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首页> 外文期刊>International Journal of Biochemistry Research & Review >Chronic Alcoholism-mediated MetabolicViolations in Albino Rats Brain
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Chronic Alcoholism-mediated MetabolicViolations in Albino Rats Brain

机译:白化病大鼠脑中慢性酒精中毒介导的代谢违规

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Aims: Despite of intensive investigation of alcoholism consequences for nervous system, the full complex of such metabolic alterations in brain remains unknown. The aim of present work was to study the influence of chronic ethanol consumption on rats’ brain contents of free amino acids, rates of CYP2E1 and CYP3A2 expression, NO-synthase activities and pro- and antioxidant system parameters. Study Design: Wistar albino male rats (body weight (BW), 160–200 g) were divided into two groups: I – alcohol, II – normal animals. Methodology: The content of amino acids in rat brain was determined using an amino acid analyzer. Brain CYP2E1 and CYP3A2 were evaluated with RT-PCR method, pro- and antioxidant system parameters – by standard methods. Results: Changes of brain free amino acids contents with alcoholism were demonstrated for 14 amino acids and their total sum. Chronic alcohol consumption caused 1.77 times increasing of CYP2D?1 mRNA expression in rat’s brain, 2.34 times – of CYP3A2 mRNA expression, 2.8 times - of cNOS activity, 42% - of TBARS formation rates. Activities of SOD and catalase were decreased 19% and 25% respectively. Conclusions: Thus investigation of alcoholism effects on brain levels of free amino acids permits to obtain complex estimation of this pathology influence on metabolic processes in brain, especially on amino acids, proteins, ATP and NADPH metabolisms. Alterations on the level of genome in our experiments were accompanied with complex alterations on the level of protein, amino acid and nitrous metabolisms.
机译:目的:尽管对酒精中毒对神经系统的后果进行了深入研究,但这种代谢变化在大脑中的完整复合物仍然未知。本研究的目的是研究长期饮酒对大鼠大脑中游离氨基酸含量,CYP2E1和CYP3A2表达速率,NO合酶活性以及前和抗氧化系统参数的影响。研究设计:Wistar白化病雄性大鼠(体重(BW),160–200 g)分为两组:I –酒精,II –正常动物。方法:使用氨基酸分析仪测定大鼠大脑中氨基酸的含量。使用RT-PCR方法,前和抗氧化剂系统参数-通过标准方法评估了大脑的CYP2E1和CYP3A2。结果:酒精中毒后脑中游离氨基酸含量的变化被证实为14种氨基酸及其总和。长期饮酒会使大鼠大脑中CYP2D?1 mRNA表达增加1.77倍,是CYP3A2 mRNA表达的2.34倍,cNOS活性的2.8倍,TBARS形成率的42%。 SOD和过氧化氢酶的活性分别降低了19%和25%。结论:因此,对酒精中毒对大脑中游离氨基酸水平的影响进行调查,可以得到这种病理学对大脑代谢过程,尤其是氨基酸,蛋白质,ATP和NADPH代谢的影响的复杂估计。在我们的实验中,基因组水平的变化伴随着蛋白质,氨基酸和亚硝酸盐代谢水平的复杂变化。

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