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绿茶多酚表没食子儿茶素-3-没食子酸酯通过调节 miR-486-5p 和肌肉生长抑制素来减轻与年龄相关的肌肉损失。

The green tea polyphenol epigallocatechin-3-gallate attenuates age-associated muscle loss via regulation of miR-486-5p and myostatin.

机构信息

Department of Life Sciences, National Cheng Kung University, Tainan, Taiwan; Department of Nursing, Shu-Zen College of Medicine and Management, Kaohsiung, Taiwan.

Department of Physical Education, National Taiwan Normal University, Taipei, Taiwan.

出版信息

Arch Biochem Biophys. 2020 Oct 15;692:108511. doi: 10.1016/j.abb.2020.108511. Epub 2020 Jul 22.

Abstract

(-)-Epigallocatechin-3-gallate (EGCG), the most abundant catechin component in green tea, has been reported to attenuate age-associated insulin resistance, lipogenesis and loss of muscle mass through restoring Akt activity in skeletal muscle in our previous and present studies. Accumulated data has suggested that polyphenols regulate signaling pathways involved in aging process such as inflammation and oxidative stress via modulation of miRNA expression. Here we found that miRNA-486-5p was significantly decreased in both aged senescence accelerated mouse-prone 8 (SAMP8) mice and late passage C2C12 cells. Thus, we further investigated the regulatory effect of EGCG on miRNA-486-5p expression in age-regulated muscle loss. SAMP8 mice were fed with chow diet containing without or with 0.32% EGCG from aged 32 weeks for 8 weeks. Early passage (<12 passages) and late passage (>30 passages) of C2C12 cells were treated without or with EGCG at concentrations of 50 μM for 24h. Our data showed that EGCG supplementation increased miRNA-486-5p expression in both aged SAMP8 mice and late passage C2C12 cells. EGCG stimulated AKT phosphorylation and inhibited FoxO1a-mediated MuRF1 and Atrogin-1 transcription via up-regulating the expression of miR-486 in skeletal muscle of 40-wk-old SAMP8 mice as well as late passage C2C12 cells. In addition, myostatin expression was increased in late passage C2C12 cells and anti-myostatin treatment upregulated the expression of miR-486-5p. Our results identify a unique mechanism of a dietary constituent of green tea and suggest that use of EGCG or compounds derived from it attenuates age-associated muscle loss via myostatin/miRNAs/ubiquitin-proteasome signaling.

摘要

(-)-表没食子儿茶素没食子酸酯(EGCG)是绿茶中含量最丰富的儿茶素成分,在我们之前和现在的研究中,已被报道通过恢复骨骼肌中的 Akt 活性来减轻与年龄相关的胰岛素抵抗、脂肪生成和肌肉质量损失。积累的数据表明,多酚通过调节 miRNA 表达来调节与衰老过程相关的信号通路,如炎症和氧化应激。在这里,我们发现 miRNA-486-5p 在老年快速衰老小鼠-prone 8(SAMP8)小鼠和晚期传代 C2C12 细胞中均显著降低。因此,我们进一步研究了 EGCG 对年龄相关肌肉减少症中 miRNA-486-5p 表达的调节作用。SAMP8 小鼠从 32 周龄起喂食含或不含 0.32% EGCG 的标准饮食 8 周。早期传代(<12 代)和晚期传代(>30 代)的 C2C12 细胞用 50μM 的 EGCG 处理 24 小时。我们的数据表明,EGCG 补充剂增加了老年 SAMP8 小鼠和晚期传代 C2C12 细胞中 miRNA-486-5p 的表达。EGCG 通过上调 miR-486 的表达,刺激 AKT 磷酸化并抑制 FoxO1a 介导的 MuRF1 和 Atrogin-1 转录,从而增加 40 周龄 SAMP8 小鼠和晚期传代 C2C12 细胞的骨骼肌中 miR-486-5p 的表达。此外,晚期传代 C2C12 细胞中的肌肉生长抑制素表达增加,抗肌肉生长抑制素治疗上调了 miR-486-5p 的表达。我们的研究结果确定了绿茶饮食成分的一种独特机制,并表明使用 EGCG 或其衍生化合物可通过肌肉生长抑制素/miRNA/泛素-蛋白酶体信号通路来减轻与年龄相关的肌肉减少症。

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