Shanghai Innovation Center of TCM Health Service, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong 999077, China.
Nutrients. 2024 Jun 6;16(11):1782. doi: 10.3390/nu16111782.
NASH (non-alcoholic steatohepatitis) is a severe liver disease characterized by hepatic chronic inflammation that can be associated with the gut microbiota. In this study, we explored the therapeutic effect of extract (GPE), a Chinese herbal extract, on methionine- and choline-deficient (MCD) diet-induced NASH mice. Based on the peak area, the top ten compounds in GPE were hydroxylinolenic acid, rutin, hydroxylinoleic acid, vanillic acid, methyl vanillate, quercetin, pheophorbide A, protocatechuic acid, aurantiamide acetate, and iso-rhamnetin. We found that four weeks of GPE treatment alleviated hepatic confluent zone inflammation, hepatocyte lipid accumulation, and lipid peroxidation in the mouse model. According to the 16S rRNA gene V3-V4 region sequencing of the colonic contents, the gut microbiota structure of the mice was significantly changed after GPE supplementation. Especially, GPE enriched the abundance of potentially beneficial bacteria such as and decreased the abundance of opportunistic pathogens such as . Moreover, RNA sequencing revealed that the GPE group showed an anti-inflammatory liver characterized by the repression of the NF-kappa B signaling pathway compared with the MCD group. Ingenuity Pathway Analysis (IPA) also showed that GPE downregulated the pathogen-induced cytokine storm pathway, which was associated with inflammation. A high dose of GPE (HGPE) significantly downregulated the expression levels of the tumor necrosis factor-α (TNF-α), myeloid differentiation factor 88 (Myd88), cluster of differentiation 14 (CD14), and Toll-like receptor 4 (TLR4) genes, as verified by real-time quantitative PCR (RT-qPCR). Our results suggested that the therapeutic potential of GPE for NASH mice may be related to improvements in the intestinal microenvironment and a reduction in liver inflammation.
非酒精性脂肪性肝炎(NASH)是一种严重的肝脏疾病,其特征为慢性肝脏炎症,可能与肠道微生物群有关。在这项研究中,我们探索了一种中药提取物(GPE)对蛋氨酸和胆碱缺乏(MCD)饮食诱导的 NASH 小鼠的治疗作用。根据峰面积,GPE 中的前 10 种化合物为羟基亚麻酸、芦丁、羟基亚油酸、香草酸、甲基香草酸、槲皮素、原卟啉 A、原儿茶酸、aurantiamide 乙酸盐和异鼠李素。我们发现,GPE 治疗 4 周可减轻小鼠模型中的融合区炎症、肝细胞脂质积累和脂质过氧化。根据结肠内容物 16S rRNA 基因 V3-V4 区测序,GPE 补充后小鼠肠道微生物群结构发生显著变化。特别是,GPE 增加了潜在有益菌如 的丰度,降低了机会性病原体如 的丰度。此外,RNA 测序显示,与 MCD 组相比,GPE 组表现出抗炎性肝特征,NF-kappa B 信号通路受到抑制。Ingenuity 通路分析(IPA)也显示,GPE 下调了与炎症相关的病原体诱导细胞因子风暴通路。高剂量 GPE(HGPE)通过实时定量 PCR(RT-qPCR)验证,显著下调了肿瘤坏死因子-α(TNF-α)、髓样分化因子 88(Myd88)、分化抗原 14(CD14)和 Toll 样受体 4(TLR4)基因的表达水平。我们的结果表明,GPE 治疗 NASH 小鼠的潜在治疗作用可能与改善肠道微环境和减轻肝脏炎症有关。