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首页|期刊导航|中国药科大学学报|基于网络药理学探讨银杏叶提取物通过激活PPARγ治疗动脉粥样硬化的机制

基于网络药理学探讨银杏叶提取物通过激活PPARγ治疗动脉粥样硬化的机制

王子元 陶惠 肖映雪 殷志琦

中国药科大学学报2025,Vol.56Issue(2):225-235,11.
中国药科大学学报2025,Vol.56Issue(2):225-235,11.DOI:10.11665/j.issn.1000-5048.2024032301

基于网络药理学探讨银杏叶提取物通过激活PPARγ治疗动脉粥样硬化的机制

Network pharmacology-based study of the mechanism of Ginkgo biloba extract(GBE)in the treatment of atherosclerosis by activating PPARγ

王子元 1陶惠 1肖映雪 2殷志琦1

作者信息

  • 1. 中国药科大学中药学院中药制药系,南京 211198
  • 2. 中国药科大学中药学院天然药物化学系,南京 211198
  • 折叠

摘要

Abstract

To investigate the effect of Ginkgo biloba extract(GBE)on lipids accumulation and the progression of atherosclerosis(AS),ApoE-/-mice fed with HFD were injected i.g.with two different doses of GBE(GBE-L 50 mg/(kg·d)or GBE-H 150 mg/(kg·d))for 9 weeks.The core targets and potential mechanisms of GBE therapy for AS were investigated using network pharmacological target prediction.Subsequently,oxidized low-density lipoprotein(ox-LDL)-induced THP-1 was used to investigate the effect of GBE on foam cell formation through oil red staining and Dil-oxLDL fluorescent staining.The mRNA alterations in cholesterol uptake and efflux receptors were detected by real-time quantitative PCR.Finally,the impact of GBE on the expression of PPARγ as the core target was assessed through Western blot and immunofluorescence.It was found that GBE improved serum lipid profile,reduced necrotic cores and lipid deposition in aortic root plaques,and decreased the level of inflammatory factors in serum of ApoE-/-mice.Moreover,GBE treatment reduced the level of intracellular lipid accumulation and inhibited cholesterol uptake and efflux to alleviate foam cell formation.GBE activated PPARγ to enhance ABCA1/ABCG1-induced cholesterol efflux in THP-1.These results suggest that GBE can suppress lipid accumulation and alleviate foam cell formation by activating PPARγ pathway.

关键词

银杏叶提取物/动脉粥样硬化/泡沫细胞/PPARγ

Key words

Ginkgo bilobaextract/atherosclerosis/foam cell/PPARγ

分类

医药卫生

引用本文复制引用

王子元,陶惠,肖映雪,殷志琦..基于网络药理学探讨银杏叶提取物通过激活PPARγ治疗动脉粥样硬化的机制[J].中国药科大学学报,2025,56(2):225-235,11.

中国药科大学学报

OA北大核心

1000-5048

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