Life-long spontaneous exercise does not prolong lifespan but improves health span in mice.

Rebeca Garcia-Valles, Mari Carmen Gomez-Cabrera, Leocadio Rodriguez-Mañas, Francisco J Garcia-Garcia, Ana Diaz, Inma Noguera, Gloria Olaso-Gonzalez, Jose Viña
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引用次数: 81

Abstract

Background: Life expectancy at birth in the first world has increased from 35 years at the beginning of the 20th century to more than 80 years now. The increase in life expectancy has resulted in an increase in age-related diseases and larger numbers of frail and dependent people. The aim of our study was to determine whether life-long spontaneous aerobic exercise affects lifespan and healthspan in mice.

Results: Male C57Bl/6J mice, individually caged, were randomly assigned to one of two groups: sedentary (n = 72) or spontaneous wheel-runners (n = 72). We evaluated longevity and several health parameters including grip strength, motor coordination, exercise capacity (VO2max) and skeletal muscle mitochondrial biogenesis. We also measured the cortical levels of the brain-derived neurotrophic factor (BDNF), a neurotrophin associated with brain plasticity. In addition, we measured systemic oxidative stress (malondialdehyde and protein carbonyl plasma levels) and the expression and activity of two genes involved in antioxidant defense in the liver (that is, glutathione peroxidase (GPx) and manganese superoxide dismutase (Mn-SOD)). Genes that encode antioxidant enzymes are considered longevity genes because their over-expression may modulate lifespan. Aging was associated with an increase in oxidative stress biomarkers and in the activity of the antioxidant enzymes, GPx and Mn-SOD, in the liver in mice. Life-long spontaneous exercise did not prolong longevity but prevented several signs of frailty (that is, decrease in strength, endurance and motor coordination). This improvement was accompanied by a significant increase in the mitochondrial biogenesis in skeletal muscle and in the cortical BDNF levels.

Conclusion: Life-long spontaneous exercise does not prolong lifespan but improves healthspan in mice. Exercise is an intervention that delays age-associated frailty, enhances function and can be translated into the clinic.

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终生自发运动不能延长小鼠寿命,但能提高健康寿命。
背景:第一世界的出生时预期寿命已从20世纪初的35岁增加到现在的80多岁。预期寿命的延长导致与年龄有关的疾病增加,体弱多病和依赖他人的人数增多。我们研究的目的是确定终身自发有氧运动是否影响小鼠的寿命和健康寿命。结果:单独笼养的雄性C57Bl/6J小鼠随机分为两组:久坐组(n = 72)和自发轮跑组(n = 72)。我们评估了寿命和一些健康参数,包括握力、运动协调、运动能力(VO2max)和骨骼肌线粒体生物发生。我们还测量了脑源性神经营养因子(BDNF)的皮质水平,BDNF是一种与大脑可塑性相关的神经营养因子。此外,我们测量了系统性氧化应激(丙二醛和蛋白羰基血浆水平)以及肝脏中参与抗氧化防御的两个基因(即谷胱甘肽过氧化物酶(GPx)和锰超氧化物歧化酶(Mn-SOD))的表达和活性。编码抗氧化酶的基因被认为是长寿基因,因为它们的过度表达可能会调节寿命。衰老与小鼠肝脏中氧化应激生物标志物和抗氧化酶GPx和Mn-SOD活性的增加有关。终生自发运动并不能延长寿命,但可以防止一些虚弱的迹象(即力量、耐力和运动协调能力的下降)。这种改善伴随着骨骼肌线粒体生物发生和皮质BDNF水平的显著增加。结论:终身自发运动不能延长小鼠寿命,但能提高健康寿命。锻炼是一种干预,可以延缓与年龄相关的虚弱,增强功能,并可以转化为临床。
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