Yang Genling, Zhang Li, Ma Li, Jiang Rong, Kuang Ge, Li Ke, Tie Hongtao, Wang Bin, Chen Xinyu, Xie Tianjun, Gong Xia, Wan Jingyuan
Laboratory Animal Center, Chongqing Medical University, Chongqing 40016, China.
Laboratory of Stem Cell and Tissue Engineering, Chongqing Medical University, Chongqing 40016, China.
Int Immunopharmacol. 2017 Sep;50:186-193. doi: 10.1016/j.intimp.2017.06.027. Epub 2017 Jun 29.
Acetaminophen (APAP) is a widely used antipyretic and analgesic drug, which is safe and effective at the therapeutic dose. Unfortunately, excessive dosage of APAP could cause severe liver injury due to lack of effective therapy. Successful therapeutic strategies are urgently requested in clinic. Glycyrrhetinic acid (GA), derived from a traditional medicine licorice, has been shown to exert anti-inflammatory and antioxidant actions. In this study, the effect and the underlying mechanism of GA on APAP-induced hepatotoxicity were explored. Our results showed that pretreatment with GA significantly reduced serum ALT and AST activities, alleviated hepatic pathological damages with hepatocellular apoptosis, down-regulated expression of CYP2E1 mRNA and protein, increased GSH levels, and reduced reactive oxygen species (ROS) productions in the liver of APAP-exposed mice. Furthermore, GA obviously inhibited APAP-induced HMGB1-TLR4 signal activation, as evaluated by reduced hepatic HMGB1 release, p-IRAK1, p-MAPK and p-IκB expression as well as the productions of TNF-α and IL-1β. In addition, GA attenuated hepatic neutrophils recruitment and macrophages infiltration caused by APAP. These findings reflected that GA could alleviate APAP-induced hepatotoxicity, the possible mechanism is associated with down-regulation of CYP2E1 expression and deactivation of HMGB1-TLR4 signal pathway.
对乙酰氨基酚(APAP)是一种广泛使用的解热镇痛药,在治疗剂量下安全有效。不幸的是,由于缺乏有效的治疗方法,过量服用APAP会导致严重的肝损伤。临床上迫切需要成功的治疗策略。甘草次酸(GA)源自传统药物甘草,已被证明具有抗炎和抗氧化作用。在本研究中,探讨了GA对APAP诱导的肝毒性的影响及其潜在机制。我们的结果表明,GA预处理显著降低了血清ALT和AST活性,减轻了肝细胞凋亡引起的肝脏病理损伤,下调了CYP2E1 mRNA和蛋白的表达,提高了GSH水平,并减少了APAP暴露小鼠肝脏中活性氧(ROS)的产生。此外,通过降低肝脏HMGB1释放、p-IRAK1、p-MAPK和p-IκB表达以及TNF-α和IL-1β的产生来评估,GA明显抑制了APAP诱导的HMGB1-TLR4信号激活。此外,GA减轻了APAP引起的肝脏中性粒细胞募集和巨噬细胞浸润。这些发现表明,GA可以减轻APAP诱导的肝毒性,其可能的机制与下调CYP2E1表达和失活HMGB1-TLR4信号通路有关。