Institute of Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Guangdong Metabolic Diseases Research Center of Integrated Chinese and Western Medicine, Guangdong Pharmaceutical University, Guangzhou, China.
Front Endocrinol (Lausanne). 2022 Jun 16;13:864703. doi: 10.3389/fendo.2022.864703. eCollection 2022.
Nonalcoholic steatohepatitis (NASH) has become a major cause of liver transplantation and liver-associated death. Targeting the gut-liver axis is a potential therapy for NASH. The Fufang Zhenzhu Tiaozhi (FTZ) capsule, a traditional Chinese medicine commonly used in clinical practice, has recently emerged as a promising drug candidate for metabolic diseases such as NASH. The present study aimed to investigate whether FTZ exerts an anti-NASH effect by targeting the gut-liver axis. Mice were fed with a high-fat diet (HFD) for 20 weeks to induce NASH. HFD-fed mice were daily intragastrically administrated with FTZ at 10 weeks after tbe initiation of HFD feeding. The mRNA levels of genes associated with the intestinal tight junction, lipid metabolism, and inflammation were determined by the q-PCR assay. Hepatic pathology was evaluated by H&E staining. The gut microbiota was analyzed by 16S rRNA gene sequencing. FTZ attenuated HFD-induced obesity, insulin resistance, and hepatic steatosis in mice. FTZ treatment decreased the elevated levels of serum aminotransferases and liver triglyceride in NASH mice. Furthermore, FTZ treatment reduced hepatic inflammatory cell infiltration and fibrosis in mice. In addition, FTZ attenuated the intestinal inflammatory response and improved intestinal barrier function. Mechanistically, FTZ-treated mice showed a different gut microbiota composition compared with that in HFD-fed mice. Finally, we identified eight differential metabolites that may contribute to the improvement of NASH with FTZ treatment. In summary, FTZ ameliorates NASH by inhibiting gut inflammation, improving intestinal barrier function, and modulating intestinal microbiota composition.
非酒精性脂肪性肝炎(NASH)已成为肝移植和与肝相关死亡的主要原因。靶向肠-肝轴是治疗 NASH 的一种潜在疗法。复方珍珠降脂胶囊是一种常用于临床实践的中药,最近作为 NASH 等代谢性疾病的有前途的药物候选物出现。本研究旨在探讨复方珍珠降脂胶囊是否通过靶向肠-肝轴发挥抗 NASH 作用。用高脂肪饮食(HFD)喂养小鼠 20 周以诱导 NASH。在 HFD 喂养开始后 10 周,用 HFD 喂养的小鼠每天用 FTZ 灌胃。通过 q-PCR 测定与肠道紧密连接、脂质代谢和炎症相关的基因的 mRNA 水平。通过 H&E 染色评估肝组织病理学。通过 16S rRNA 基因测序分析肠道微生物群。FTZ 减轻了 HFD 诱导的肥胖、胰岛素抵抗和肝脂肪变性。FTZ 治疗降低了 NASH 小鼠血清转氨酶和肝甘油三酯的升高水平。此外,FTZ 治疗减少了小鼠肝脏炎性细胞浸润和纤维化。此外,FTZ 减轻了肠道炎症反应并改善了肠道屏障功能。在机制上,与 HFD 喂养的小鼠相比,FTZ 治疗的小鼠表现出不同的肠道微生物群组成。最后,我们确定了八种可能有助于改善 FTZ 治疗 NASH 的差异代谢物。总之,FTZ 通过抑制肠道炎症、改善肠道屏障功能和调节肠道微生物群组成来改善 NASH。