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[铁给药所致氧化应激中脑内内源性脂质过氧化的激活及其维生素E预防]

[Activation of endogenous lipid peroxidation in the brain in oxidation stress caused by administration of iron and its prevention by vitamin E].

作者信息

Kaĭnova G M, Markovska D, Staneva D, Kagan V E

出版信息

Biull Eksp Biol Med. 1990 Jan;109(1):35-7.

PMID:2334794
Abstract

Looking for an appropriate model of accelerated aging in vivo we investigated the content of endogenous products of lipid peroxidation (LP) in the rat brain after single or 4 day-lasting intramuscular injection of complex-bind iron (ferum Hausman, 50 mg/kg body weight) like promoter of LP. We found that the single administration of this iron complex fails to induce endogenous LP; after 4 day-application of iron we observed significant increase in content of primary (lipid peroxides) and final (fluorescent) products of LP. Iron-promoted activation of endogenous LP could be abolished by animal pretreatment with the natural antioxidant alpha-tocopherol. The calcium antagonist nifedipine didn't affect the content of endogenous LP products neither alone nor in combination with alpha-tocopherol.

摘要

为寻找合适的体内加速衰老模型,我们研究了单次或连续4天肌肉注射复合结合铁(豪斯曼铁,50mg/kg体重)(作为脂质过氧化(LP)的促进剂)后大鼠脑内脂质过氧化内源性产物的含量。我们发现,单次给予这种铁复合物未能诱导内源性LP;在应用铁4天后,我们观察到LP的初级(脂质过氧化物)和最终(荧光)产物含量显著增加。用天然抗氧化剂α-生育酚对动物进行预处理可消除铁促进的内源性LP激活。钙拮抗剂硝苯地平单独使用或与α-生育酚联合使用均不影响内源性LP产物的含量。

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