Jamal Mohammad H, Ali Hamad, Dashti Ali, Al-Abbad Jasim, Dashti Husain, Mathew Chako, Al-Ali Waleed, Asfar Sami
Department of Surgery, Faculty of Medicine, Health Sciences Center, Kuwait University Kuwait.
Department of Medical Laboratory Sciences (MLS), Faculty of Allied Health Sciences, Health Sciences Center, Kuwait University Kuwait.
Int J Clin Exp Pathol. 2015 Jan 1;8(1):649-54. eCollection 2015.
The aim of this study was to investigate the effect of epigallocatechin gallate (EGCG) on uncoupling protein 2 regulation in an acute liver injury-animal model.
Twenty seven male Wistar rats were divided into three groups: control group (n = 9), TAA group (n = 9): acute liver injury was induced by the intraperitoneal injection of thioacetamide (200 mg/kg) and EGCG/TAA (n = 9 rats): Epigallocatechin gallate was given two weeks prior to the induction of acute liver injury by thioacetamide. The levels of uncoupling protein 2, CRP, TNF-α and interleukins (IL) 6 and 18 were analyzed in the liver using PCR analysis.
Q-PCR analysis showed that the genetic expression of UCP2, TNF-α and CRP in the EGCG/TAA group was the least in comparison to other groups (P ≤ 0.005). The IL-6 and IL-18 were upregulated after induction of acute liver injury, but this upregulation was significantly less in the group that received epigallocatechin gallate (EGCG/TAA) compared to the TAA group. In addition, histological examination showed a reduction in hepatocyte injury in EGCG/TAA compared to the TAA group.
Epigallocatechin gallate administration prior to induction of acute liver injury down-regulates uncoupling protein 2 expression and reduces IL-6, IL-18, TNF-α and CRP.
本研究旨在探讨表没食子儿茶素没食子酸酯(EGCG)对急性肝损伤动物模型中解偶联蛋白2调节的影响。
将27只雄性Wistar大鼠分为三组:对照组(n = 9)、TAA组(n = 9):通过腹腔注射硫代乙酰胺(200 mg/kg)诱导急性肝损伤,以及EGCG/TAA组(n = 9只大鼠):在通过硫代乙酰胺诱导急性肝损伤前两周给予表没食子儿茶素没食子酸酯。使用PCR分析肝脏中解偶联蛋白2、CRP、TNF-α和白细胞介素(IL)6和18的水平。
Q-PCR分析显示,与其他组相比,EGCG/TAA组中UCP2、TNF-α和CRP的基因表达最少(P≤0.005)。急性肝损伤诱导后IL-6和IL-18上调,但与TAA组相比,接受表没食子儿茶素没食子酸酯的组(EGCG/TAA)中这种上调明显较少。此外,组织学检查显示,与TAA组相比,EGCG/TAA组肝细胞损伤减少。
在诱导急性肝损伤前给予表没食子儿茶素没食子酸酯可下调解偶联蛋白2的表达,并降低IL-6、IL-18、TNF-α和CRP。