亚甲蓝和LY83583对神经元一氧化氮合酶和nadph -脱氢酶的影响

Dasan Luo, Sheela Das, Steven R. Vincent
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引用次数: 94

摘要

亚甲基蓝和6-苯胺-5,8-喹啉吡啶(LY83583)常被用作可溶性胍基环化酶的“选择性”抑制剂。我们报道,在体外实验中,这两种化合物都是大鼠小脑一氧化氮合酶活性的有效抑制剂。亚甲基蓝的Ki值为2.7 μM, LY83583的Ki值为15.8 μM。此外,亚甲基蓝抑制NADPH-diaphorase与一氧化氮合酶相关的组织化学反应,而LY83583不抑制。我们的研究结果表明,这些药物的许多作用归因于抑制胍基环化酶,可能源于它们对一氧化氮合酶活性的直接抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of methylene blue and LY83583 on neuronal nitric oxide synthase and NADPH-diaphorase

Methylene blue and 6-anilino-5,8-quinolinedine (LY83583) have often been used as ‘selective’ inhibitors of soluble guanylyl cyclase. We report that in vitro assays, both these compounds were potent inhibitors of rat cerebellar nitric oxide synthase activity. Methylene blue had an apparent Ki of 2.7 μM, while for LY83583 the Ki was 15.8 μM. Furthermore, methylene blue, but not LY83583, inhibited the NADPH-diaphorase histochemical reaction associated with nitric oxide synthase. Our results indicate that many of the effects of these drugs which have been attributed to inhibition of guanylyl cyclase, may derive from their direct inhibition of nitric oxide synthase activity instead.

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