Zhang Ruonan, Sun Xuewei, Lu Han, Zhang Xinrui, Zhang Mingyan, Ji Xuewen, Yu Xinyi, Tang Chengliang, Wu Zihan, Mao Yinghua, Zhu Jin, Ji Minjun, Yang Zhan
Department of Pathogen Biology, Nanjing Medical University, Nanjing, China.
Huadong Medical Institute of Biotechniques, Nanjing, China.
Microb Biotechnol. 2025 Jan;18(1):e70083. doi: 10.1111/1751-7915.70083.
Acetaminophen induced acute liver injury (ALI) has a high incidence and is a serious medical problem, but there is a lack of effective treatment. The enterohepatic axis is one of the targets of recent attention due to its important role in liver diseases. Disulfiram (DSF) is a multitarget drug that has been proven to play a role in a variety of liver diseases and can affect intestinal flora, but whether it can alleviate ALI is not clear. We utilised bacterial 16S rRNA gene profiling, antimicrobial treatments, and faecal microbiota transplantation tests to explore whether DSF therapy for ALI is dependent on gut microbiota. Our findings indicate that DSF primarily restores intestinal microbiome balance by modulating the abundance of Akkermansia muciniphila (A. muciniphila), leading to significant alleviation of ALI symptoms in a gut microbiota dependent manner. We also found that A. muciniphila can promote the activation of PI3K/Akt pathway, correct the Bcl-2/Bax ratio, and further inhibit hepatocyte apoptosis. In conclusion, DSF ameliorates ALI by modulating the intestinal microbiome and activating the PI3K/AKT pathway through A. muciniphila.
对乙酰氨基酚诱导的急性肝损伤(ALI)发病率高,是一个严重的医学问题,但缺乏有效的治疗方法。肠肝轴因其在肝脏疾病中的重要作用而成为近期关注的靶点之一。双硫仑(DSF)是一种多靶点药物,已被证明在多种肝脏疾病中发挥作用,且能影响肠道菌群,但它是否能减轻ALI尚不清楚。我们利用细菌16S rRNA基因谱分析、抗菌治疗和粪便微生物群移植试验,探讨DSF治疗ALI是否依赖于肠道微生物群。我们的研究结果表明,DSF主要通过调节嗜黏蛋白阿克曼氏菌(A. muciniphila)的丰度来恢复肠道微生物群平衡,从而以肠道微生物群依赖的方式显著减轻ALI症状。我们还发现,A. muciniphila可促进PI3K/Akt通路的激活,纠正Bcl-2/Bax比值,并进一步抑制肝细胞凋亡。总之,DSF通过调节肠道微生物群并通过A. muciniphila激活PI3K/AKT通路来改善ALI。