期刊文献+

有氧运动改善高脂膳食诱导的胰岛素抵抗:增强骨骼肌线粒体融合与分裂及功能 被引量:11

Adaptation of Mitochondrial Dynamics Is Probably Involved in Aerobic Exercise Prevention of Insulin Resistance Induced by High-fat-diets in Mice
下载PDF
导出
摘要 目的:研究高脂膳食诱导胰岛素抵抗(IR)发生中骨骼肌线粒体融合与分裂的改变和长期耐力训练对其影响,为深入探讨IR发生的分子病理学机制以及运动防治IR的机制提供依据。方法:雄性C57BL/6小鼠通过8周高脂膳食诱导IR,再分别将正常和IR小鼠分为安静组和运动组,即正常膳食对照组(NS)、正常膳食运动组(NE)、高脂膳食对照组(HS)、高脂膳食运动组(HE),各运动组进行8周有氧运动训练。检测空腹血糖、胰岛素。提取骨骼肌线粒体测定呼吸功能和ATP合成酶活力。实时荧光定量PCR和Western blot分别测定骨骼肌Mfn2、Opa1、Drp1、Fis1的mRNA和蛋白表达。结果:(1)HS组小鼠空腹血糖、胰岛素和胰岛素抵抗指数均显著高于NS组(P<0.01);骨骼肌线粒体态3呼吸速率、呼吸控制比和ATP酶合成活力均显著低于NS组(P<0.01);Mfn2蛋白显著低于NS组(P<0.01),Drp1和Fis1显著高于NS组(P<0.01)。(2)HE组小鼠空腹血糖、胰岛素和胰岛素抵抗指数均显著高于HS组(P<0.01);骨骼肌线粒体态3呼吸速率、RCR和ATP酶合成活力均显著高于HS组(P<0.01);Mfn2、Opa1和Drp1蛋白显著高于HS组(P<0.01,P<0.05,P<0.01)。结论:高脂膳食诱导IR的小鼠骨骼肌线粒体趋于分裂,呼吸功能和ATP合成能力下降,可能是高脂膳食诱导IR的机制之一。长期有氧运动训练使正常和IR小鼠骨骼肌线粒体融合和分裂均增强,促进线粒体呼吸功能和ATP合成能力,有利于预防和改善IR。 Objective To investigate the effect of long-term aerobic exercise on skeletal muscle mitochondrial dynamics (fusion and fission) and its function on insulin resistance (IR) induced by high-fat-diet in mice. Methods C57BL/6 mice were fed with high fat diet for 8 weeks to induce IR. Then, normal mice and IR mice divided into 4 groups: normal diet control (NS) , normal diet plus exercise (NE) , high-fat diet control (HS) and high-fat diet plus exercise (HE) . Mice were fed and/or trained for 8 weeks. Fasting blood glucose concentration and fasting serum insulin level weremeasured to evaluate IR. Respiratory control ratio (RCR) and ATP synthesis activity in isolated skeletal muscle mitochondria were detected. Skeletal muscle mRNA and Protein levels of Mfn2, Opal and Drpl, Fisl were measured by Real-time PCR and Western-blot respectively. Results ( 1 ) Compare with NS group, the fast blood glucose, fast serum insulin and HOMA-IR of mice in HS group were significantly higher (P 〈 0.01 ) . The skeletal muscle mitochondrial respiratory rate of states 3, RCR and ATP synthesis activity were significantly lower (P 〈 0.01 ) . The protein level of Mfn2 was significantly lower (P 〈 0.01 ) , Drpl and Fisl were significantly higher (P 〈 0.01 ) . (2) Compare with HS group, the fast blood glucose, fast serum insulin and HOMA-IR of mice in HE group were significantly lower (P 〈 0.01 ) . The skeletal muscle mitochondrial respiratory rate of states 3, RCR and ATP synthesis activity of mice in HE group were significantly higher (P 〈 0.01 ) . The protein levels of Mfn2, Opal and Drplwere significantly higher (P 〈 0.01, P 〈 0.05, P 〈 0.01 ) . Conclusion The mitochondria of the IR mice induced by high fat diet inclined to fission; the decreased of mitochondrial respiratory function and ATP synthesis activity, might be involved in the pathogenesis of high fat diet induced IR. Long-time aerobic training enhanced both fusion and fission of skeletal muscle mitochondria and improved the respiratory function and ATP synthesis activity of mitochondria, might be helpful to prevent and cure IR.
出处 《中国运动医学杂志》 CAS CSCD 北大核心 2012年第1期24-30,共7页 Chinese Journal of Sports Medicine
基金 国家自然科学基金(30871214 30771048) 天津市应用基础及前沿技术研究计划(09JCYBJC12000) 天津市高校科技发展基金(20072612)共同资助
关键词 骨骼肌 线粒体融合与分裂 胰岛素抵抗 有氧运动 skeletal muscle, mitochondrial fusion and fission, insulin resistance, aerobic exer-cise
  • 相关文献

