Lipid peroxidation and glutathione levels after cortical injection of ferric chloride in rats: effect of trimetazidine and deferoxamine.

T Suzer, E Coskun, S Demir, K Tahta
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Abstract

Intracortical injection of iron salts causes seizures. Oxidation of lipids in neural membranes by reactive oxygen species is involved in the mechanism responsible for iron-induced seizures as a model of posttraumatic epilepsy. In this study, we examined the effect of trimetazidine (TMZ) and deferoxamine (DFO) on lipid peroxidation after cortical injection of 5 microliters of an aqueous solution containing 100 mM of ferric chloride (FeCl3) in rats. Animals were divided into four groups (n = 7 each) and treated as follows: group 1, saline injection into the cortex (control group); group 2, iron injection into the cortex (injury group); group 3, iron injection into the cortex plus TMZ; group 4, iron injection into the cortex plus DFO. The animals were killed 3 h after injections, and the levels of malondialdehyde (MDA), a lipid peroxidation product, and reduced glutathione (GSH) were measured. A significant elevation of MDA was observed in group 2 (P < 0.05). MDA levels were found to be lower in both the TMZ-treated (P < 0.05) and DFO-treated (P < 0.05) groups than in the injury group. Tissue GSH levels were significantly decreased in group 2 (P < 0.05). GSH levels were increased in the TMZ-treated (P < 0.05) and DFO-treated (P < 0.05) groups compared to the injury group. The results of our study suggest that lipid peroxidation is a critical event in iron-induced epilepsy and that treatment with TMZ and DFO is effective in preventing the formation of free radicals and reducing lipoperoxides in brain tissue.

大鼠皮质注射三氯化铁后脂质过氧化和谷胱甘肽水平:曲美他嗪和去铁胺的影响。
皮质内注射铁盐会引起癫痫发作。作为创伤后癫痫的一种模型,神经膜中的脂质被活性氧氧化参与了铁诱导癫痫发作的机制。在这项研究中,我们研究了曲美他嗪(TMZ)和去铁胺(DFO)对大鼠皮质注射5微升含有100 mM氯化铁(FeCl3)的水溶液后脂质过氧化的影响。将动物分为4组,每组7只,分别进行如下处理:1组,皮质内注射生理盐水(对照组);2组,皮质注射铁(损伤组);3组,皮质铁注射加TMZ;第4组,皮质铁注射加DFO。注射后3 h处死动物,测定脂质过氧化产物丙二醛(MDA)和还原性谷胱甘肽(GSH)水平。2组大鼠MDA水平显著升高(P < 0.05)。tmz处理组和dfo处理组的MDA水平均低于损伤组(P < 0.05)。组2组织GSH水平显著降低(P < 0.05)。与损伤组相比,tmz处理组和dfo处理组GSH水平均升高(P < 0.05)。我们的研究结果表明,脂质过氧化是铁诱导癫痫的一个关键事件,用TMZ和DFO治疗可以有效地防止自由基的形成和减少脑组织中的脂质过氧化物。
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