Liqustri lucidi Fructus inhibits hepatic injury and functions as an antioxidant by activation of AMP-activated protein kinase in vivo and in vitro

被引:29
|
作者
Seo, Hye Lim [1 ]
Baek, Su Youn [1 ]
Lee, Eun Hye [1 ,2 ]
Lee, Ju-Hee [1 ,3 ]
Lee, Seul-Gi [1 ]
Kim, Kwang-Youn [1 ,4 ]
Jang, Mi Hee [1 ]
Park, Min-Hui [1 ,2 ,5 ]
Kim, Joung-Hee [5 ,6 ]
Kim, Keuk-Jun [5 ]
Lee, Hyeong Sik [2 ]
Ahn, Soon-Cheol [4 ]
Lee, Jong Rok [7 ]
Park, Sook Jahr [1 ]
Kim, Sang Chan [1 ]
Kim, Young Woo [1 ]
机构
[1] Daegu Haany Univ, Coll Oriental Med, Med Res Ctr MRC GHF, Gyongsan, South Korea
[2] Daegu Haany Univ, Dept Med Sci, Gyongsan, South Korea
[3] Dongguk Univ, Coll Oriental Med, Gyeongju, South Korea
[4] Pusan Natl Univ, Dept Microbiol & Immunol, Sch Med, Yagnsan, South Korea
[5] Daekyeung Coll, Dept Biomed Lab Sci, Gyongsan, South Korea
[6] Changwon Natl Univ, Dept Bio Hlth Sci, Coll Nat Sci, Chang Won, South Korea
[7] Daegu Haany Univ, Dept Pharmaceut Engn, Gyongsan, South Korea
基金
新加坡国家研究基金会;
关键词
AMPK; LKB1; Ligustri lucidi Fructus; Liver injury; CCl4; MITOCHONDRIAL PERMEABILITY TRANSITION; CAUSES CELL-DEATH; OXIDATIVE STRESS; ARACHIDONIC-ACID; LIGUSTRUM-LUCIDUM; CHLOROGENIC ACID; FRUIT EXTRACT; FEMALE RATS; APOPTOSIS; IRON;
D O I
10.1016/j.cbi.2016.11.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Medicinal herbs are used to treat or prevent various diseases, and function to regulate protective mechanisms as nutraceuticals. Fructus Ligustri lucidi is the fruit of Ligustrum lucidum and has been used for its tonic effects on the liver. This study was designed to examine the effects of Fructus Ligustri lucidi water extract (FLL) against severe oxidative stress and mitochondrial impairment in vivo and in vitro and to elucidate its cellular mechanisms of action. Treatment of HepG2 cells with arachidonic acid (AA) + iron successfully induced oxidative stress and apoptosis, as indicated by depletion of glutathione, formation of ROS, decreses in mitochondrial membrane potential (Delta Psi m), and altered expression of apoptosis-related proteins, such as procaspase-3 and Bcl-xL. FLL treatment significantly blocked these pathological changes and the mitochondrial dysfunction caused by AA + iron, which were similar with the effect of aminoimidazole-carboxamide-beta-D-ribofuranoside (AICAR). Moreover, FLL induced the activation of AMP-activated protein kinase (AMPK), which was mediated by its upstream kinase LKB1. Inhibition or activation of AMPK revealed the role of AMPK in cellular protection conferred by FLL in LKB1deficient cells. In mice, oral administration of 100 mg/kg FLL activated AMPK in the liver, and protected against oxidative stress and liver injury induced by CCl4 injection. Among the components of FLL, chlorogenic acid was found to be responsible for the protection of hepatocytes against AA + iron-induced cellular damage. Overall, our results confirmed that FLL has the ability to protect hepatocytes against oxidative injury through regulation of the AMPK signaling pathway. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:57 / 68
页数:12
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