参考文献22

  • 1Hawley JA.Exercise as a therapeutic intervention for theprevention and treatment of insulin resistance.DiabetesMetab Res Rev,2004,20(5):383-393.
  • 2Schenk S,Horowitz JF.Acute exercise increases triglyc-eride synthesis in skeletal muscle and prevents fatty acid-induced insulin resistance.J Clin Invest,2007,117(6):1690-1698.
  • 3Lowell BB,Shulman GI.Mitochondrial dysfunction andtype 2 diabetes.Science,2005,307(5708):384-387.
  • 4Kelley DE,He J,Menshikova EV,et al.Dysfunctionof mitochondria in human skeletal muscle in type 2 diabe-tes.Diabetes,2002,51(10):2944-2950.
  • 5Hoppeler H,Fluck M.Plasticity of skeletal muscle mito-chondria:structure and function.Med Sci Sports Exerc,2003,35(1):95-104.
  • 6Civitarese AE,Ravussin E.Mitochondrial energeticsand insulin resistance.Endocrinology,2008,149(3):950-954.
  • 7De Souza C T,Araujo EP,Bordin S,et al.Consump-tion of a fat-rich diet activates a proinflammatory responseand induces insulin resistance in the hypothalamus.Endo-crinology,2005,146(10):4192-4199.
  • 8Kraegen EW,Cooney GJ,Turner N.Muscle insulinresistance:A case of fat overconsumption,not mito-chondrial dysfunction.PNAS,2008,105(22):7627-7628.
  • 9Holloszy JO.Skeletal muscle‘mitochondrial deficiency’does not mediate insulin resistance.Am J Clin Nutr,2009,89(suppl):463S-6S.
  • 10Meeusen S,Mccaffery JM,Nunnari J.Mitochondrialfusion intermediates revealed in vitro.Science,2004,305(5691):1747-1752.

同被引文献203

  • 1克日阿且,刘桠,朱建伟,朱茜如,康健,张翕宇.以“脾胃转枢”理论辨治2型糖尿病血糖波动[J].辽宁中医杂志,2022,49(6):67-69. 被引量:7
  • 2戴霞,陈青云,薛月桂,陈莹,游越西,周爱民,林健云.糖尿病运动处方的开发及量化测评[J].广西医学院学报,2008,18(2):224-226. 被引量:20
  • 3Rayaz Ahmed Malik,王玉珍.糖尿病神经病变的诊断[J].国外医学(内分泌学分册),2004,24(5):299-300. 被引量:16
  • 4李立明,饶克勤,孔灵芝,姚崇华,向红丁,翟凤英,马冠生,杨晓光,中国居民营养与健康状况调查技术执行组.中国居民2002年营养与健康状况调查[J].中华流行病学杂志,2005,26(7):478-484. 被引量:1783
  • 5蒋春笋,肖伟明,陈佺.线粒体分裂、融合与细胞凋亡[J].生物物理学报,2007,23(4):256-264. 被引量:12
  • 6P. J. Scarpace,M. Matheny,N. Tümer,K. Y. Cheng,Y. Zhang.Leptin resistance exacerbates diet-induced obesity and is associated with diminished maximal leptin signalling capacity in rats[J]. Diabetologia . 2005 (6)
  • 7H. Münzberg,M. Bj?rnholm,S. H. Bates,M. G. Myers.Leptin receptor action and mechanisms of leptin resistance[J]. CMLS Cellular and Molecular Life Sciences . 2005 (6)
  • 8Christian K Roberts,R.James Barnard,Kai Hui Liang,Nosratola D Vaziri.Effect of diet on adipose tissue and skeletal muscle VLDL receptor and LPL: implications for obesity and hyperlipidemia[J]. Atherosclerosis . 2002 (1)
  • 9Rexford S. Ahima,Jeffrey S. Flier.Leptin[J]. Annual Review of Physiology . 2000
  • 10Rube DA,van der Bliek AM.Mitochondrial morphology is dynamic and varied.Mol Cell Biochem,2004,256:331-339.

引证文献11

二级引证文献92

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