首页> 美国卫生研究院文献>other >Reversal of Muscle Atrophy by Zhimu-Huangbai Herb-Pair via Akt/mTOR/FoxO3 Signal Pathway in Streptozotocin-Induced Diabetic Mice
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Reversal of Muscle Atrophy by Zhimu-Huangbai Herb-Pair via Akt/mTOR/FoxO3 Signal Pathway in Streptozotocin-Induced Diabetic Mice

机译:知母-黄柏对通过链脲佐菌素诱导的糖尿病小鼠的Akt / mTOR / FoxO3信号通路逆转肌肉萎缩

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摘要

Skeletal muscle atrophy is one of the serious complications of diabetes. Zhimu-Huangbai herb-pair (ZB) is widely used in Chinese traditional medicine formulas for treating Xiaoke (known as diabetes) and its complications. However, the effect of ZB on reversal of muscle atrophy and the underlying mechanisms remain unknown. In this research, we investigated the effect and possible mechanisms of ZB on skeletal muscle atrophy in diabetic mice. Animal model of diabetic muscle atrophy was developed by high fat diet (HFD) feeding plus streptozotocin (STZ) injection. After oral adminstration of ZB for 6 weeks, the effects of ZB on reversal of muscle atrophy and the underlying mechanisms were evaluated by biochemical, histological and western blot methods. The skeletal muscle weight, strength, and cross-sectional area of diabetic mice were significantly increased by ZB treatment. Biochemical results showed that ZB treatment reduced the serum glucose level, and elevated the serum insulin-like growth factor 1 (IGF-1) and insulin levels significantly compared with untreated diabetic group. The western blot results showed that ZB activated the mTOR signal pathway, shown as increased phosphorylations (p-) of Akt, mTOR, Raptor, S6K1 and reduced Foxo3 expression compared with the model group. ZB could reverse muscle atrophy in diabetic mice. This may be through activation of mTOR signaling pathway that promotes protein synthesis, and inactivation foxo3 protein that inhibits protein degradation. These findings suggested that ZB may be considered as a potential candidate drug in treatment of diabetic muscle atrophy.
机译:骨骼肌萎缩是糖尿病的严重并发症之一。知母-黄柏草药对(ZB)被广泛用于中药配方中,用于治疗小柯(称为糖尿病)及其并发症。但是,ZB对肌萎缩的逆转及其潜在机制的作用仍未知。在这项研究中,我们研究了ZB对糖尿病小鼠骨骼肌萎缩的影响及其可能的机制。通过高脂饮食(HFD)喂养和链脲佐菌素(STZ)注射建立了糖尿病肌肉萎缩的动物模型。口服ZB 6周后,通过生化,组织学和Western blot方法评估ZB对肌肉萎缩逆转的作用及其潜在机制。 ZB处理可显着增加糖尿病小鼠的骨骼肌重量,强度和横截面积。生化结果显示,与未治疗的糖尿病组相比,ZB治疗可降低血清葡萄糖水平,并显着提高血清胰岛素样生长因子1(IGF-1)和胰岛素水平。蛋白质印迹结果表明,与模型组相比,ZB激活了mTOR信号通路,表现为Akt,mTOR,Raptor,S6K1的磷酸化增强(p-)和Foxo3表达降低。 ZB可以逆转糖尿病小鼠的肌肉萎缩。这可能是通过激活可促进蛋白质合成的mTOR信号通路,以及使抑制蛋白质降解的foxo3蛋白质失活而实现的。这些发现表明,ZB可能被认为是治疗糖尿病性肌萎缩症的潜在候选药物。

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