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二甲双胍改变老年人抵抗训练中骨骼肌转录组的适应性。

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

机构信息

Institute for Aging Research, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Department of Medicine, Division of Endocrinology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Aging (Albany NY). 2020 Oct 18;12(20):19852-19866. doi: 10.18632/aging.104096.

DOI:10.18632/aging.104096
PMID:33071237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7655218/
Abstract

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.

摘要

来自临床试验和观察性研究的证据表明,渐进式抗阻运动训练(PRT)和二甲双胍均可延缓多种与年龄相关的疾病。此前,我们完成了一项临床试验,测试了 14 周 PRT+二甲双胍(metPRT)与 PRT+安慰剂(plaPRT)对老年人肌肉肥大的影响。我们发现二甲双胍抑制了 PRT 引起的肌肉肥大反应。为了了解二甲双胍对 PRT 的抑制作用的潜在机制,我们分析了 23 名 metPRT 和 24 名 plaPRT 参与者的肌肉转录组。PRT 显著增加了细胞外基质重塑途径中参与的基因的表达,并下调了两组的 RNA 处理途径,但与 plaPRT 相比,二甲双胍减弱了这些途径中差异表达基因的数量。通路分析表明,metPRT 特有的基因调节与衰老相关的通路,如细胞衰老和自噬。与年轻志愿者的静息肌肉相比,老年人基线活检中的差异表达基因在 plaPRT 后的 PRT 中减少,而在 metPRT 中进一步减少。我们认为,尽管二甲双胍可能会抑制 PRT 诱导的促进肌肉肥大的途径,但在 PRT 期间联合使用二甲双胍可能对老年人肌肉中与衰老相关的途径有有益的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/c87b970b84fa/aging-12-104096-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/f7f491133c94/aging-12-104096-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/d3233e0101d6/aging-12-104096-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/c87b970b84fa/aging-12-104096-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/f7f491133c94/aging-12-104096-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/d3233e0101d6/aging-12-104096-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95d2/7655218/c87b970b84fa/aging-12-104096-g003.jpg

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