Comprehensive interrogation of human skeletal muscle reveals a dissociation between insulin resistance and mitochondrial capacity

Author:

Whytock Katie L.1ORCID,Pino Maria F.1,Sun Yifei2,Yu GongXin1,De Carvalho Flavia G.1,Yeo Reichelle X.1ORCID,Vega Rick B.1,Parmar Gaganvir3,Divoux Adeline1,Kapoor Nidhi1,Yi Fancaho1,Cornnell Heather1,Patten David A.3,Harper Mary-Ellen3ORCID,Gardell Stephen J.1,Smith Steven R.1,Walsh Martin J.2,Sparks Lauren M.1ORCID

Affiliation:

1. Translational Research Institute, AdventHealth, Orlando, Florida, United States

2. Icahn School of Medicine at Mount Sinai, New York City, New York, United States

3. Department of Biochemistry Microbiology and Immunology, Faculty of Medicine, Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada

Abstract

Whether impaired mitochondrial capacity contributes to skeletal muscle insulin resistance is debated. Our multifactorial analysis shows no differences in skeletal muscle mitochondrial content, mitochondrial capacity, and mitochondrial molecular profiles between obese individuals with and without T2D that had comparable levels of confounding factors (BMI, age, aerobic capacity). We highlight that lean, active individuals have enhanced skeletal muscle mitochondrial capacity that is also reflected at the level of DNA methylation and gene transcription.

Funder

American Diabetes Association

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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