Effect of orlistat on lipid peroxidation, Na+, K+ ATPase, glutathione and serotonin in rat brain.

D Calderón Guzmán, E Hernández García, A Juárez Jacobo, L Segura Abarca, G Barragán Mejía, R Rodríguez Pérez, H Juárez Olguín
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Abstract

The aim of this study was to evaluate the effect of orlistat, a drug used in weight loss, on 5-HT and indicators of oxidative stress in rat brain. Orlistat, 12 mg/kg was administered to Wistar rats as single dose or successive doses on 3 consecutive days. Blood glucose and oxidative stress indicators were detected by measurement of lipid peroxidation, Na+, K+ ATPase, glutathione and serotonin levels using previous validated methods. The levels of glucose decreased in rats receiving successive doses. The activity of Na+, K+ ATPase and total ATPase was reduced in rats receiving successive doses, while the level of lipid peroxidation increased slightly in both groups. Glutathione underwent significant reduction in the successive doses group (p < 0.05). 5-HT increased significantly after single dose treatment (p < 0.05). Orlistat can induce pro-oxidant effects in the brain due to alteration of serotonergic metabolism and the reduction of glutathione.

奥利司他对大鼠脑脂质过氧化、Na+、K+ atp酶、谷胱甘肽和血清素的影响。
本研究旨在评价奥利司他对大鼠脑内5-羟色胺及氧化应激指标的影响。奥利司他,12 mg/kg, Wistar大鼠单次或连续给药,连续3天。血糖和氧化应激指标通过测定脂质过氧化、Na+、K+ atp酶、谷胱甘肽和血清素水平检测。连续给药的大鼠葡萄糖水平下降。连续给药组大鼠Na+、K+ atp酶活性和总atp酶活性均降低,脂质过氧化水平均略有升高。连续给药组谷胱甘肽显著降低(p < 0.05)。单次给药后5-HT显著升高(p < 0.05)。奥利司他可以通过改变血清素代谢和谷胱甘肽的减少而在大脑中诱导促氧化作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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