The Effect of Alpha Lipoic Acid and Melatonin on the progression of Streptozotocin-induced diabetic cardiomyopathy in rats

R. Mehanna, P. Hassaan, H. Nomeir, F. Dwedar
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引用次数: 1

Abstract

Background: Diabetic cardiomyopathy (DCM) is a major cause of diabetes-related morbidity and mortality. Alpha lipoic acid (ALA) and Melatonin (Mel) have gained a considerable amount of attention as antioxidants, their effect on the progression of DCM has not yet determined. Aim: To evaluate effects of ALA and Mel on AMP-activated protein kinase (AMPK) activity and the state of oxidative stress (OS) in DCM in rats. It also aims at correlating the pathogenesis of DCM to AMPK activity. Methods: 60 rats were divided into 6 groups (n=10); control (CG), C + ALAG, C + MelG, Diabetic (DG), D + ALAG and D + MelG. Diabetes was induced by 60mg/Kg streptozotocin. ALA and Mel were given in a dose of 100 mg/kg/day and 10 mg/kg/day respectively for 12 weeks. The heart/body weight (Ht/BW) ratio, AMPK activity and oxidative state in cardiac tissue, serum cardiac enzymes (serum lactate dehydrogenase "LDH" and creatine kinase "CK"), lipid profile, fasting glucose level and histologic examination were assessed at the end of the study. Results: Ht/BW and OS increased in DG compared to CG, decreased subsequently by ALA and Mel treatment with no significant difference between both groups. LDH and CK were higher in DG as compared to CG. Cardiac AMPK activity was decreased in DCM and increased subsequently by ALA and Mel treatment. Normal cardiac architecture was restored by both of them. ALA and Mel showed a hypolipidemic effect while ALA had a hypoglycemic effect. Conclusions: ALA and Mel enhanced AMPK activity, and antioxidant activity in the heart thus decreased the progression of cardiac dysfunction.
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α硫辛酸和褪黑素对链脲佐菌素诱导的大鼠糖尿病性心肌病进展的影响
背景:糖尿病性心肌病(DCM)是糖尿病相关发病和死亡的主要原因。α硫辛酸(ALA)和褪黑素(Mel)作为抗氧化剂已引起相当多的关注,但它们对DCM进展的影响尚未确定。目的:探讨ALA和Mel对DCM大鼠amp活化蛋白激酶(AMPK)活性及氧化应激状态的影响。它还旨在将DCM的发病机制与AMPK活性联系起来。方法:将60只大鼠分为6组(n=10);control (CG)、C + ALAG、C + MelG、Diabetic (DG)、D + ALAG和D + MelG。用60mg/Kg链脲佐菌素诱导糖尿病。ALA和Mel分别以100 mg/kg/天和10 mg/kg/天的剂量给予12周。在研究结束时,评估心脏/体重(Ht/BW)比、心脏组织AMPK活性和氧化状态、血清心脏酶(血清乳酸脱氢酶“LDH”和肌酸激酶“CK”)、血脂、空腹血糖水平和组织学检查。结果:与CG相比,DG组的Ht/BW和OS升高,ALA和Mel治疗组的Ht/BW和OS降低,两组差异无统计学意义。LDH和CK在DG中的含量高于CG。心肌AMPK活性在DCM时降低,ALA和Mel治疗后升高。心脏结构均恢复正常。ALA和Mel具有降血脂作用,ALA具有降血糖作用。结论:ALA和Mel增强AMPK活性和心脏抗氧化活性,从而减缓心功能障碍的进展。
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