热量限制通过AMPK-SIRT1-线粒体通路延缓小鼠骨骼肌衰老

蒲荣喜; 白川川; 解栋梁; 吴韦铷; 舒彬; 杨忠

doi:10.16016/j.1000-5404.201610056

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热量限制通过AMPK-SIRT1-线粒体通路延缓小鼠骨骼肌衰老

更新时间：2026-01-09

- 热量限制通过AMPK-SIRT1-线粒体通路延缓小鼠骨骼肌衰老
- Calorie restriction delays skeletal muscle aging through AMPK-SIRT1-mitochondria pathway in mice
- 第三军医大学学报 2017年39卷第6期页码：548-552
- 作者机构：
  
  1.400038 重庆，第三军医大学西南医院检验系临床血液学教研室
  2.401121 重庆，重庆医科大学附属大学城医院康复中心
- 作者简介：
  
  [杨忠,E-mail:zyang@tmmu.edu.cn Yang Zhong, E-mail: zyang@tmmu.edu.cn
- 基金信息：
  
  国家自然科学基金面上项目(31571242)
- DOI：10.16016/j.1000-5404.201610056
  中图分类号： R151.1; R322.74; R339.34
- 收稿：2016-10-11，
  
  修回：2016-11-09，
  
  纸质出版：2017-06
- 稿件说明：
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蒲荣喜, 白川川, 解栋梁, 等. 热量限制通过AMPK-SIRT1-线粒体通路延缓小鼠骨骼肌衰老[J]. 第三军医大学学报, 2017,39(6):548-552.

Rongxi Pu, Chuanchuan Bai, Dongliang Xie, et al. Calorie restriction delays skeletal muscle aging through AMPK-SIRT1-mitochondria pathway in mice[J]. Journal of Third Military Medical University, 2017, 39(6): 548-552.
蒲荣喜, 白川川, 解栋梁, 等. 热量限制通过AMPK-SIRT1-线粒体通路延缓小鼠骨骼肌衰老[J]. 第三军医大学学报, 2017,39(6):548-552. DOI： 10.16016/j.1000-5404.201610056.

Rongxi Pu, Chuanchuan Bai, Dongliang Xie, et al. Calorie restriction delays skeletal muscle aging through AMPK-SIRT1-mitochondria pathway in mice[J]. Journal of Third Military Medical University, 2017, 39(6): 548-552. DOI： 10.16016/j.1000-5404.201610056.

摘要

目的

观察热量限制对老化进程中小鼠骨骼肌线粒体等生物学性状的影响，探讨热量限制生物效应的分子机制。

方法

13月龄C57BL/6雄性小鼠30只，按照简单随机抽样法分为自由进食组和热量限制组，每周按照自由进食组前1周平均摄食量的60%饲养热量限制小鼠。热量限制12周后，测量骨骼肌衰减指数、胫前肌等肌纤维密度及相对横截面积，透射电镜观察骨骼肌线粒体变化，Western blot检测PGC1α、AMPKα、p-AMPKα及SIRT1等的表达，并比较老年鼠与成年鼠的表达差异。

结果

①与自由进食组比较，热量限制组骨骼肌衰减指数变化不明显，胫前肌等肌纤维密度显著升高 (

0.01)，相对横截面积降低 (

0.01)；②电镜观察显示：与自由进食组比较，热量限制组骨骼肌线粒体长度和宽度均增加 (

0.05，

0.01)，相对密度增加 (

0.01)，PGC1α表达升高 (

0.05)；③与自由进食组比较，热量限制组骨骼肌AMPK的磷酸化水平升高 (

0.01)，同时SIRT1表达也升高 (

0.05)；④与成年鼠比较，老年鼠骨骼肌AMPK磷酸化水平下降 (

0.05)，SIRT1和PGC1α的表达也均下降 (

0.05)。

结论

热量限制能显著促进老化进程中骨骼肌线粒体的生成及活性，这一作用可能通过激活AMPK信号途径实现。

Abstract

Objective

To observe the effects of calorie restriction (CR) on the biological characteristics of mouse skeletal muscle mitochondria during the aging process

and explore the molecular mechanism of the biological effects of CR.

Methods

Thirty C57BL/6 male mice

13 months old

were randomly divided into 2 groups: free eating (ad libitum

AL) group and CR group

and the CR group was fed with 60% consumption of the AL group. After 12 weeks of CR

the sarcopenia index of skeletal muscle

and the myofiber density and cross section area in tibialis anterior muscle were measured. The changes of skeletal muscle mitochondria were observed with transmission electron microscopy. The expression levels of AMPKα

p-AMPKα

SIRT1

and PGC1α were detected by Western blotting

and those of AMPKα and SIRT1 in the normal adult mice and aged mice were compared.

Results

Compared with the AL group

the sarcopenia index did not change significantly

the myofiber density was increased significantly (

0.01)

and the relative cross-sectional area was decreased (

0.01) in the CR group. Electron microscope observation showed that the length and width of skeletal muscle mitochondria in the CR group were significantly increased (

0.05

0.01)

the relative density was significantly increased (

0.01)

and the expression of PGC1α was significantly increased (

0.05). The phosphorylation of AMPK in skel

etal muscle was enhanced by CR

and the expression levels of SIRT1 and PGC1α were significantly increased (

0.05). Compared with the normal adult mice

the phosphorylation of AMPK and the expression of SIRT1 and PGC1α in the aged mice were significantly decreased (

0.05).

Conclusion

CR can significantly promote the biogenesis and activity of mitochondria in the aging skeletal muscle

which may be regulated by activating AMPK signaling pathway.

关键词

Keywords

references

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