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Preventive effects of the butanol fraction of Justicia procumbens L. against dexamethasone-induced muscle atrophy in C2C12 myotubesopen access

Authors
Kim, Jae -YongKim, Hye MiKim, Ji HoonLee, Ju-HeeZhang, KaixuanGuo, ShuoLee, Do HyunGao, Eun MeiSon, Rak HoKim, Seong-MinKim, Chul Young
Issue Date
Nov-2022
Publisher
Cell Press
Keywords
Justicia procumbens L; Muscle atrophy; Dexamethasone; Protein degradation
Citation
Heliyon, v.8, no.11, pp 1 - 9
Pages
9
Indexed
SCIE
SCOPUS
Journal Title
Heliyon
Volume
8
Number
11
Start Page
1
End Page
9
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111572
DOI
10.1016/j.heliyon.2022.e11597
ISSN
2405-8440
Abstract
Skeletal muscle atrophy is associated with many diseases including cancer, inflammatory diseases, neuromuscular diseases, and acute critical illness. Justicia procumbens L. has been used as a herbal remedy, but the pharmaco-logical effect of J. procumbens on muscle atrophy has not yet been reported. Herein, we investigate the anti -atrophic effect of the n-butanol fraction of J. procumbens (JPBuFr) on dexamethasone (DEX)-induced muscle at-rophy in C2C12 myotubes. The myotubes diameter, MHC positive area, ROS production, and mitochondria contents were observed under a fluorescence microscope, and various proteins related to degradation or synthesis were analyzed by western blots. JPBuFr significantly attenuated a reduction of myotube diameter, mitochondrial content, ATP level, myosin heavy chain, and myogenin expression induced by DEX. Furthermore, co-treatment of DEX and JPBuFr not only increased phosphorylation of Akt, mTOR, and p70S6K proteins but also decreased reactive oxygen species production and expression of protein degradation factors (MuRF1, Atrogin-1, FoxO3a) compared to DEX treatment. These results suggest that JPBuFr may provide potential protective effects against muscle atrophy, giving it potential for the development of anti-atrophic health functional foods.
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