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Effect of DL-alpha-lipoic acid on cyclophosphamide induced lysosomal changes in oxidative cardiotoxicity.

机译:DL-α-硫辛酸对环磷酰胺诱导的溶酶体氧化性心脏毒性变化的影响。

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摘要

Cyclophosphamide (CP), one of the widely prescribed antineoplastic drugs can cause fatal cardiotoxicity. The present study is aimed at evaluating the cardioprotective role of lipoic acid in CP induced toxicity. Male albino rats of Wistar strain were divided into four groups and treated as follows: Group I served as control, Group II received a single dose of CP (200 mg/kg b.wt., i.p.), Group III received lipoic acid (25 mg/kg b.wt., orally) for 10 days, and Group IV received CP immediately followed by lipoic acid for 10 days. In CP administered rats, the levels of protein carbonyl and 8-hydroxy-2-deoxyguanosine were increased significantly (P<0.001) indicating oxidative changes in the heart tissue. The activities of lysosomal acid hydrolases, beta-Glu, beta-Gal, NAG, Cat-D and ACP increased significantly (P<0.001) in the serum as well as in the heart tissue after CP administration. An increase in hydroxyproline was observed in CP induced rats. Lipoic acid effectively reverted these abnormal biochemicalchanges to near normalcy. These observations highlight the protective role of lipoic acid in CP induced cardiotoxicity.
机译:环磷酰胺(CP)是广泛使用的抗肿瘤药物之一,可引起致命的心脏毒性。本研究旨在评估硫辛酸在CP诱导的毒性中的心脏保护作用。将Wistar品系的雄性白化病大鼠分为四组,并进行如下处理:第一组为对照组,第二组接受单剂量的CP(200 mg / kg b.wt.,ip),第三组接受硫辛酸(25口服),持续10天,第IV组立即接受CP,然后接受硫辛酸治疗10天。在CP给药的大鼠中,羰基蛋白和8-羟基-2-脱氧鸟苷的蛋白水平显着增加(P <0.001),表明心脏组织中的氧化变化。给予CP后,血清和心脏组织中的溶酶体酸水解酶,β-Glu,β-Gal,NAG,Cat-D和ACP的活性显着增加(P <0.001)。在CP诱导的大鼠中观察到羟脯氨酸的增加。硫辛酸有效地将这些异常的生化变化恢复到接近常态。这些观察结果突出了硫辛酸在CP诱导的心脏毒性中的保护作用。

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