基于网络药理学探究黄诺玛苷对非酒精性脂肪肝的降脂作用

魏晓丽; 郭艳丽; 张永威; 冉峥; 兰怡; 王丽凤; 毛新民

doi:10.16016/j.1000-5404.202009246

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基于网络药理学探究黄诺玛苷对非酒精性脂肪肝的降脂作用

基础医学 | 更新时间：2026-01-09

- 基于网络药理学探究黄诺玛苷对非酒精性脂肪肝的降脂作用
- Lipid-lowering effect of flavanomarein on non-alcoholic fatty liver disease based on network pharmacology
- 第三军医大学学报 2021年43卷第5期页码：383-394
- 作者机构：
- 作者简介：
- 基金信息：
  
  国家自然科学基金地区项目(81460636);国家自然科学基金联合基金项目(U1303233)
- DOI：10.16016/j.1000-5404.202009246
  中图分类号：
- 收稿：2020-09-29，
  
  纸质出版：2021-03-15
- 稿件说明：
移动端阅览
魏晓丽, 郭艳丽, 张永威, 等. 基于网络药理学探究黄诺玛苷对非酒精性脂肪肝的降脂作用[J]. 第三军医大学学报, 2021,43(5):383-394.

Xiaoli WEI, Yanli GUO, Yongwei ZHANG, et al. Lipid-lowering effect of flavanomarein on non-alcoholic fatty liver disease based on network pharmacology[J]. Journal of Third Military Medical University, 2021, 43(5): 383-394.
魏晓丽, 郭艳丽, 张永威, 等. 基于网络药理学探究黄诺玛苷对非酒精性脂肪肝的降脂作用[J]. 第三军医大学学报, 2021,43(5):383-394. DOI： 10.16016/j.1000-5404.202009246.

Xiaoli WEI, Yanli GUO, Yongwei ZHANG, et al. Lipid-lowering effect of flavanomarein on non-alcoholic fatty liver disease based on network pharmacology[J]. Journal of Third Military Medical University, 2021, 43(5): 383-394. DOI： 10.16016/j.1000-5404.202009246.

摘要

Abstract

Objective

To explore the targets and signaling pathways of flavanomarein in the treatment of non-alcoholic fatty liver disease (NAFLD) by network pharmacology

and to investigate the effect and mechanisms in the treatment.

Methods

① The potential active targets of flavanomarein were retrieved in the Swiss Target Pr

ediction database

and the disease-related targets were searched in the DisGeNET database. The prediction targets of lipid metabolism of NAFLD regulated by flavanomarein was obtained through Venn analysis. The Biso Genet database was used to construct the protein-protein interaction (PPI) network diagram

the Metascape database was used to analyze GO functional enrichment and KEGG pathway enrichment

and the Cytoscape software was used to draw the "target-pathway" network diagram. ② NAFLD db/db mice was employed for

in vivo

verification. Thirty male db/db mice were randomly divided into db/m group

db/db model group

and db/db+flavanomarein group (50 mg/kg). After the administration of 0.5% sodium carboxymethyl cellulose solution and flavanomarein for 12 weeks

the mice were sacrificed

and the liver contents of TG

GSH and GSSG was detected. HE staining and oil red O staining were used to observe the pathological changes of the liver. qRT-PCR and Western blotting were used to detect the mRNA and protein levels of key molecules in the lipid metabolism in the liver. ③HepG2 cells were treated with free fatty acids (FFAs

oleic acid∶palmitic acid =2∶1) and divided into normal group

FFAs treatment group (500 μmol/L)

and FFAs+ low

medium and high concentrations of flavanomarein (25

100 μmol/L) for 24 h. Oil red O staining was used to detect the TG content in HepG2 cells. qRT-PCR and Western blotting were used to detect the mRNA and protein levels of key molecules in the lipid metabolism of HepG2 cells.

Results

① A total of 29 core targets of flavanomarein docking NAFLD were screened through Venn analysis

including peroxisome proliferator-activated receptor-gamma (PPARγ)

vascular endothelial growth factor (VEGF)

and mitogen-activated protein kinase 14 (MAPK14). The GO analysis enriched 6 molecular functions

20 biological processes and 5 cellular components. KEGG analysis enriched 40 key signaling pathways related to the effect of flavanomarein on NAFLD

which

mainly focuses on the AMPK lipid metabolism pathway

insulin resistance (IR) pathway

and apoptosis pathway. ② The results of animal experiments showed that flavanomarein treatment reduced TG level in the NAFLD mice (

0.05) and improved the ratio of GSH/GSSG (

0.05). HE and oil red O staining showed that flavanomarein could reverse hepatocyte enlargement and reduce lipid drop infiltration of hepatocytes. qRT-PCR results showed that the treatment decreased the mRNA levels of ACC1

SCD1

and FASN for lipid synthesis (

0.05)

while increased those of ACOX-1 and CPT1α for β-oxidation (

0.05). Western blot assay results indicated that the expression levels of SREBP and FASN were obviously lower (

0.05)

and those of PPARγ and PPARα were increased (

0.05) in the flavanomarein group than the model group. ③

In vitro

cell experiments showed that flavanomarein reduced the TG content of HepG2 cells (

0.05) and the expression of SREBP

SCD1 and ACC1

but increased the levels of CPT1α and ACOX-1 mRNA (

0.05). And

the protein expression of SREBP and FASN was also significantly reduced (

0.05).

Conclusion

Flavanomarein may play a therapeutic role in NAFLD by improving oxidative stress

up-regulating fatty acid β-oxidation

reducing lipid synthesis through regulating the PPARγ/SREBP/FASN signaling pathway.

关键词

Keywords

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