Proteomic Analysis of Skeletal Muscle and White Adipose Tissue after Aerobic Exercise Training in High Fat Diet Induced Obese Mice

Author:

Chou Tzu-Jung12ORCID,Lu Chia-Wen234ORCID,Lin Li-Yu56ORCID,Hsu Yi-Ju5,Huang Chi-Chang5ORCID,Huang Kuo-Chin134ORCID

Affiliation:

1. Department of Family Medicine, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu 300, Taiwan

2. Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei 100, Taiwan

3. Department of Family Medicine, National Taiwan University Hospital, Taipei 100, Taiwan

4. Department of Family Medicine, National Taiwan University College of Medicine, Taipei 100, Taiwan

5. Graduate Institute of Sports Science, National Taiwan Sport University, Taoyuan 333, Taiwan

6. Graduate Institute of Physiology, National Taiwan University College of Medicine, Taipei 100, Taiwan

Abstract

Obesity is associated with excessive fat accumulation in adipose tissue and other organs, such as skeletal muscle, whereas aerobic exercise (AE) plays an important role in managing obesity through profound protein regulation. Our study aimed to investigate the impact of AE on proteomic changes in both the skeletal muscle and the epididymal fat pad (EFP) of high-fat-diet-induced obese mice. Bioinformatic analyses were performed on differentially regulated proteins using gene ontology enrichment analysis and ingenuity pathway analysis. Eight weeks of AE significantly reduced body weight, increased the serum FNDC5 level, and improved the homeostatic model assessment of insulin resistance. A high-fat diet caused alterations in a subset of proteins involved in the sirtuin signaling pathway and the production of reactive oxygen species in both skeletal muscle and EFP, leading to insulin resistance, mitochondrial dysfunction, and inflammation. On the other hand, AE upregulated skeletal muscle proteins (NDUFB5, NDUFS2, NDUFS7, ETFD, FRDA, and MKNK1) that enhance mitochondrial function and insulin sensitivity. Additionally, the upregulation of LDHC and PRKACA and the downregulation of CTBP1 in EFP can promote the browning of white adipose tissue with the involvement of FNDC5/irisin in the canonical pathway. Our study provides insights into AE-induced molecular responses and may help further develop exercise-mimicking therapeutic targets.

Funder

Ministry of Science and Technology of Taiwan

National Taiwan University Hospital Hsin Chu Branch

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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