Tu Guifang, Gong Xiangwen, Yang Qinhe, Li Yuanyuan, Wang Guanlong, Liang Yinji, Zhang Yupei, Yan Haizhen, Lin Chunmei, Zhang Jinwen
School of Chinese Medicine, Jinan University, Guangzhou 510632, China.
J Tradit Chin Med. 2018 Aug;38(4):535-547.
To investigate effects of the extracts from soothing-liver and invigorating-spleen formulas on the injury due to oxidative stress, mediated by the Nuclear factor-like 2 (Nrf2)-Antioxidant response element (ARE) pathway, in the hepatocytes of rats with non-alcoholic fatty liver disease (NAFLD) induced by high-fat diet.
Soothing-liver and invigorating-spleen formula mixtures were prepared for five groups: normal, model, soothing-liver formula group (SLG), invigorating-spleen formula group (ISG), integrated formula group (IG). The rat model of NAFLD was induced by feeding rats a high-fat diet (HFD). After 16 weeks, the hepatic tissue was examined following Haematoxylin-Eosin (H&E) staining and with Transmission electron microscopy (TEM). Levels of hepatic lipids, serum lipids and hepatic functions were measured using a biochemical analyser. Hepatocytes were isolated from the livers of rats and were identified by cellar immunohistochemistry, cellular immunofluorescence and flow cytometry. The expression levels of Nrf2, Kelch-like epichlorohydrin-associated protein 1 (Keap-1), haeme oxygenase-1 (HO-1) and NAD(P)H: quinone oxidoreductase 1 (NQO1) mRNAs were assessed by real-time fluorescence quantitative PCR. Nrf2, Keap-1, HO-1 and NQO1 proteins were measured by Western blotting. Finally, the levels of oxidative stress factors Superoxide Dismutase (SOD), malonaldehyde (MDA) and Glutathione peroxidase (GSH-Px) in hepatocytes were measured by WST-1, TBA and colorimetry.
The H & E and TEM results showed that the NAFLD model rats successfully reproduced typical pathogenetic and histopathological features. The liver function and levels of hepatic lipids and serum lipids from the model rats were dramatically increased. Compared with the model group, the levels of hepatic lipids, serum lipids and hepatic function in the treatment groups were ameliorated to different degrees. The yields of purified hepatocytes in each rat were 4-5 ¡Á 108. The viability of the isolated hepatocytes was higher than 95%, with a purity over 93.2%. Cellular immunohistochemistry analysis showed that the hepatocytes were brown, while in the cellular immunofluorescence analysis, the hepatocytes showed green fluorescence. The expression levels of Nrf2, Keap-1, HO-1 and NQO1 mRNA and protein in the hepatocytes were significantly higher in the model group than in the normal group (P < 0.05, P < 0.01). Compared with the model group, the expression of Nrf2, Keap-1, HO-1 and NQO-1 mRNAs and proteins in all treatment groups increased, especially in the IG (P < 0.01).
The extracts from soothing-liver and invigorating-spleen formulas may protect the liver against the injury induced by oxidative stress in hepatocytes by influencing the Nrf2-ARE pathway, which may be the mechanism having the potential for prevention and treatment of NAFLD.
探讨疏肝健脾方提取物对高脂饮食诱导的非酒精性脂肪性肝病(NAFLD)大鼠肝细胞氧化应激损伤的影响及其通过核因子样2(Nrf2)-抗氧化反应元件(ARE)通路介导的作用机制。
将大鼠分为正常组、模型组、疏肝方组(SLG)、健脾方组(ISG)、合方组(IG),共5组,制备疏肝健脾方合剂。采用高脂饮食(HFD)诱导大鼠建立NAFLD模型。16周后,采用苏木精-伊红(H&E)染色和透射电子显微镜(TEM)观察肝组织情况。使用生化分析仪检测肝脂质、血脂及肝功能水平。从大鼠肝脏中分离肝细胞,通过细胞免疫组化、细胞免疫荧光和流式细胞术进行鉴定。采用实时荧光定量PCR检测Nrf2、 Kelch样环氧氯丙烷相关蛋白1(Keap-1)、血红素加氧酶-1(HO-1)和NAD(P)H:醌氧化还原酶1(NQO1)mRNA的表达水平。通过蛋白质免疫印迹法检测Nrf2、Keap-1、HO-1和NQO1蛋白。最后,采用WST-1法、硫代巴比妥酸(TBA)法和比色法检测肝细胞中氧化应激因子超氧化物歧化酶(SOD)、丙二醛(MDA)和谷胱甘肽过氧化物酶(GSH-Px)的水平。
H&E染色和TEM结果显示,NAFLD模型大鼠成功复制了典型的发病机制和组织病理学特征。模型组大鼠肝功能及肝脂质、血脂水平显著升高。与模型组相比,各治疗组肝脂质、血脂水平及肝功能均有不同程度改善。每只大鼠纯化肝细胞产量为4-5×10⁸。分离的肝细胞活力高于95%,纯度超过93.2%。细胞免疫组化分析显示肝细胞呈棕色,细胞免疫荧光分析显示肝细胞呈绿色荧光。模型组肝细胞中Nrf2、Keap-1、HO-1和NQO1 mRNA及蛋白表达水平显著高于正常组(P<0.05,P<0.01)。与模型组相比,各治疗组Nrf2、Keap-1、HO-1和NQO-1 mRNA及蛋白表达均升高,尤其在合方组(IG)升高明显(P<0.01)。
疏肝健脾方提取物可能通过影响Nrf2-ARE通路保护肝细胞免受氧化应激损伤,这可能是其防治NAFLD的潜在机制。