首页> 外文期刊>Journal of pharmacological sciences. >Inactivation of membrane surface ecto-5'-nucleotidase by sodium nitroprusside in C6 glioma cells.
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Inactivation of membrane surface ecto-5'-nucleotidase by sodium nitroprusside in C6 glioma cells.

机译:硝普钠在C6胶质瘤细胞中灭活膜表面ecto-5'-核苷酸酶。

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摘要

Ecto-5'-nucleotidase (NT5E), a predominant enzyme that produces extracellular adenosine from AMP, plays an important role in a variety of physiological and pathophysiological processes. This study was performed to identify agents that affect NT5E activity using C6 glioma cells. When cells were incubated with sodium nitroprusside (SNP), phorbol 12-myristate 13-acetate, forskolin, lipopolysaccharide, or interferon-gamma, only SNP inhibited NT5E activity in a time- and concentration-dependent manner (IC(50) = 1.2 microM). The inhibitory effect of SNP was long-lasting even after SNP washout; and its action was not mimicked by nitric oxide generating agents, 8-bromo cyclic GMP, ferricyanide, ferrocyanide, or sodium cyanide. SNP did not change NT5E mRNA level or membrane surface protein expression. Similar to SNP, Fe(2+) inhibited NT5E activity, but to a lesser extent. Although Fe(2+) is known to increase oxidative stress, Fe(2+)-mediated oxidative stress was not involved in SNP inhibition of NT5E because the inhibition of NT5E by SNP was not affected by superoxide dismutase and catalase. In contrast, addition of Zn(2+), an essential metal co-factor of NT5E activity, prevented SNP from inhibiting NT5E. These results suggest that SNP disrupts a critical Zn(2+)-dependent enzyme activity and might be useful as a pharmacological tool for inhibiting NT5E.
机译:Ecto-5'-核苷酸酶(NT5E)是一种主要的酶,可从AMP产生细胞外腺苷,在多种生理和病理生理过程中均起着重要作用。进行这项研究是为了鉴定使用C6胶质瘤细胞影响NT5E活性的药物。当将细胞与硝普钠(SNP),佛波醇12-肉豆蔻酸酯13-乙酸酯,毛喉素,脂多糖或干扰素-γ一起温育时,只有SNP以时间和浓度依赖性方式抑制NT5E活性(IC(50)= 1.2 microM )。即使冲洗掉SNP,SNP的抑制作用仍然持久。一氧化氮生成剂,8-溴环GMP,铁氰化物,亚铁氰化物或氰化钠不能模仿其作用。 SNP不会改变NT5E mRNA水平或膜表面蛋白表达。类似于SNP,Fe(2+)抑制NT5E活性,但程度较小。尽管已知Fe(2+)会增加氧化应激,但Fe(2+)介导的氧化应激并不参与NT5E的SNP抑制,因为SNP抑制NT5E不受超氧化物歧化酶和过氧化氢酶的影响。相反,添加Zn(2 +)(NT5E活性的必需金属辅助因子)可防止SNP抑制NT5E。这些结果表明,SNP破坏了关键的Zn(2+)依赖酶活性,可能用作抑制NT5E的药理学工具。

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