期刊文献+

运动激活自噬对小鼠骨骼肌抗氧化防御功能的影响 被引量:1

Effects of Exercise Induced Autophagy on Antioxidant Defense Function of Skeletal Muscles in Mice
下载PDF
导出
摘要 目的:探讨一次性力竭运动能否激活骨骼肌自噬及运动性自噬对骨骼肌抗氧化防御功能的影响,为运动性自噬与骨骼肌抗氧化防御功能之间的发生机制提供实验依据。方法:30只健康雄性4周龄C57BL/6小鼠随机分为安静对照组(n=6)和运动组(n=24),运动组进行一次性力竭跑台运动,分别于运动完成后的0 h(n=6)、6 h(n=6)、12 h(n=6)和24 h(n=6)取小鼠两侧腓肠肌,采用黄嘌呤氧化酶法测定腓肠肌锰超氧化物歧化酶(Mn SOD)、总超氧化物歧化酶(T-SOD)和铜锌超氧化物歧化酶(Cuzn SOD)的活性;比色法测定腓肠肌总抗氧化能力(T-AOC)的含量;荧光定量PCR和Western Blot分别检测腓肠肌自噬相关因子Beclin1、P62和B淋巴细胞瘤-2(Bcl2)的m RNA和蛋白表达。结果:与安静对照组相比,(1)小鼠腓肠肌Beclin1 m RNA表达在运动后0 h、6 h均极显著升高(P<0.01),P62 m RNA表达在运动后24 h极显著升高(P<0.01);P62蛋白表达在运动后0 h、12 h和24 h均显著下降(P<0.05或P<0.01),Bcl2蛋白表达在运动后0 h、6 h和12 h均显著升高(P<0.05或P<0.01);(2)Mn SOD和Cuzn SOD活性在0 h均显著升高(P<0.05),T-SOD活性在6 h极显著下降(P<0.01),T-AOC含量在运动后6 h、12 h、24 h均显著升高(P<0.05或P<0.01);P62蛋白表达与T-AOC含量呈负相关。结论:一次性力竭跑台运动可在一定程度上激活骨骼肌自噬相关因子Beclin1 m RNA和P62蛋白的表达,可适度提高自噬;且自噬相关因子P62蛋白表达与骨骼肌抗氧化防御功能具有相关性,这可能是运动增加骨骼肌抗氧化防御功能的分子机理之一。 Objective To explore whether a single bout of exhaustive exercise can activate autophagyin mice skeletal muscles and to investigate the effect and possible mechanisms of exercise-induced au-tophagy on antioxidant defense function in vivo. Methods Thirty healthy 4-week-old male C57 BL/6 mice were randomly divided into a control group(n=6) and an exercise group(n=24). The latter wassubjected to a single bout of exhaustive treadmill exercise. Gastrocnemius muscles of 6 mice on bothsides were then isolated right after,as well as 6 h,12 h and 24 h after the running. The manganese superoxide dismutase(Mn SOD),total superoxide dismutase(T-SOD) and Copper-Zinc superoxide dismutase(Cuzn SOD) activities were determined using the xanthine oxidase method and the content of the totalanti-oxygen capability(T-AOC) using the colorimetric method. The expression of Beclin1,P62 andBcl2 m RNAs,as well as their proteins were determined using the fluorescent quantitative PCR andWestern blotting. Results The expression of Beclin1 m RNA in gastrocnemius muscles of the exercisegroup increased more significantly than that of the control group right after the exercise,as well as 6 hours later(P〈0.01). P62 m RNA expression also increased significantly(P〈0.01) 24 h after the exercise.In contrast,the expression of P62 protein at 0 h,12 h and 24 h after the exercise decreased more signifi-cantly(P〈0.05 or P〈0.01) than that of the control group. Similarly,the expression of Bcl2 protein at0 h,6 h and 12 h increased significantly(P〈0.05 or P〈0.01). The Mn SOD and Cuzn SOD activity in-creased significantly right after the exercise(P〈0.05). The T-SOD activity decreased significantly(P〈0.01) 6 h after the exercise. T-AOC content increased significantly 6 h,12 h and 24 h after the exercise(P〈0.05 or P〈0.01). The P62 protein expression was negatively correlated with T-AOC content. Conclusion The single bout of exhaustive treadmill exercise can activate the expression of such autophagy-related factors as Beclin1 m RNA and P62 protein and increase the autophagy to a certain extent tomaintain antioxidant defensive function of the skeletal muscle.
作者 王平 Chun-Guang LI 崔迪 邱守涛 漆正堂 李娅晖 丁树哲 Wang Ping;Chun-Guang LI;Cui Di;Qi Zhengtang;Qiu Shoutao;Li Yahui;Ding Shuzhe(School of Physical Education and Health, Hangzhou Normal University, Hangzhou 311121, China;National Institute of Complementary Medicine, Western Sydney University, Sydney 2751,Australia;Key Laboratory of Adolescent Health Assessment and Exercise Intervention, Ministry of Education, East China Normal University, Shanghai 200241, China;School of Life Science and Biotechnology, Shanghai Jiao Tong University ,Shanghai 200240, China)
出处 《中国运动医学杂志》 CAS CSCD 北大核心 2018年第1期49-56,共8页 Chinese Journal of Sports Medicine
基金 国家自然科学基金(31171142) 浙江省教育厅课题(Y201328990) 杭州师范大学博士启动金(PE13002004028)
关键词 运动 自噬 骨骼肌 抗氧化防御功能 exercise,autophagy, skeletal muscle, antioxidant defense function
  • 相关文献

