褪黑素对阿霉素所致大鼠脑氧化应激的抗氧化作用。

Revista espanola de fisiologia Pub Date : 1997-09-01
P Montilla, I Túnez, M C Muñoz, J V Soria, A López
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引用次数: 0

摘要

研究了褪黑素对大鼠大剂量阿霉素(AD,盐酸阿霉素)诱导的血浆、下丘脑和大脑皮层氧化应激的影响,以及脂过氧化物的变化和过氧化氢酶活性(CAT)水平的影响。在给予单次高剂量AD (25mg /kg, i.p.)后,在氧化应激诱导前后三天每天注射褪黑激素。注射AD后,血浆、下丘脑和大脑皮层中的脂过氧化物显著增加,而褪黑激素可以阻止这种情况。AD使下丘脑的CAT活性平均值下降,同时给予褪黑激素可使其恢复并增加。AD、褪黑素或AD +褪黑素在血浆和脑皮层的CAT活性没有改变。这些结果,特别是与脂过氧化物含量变化有关的结果,表明褪黑素在大鼠神经和神经外水平上都具有强大的抗氧化作用。褪黑激素存在时CAT的变化表明,松果体激素的清扫剂作用与大脑下丘脑区域的高氧化活性之间存在关系。当这些结果结合在一起时,他们还表明,褪黑激素除了产生神经外作用外,还可以作为一种强大的抗氧化剂,在神经和神经外组织中富含易氧化的脂质,如大脑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antioxidative effect of melatonin in rat brain oxidative stress induced by Adriamycin.

The effect of melatonin administration on the oxidative stress induced by a high dose of Adriamycin (AD, doxorubicin hydrochloride) in plasma, hypothalamus and brain cortex of rats, as well as lipoperoxide changes, and catalase activity (CAT) levels have been studied. After administration of a single high AD dosis (25 mg/kg, i.p.), melatonin was injected daily three days before and after oxidative stress induction. The AD injection produced a significant lipoperoxide increase in plasma, hypothalamus and brain cortex, which was prevented by melatonin. CAT activity mean values decreased in hypothalamus by AD, effect which was reverted and increased by simultaneous melatonin administration. CAT activity was not changed after AD, melatonin or AD + melatonin administration in plasma and brain cortex. These results, especially those concerning lipoperoxide content changes, showed a powerful antioxidative effect of melatonin at both neural and extraneural levels in rats. CAT changes in the presence of melatonin suggest that there is a relationship between a scavenger role of the pineal hormone and a high oxidative activity in the brain hypothalamy area. When these results are taken together, they also show that melatonin, besides, producing the extraneural effect, can act as a powerful antioxidative agent in organs such as the brain, very rich in lipid susceptible to oxidation in the neuronal as well as the extraneuronal tissues.

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