大鼠脑组织中一氧化氮合酶测定
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The Measurement of Nitric Oxide Synthase in Rats' Brain
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    摘要:

    在含有一氧化氮合酶(NOS)底物左族精氨酸(L-Arg), 辅助因子还原性辅酶Ⅱ(NADPH)、四氢生物蝶呤(BH4)、黄素单核苷酸(FMN), 黄素腺嘌呤二核苷酸(FAD)以及Ca2+、钙调蛋白等溶液中加入大鼠脑组织匀浆离心上清液, 组成酶反应体系. 37℃温育80min, 应用N-(1-萘基)-乙二胺、对氨基苯磺酸的重氮、偶氮反应测定酶反应体系中一定时间内NO代谢产物NO-2浓度变化, 建立一种简便的NOS活性测定方法. 反应体系最佳pH为7.4, Km=0.1mmol/L, 体系内NO-2生成量与加入样品量之间有良好线性关系(r=0.998). 此方法简单、方便、重复性好, 批内CV为3.69%, 批间CV为5.16%. 10只健康大鼠脑组织中NOS活性为(39.61±7.64)nmol/(min·g).

    Abstract:

    An enzyme reaction system which contains L-Arg、NADPH、FAD、FMN、BH4、Ca2+ etc,has been studied to determine the activity of nitric oxide synthase (NOS) in rats'brain. Alter being incubated at 37℃ for 80 min in dark with samples,the sulfanilic acid and N-(1-naphthyl)-ethylenediammonium was added to the reaction system to measure the concentration of produced nitrite in system.It was found that the optimum pH for the enzyme reaction was 7.4,Km was 0.1 mmol/L.There was a relationship between the amounts of sample and nitrite concentration in the system. This method is simple and convenient. Intra-assay CV value is 3.69% and inter-assay CV value is 5.16%. The specific activity of nitric oxide synthase in ten rats' brains is (39.61±7.64)nmol/(min·g).

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王成彬,田亚平,沈文梅,汪德清,蒋赐恩.大鼠脑组织中一氧化氮合酶测定[J].生物化学与生物物理进展,1996,23(6):548-551

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  • 收稿日期:1995-11-21
  • 最后修改日期:1996-07-17
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