Yinchenhao Tang alleviates high fat diet induced NAFLD by increasing NR1H4 and APOA1 expression

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-07-01 DOI:10.1016/j.jtcme.2023.02.010
Li Xu, Hongliang Cui
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引用次数: 1

Abstract

Background and aim

Traditional Chinese medicine Yinchenhao Tang (YCHT) demonstrated benefits when treating nonalcoholic fatty liver disease (NAFLD), but the dose effects and potential targets are still ambiguous. In this study, different concentrations of YCHT were employed to treat NAFLD and the underlying therapeutic targets were investigated.

Experimental procedure

Kunming mice were fed with high fat diet (HFD) for 8 weeks to induce NAFLD, then treated with 3 different concentrations of YCHT. Hepatic pathological changes and serum lipid levels were examined. Network pharmacology was applied to screen the potential targets of YCHT for NAFLD modulation. NR1H4 and APOA1 expression was evaluated by QPCR and western blotting. Immunohistochemistry (IHC) staining was conducted to visualize the localization pattern of NR1H4 and APOA1 in the liver.

Results

YCHT significantly reduced liver lipid storage and improved the liver pathological status of NAFLD mice. The serum lipid levels, as well as alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, were remarkably reduced by the middle and high dose YCHT. There are 35 potential targets for YCHT to regulate NAFLD. HFD suppressed both RNA and protein expression of NR1H4 and APOA1, while YCHT elevated NR1H4 and APOA1 expression. IHC staining indicated that NR1H4 was mainly located in the cell nucleus and the APOA1 signal was observed at the liver sinusoid or cytoplasm.

Conclusion

YCHT can effectively ameliorate HFD induced NAFLD by modulating the promising targets of NR1H4 and APOA1.

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银陈浩汤通过提高NR1H4和APOA1的表达来缓解高脂饮食诱导的NAFLD
背景与目的中药茵陈蒿汤(YCHT)治疗非酒精性脂肪性肝病(NAFLD)疗效显著,但其剂量效应和潜在靶点尚不明确。在本研究中,采用不同浓度的YCHT治疗NAFLD,并研究了潜在的治疗靶点。实验方法昆明小鼠采用高脂饮食(HFD)诱导NAFLD 8周,然后用3种不同浓度的YCHT处理。检查肝脏病理变化和血脂水平。应用网络药理学筛选YCHT调节NAFLD的潜在靶点。通过QPCR和蛋白质印迹评估NR1H4和APOA1的表达。进行免疫组织化学(IHC)染色以观察NR1H4和APOA1在肝脏中的定位模式。结果YCHT能显著降低NAFLD小鼠的肝脏脂质蓄积,改善其肝脏病理状态。中高剂量YCHT可显著降低血清脂质水平以及丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)水平。YCHT有35个潜在的靶点来调节NAFLD。HFD抑制NR1H4和APOA1的RNA和蛋白质表达,而YCHT升高NR1H4及APOA1表达。IHC染色显示NR1H4主要位于细胞核,APOA1信号主要分布于肝窦或细胞质。结论YCHT可通过调节NR1H4和APOA1的靶点,有效改善HFD诱导的NAFLD。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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