Abstract
Background: Reduced physical activity and increased intake of calorically-dense diets are the main risk factors for obesity, glucose intolerance, and type 2 diabetes. Chronic overnutrition and hyperglycemia can alter gene expression, contributing to long-term obesity complications. While caloric restriction can reduce obesity and glucose intolerance, it is currently unknown whether it can effectively reprogram transcriptome to a pre-obesity level. The present study addressed this question by the preliminary examination of the transcriptional dynamics in skeletal muscle after exposure to overnutrition and following caloric restriction. Results: Six male rhesus macaques of 12-13 years of age consumed a high-fat western-style diet for 6 months and then were calorically restricted for 4 months without exercise. Skeletal muscle biopsies were subjected to longitudinal gene expression analysis using next-generation whole-genome RNA sequencing. In spite of significant weight loss and normalized insulin sensitivity, the majority of WSD-induced (n = 457) and WSD-suppressed (n = 47) genes remained significantly dysregulated after caloric restriction (FDR ≤0.05). The MetacoreTM pathway analysis reveals that western-style diet induced the sustained activation of the transforming growth factor-β gene network, associated with extracellular matrix remodeling, and the downregulation of genes involved in muscle structure development and nutritional processes. Conclusions: Western-style diet, in the absence of exercise, induced skeletal muscle transcriptional programing, which persisted even after insulin resistance and glucose intolerance were completely reversed with caloric restriction.
| Original language | English |
|---|---|
| Article number | 411 |
| Journal | BMC Genomics |
| Volume | 18 |
| Issue number | 1 |
| DOIs | |
| State | Published - May 25 2017 |
Bibliographical note
Publisher Copyright:© 2017 The Author(s).
Funding
This work was supported by National Institutes of Health Grants R21 AG047543 (to O.V.), P51 OD011092 for the operation of the Oregon National Primate Research Center, AG043896-01 (to I.M.), and the National Science Foundation Grant ABI-0957099 (to I.M.). These funding sources covered animal and housing costs, labor, experimental procedures, data analysis, computational and publication fees.
| Funders | Funder number |
|---|---|
| National Science Foundation Arctic Social Science Program | ABI-0957099 |
| National Institutes of Health (NIH) | R21 AG047543, P51 OD011092 |
| National Institute on Aging | R21AG043896 |
| Oregon National Primate Research Center | AG043896-01 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Caloric restriction
- High-fat diet
- Insulin resistance
- Obesity
- Skeletal muscle
ASJC Scopus subject areas
- Biotechnology
- Genetics
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