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肥胖个体的骨骼肌中是否存在代谢程序?

Is there a metabolic program in the skeletal muscle of obese individuals?

作者信息

Houmard Joseph A, Pories Walter J, Dohm G Lynis

机构信息

Department of Exercise and Sport Science, College of Health and Human Performance, East Carolina University, Greenville, NC 27834, USA.

出版信息

J Obes. 2011;2011:250496. doi: 10.1155/2011/250496. Epub 2011 Apr 26.

Abstract

Severe obesity (BMI ≥ 40 kg/m(2)) is associated with multiple defects in skeletal muscle which contribute to insulin resistance and a reduction in fatty acid oxidation (FAO) in this tissue. These metabolic derangements are retained in human skeletal muscle cells raised in culture. Together, these findings are indicative of a dysfunctional global metabolic program with severe obesity which is of an epigenetic or genetic origin. Weight loss via gastric bypass surgery can "turn off" and/or correct components of this metabolic program as insulin sensitivity is restored; however, the impairment in FAO in skeletal muscle remains evident. Physical activity can improve FAO and insulin action, indicating that this patient population is not exercise resistant and that exercise offers a pathway to circumvent the abnormal program. Findings presented in this review will hopefully increase the understanding of and aid in preventing and/or treating the severely obese condition.

摘要

重度肥胖(体重指数≥40kg/m²)与骨骼肌的多种缺陷相关,这些缺陷会导致胰岛素抵抗以及该组织中脂肪酸氧化(FAO)减少。这些代谢紊乱在培养的人骨骼肌细胞中依然存在。综合来看,这些发现表明重度肥胖存在一个源于表观遗传或遗传的功能失调的整体代谢程序。通过胃旁路手术减重可在恢复胰岛素敏感性的同时“关闭”和/或纠正该代谢程序的某些组成部分;然而,骨骼肌中脂肪酸氧化的损害依然明显。体育活动可改善脂肪酸氧化和胰岛素作用,这表明该患者群体并非运动抵抗型,且运动提供了一条规避异常程序的途径。本综述中呈现的研究结果有望增进对重度肥胖症的理解,并有助于预防和/或治疗该疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b175/3092539/62be0cbf1e80/JOBES2011-250496.001.jpg

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