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肥胖人群中中等强度运动和体重减轻诱导的骨骼肌线粒体生物合成特征

Characteristics of skeletal muscle mitochondrial biogenesis induced by moderate-intensity exercise and weight loss in obesity.

作者信息

Menshikova Elizabeth V, Ritov Vladimir B, Ferrell Robert E, Azuma Koichiro, Goodpaster Bret H, Kelley David E

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

J Appl Physiol (1985). 2007 Jul;103(1):21-7. doi: 10.1152/japplphysiol.01228.2006. Epub 2007 Mar 1.

Abstract

There are fewer mitochondria and a reduced oxidative capacity in skeletal muscle in obesity. Moderate-intensity physical activity combined with weight loss increase oxidative enzyme activity in obese sedentary adults; however, this adaptation occurs without a significant increase in mitochondrial DNA (mtDNA), which is unlike the classic pattern of mitochondrial biogenesis induced by vigorous activity. The objective of this study was to examine the hypothesis that the mitochondrial adaptation to moderate-intensity exercise and weight loss in obesity induces increased mitochondrial cristae despite a lack of mtDNA proliferation. Content of cardiolipin and mtDNA and enzymatic activities of the electron transport chain (ETC) and tricarboxylic acid cycle were measured in biopsy samples of vastus lateralis muscle obtained from sedentary obese men and women before and following a 4-mo walking intervention combined with weight loss. Cardiolipin increased by 60% from 47 +/- 4 to 74 +/- 8 microg/mU CK (P < 0.01), but skeletal muscle mtDNA content did not change significantly (1,901 +/- 363 to 2,169 +/- 317 Rc, where Rc is relative copy number of mtDNA per diploid nuclear genome). Enzyme activity of the ETC increased (P < 0.01); that for rotenone-sensitive NADH-oxidase (96 +/- 1%) increased more than for ubiquinol-oxidase (48 +/- 6%). Activities for citrate synthase and succinate dehydrogenase increased by 29 +/- 9% and 40 +/- 6%, respectively. In conclusion, moderate-intensity physical activity combined with weight loss induces skeletal muscle mitochondrial biogenesis in previously sedentary obese men and women, but this response occurs without mtDNA proliferation and may be characterized by an increase in mitochondrial cristae.

摘要

肥胖状态下,骨骼肌中的线粒体数量减少且氧化能力降低。对于久坐不动的肥胖成年人,中等强度的体育活动与体重减轻相结合可增加氧化酶活性;然而,这种适应性变化并未伴随线粒体DNA(mtDNA)显著增加,这与剧烈运动诱导的经典线粒体生物发生模式不同。本研究的目的是检验以下假设:肥胖人群线粒体对中等强度运动和体重减轻的适应性变化会导致线粒体嵴增加,尽管mtDNA没有增殖。在一项为期4个月的步行干预并结合体重减轻前后,对久坐不动的肥胖男性和女性的股外侧肌活检样本进行检测,测量心磷脂含量、mtDNA以及电子传递链(ETC)和三羧酸循环的酶活性。心磷脂含量从47±4微克/毫单位肌酸激酶增加到74±8微克/毫单位肌酸激酶,增幅为60%(P<0.01),但骨骼肌mtDNA含量没有显著变化(从1901±363到2169±317 Rc,其中Rc是每个二倍体核基因组中mtDNA的相对拷贝数)。ETC的酶活性增加(P<0.01);对鱼藤酮敏感的NADH氧化酶活性增加(96±1%),高于泛醇氧化酶(48±6%)。柠檬酸合酶和琥珀酸脱氢酶的活性分别增加了29±9%和40±6%。总之,中等强度的体育活动与体重减轻相结合可诱导久坐不动的肥胖男性和女性骨骼肌发生线粒体生物发生,但这种反应不伴随mtDNA增殖,其特征可能为线粒体嵴增加。

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