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脂酸可逆转大鼠脑内由杀虫剂引起的氧化损伤和炎症。

The oxidative damage and inflammation caused by pesticides are reverted by lipoic acid in rat brain.

机构信息

Cátedra de Bioquímica y Biología Molecular, Universidad Nacional de La Plata, La Plata, Argentina.

出版信息

Neurochem Int. 2012 Dec;61(7):1231-41. doi: 10.1016/j.neuint.2012.09.003. Epub 2012 Sep 17.

DOI:10.1016/j.neuint.2012.09.003
PMID:22995786
Abstract

We have previously demonstrated that the administration of low doses of dimethoate, glyphosate and zineb to rats (i.p. 1/250 LD50, three times a week for 5weeks) provokes severe oxidative stress (OS) in specific brain regions: substantia nigra, cortex and hippocampus. These effects were also observed in plasma. Lipoic acid (LA) is considered an "ideal antioxidant" due to its ability to scavenge reactive species, reset antioxidant levels and cross the blood-brain barrier. To investigate its protective effect we administered LA (i.p. 25, 50 and 100mg/kg) simultaneously with the pesticide mixture (PM) for 5weeks. After suppression of PM administration, we evaluated the restorative effect of LA for a further 5weeks. LA prevented OS and the production of nitrites+nitrates [NOx] caused by PM in a dose-dependent manner. The PM-induced decrease in reduced glutathione and α-tocopherol levels in all brain regions was completely restored by LA at both high doses. PM administration also caused an increase in prostaglandins E(2) and F(2α) in brain that was reduced by LA in a dose-dependent fashion. Taking into account the relationship between OS, inflammation and apoptosis, we measured caspase and calpain activity. Only milli- and micro-calpain isoforms were increased in the PM-treated group and LA reduced the activities to basal levels. We also demonstrated that interrupting PM administration is not enough to restore the levels of all the parameters measured and that LA is necessary to achieve basal status. In our experimental model LA displayed a protective role against pesticide-induced damage, suggesting that LA administration is a promising therapeutic strategy to cope with disorders suspected to be caused by OS generators, especially in brain.

摘要

我们之前的研究表明,给大鼠腹腔内注射低剂量的乐果、草甘膦和代森锌(1/250LD50,每周三次,共 5 周)会引起特定脑区(黑质、皮质和海马体)的严重氧化应激(OS)。这些影响也在血浆中观察到。硫辛酸(LA)因其能够清除活性物质、重置抗氧化水平和穿过血脑屏障而被认为是一种“理想的抗氧化剂”。为了研究其保护作用,我们同时给予 LA(腹腔内注射 25、50 和 100mg/kg)和农药混合物(PM)5 周。在抑制 PM 给药后,我们进一步评估了 LA 的恢复作用 5 周。LA 以剂量依赖的方式预防了 PM 引起的 OS 和亚硝酸盐+硝酸盐[NOx]的产生。LA 完全恢复了 PM 引起的所有脑区还原型谷胱甘肽和α-生育酚水平的降低。PM 给药还导致脑内前列腺素 E(2)和 F(2α)增加,LA 以剂量依赖的方式降低了它们的含量。考虑到 OS、炎症和细胞凋亡之间的关系,我们测量了半胱天冬酶和钙蛋白酶的活性。只有毫微微和微钙蛋白酶同工型在 PM 处理组中增加,LA 将其活性降低到基础水平。我们还证明,中断 PM 给药不足以恢复所有测量参数的水平,LA 是达到基础状态所必需的。在我们的实验模型中,LA 显示出对农药诱导损伤的保护作用,表明 LA 给药是一种有前途的治疗策略,可用于应对疑似由 OS 生成器引起的疾病,尤其是在大脑中。

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