Li Jie, Yang Xiujuan, Lian Xiaolong, Li Baojian, Ma Quhuan, Yang Lingling, Gao Guangmiao, Deng Yi, Yang Zhijun
School of Pharmaceutical Science, Gansu University of Traditional Chinese Medicine, Lanzhou, Gansu, China.
Department of pharmacy, Qinghai University Medical College, Xining, China.
Front Pharmacol. 2025 Mar 20;16:1557125. doi: 10.3389/fphar.2025.1557125. eCollection 2025.
Cisplatin (CP), a widely used antineoplastic drug, could induce hepatotoxicity and is also one of the most common reasons for drug-induced liver injury (DILI). Licorice (Chinese name GanCao, GC) is a commonly used herbal drug in traditional Chinese medicine (TCM) that has been shown to treat liver diseases and DILI. CP has been documented to induce apoptosis through the promotion of endoplasmic reticulum (ER) stress. However, the exact role of ER stress in the pathogenesis of CP-induced hepatotoxicity remains unclear. A rat DILI model was constructed through intraperitoneal injection of CP, and the anti-DILI effect of GC was detected by liver coefficients, liver function tests, pathological staining, and oxidative stress indices. Additionally, the ER stress and apoptosis indices were investigated by quantitative real-time PCR (qRT-PCR), Western blotting, and immunofluorescence (IF) on CP-induced toxicity in rat liver tissues and LO2 cells. In the model group, liver function indicators significantly elevated, liver lesions more pronounced, and the reactive oxygen species (ROS) level in the liver increased, the expression of ER stress markers, apoptosis factors, and indicators related to the protein kinase RNA-like ER kinase/activating transcription factor 4/C/EBP homologous protein (PERK/ATF4/CHOP) pathway significantly elevated. Treatment of the CP-induced toxicity in the rat model with GC significantly improved liver function, reduced liver lesions, decreased liver ROS. In addition, GC significantly inhibited the expression of ER stress markers, apoptosis factors, and indicators related to PERK/ATF4/CHOP pathway, demonstrating the anti-CP-induced hepatotoxicity effect of GC. In this study, we verified the protective effect of GC in CP-induced hepatotoxicity in rats and clarified its mechanisms related to ER stress and apoptosis.
顺铂(CP)是一种广泛使用的抗肿瘤药物,可诱发肝毒性,也是药物性肝损伤(DILI)最常见的原因之一。甘草(中文名甘草,GC)是中药中常用的草药,已被证明可治疗肝脏疾病和DILI。已有文献记载CP通过促进内质网(ER)应激诱导细胞凋亡。然而,ER应激在CP诱导的肝毒性发病机制中的确切作用仍不清楚。通过腹腔注射CP构建大鼠DILI模型,并通过肝脏系数、肝功能测试、病理染色和氧化应激指标检测GC的抗DILI作用。此外,通过定量实时PCR(qRT-PCR)、蛋白质免疫印迹法和免疫荧光(IF)研究CP诱导的大鼠肝组织和LO2细胞毒性中的ER应激和细胞凋亡指标。模型组肝功能指标显著升高,肝脏病变更明显,肝脏中活性氧(ROS)水平升高,ER应激标志物、细胞凋亡因子以及与蛋白激酶RNA样内质网激酶/激活转录因子4/C/EBP同源蛋白(PERK/ATF4/CHOP)通路相关的指标表达显著升高。用GC治疗CP诱导的大鼠模型毒性可显著改善肝功能,减轻肝脏病变,降低肝脏ROS水平。此外,GC显著抑制ER应激标志物、细胞凋亡因子以及与PERK/ATF4/CHOP通路相关指标的表达,证明了GC对CP诱导的肝毒性具有保护作用。在本研究中,我们验证了GC对CP诱导的大鼠肝毒性的保护作用,并阐明了其与ER应激和细胞凋亡相关的机制。