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首页> 外文期刊>International Journal of Pharmacology >Asiatic Acid Improves Diabetes-Induced Muscle Atrophy in Mice
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Asiatic Acid Improves Diabetes-Induced Muscle Atrophy in Mice

机译:亚洲酸改善糖尿病诱导的小鼠肌肉萎缩

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Background and Objective: Diabetic amyotrophy is one of serious muscular complications in diabetes. Asiatic Acid (AA) possessed multiple pharmacological actions in diabetic complications. However, the potential role of AA on diabetic myopathy has been not reported to date. Current study aimed to estimate improvement effect of AA on diabetic-associated muscle atrophy in mice. Materials and Methods: Mice were intraperitoneal injection with streptozocin (STZ, 50 mg kgG1 ) for 5 days to establish diabetic model. When blood glucose concentration was above 16.7 mmol/L, mice were treated with AA (30 mg/kg/day) for 8 weeks. Then, mice were euthanized to collect blood and muscle samples for further research. Results: Our data demonstrated that AA significantly reduced blood glucose concentration and led to a significant decrease in serum glucose (Glu), triglyceride (TG), cholesterol (TC), Creatine Kinase (CK), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea (BUN) and creatinine (Cre) in diabetic mice. Moreover, AA significantly increased myofiber size and weight of gastrocnemius and enhanced grip strength to improve muscle atrophy. In skeletal muscle, AA significantly relieved Atrogin-1, MuRF-1, TNF-a, IL-6 and Bax expressions and elevated Nrf-1, Pgc-1" and Bcl-2 expressions in diabetic mice. Conclusion: AA produced beneficial effects against diabetic amyotrophy through its accommodation of inflammatory response, mitochondrial dysfunction and apoptosis in mice. These biological functions suggested AA could be used as a novel medicine for improvement of diabetes-induced skeletal muscle atrophy.
机译:背景和目的:糖尿病肌萎缩是糖尿病患者严重的肌肉起源之一。亚洲酸(AA)具有糖尿病并发症的多种药理作用。然而,迄今未报告AA对糖尿病肌病的潜在作用。目前的研究旨在估算AA对小鼠糖尿病相关肌肉萎缩的改善效果。材料和方法:小鼠与链霉菌(STZ,50mg Kgg1)腹腔注射5天以建立糖尿病模型。当血糖浓度高于16.7mmol / L时,用Aa(30mg / kg /天)处理小鼠8周。然后,使小鼠安乐死以收集血液和肌肉样品进行进一步研究。结果证明,AA显着降低血糖浓度,并导致血清葡萄糖(GLU),甘油三酯(TG),胆固醇(TC),乳酸脱氢酶(LDH),天冬氨酸氨基转移酶( AST),糖苷氨基转移酶(ALT),血液尿素(BUN)和糖尿病小鼠的肌酐(CRE)。此外,AA显着增加了肌纤维尺寸和胃肠炎的重量,提高了握力,以改善肌肉萎缩。在骨骼肌中,AA显着减轻了糖尿病小鼠中的亚毒素-1,Murf-1,TNF-A,IL-6和BCL-2表达的升高和Bcl-2表达。结论:AA产生有益效果通过其通过其对小鼠的炎症反应,线粒体功能障碍和细胞凋亡的容纳来对抗糖尿病肌萎缩。这些生物学功能表明AA可以用作改善糖尿病诱导的骨骼肌萎缩的新药。

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