Gardeniae Fructus Extract Alleviates Dexamethasone-Induced Muscle Atrophy in Mice

被引:2
|
作者
Lee, Jin A. [1 ]
Lee, Se Hui [1 ]
Shin, Mi-Rae [1 ]
Park, Hae-Jin [2 ]
Roh, Seong-Soo [1 ,3 ]
机构
[1] Daegu Haany Univ, Coll Korean Med, Dept Herbol, Daegu, South Korea
[2] DHU Bio Convergence Testing Ctr, Gyongsan, South Korea
[3] Daegu Haany Univ, Coll Korean Med, 136 Shinchendong Ro, Daegu 42158, South Korea
基金
新加坡国家研究基金会;
关键词
dexamethasone; Gardeniae Fructus; muscle atrophy; OXIDATIVE STRESS; ATROGIN-1;
D O I
10.1089/jmf.2022.K.0038
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Muscle atrophy (MA) is a case in which protein degeneration occurs excessively due to an imbalance between protein synthesis and breakdown, and is characterized by decreased muscle mass and weakened muscle strength. Despite mounting concern about MA, the number of patients with MA is increasing every year. The aim of the present study was to assess the impact of Gardeniae Fructus (GF) hot water extract on dexamethasone (DEX)-induced MA in mice. C57BL/6N mice were grouped (n = 8) as follows: Normal mice (Normal), MA mice were treated with distilled water (Control), MA mice were treated with GF 100 mg/kg (GF100), MA mice were treated with GF 200 mg/kg (GF200). For 10 days, DEX (25 mg/kg body weight, i.p.) injection was used to induce MA, and GF was administered. GF treatment restored the muscle weight decreased due to MA, and in particular, the weights of EDL+TA and Sol were significantly increased in the GF200 group. Also, it was confirmed that the swimming time was improved in the GF200 group. In addition, the expression of NADPH oxidase related to oxidative stress was significantly reduced, and protective (insulin-like growth factor I/phosphoinositide 3-kinase/protein kinase B pathway) and catabolic (AMP-activated kinase [AMPK]/sirtuin 1 [SIRT1]/proliferator-activated receptor-gamma coactivator-1 alpha (PGC-1 alpha)-forkhead box O (FOXO) pathway) pathways were significantly modulated. These results demonstrate that GF regulates muscle protein synthesis and catabolic pathways, and in particular, it is judged to improve MA by regulating the proteolytic AMPK/SIRT1/PGC-1 alpha-FOXO pathway.
引用
收藏
页码:882 / 891
页数:10
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