Lan Qingping, Ren Zhitao, Chen Yan, Cui Guozhen, Choi I Cheong, Ung Carolina Oi Lam, Yu Hon Ho, Lee Simon Ming-Yuen
State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Macao, China.
Zun Yi Medical University- Zhuhai Campus, Zhuhai, China.
Chin Med. 2021 Mar 16;16(1):27. doi: 10.1186/s13020-021-00434-1.
Non-alcoholic steatohepatitis (NASH) is an advanced form of non-alcoholic fatty liver disease (NAFLD) for which there is yet any standard pharmacotherapy. Traditional Chinese medicine formula such as Qushihuayu (QSHY) composing of multiple bioactive compounds has been used to treat NAFLD and NASH and shows beneficial effects over single compound treatment. This study aimed to investigate the mechanism of hepatoprotective effect of QSHY formula using a rat model.
Six-weeks old male Wistar rats were given methionine/choline supplemented (MCS) diet for 8 weeks and used as the blank control. Another 7 rats, which received methionine/choline deficient (MCD) diet in the first 6 weeks and a MCS&MCD (1:1) mixture diet in the last 2 weeks, were used as the model group. The groups of QSHY pre-treatment, low dosage, medium dosage and high dosage were given the same diet as the model group. Except for pre-treatment group (1 week in advanced of other groups), all QSHY treatment groups received QSHY formula by gavage every day since the MCD diet started.
In the MCD diet group, the QSHY formula decreased the serum ALT and AST levels, lipid droplets, inflammation foci, FAS and α-SMA protein expression than MCD diet group. MAPK pathways phospharylation were markedly depressed by the QSHY formula. Moreover, QSHY formula enhanced PPAR-γ and p-p65 translocating into nucleus. The administration of QSHY increased hepatic mRNA levels of Transcription Factor 1 alpha (HNF1A), Hepatocyte Nuclear Factor 4 alpha (HNF4A) and Forkhead box protein A3 (FOXA3) which play a pivotal role in Hepatic stellate cell (HSCs) reprogramming.
These findings suggest that QSHY formula exerts a hepatoprotective effect against steatosis and fibrosis presumably via depressed MAPK pathways phosphorylation, reinforcement of PPAR-γ and p-p65 translocating into nucleus and enhanced HSCs reprogramming.
非酒精性脂肪性肝炎(NASH)是非酒精性脂肪性肝病(NAFLD)的一种晚期形式,目前尚无标准的药物治疗方法。由多种生物活性化合物组成的中药方剂如祛瘀化淤(QSHY)已被用于治疗NAFLD和NASH,且相较于单一化合物治疗显示出有益效果。本研究旨在使用大鼠模型探究QSHY方剂肝保护作用的机制。
六周龄雄性Wistar大鼠给予补充蛋氨酸/胆碱(MCS)的饮食8周作为空白对照。另外7只大鼠,在前6周给予蛋氨酸/胆碱缺乏(MCD)饮食,后2周给予MCS和MCD(1:1)混合饮食,作为模型组。QSHY预处理组、低剂量组、中剂量组和高剂量组给予与模型组相同的饮食。除预处理组(比其他组提前1周)外,所有QSHY治疗组自MCD饮食开始后每天通过灌胃给予QSHY方剂。
在MCD饮食组中,QSHY方剂降低了血清ALT和AST水平、脂滴、炎症灶、FAS和α-SMA蛋白表达。QSHY方剂显著抑制了MAPK通路的磷酸化。此外,QSHY方剂增强了PPAR-γ和p-p65向细胞核的转位。给予QSHY增加了转录因子1α(HNF1A)、肝细胞核因子4α(HNF4A)和叉头框蛋白A3(FOXA3)的肝脏mRNA水平,这些在肝星状细胞(HSCs)重编程中起关键作用。
这些发现表明,QSHY方剂可能通过抑制MAPK通路磷酸化、增强PPAR-γ和p-p65向细胞核的转位以及增强HSCs重编程,对脂肪变性和纤维化发挥肝保护作用。