Hepatoprotective Effect of Jianpi Huoxue Formula on Nonalcoholic Fatty Liver Disease Induced by Methionine-Choline-Deficient Diet in Rat

被引:15
作者
Feng, Yu [1 ,2 ]
Chen, Yan [1 ,2 ]
Yang, Binrui [1 ,2 ]
Lan, Qingping [1 ,2 ]
Wang, Tao [3 ]
Cui, Guozhen [1 ,2 ,3 ]
Ren, Zhitao [1 ,2 ]
Choi, I. Cheong [4 ]
Leung, George Pak-Heng [5 ]
Yan, Fenggen [6 ]
Chen, Dacan [6 ]
Yu, Hon Ho [4 ]
Lee, Simon Ming Yuen [1 ,2 ]
机构
[1] Univ Macau, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Univ Macau, Inst Chinese Med Sci, Macau, Peoples R China
[3] Zhuhai Campus Zunyi Med Univ, Dept Bioengn, Zhuhai, Peoples R China
[4] Kiang Wu Hosp, Dept Gastroenterol, Macau, Peoples R China
[5] Univ Hong Kong, Dept Pharmacol & Pharm, Hong Kong, Peoples R China
[6] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Guangdong Prov Hosp Chinese Med, Guangzhou, Guangdong, Peoples R China
关键词
TRADITIONAL CHINESE MEDICINE; OXIDATIVE STRESS; HEPATIC STEATOSIS; ANIMAL-MODELS; STEATOHEPATITIS; PATHOGENESIS; EPIDEMIOLOGY; INFLAMMATION; PREVALENCE; GUIDELINE;
D O I
10.1155/2019/7465272
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In parallel with the prevalence metabolic syndrome, nonalcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease in most countries. It features a constellation of simple steatosis, nonalcoholic steatohepatitis (NASH), fibrosis, cirrhosis, and even hepatocellular carcinoma. There are no approved drugs for effective management of NAFLD and NASH. Jianpi Huoxue formula (JPHX) mainly consists of Atractylodes macrocephal (Baizhu), Salvia miltiorrhiza (Danshen), Rasux Paeonia Alba (Baishao), Rhizoma Alismatis (Zexie), and Fructus Schisandrae Chinensis (Wuweizi), which may have beneficial effects on NAFLD. The aim of the study was to identify the effect of JPHX on NAFLD. A NAFLD model was induced by methionine-choline-deficient food (MCD) in Wistar rats and orally administered with simultaneous JPHX, once a day for 8 weeks. Hepatocellular injury, lipid profile, inflammation, fibrosis, and apoptosis were evaluated. The results showed that JPHX significantly decreased the abnormal serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels compared with the MCD model (P<0.05). Furthermore, JPHX protected MCD diet-fed rats from accumulation of hepatic triglycerides (TG) and total cholesterol (TC). Histological examination demonstrated that JPHX noticeably normalized the NAFLD activity score (NAS). Moreover, JPHX ameliorated liver inflammation by decreasing TNF-alpha levels and reduced collagen and matrix metalloproteinases in MCD diet-fed rats. In addition, JPHX prevented rats from MCD-induced cellular apoptosis, as suggested by TUNEL staining, and suppressed the activation of caspase 3 and 7 proteins. JPHX also inhibited the phosphorylation of JNK. In conclusion, JPHX exhibited a hepatoprotective effect against NAFLD in an MCD experimental model.
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页数:12
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