Toledo Frederico G S, Watkins Simon, Kelley David E
Division of Endocrinology and Metabolism, Department of Medicine, University of Pittsburgh School of Medicine, 807N Montefiore Hospital, 3459 5th Avenue, Pittsburgh, PA 15213, USA.
J Clin Endocrinol Metab. 2006 Aug;91(8):3224-7. doi: 10.1210/jc.2006-0002. Epub 2006 May 9.
In obesity, skeletal muscle insulin resistance may be associated with smaller mitochondria.
Our objective was to examine the effect of a lifestyle-modification intervention on the content and morphology of skeletal muscle mitochondria and its relationship to insulin sensitivity in obese, insulin-resistant subjects.
In this prospective interventional study, intermyofibrillar mitochondrial content and size were quantified by transmission electron microscopy with quantitative morphometric analysis of biopsy samples from vastus lateralis muscle. Systemic insulin sensitivity was measured with euglycemic hyperinsulinemic clamps.
The study took place at a university-based clinical research center.
Eleven sedentary, overweight/obese volunteers without diabetes participated in the study.
Intervention included 16 wk of aerobic training with dietary restriction of 500-1000 kcal/d.
We assessed changes in mitochondrial content and size and changes in insulin sensitivity.
The percentage of myofiber volume occupied by mitochondria significantly increased from 3.70 +/- 0.31 to 4.87 +/- 0.33% after intervention (P = 0.01). The mean individual increase was 42.5 +/- 18.1%. There was also a change in the mean cross-sectional mitochondrial area, increasing from a baseline of 0.078 +/- 0.007 to 0.091 +/- 0.007 microm(2) (P < 0.01), a mean increase of 19.2 +/- 6.1% per subject. These changes in mitochondrial size and content highly correlated with improvements in insulin resistance (r = 0.68 and 0.72, respectively; P = 0.01).
A combined intervention of weight loss and physical activity in previously sedentary obese adults is associated with enlargement of mitochondria and an increase in the mitochondrial content in skeletal muscle. These findings indicate that in obesity with insulin resistance, ultrastructural mitochondrial plasticity is substantially retained and, importantly, that changes in the morphology of mitochondria are associated with improvements in insulin resistance.
在肥胖症中,骨骼肌胰岛素抵抗可能与较小的线粒体有关。
我们的目的是研究生活方式改变干预对肥胖、胰岛素抵抗受试者骨骼肌线粒体含量和形态的影响及其与胰岛素敏感性的关系。
在这项前瞻性干预研究中,通过透射电子显微镜对来自股外侧肌活检样本进行定量形态分析,以量化肌原纤维间线粒体的含量和大小。采用正常血糖高胰岛素钳夹技术测量全身胰岛素敏感性。
该研究在一个大学临床研究中心进行。
11名无糖尿病的久坐不动、超重/肥胖志愿者参与了该研究。
干预包括16周的有氧运动训练以及每天500 - 1000千卡的饮食限制。
我们评估了线粒体含量和大小的变化以及胰岛素敏感性的变化。
干预后,线粒体占肌纤维体积的百分比从3.70±0.31显著增加至4.87±0.33%(P = 0.01)。个体平均增加量为42.5±18.1%。平均线粒体横截面积也有变化,从基线的0.078±0.007增加至0.091±0.007平方微米(P < 0.01),每个受试者平均增加量为19.2±6.1%。线粒体大小和含量的这些变化与胰岛素抵抗的改善高度相关(分别为r = 0.68和0.72;P = 0.01)。
对于先前久坐不动的肥胖成年人,减肥与体育活动相结合的干预措施与线粒体增大以及骨骼肌线粒体含量增加有关。这些发现表明,在伴有胰岛素抵抗的肥胖症中,线粒体超微结构可塑性基本得以保留,重要的是,线粒体形态的变化与胰岛素抵抗的改善有关。