姜黄素对肥胖雄性白化大鼠奥利司他相关毒性的肝、肾和小脑抗毒作用

Eman H. Kandil, Samah M. Arisha
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引用次数: 1

摘要

背景:奥利司他是治疗超重的常用药物之一,使用奥利司他可能会引起一些副作用。姜黄素是一种从姜黄根茎中分离出来的黄色酚类化合物,具有抗氧化和抗炎作用。目的:探讨姜黄素对肥胖白化大鼠奥利司他诱发的肝肾和小脑毒性的保护作用。材料与方法:40只成年雄性白化大鼠,随机分为4组;第一组:对照组。第二组:姜黄素组;第三组:奥利司他组。IV组大鼠给予奥利司他(32mg/kg/d),然后给予姜黄素(200mg/kg体重,每周3次,连用6周)。结果:奥利司他给药后大鼠肝脏出现胞浆变性,胞浆内多空泡,细胞核染色深。同样,部分肾小球萎缩或断裂,小脑皮质海绵状病变,浦肯野细胞、颗粒细胞和分子细胞变性。经奥利司他和姜黄素处理后,大鼠肝、肾和小脑的组织病理变化均较对照组恢复。与奥利司他处理大鼠相比,Kupffer细胞数量、肾小球直径、Bowman间隙宽度和肾小管尺寸明显降低,上皮高度恢复正常。MDA、多巴胺、谷氨酸水平显著降低,SOD活性显著升高。经姜黄素处理后,奥利司他处理后的PCNA和Bcl2表达的升高明显降低。结论:本研究认为姜黄素可能在改善奥利司他治疗后的肝肾和小脑毒性方面具有潜在的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatorenal and cerebellar anti-toxic effects of curcumin against orlistat associated toxicity in obese male albino rats
Background : Orlistat is one of the common medicines in treating overweight, and its use may cause several side effects. Curcumin, a yellow phenolic compound isolated from Curcuma longa's rhizome, possesses several pharmaceutical effects due to its antioxidant and anti-inflammatory properties. Aim: This work aimed to test the possible protective effect of curcumin against orlistat-induced hepatorenal and cerebellar toxicities in obese albino rats. Material and Methods: Forty adult male albino rats were equally separated into four groups; Group I: the control group. Group II: curcumin group; Group III: orlistat group. Group IV, rats were given orlistat ((32mg/kg/day ) ) then curcumin (200mg/kg body weight three times per week for six weeks). Results: In the liver of rats treated with orlistat, the hepatic cells appeared with degenerated cytoplasm containing many vacuoles and darkly stained nuclei. similarly, some glomeruli in the kidney were atrophic or fractured, the cerebellar cortex is spongiosis, and the Purkinje cells, granule, and molecular cells were degenerated. When rats were treated with orlistat and curcumin, the liver, kidney, and cerebellar the histopathological changes were relatively recovered to the control ones. The number of Kupffer cells, glomerular diameter, Bowman’s space width, and the dimensions of the renal tubules significantly decreased, and the epithelial height retrains normal as compared to orlistat treated rats. The levels of MDA, dopamine, and glutamate significantly decreased, and the activity of SOD significantly increased. The rising in PCNA and Bcl2 expression after orlistat is significantly decreased in the studied organs after curcumin treatment. Conclusion: This study concluded that curcumin may have a potential role in improving hepatorenal and cerebellar toxicities after orlistat treatment.
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