Metformin alters skeletal muscle transcriptome adaptations to resistance training in older adults

被引:26
|
作者
Kulkarni, Ameya S. [1 ,2 ]
Peck, Bailey D. [3 ]
Walton, R. Grace [3 ]
Kern, Philip A. [4 ,5 ]
Mar, Jessica C. [6 ]
Windham, Samuel T. [7 ,8 ]
Bamman, Marcas M. [7 ,9 ,10 ]
Barzilai, Nir [1 ,2 ]
Peterson, Charlotte A. [3 ]
机构
[1] Albert Einstein Coll Med, Inst Aging Res, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Div Endocrinol, Bronx, NY 10461 USA
[3] Univ Kentucky, Coll Hlth Sci, Ctr Muscle Biol, Lexington, KY 40504 USA
[4] Univ Kentucky, Dept Internal Med, Div Endocrinol, Lexington, KY 40504 USA
[5] Univ Kentucky, Barnstable Brown Diabet & Obes Ctr, Lexington, KY 40504 USA
[6] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld, Australia
[7] Univ Alabama Birmingham, Ctr Exercise Med, Birmingham, AL 35233 USA
[8] Univ Alabama Birmingham, Sch Med, Dept Surg, Birmingham, AL 35233 USA
[9] Univ Alabama Birmingham, Sch Med, Dept Cell Dev & Integrat Biol, Birmingham, AL 35233 USA
[10] Birmingham VA Med Ctr, Geriatr Res Educ & Clin Ctr, Birmingham, AL 35233 USA
来源
AGING-US | 2020年 / 12卷 / 20期
关键词
aging; metformin; strength training; exercise-drug interaction; gene expression; REPURPOSING METFORMIN; EXTRACELLULAR-MATRIX; EXERCISE; SARCOPENIA; HALLMARKS; MEN;
D O I
10.18632/aging.104096
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Evidence from clinical trials and observational studies suggests that both progressive resistance exercise training (PRT) and metformin delay a variety of age-related morbidities. Previously, we completed a clinical trial testing the effects of 14 weeks of PRT + metformin (metPRT) compared to PRT with placebo (plaPRT) on muscle hypertrophy in older adults. We found that metformin blunted PRT-induced muscle hypertrophic response. To understand potential mechanisms underlying the inhibitory effect of metformin on PRT, we analyzed the muscle transcriptome in 23 metPRT and 24 plaPRT participants. PRT significantly increased expression of genes involved in extracellular matrix remodeling pathways, and downregulated RNA processing pathways in both groups, however, metformin attenuated the number of differentially expressed genes within these pathways compared to plaPRT. Pathway analysis showed that genes unique to metPRT modulated aging-relevant pathways, such as cellular senescence and autophagy. Differentially expressed genes from baseline biopsies in older adults compared to resting muscle from young volunteers were reduced following PRT in plaPRT and were further reduced in metPRT. We suggest that although metformin may blunt pathways induced by PRT to promote muscle hypertrophy, adjunctive metformin during PRT may have beneficial effects on aging-associated pathways in muscle from older adults.
引用
收藏
页码:19852 / 19866
页数:15
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