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α-硫辛酸可预防氰化钾诱导的癫痫发作和死亡。

Alpha-lipoic acid protects against potassium cyanide-induced seizures and mortality.

作者信息

Abdel-Zaher Ahmed O, Abdel-Hady Randa H, Abdel Moneim Wafaa M, Salim Safa Y

机构信息

Department of Pharmacology, Faculty of Medicine, Assiut University, Assiut, Egypt.

出版信息

Exp Toxicol Pathol. 2011 Jan;63(1-2):161-5. doi: 10.1016/j.etp.2009.11.004. Epub 2009 Dec 3.

Abstract

This study was proposed to investigate the potential protective effect of alpha-lipoic acid (α-LA) against potassium cyanide (KCN)-induced seizures and lethality in mice. The intraperitoneal ED(50) value of KCN, as measured by induction of clonic and tonic seizures was increased by pretreatment of mice with α-LA (25, 50 and 100 mg/kg) intraperitoneally in a dose-dependent manner. Similarly, the intraperitoneal LD(50) value of KCN, based on 24h mortality, was increased by pretreatment with α-LA in a dose-dependent manner. Intraperitoneal injection of the estimated ED(50) of KCN (4.8 mg/kg) into mice increased, 1h later, nitric oxide (NO) production and brain glutamate and malondialdehyde (MDA) levels. The estimated ED(50) of KCN also decreased brain intracellular reduced glutathione (GSH) level and glutathione peroxidase (GSH-Px) activity in these animals. Administration of the estimated LD(50) of KCN (6 mg/kg) produced, 24h later, similar marked biochemical alterations in surviving animals. Pretreatment of mice with α-LA inhibited; dose-dependently KCN (ED(50) and LD(50))-induced an increase in NO production and brain MDA level as well as a decrease in brain intracellular GSH level and GSH-Px activity. The elevation induced by KCN in brain glutamate level was not inhibited by α-LA. It can be concluded that the protective effect of α-LA against KCN-induced seizures and lethality may be due to inhibition of NO overproduction and maintenance of intracellular antioxidant defense mechanisms.

摘要

本研究旨在探讨α-硫辛酸(α-LA)对小鼠氰化钾(KCN)诱导的惊厥和致死作用的潜在保护作用。通过诱导阵挛性和强直性惊厥测定的KCN腹腔半数有效剂量(ED50)值,在小鼠腹腔注射α-LA(25、50和100mg/kg)预处理后呈剂量依赖性增加。同样,基于24小时死亡率的KCN腹腔半数致死剂量(LD50)值,在α-LA预处理后也呈剂量依赖性增加。向小鼠腹腔注射估计的KCN ED50(4.8mg/kg),1小时后,一氧化氮(NO)生成量、脑谷氨酸和丙二醛(MDA)水平增加。估计的KCN ED50还降低了这些动物脑内细胞内还原型谷胱甘肽(GSH)水平和谷胱甘肽过氧化物酶(GSH-Px)活性。注射估计的KCN LD50(6mg/kg),24小时后,存活动物出现类似的明显生化改变。用α-LA预处理小鼠可剂量依赖性地抑制KCN(ED50和LD50)诱导的NO生成增加、脑MDA水平升高以及脑内细胞内GSH水平和GSH-Px活性降低。α-LA未抑制KCN诱导的脑谷氨酸水平升高。可以得出结论,α-LA对KCN诱导的惊厥和致死作用的保护作用可能是由于抑制NO过量生成和维持细胞内抗氧化防御机制。

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