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有氧运动和脂肪酸补充对全球和基因特异性 DNA 甲基化的影响。

Impact of aerobic exercise and fatty acid supplementation on global and gene-specific DNA methylation.

机构信息

a Translational Chemical Biology Research Group, School of Sport, Exercise and Health Sciences , Loughborough University , Loughborough , UK.

b National Centre for Sport and Exercise Medicine, School of Sport, Exercise and Health Sciences , Loughborough University , Loughborough , UK.

出版信息

Epigenetics. 2019 Mar;14(3):294-309. doi: 10.1080/15592294.2019.1582276. Epub 2019 Mar 18.

Abstract

Lifestyle interventions, including exercise and dietary supplementation, can modify DNA methylation and exert health benefits; however, the underlying mechanisms are poorly understood. Here we investigated the impact of acute aerobic exercise and the supplementation of omega-3 polyunsaturated fatty acids (n-3 PUFA) and extra virgin olive oil (EVOO) on global and gene-specific (PPARGC1A, IL6 and TNF) DNA methylation, and DNMT mRNA expression in leukocytes of disease-free individuals. Eight trained male cyclists completed an exercise test before and after a four-week supplementation of n-3 PUFA and EVOO in a double-blind, randomised, repeated measures design. Exercise triggered global hypomethylation (Pre 79.2%; Post 78.7%; p = 0.008), alongside, hypomethylation (Pre 6.9%; Post 6.3%; p < 0.001) and increased mRNA expression of PPARGC1A (p < 0.001). Associations between PPARGC1A methylation and exercise performance were also detected. An interaction between supplement and trial was detected for a single CpG of IL6 indicating increased DNA methylation following n-3 PUFA and decreased methylation following EVOO (p = 0.038). Global and gene-specific DNA methylation associated with markers of inflammation and oxidative stress. The supplementation of EVOO reduced DNMT1 mRNA expression compared to n-3 PUFA supplementation (p = 0.048), whereas, DNMT3a (p = 0.018) and DNMT3b (p = 0.046) mRNA expression were decreased following exercise. In conclusion, we demonstrate that acute exercise and dietary supplementation of n-3 PUFAs and EVOO induce DNA methylation changes in leukocytes, potentially via the modulation of DNMT mRNA expression. Future studies are required to further elucidate the impact of lifestyle interventions on DNA methylation.

摘要

生活方式干预,包括运动和饮食补充,可以改变 DNA 甲基化并产生健康益处;然而,其潜在机制尚不清楚。在这里,我们研究了急性有氧运动以及补充 ω-3 多不饱和脂肪酸(n-3 PUFA)和特级初榨橄榄油(EVOO)对白细胞全基因组和特定基因(PPARGC1A、IL6 和 TNF)DNA 甲基化以及 DNMT mRNA 表达的影响,这些白细胞均取自无疾病个体。8 名训练有素的男性自行车运动员在双盲、随机、重复测量设计中,在四周补充 n-3 PUFA 和 EVOO 前后完成了一项运动测试。运动导致全基因组低甲基化(Pre 79.2%;Post 78.7%;p = 0.008),同时 PPARGC1A 也发生低甲基化(Pre 6.9%;Post 6.3%;p < 0.001),mRNA 表达增加(p < 0.001)。还检测到 PPARGC1A 甲基化与运动表现之间的关联。IL6 的一个 CpG 检测到补充剂和试验之间的相互作用,表明 n-3 PUFA 后 DNA 甲基化增加,EVOO 后甲基化减少(p = 0.038)。全基因组和特定基因的 DNA 甲基化与炎症和氧化应激标志物相关。与 n-3 PUFA 补充相比,特级初榨橄榄油补充降低了 DNMT1 mRNA 表达(p = 0.048),而运动后 DNMT3a(p = 0.018)和 DNMT3b(p = 0.046)mRNA 表达降低。总之,我们证明急性运动和饮食补充 n-3 PUFAs 和 EVOO 会导致白细胞中的 DNA 甲基化变化,这可能是通过调节 DNMT mRNA 表达实现的。需要进一步的研究来阐明生活方式干预对 DNA 甲基化的影响。

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