抗抑郁药物对狗脑缩氨基脲敏感胺氧化酶的影响。

Toshio Obata, Masahiro Aomine
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引用次数: 0

摘要

本研究考察了其他环类抗抑郁药,如双环药物齐默尔定、三环药物丙咪嗪、四环药物马普替林和非环类药物诺非芬,是否能抑制狗脑中氨基脲敏感胺氧化酶(SSAO)的活性。用100nm克劳格林和100nm去戊烯醇治疗后,4种抗抑郁药物均能抑制狗脑SSAO活性。丙咪嗪的抑制作用最强,其次是马普替林、齐默丁和诺非芬。四种药物均为犬脑SSAO的非竞争性抑制剂。与其他类型的抗抑郁药物相比,我们发现三环类抗抑郁药物丙咪嗪是狗脑SSAO活性最具选择性的抑制剂。
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 antidepressant drug on semicarbazide-sensitive amine oxidase (SSAO) in dog brain.

The present study examined whether or not other cyclic antidepressants, such as the dicyclic drug zimeldine, the tricyclic drug imipramine, and tetracyclic drug maprotiline, and the noncyclic drug nomifensine, inhibit semicarbazide-sensitive amine oxidase (SSAO) activity in dog brain. After treatment with 100 nM clorgyline and 100 nM deprenyl, all four antidepressant drugs inhibit SSAO activity in dog brain. The most potent of inhibition was observed by imipramine, followed by maprotiline, zimeldine and nomifensine. All four drugs are noncompetitive inhibitor of SSAO in dog brain. We found the tricyclic antidepressant drug imipramine to be the most selective inhibitors of SSAO activity in dog brain, as compared with other type of antidepressant drugs.

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