{"title":"亚甲蓝和LY83583对神经元一氧化氮合酶和nadph -脱氢酶的影响","authors":"Dasan Luo, Sheela Das, Steven R. Vincent","doi":"10.1016/0922-4106(95)00084-4","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>K</em><sub>i</sub> of 2.7 μM, while for LY83583 the <em>K</em><sub>i</sub> 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.</p></div>","PeriodicalId":100502,"journal":{"name":"European Journal of Pharmacology: Molecular Pharmacology","volume":"290 3","pages":"Pages 247-251"},"PeriodicalIF":0.0000,"publicationDate":"1995-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0922-4106(95)00084-4","citationCount":"94","resultStr":"{\"title\":\"Effects of methylene blue and LY83583 on neuronal nitric oxide synthase and NADPH-diaphorase\",\"authors\":\"Dasan Luo, Sheela Das, Steven R. Vincent\",\"doi\":\"10.1016/0922-4106(95)00084-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <em>K</em><sub>i</sub> of 2.7 μM, while for LY83583 the <em>K</em><sub>i</sub> 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.</p></div>\",\"PeriodicalId\":100502,\"journal\":{\"name\":\"European Journal of Pharmacology: Molecular Pharmacology\",\"volume\":\"290 3\",\"pages\":\"Pages 247-251\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0922-4106(95)00084-4\",\"citationCount\":\"94\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmacology: Molecular Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0922410695000844\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Molecular Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0922410695000844","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.