参考文献3

二级参考文献109

  • 1Lecker SH, Goldberg AL, Mitch WE. Protein degradation by the ubiquitin-proteasome pathway in normal and disease states. J Am Soc Nephrol,2006,17(7) : 1807-1819.
  • 2Mammucari C, Schiaffino S, Sandri M. Downstream of AKT: FOXO3 and mTOR in the regulation of autophagy in skele- tal muscle. Autophagy, 2007,4 (4) : 524-526.
  • 3Furuno K,Goodman MN,Goldberg AL. Role of different proteolytic systems in the degradation of muscle proteins during denervation ~rophy. J Biol Chem,1990,25,265 (15):8550-8557.
  • 4Mizushima N,Yamamoto A, Matsui M, et al. In vivo analy- sis of autophagy in response to nutrient starvation using transgenic mice expressing a fluorescent autophagosome marker. Mol Biol Cell, 2004,15 (3) : 1101-1111.
  • 5Wildey GM,Howe PH. Runxl is a co-activator with FOX- 03 to mediate transforming growth factor beta (TGFbeta)- induced Bim transcription in hepatic cells. J Biol Chem, 2009,24,284(30) : 20227-20239.
  • 6Tassa A, Roux MP, Attaix D, et al. Class III phosphoinosi- tide 3-kinase--BBeclinl complex mediates the amino acid-dependent regulation of autophagy in C2C12 my- otubes. Biochem J ,2003,376(Pt 3):577-586.
  • 7Tracy K,Macleod KF. Regulation of mitochondrial integri- ty,autophagy and cell survival by BNIP3. Autophagy, 2007,3(6) :616-619.
  • 8ARNDT V, DICK N, TAWO R, et al. Chaperone-assisted selec- tive autophagy is essential for muscle maintenanceEJ-]. Curr Biol, 2010,20 (2) : 143-148.
  • 9BONALDO P, SANDRI M. Cellular and molecular mechanisms of muscle atrophy[J]. Dis Model Mech, 2013,6 (1) : 25-39.
  • 10CANTO C, GERHART-HINES Z, FEIGE J N, et al. AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity[J]. Nature,2009,458(7241) :1056-1060.

共引文献26

同被引文献5

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部