Translational Chemical Biology Research Group, School of Sport, Exercise and Health Sciences, Loughborough University, Epinal Way, Loughborough LE11 3TU, UK.
National Centre for Sport and Exercise Medicine, School of Sport, Exercise and Health Sciences, Loughborough University, Epinal Way, Loughborough LE11 3TU, UK.
Genes (Basel). 2023 Feb 13;14(2):478. doi: 10.3390/genes14020478.
Physical inactivity and a poor diet increase systemic inflammation, while chronic inflammation can be reduced through exercise and nutritional interventions. The mechanisms underlying the impacts of lifestyle interventions on inflammation remain to be fully explained; however, epigenetic modifications may be critical. The purpose of our study was to investigate the impacts of eccentric resistance exercise and fatty acid supplementation on DNA methylation and mRNA expression of and in skeletal muscle and leukocytes. Eight non-resistance exercise-trained males completed three bouts of isokinetic eccentric contractions of the knee extensors. The first bout occurred at baseline, the second occurred following a three-week supplementation of either omega-3 polyunsaturated fatty acid or extra virgin olive oil and the final bout occurred after eight-weeks of eccentric resistance training and supplementation. Acute exercise decreased skeletal muscle DNA methylation by 5% ( = 0.031), whereas DNA methylation increased by 3% ( = 0.01). Leukocyte DNA methylation was unchanged following exercise ( > 0.05); however, three hours post-exercise the DNA methylation decreased by 2% ( = 0.004). In skeletal muscle, increased and mRNA expression levels were identified immediately post-exercise ( < 0.027); however, the leukocyte mRNA expression was unchanged. Associations between DNA methylation and markers of exercise performance, inflammation and muscle damage were identified ( < 0.05). Acute eccentric resistance exercise is sufficient to induce tissue-specific DNA methylation modifications to and ; however, neither eccentric training nor supplementation was sufficient to further modify the DNA methylation.
缺乏身体活动和不良饮食会增加全身炎症,而运动和营养干预可以减少慢性炎症。生活方式干预对炎症影响的机制仍有待充分解释;然而,表观遗传修饰可能是关键。我们的研究目的是调查离心抗阻运动和脂肪酸补充对骨骼肌和白细胞中 和 基因的 DNA 甲基化和 mRNA 表达的影响。8 名非抗阻运动训练男性完成了 3 次膝关节伸肌等速离心收缩。第一回合在基线时进行,第二回合在补充欧米伽-3 多不饱和脂肪酸或特级初榨橄榄油 3 周后进行,第三回合在进行 8 周离心抗阻训练和补充后进行。急性运动使骨骼肌 基因的 DNA 甲基化减少了 5%(=0.031),而 基因的 DNA 甲基化增加了 3%(=0.01)。运动后白细胞的 DNA 甲基化没有变化(>0.05);然而,运动后 3 小时, 基因的 DNA 甲基化减少了 2%(=0.004)。在骨骼肌中,运动后立即发现 和 mRNA 表达水平增加(<0.027);然而,白细胞的 mRNA 表达没有变化。DNA 甲基化与运动表现、炎症和肌肉损伤标志物之间存在相关性(<0.05)。急性离心抗阻运动足以诱导 和 基因的组织特异性 DNA 甲基化修饰;然而,离心训练和补充都不足以进一步修饰 DNA 甲基化。