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亚急性氰化物暴露后大鼠不同器官中某些抗氧化酶的活性和基因表达谱:α-酮戊二酸的作用

Activity and gene expression profile of certain antioxidant enzymes in different organs of rats after subacute cyanide exposure: effect of alpha-ketoglutarate.

作者信息

Hariharakrishnan Janardhanan, Anand Tamatam, Satpute Ravindra M, Jayaraj Ravindran, Prasad G B K S, Bhattacharya Rahul

机构信息

Division of Pharmacology and Toxicology, Defence Research and Development Establishment, Gwalior, India.

出版信息

Drug Chem Toxicol. 2009;32(3):268-76. doi: 10.1080/01480540902882218.

Abstract

Oxidative stress plays a crucial role in mediating cyanide toxicity. The present study addresses the effect of cyanide on activity and gene-expression profile of certain antioxidant enzymes and the expression of heat shock protein (HSP-70) in different organs of rats. Rats were treated with 0.50 LD(50) (7.0 mg/kg) of potassium cyanide (KCN; oral) and/or alpha-ketoglutarate (A-KG; 1.0 g/kg; oral) daily for 14 days, and various biochemical variables were measured in brain, liver, and kidney after 7 and 14 days of treatments and a 7-day recovery period. Cyanide significantly reduced the activity of glutathione peroxidase (GPx), glutathione reductase (GR), superoxide dismutase (SOD), and catalase (CA) in all the organs after 7 days, while the activity of GPx in brain, liver, and kidney, GR in liver, and CA in brain remained diminished up to 14 days. The gene-expression profile of corresponding enzymes did not show any difference between the control and treatment groups. Elevated levels of malondialdehyde were observed in brain and kidney 7 and 14 days after cyanide. Cyanide also increased the expression of HSP-70 activity in brain after 7 days alone. Regression of toxicity was observed after the withdrawal of KCN. Treatment of A-KG was found to prevent all the biochemical alterations caused by cyanide. This study reveals that oxidative stress caused by cyanide was independent of the expression of antioxidant enzyme activity at the gene level, and all changes responded favorably to A-KG, indicating its therapeutic potential.

摘要

氧化应激在介导氰化物毒性中起关键作用。本研究探讨了氰化物对大鼠不同器官中某些抗氧化酶的活性和基因表达谱以及热休克蛋白(HSP - 70)表达的影响。大鼠每日经口给予0.50 LD(50)(7.0毫克/千克)的氰化钾(KCN)和/或α - 酮戊二酸(A - KG;1.0克/千克;经口),持续14天,在处理7天、14天后以及7天恢复期后,测量脑、肝和肾中的各种生化变量。7天后,氰化物显著降低了所有器官中谷胱甘肽过氧化物酶(GPx)、谷胱甘肽还原酶(GR)、超氧化物歧化酶(SOD)和过氧化氢酶(CA)的活性,而脑、肝和肾中的GPx活性、肝中的GR活性以及脑中的CA活性在14天内仍持续降低。相应酶的基因表达谱在对照组和处理组之间未显示出任何差异。氰化物处理7天和14天后,在脑和肾中观察到丙二醛水平升高。氰化物还仅在7天后增加了脑中HSP - 70的活性表达。停用KCN后观察到毒性消退。发现A - KG处理可预防氰化物引起的所有生化改变。本研究表明,氰化物引起的氧化应激在基因水平上与抗氧化酶活性的表达无关,并且所有变化对A - KG均有良好反应,表明其具有治疗潜力。

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