...
首页> 外文期刊>The British Journal of Nutrition >The preventive effect of beta-carotene on denervation-induced soleus muscle atrophy in mice.
【24h】

The preventive effect of beta-carotene on denervation-induced soleus muscle atrophy in mice.

机译:β-胡萝卜素对神经支配引起的比目鱼肌萎缩症的预防作用。

获取原文
获取原文并翻译 | 示例
           

摘要

Muscle atrophy increases the production of reactive oxygen species and the expression of atrophy-related genes, which are involved in the ubiquitin-proteasome system. In the present study, we investigated the effects of beta-carotene on oxidative stress (100 muM-H2O2)-induced muscle atrophy in murine C2C12 myotubes. beta-Carotene (10 muM) restored the H2O2-induced decreased levels of myosin heavy chain and tropomyosin (P< 0.05, n 3) and decreased the H2O2-induced increased levels of ubiquitin conjugates. beta-Carotene reduced the H2O2-induced increased expression levels of E3 ubiquitin ligases (Atrogin-1 and MuRF1) and deubiquitinating enzymes (USP14 and USP19) (P< 0.05, n 3) and attenuated the H2O2-induced nuclear localisation of FOXO3a. Furthermore, we determined the effects of beta-carotene on denervation-induced muscle atrophy. Male ddY mice (8 weeks old, n 30) were divided into two groups and orally pre-administered micelle with or without beta-carotene (0.5 mg once daily) for 2 weeks, followed by denervation in the right hindlimb. beta-Carotene was further administered once daily until the end of the experiment. At day 3 after denervation, the ratio of soleus muscle mass in the denervated leg to that in the sham leg was significantly higher in beta-carotene-administered mice than in control vehicle-administered ones (P< 0.05, n 5). In the denervated soleus muscle, beta-carotene administration significantly decreased the expression levels of Atrogin-1, MuRF1, USP14 and USP19 (P< 0.05, n 5) and the levels of ubiquitin conjugates. These results indicate that beta-carotene attenuates soleus muscle loss, perhaps by repressing the expressions of Atrogin-1, MuRF1, USP14 and USP19, at the early stage of soleus muscle atrophy
机译:肌肉萎缩增加了活性氧的产生以及与遍在蛋白-蛋白酶体系统有关的萎缩相关基因的表达。在本研究中,我们研究了β-胡萝卜素对氧化应激(100μM-H 2 O 2 )诱导的小鼠C2C12肌管肌萎缩的影响。 β-胡萝卜素(10μM)恢复了H 2 O 2 诱导的肌球蛋白重链和原肌球蛋白水平降低(P <0.05,n 3)并降低了H < sub> 2 O 2 诱导的泛素结合物水平升高。 β-胡萝卜素降低了H 2 O 2 诱导的E3泛素连接酶(Atrogin-1和MuRF1)和去泛素化酶(USP14和USP19)的表达水平(P < 0.05,n 3)并减弱H 2 O 2 诱导的FOXO3a核定位。此外,我们确定了β-胡萝卜素对失神经引起的肌肉萎缩的影响。将雄性ddY小鼠(8周大,n = 30)分为两组,口服含或不含β-胡萝卜素的胶束(每天一次0.5 mg)持续2周,然后在右后肢去神经支配。每天一次进一步施用β-胡萝卜素,直到实验结束。去神经后第3天,给予β-胡萝卜素的小鼠的去神经支腿比目鱼腿的比目鱼肌质量比明显高于对照组赋形剂的小鼠(P <0.05,n 5)。在失神经的比目鱼肌中,β-胡萝卜素给药显着降低了Atrogin-1,MuRF1,USP14和USP19的表达水平(P <0.05,n 5)和泛素结合物的水平。这些结果表明,在比目鱼肌萎缩的早期阶段,β-胡萝卜素可能通过抑制Atrogin-1,MuRF1,USP14和USP19的表达来减轻比目鱼肌的损失。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号