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Protective Effect of L-Carnitine and Coenzyme Q10 on CCl4-Induced Liver Injury in Rats

机译:左旋肉碱和辅酶Q10对CCl4诱导的大鼠肝损伤的保护作用

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摘要

This study provides an information about the mechanisms of liver injury induced by CCl4, and determines the influence of administration of L-carnitine or/and CoQ10 as prophylactic agents against CCl4 deteriorative effect. The study was carried out on 80 adult male albino rats divided into eight groups, 10 animals each, as follows: four normal groups (control, treated with L-carnitine, treated with CoQ10, and treated with a combination of Lcarnitine and CoQ10) and four liver injury groups treated with CCl4 (control, treated with L-carnitine, treated with CoQ10, and treated with a combination of L-carnitine and CoQ10). Liver injury was induced by s.c. injection of a single dose of CCl4 (1 ml/kg). L-carnitine (50 mg/kg/day) was given i.p. for four successive days 24 hours before CCl4 injection, and CoQ10 (200 mg/kg) was given as a single i.p. dose 24 hours before CCl4 injection. Animals were sacrificed 24 hours after CCl4 injection, blood samples were withdrawn and liver tissue samples were homogenized. The levels of the following parameters were determined: hepatic reduced glutathione, serum ALT and AST, hepatic lipid peroxides, hepatic vitamin C, hepatic and serum total protein, serum albumin, serum sialic acid, serum nitrite, and serum and hepatic total LDH activities and LDH isoenzymes. The obtained data revealed that CCl4 injection produced a significant decrease in reduced glutathione content, vitamin C, total protein and albumin levels. However, there was a significant increase in serum ALT and AST activities, lipid peroxides, sialic acid, nitric oxide, serum and hepatic total LDH activities. On the other hand, groups treated with L-carnitine or/and CoQ10 prior to CCl4 injection showed an improvement in most parameters when compared with cirrhotic control group. It has been concluded that L-carnitine and coenzyme Q10 have a pronounced prophylactic effect against liver damage induced by halogenated alkanes such as carbon tetrachloride.
机译:这项研究提供了有关CCl4诱导的肝损伤机制的信息,并确定了服用L-肉碱或/和CoQ10作为预防CCl4恶化作用的药物的影响。该研究是对80只成年雄性白化病大鼠进行的,分为八组,每组十只,如下:四个正常组(对照组,左旋肉碱治疗,辅酶Q10处理,左卡尼汀和辅酶Q10联合治疗)和用CCl4治疗的四个肝损伤组(对照组,左旋肉碱治疗,辅酶Q10治疗以及左旋肉碱和辅酶Q10的组合治疗)。肝损伤是由皮下注射引起的。注射单剂量的CCl4(1 ml / kg)。腹腔注射左旋肉碱(50 mg / kg /天)。在注射CCl4前24小时连续四天服用CoQ10(200 mg / kg)。注射CCl4前24小时服用。注射CCl4后24小时处死动物,抽取血液样本,并匀浆肝组织样本。确定以下参数的水平:肝还原型谷胱甘肽,血清ALT和AST,肝脂质过氧化物,肝维生素C,肝和血清总蛋白,血清白蛋白,血清唾液酸,血清亚硝酸盐以及血清和肝总LDH活性,以及LDH同工酶。获得的数据表明,注射CCl4可以显着降低降低的谷胱甘肽含量,维生素C,总蛋白和白蛋白水平。但是,血清ALT和AST活性,脂质过氧化物,唾液酸,一氧化氮,血清和肝脏的总LDH活性显着增加。另一方面,与肝硬化对照组相比,在注射CCl4之前用L-肉碱或/和CoQ10治疗的组在大多数参数上都有改善。已经得出结论,左旋肉碱和辅酶Q10对卤代烷烃(如四氯化碳)引起的肝损害具有明显的预防作用。

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