Department of Gastroenterology, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, Fujian, People's Republic of China.
Institute for Microbial Ecology, School of Medicine, Xiamen University, Xiamen, Fujian, People's Republic of China.
Inflammation. 2024 Dec;47(6):2000-2012. doi: 10.1007/s10753-024-02021-6. Epub 2024 Apr 13.
Autoimmune hepatitis (AIH) is a severe immune-mediated inflammatory liver disease that currently lacks feasible drug treatment methods. Our study aimed to evaluate the protective effect of succinic acid against AIH and provide a reliable method for the clinical treatment of AIH. We performed an in vivo study of the effects of succinic acid on concanavalin A (ConA)-induced liver injury in mice. We examined liver transaminase levels, performed hematoxylin and eosin (HE) staining, and observed apoptotic phenotypes in mice. We performed flow cytometry to detect changes in the number of neutrophils and monocytes, and used liposomes to eliminate the liver Kupffer cells and evaluate their role. We performed bioinformatics analysis, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and western blotting to detect mitochondrial apoptosis-induced changes in proteins from the B-cell lymphoma 2(Bcl-2) family. Succinic acid ameliorated ConA-induced AIH in a concentration-dependent manner, as reflected in the survival curve. HE and TUNEL staining and terminal deoxynucleotidyl transferase dUTP nick end labeling revealed decreased alanine transaminase and aspartate aminotransferase levels, and reduced liver inflammation and apoptosis. RT-qPCR and enzyme-linked immunosorbent assay revealed that succinic acid significantly reduced liver pro-inflammatory cytokine levels. Flow cytometry revealed significantly decreased levels of liver neutrophils. Moreover, the protective effect of succinic acid disappeared after the Kupffer cells were eliminated, confirming their important role in the effect. Bioinformatics analysis, RT-qPCR, and western blotting showed that succinic acid-induced changes in proteins from the Bcl-2 family involved mitochondrial apoptosis, indicating the molecular mechanism underlying the protective effect of succinic acid. Succinic acid ameliorated ConA-induced liver injury by regulating immune balance, inhibiting pro-inflammatory factors, and promoting anti-apoptotic proteins in the liver. This study provides novel insights into the biological functions and therapeutic potential of succinic acid in the treatment of autoimmune liver injury.
自身免疫性肝炎(AIH)是一种严重的免疫介导的炎症性肝病,目前缺乏可行的药物治疗方法。本研究旨在评估琥珀酸对 AIH 的保护作用,为 AIH 的临床治疗提供可靠方法。我们进行了琥珀酸对伴刀豆球蛋白 A(ConA)诱导的小鼠肝损伤的体内研究。我们检测了肝转氨酶水平,进行了苏木精和伊红(HE)染色,并观察了小鼠的凋亡表型。我们通过流式细胞术检测中性粒细胞和单核细胞数量的变化,并用脂质体消除肝枯否细胞并评估其作用。我们进行了生物信息学分析、逆转录定量聚合酶链反应(RT-qPCR)和 Western blot 检测 B 细胞淋巴瘤 2(Bcl-2)家族蛋白的线粒体凋亡诱导变化。琥珀酸以浓度依赖的方式改善 ConA 诱导的 AIH,表现在生存曲线上。HE 和 TUNEL 染色和末端脱氧核苷酸转移酶 dUTP 缺口末端标记显示丙氨酸转氨酶和天冬氨酸转氨酶水平降低,肝炎症和凋亡减少。RT-qPCR 和酶联免疫吸附试验显示,琥珀酸显著降低了肝前炎症细胞因子水平。流式细胞术显示肝中性粒细胞水平显著降低。此外,在消除枯否细胞后,琥珀酸的保护作用消失,证实了它们在该作用中的重要作用。生物信息学分析、RT-qPCR 和 Western blot 显示,琥珀酸诱导的 Bcl-2 家族蛋白变化涉及线粒体凋亡,表明了琥珀酸保护作用的分子机制。琥珀酸通过调节免疫平衡、抑制前炎症因子和促进肝内抗凋亡蛋白来改善 ConA 诱导的肝损伤。本研究为琥珀酸在治疗自身免疫性肝损伤中的生物学功能和治疗潜力提供了新的见解。