肝转录组揭示血府逐瘀汤改善高脂饮食诱导的非酒精性脂肪肝的潜在靶点

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Hao Tang , Jun Wang , Yi Fang , Yixiao Yin , Wei Liu , Yiyang Hu , Jinghua Peng
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引用次数: 0

摘要

背景与目的学府饮片(XZD)是一种传统中药方剂,最早见于中国古代清代,以前曾被证实可改善肝脂肪变性。本研究评估了XZD对高脂饮食(HFD)诱导的非酒精性脂肪肝(NAFLD)小鼠的影响,并检测了肝脏转录组,以揭示XZD的潜在机制。奥贝胆酸作为对照药。对体重、食物摄入量和胰岛素抵抗稳态模型评估指数(HOMA-IR)进行了分析。通过血红素和伊红染色切片观察肝组织学,并用非酒精性脂肪肝活动评分(NAS)进行量化。肝细胞中的脂质通过油红染色显现。测量丙氨酸氨基转移酶(ALT)和肝甘油三酯(TG)。结果 XZD改善了非酒精性脂肪肝小鼠的肝组织学,同时降低了空腹胰岛素、HOMA-IR、NAS、ALT和肝TG。XZD能显著逆转非酒精性脂肪肝的肝脏转录组,尤其是富集在花生四烯酸代谢、脂肪酸降解、细胞因子-细胞因子受体相互作用和细胞外基质(ECM)-受体相互作用通路中的基因。肝脏定量代谢组学分析证实脂肪酸降解是 XZD 的关键靶向途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hepatic transcriptome discloses the potential targets of Xuefu Zhuyu Decoction ameliorating non-alcoholic fatty liver disease induced by high-fat diet

Hepatic transcriptome discloses the potential targets of Xuefu Zhuyu Decoction ameliorating non-alcoholic fatty liver disease induced by high-fat diet

Background and Aim

Xuefu Zhuyu decoction (XZD), a traditional Chinese medicinal formula, was firstly recorded in the Qing dynasty of ancient China and previously demonstrated to ameliorate hepatic steatosis. In the present study, the effects of XZD on non-alcoholic fatty liver disease (NAFLD) induced by high-fat diet (HFD) were evaluated in mice and the hepatic transcriptome was detected to disclose the potential mechanisms of XZD.

Experimental procedure

The effects of XZD (low- and high-dosage) on NAFLD induced by HFD for 16 weeks were evaluated. Obeticholic acid was used as control drug. Body weight, food intake and index of homeostatic model assessment for insulin resistance (HOMA-IR) were analyzed. Hepatic histology were observed in haematoxylin and eosin stained sections and quantified with NAFLD activity score (NAS). Lipid in hepatocytes was visualized by Oil red staining. Alanine aminotransferase (ALT) and hepatic triglyceride (TG) was measured. The hepatic transcriptom was detected with RNA-sequencing and validated with real-time polymerase chain reaction, western-blotting and hepatic quantitative metabolomics.

Results

XZD ameliorated hepatic histology of NAFLD mice, accompanied with decreasing fasting insulin, HOMA-IR, NAS, ALT and hepatic TG. The hepatic transcriptom of NAFLD was significantly reversed by XZD treatment, especially the genes enriched in the pathways of arachidonic acid metabolism, fatty acid degradation, cytokine-cytokine receptor interaction and extracellular matrix (ECM) -receptor interaction. The hepatic quantitative metabolomics analysis confirmed fatty acid degradation as the key targeting pathway of XZD.

Conclusions

XZD ameliorated NAFLD induced by HFD, which probably correlated closely to the pathways of fatty acid degradation.

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CiteScore
7.20
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