake, intact MAO), a 'mobilization' of vesicular 3H-noradrenaline is a prerequisite for substantial release.

摘要

在大鼠输精管(预先加载3H-(-)-去甲肾上腺素)中分析了间接作用拟交感神经胺的作用方式。当单胺氧化酶(MAO)、儿茶酚-O-甲基转移酶和囊泡摄取被抑制时(即当轴浆中3H-去甲肾上腺素浓度较高时),所有神经元摄取的底物都会诱导载体介导的3H-去甲肾上腺素外向转运,这严格依赖于底物对神经元摄取的Km值。然而,当MAO和囊泡摄取未被抑制时,一些神经元摄取的底物比其他底物更能释放3H-去甲肾上腺素;显然,当轴浆3H-去甲肾上腺素浓度非常低时(完整的囊泡摄取,完整的MAO),囊泡3H-去甲肾上腺素的“动员”是大量释放的先决条件。

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