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


Journal

Archives of biochemistry and biophysics
ISSN: 1096-0384
Titre abrégé: Arch Biochem Biophys
Pays: United States
ID NLM: 0372430

Informations de publication

Date de publication:
15 10 2020
Historique:
received: 29 04 2020
revised: 14 07 2020
accepted: 16 07 2020
pubmed: 28 7 2020
medline: 20 11 2020
entrez: 26 7 2020
Statut: ppublish

Résumé

(-)-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.

Identifiants

pubmed: 32710883
pii: S0003-9861(20)30520-8
doi: 10.1016/j.abb.2020.108511
pii:
doi:

Substances chimiques

MIRN486 microRNA, mouse 0
MicroRNAs 0
Mstn protein, mouse 0
Muscle Proteins 0
Myostatin 0
Tea 0
Catechin 8R1V1STN48
epigallocatechin gallate BQM438CTEL

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

108511

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Yun-Ching Chang (YC)

Department of Life Sciences, National Cheng Kung University, Tainan, Taiwan; Department of Nursing, Shu-Zen College of Medicine and Management, Kaohsiung, Taiwan. Electronic address: ychang@ms.szmc.edu.tw.

Hung-Wen Liu (HW)

Department of Physical Education, National Taiwan Normal University, Taipei, Taiwan. Electronic address: hwliu@ntnu.edu.tw.

Yin-Ching Chan (YC)

Department of Food and Nutrition, Providence University, Taichung, Taiwan. Electronic address: ycchan@pu.edu.tw.

Shu-Hui Hu (SH)

Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung, Taiwan. Electronic address: suhuhu@cc.kmu.edu.tw.

Ming-Yi Liu (MY)

Department of Long Term Care, Wu Feng University, Chiayi County, Taiwan; Department of Senior Welfare and Services, Southern Taiwan University of Science and Technology. No. 1, Nan-Tai Street, Yongkang Dist., Tainan City, Taiwan. Electronic address: liumiyi@gmail.com.

Sue-Joan Chang (SJ)

Department of Life Sciences, National Cheng Kung University, Tainan, Taiwan. Electronic address: sjchang@mail.ncku.edu.tw.

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Classifications MeSH