|本期目录/Table of Contents|

[1]周新凤,宋佳音,王丹,等.基于网络药理学的参桂胶囊治疗2型糖尿病作用机制研究[J].天津医科大学学报,2023,29(01):21-26,40.
 ZHOU Xin-feng,SONG Jia-yin,WANG Dan,et al.Network pharmacology-based prediction of mechanism in Shengui capsule on type 2 diabetes mellitus[J].Journal of Tianjin Medical University,2023,29(01):21-26,40.
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基于网络药理学的参桂胶囊治疗2型糖尿病作用机制研究(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
29卷
期数:
2023年01期
页码:
21-26,40
栏目:
网络药理学专题
出版日期:
2023-01-20

文章信息/Info

Title:
Network pharmacology-based prediction of mechanism in Shengui capsule on type 2 diabetes mellitus
文章编号:
1006-8147(2023)01-0021-07
作者:
周新凤1宋佳音1王丹2杨子君1刘甜甜1崔妍3吴晓辉1
(1.天津医科大学药学院临床药学系,天津 300070;2. 天津医科大学朱宪彝纪念医院药剂科,天津 300134;3.天津医科大学基础医学院病原生物学系,天津 300070)
Author(s):
ZHOU Xin-feng1SONG Jia-yin1WANG Dan2YANG Zi-jun1LIU Tian-tian1CUI Yan3WU Xiao-hui1
(1.Department of Clinical Pharmacy,College of Pharmacy,Tianjin Medical University,Tianjin 300070,China; 2. Pharmacy Department,Chu Hsien-I Memorial Hospital,Tianjin Medical University,Tianjin 300134,China; 3. Department of Pathogen Biology,School of Basic Medical Sciences,Tianjin Medical University,Tianjin 300070,China)
关键词:
参桂胶囊网络药理学2型糖尿病活性成分
Keywords:
Shengui capsule network pharmacology type 2 diabetes mellitus active ingredient
分类号:
R781.4
DOI:
-
文献标志码:
A
摘要:
目的:通过网络药理学研究参桂胶囊(SGC)治疗2型糖尿病(T2DM)的作用机制。方法:使用中药系统药理学分析平台(TCMSP)检索SGC中的主要活性成分及靶点,治疗靶标数据库(TTD)、比较毒性基因组学数据库(CTD)、在线孟德尔遗传(OMIM)、GeneCards数据库获取T2DM靶点,进而筛选出中药和疾病的共同靶点。采用Cytoscape3.8.2软件构建“成分-靶点”网络图,并通过Metascape对共同靶点进行GO和KEGG富集分析预测SGC主要作用通路。结果:分析显示SGC中的人参皂苷、咖啡酸、油酸、肉桂醛和β-谷甾醇为主要活性成分,核心靶点有胰岛素(INS)、白细胞介素-6(IL-6)、肿瘤坏死因子(TNF)、过氧化物酶体增殖物激活受体-γ(PPAR-γ)等。主要涉及低氧诱导因子-1(HIF-1)、晚期糖基化终末产物(AGE)-糖基化终末产物受体(RAGE)信号通路、 cAMP信号通路等。结论:揭示了SGC可通过“多成分、多靶点、多途径”作用机制对抗T2DM,为今后研究SGC治疗T2DM提供了文献依据。
Abstract:
Objective: To predict the mechanism of Shengui capsule(SGC) in the treatment of type 2 diabetes mellitus(T2DM) by network pharmacology method. Methods:The main active ingredients and their targets of SGC were searched by Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform(TCMSP). Therapeutic Target Database(TTD),Comparative Toxicogenomics Database (CTD),Online Mendelian Inheritance in Man(OMIM) and GeneCards were used to obtain the related targets of T2DM,then the common targets of traditional Chinese medicine and disease were screened out. The "ingredients-target" network diagram was constructed with Cytoscape3.8.2 software. GO and KEGG enrichment analysis were performed on the common targets by Metascape to predict the main pathway of SGC. Results: Analysis showed that ginsenoside,caffeic acid,oleic acid,cinnamaldehyde and β-sitosterol were the main active ingredients in SGC,and the core targets were insulin(INS),interleukin-6(IL6),tumor necrosis factor(TNF),peroxisome proliferator-activated receptor gamma(PPARG),etc. It mainly involved hypoxia-inducible factor-1(HIF-1),advanced glycation end product(AGE) -glycation end product receptor(RAGE)signaling pathway,cyclic adenosine monophosphate(cAMP) signaling pathway,etc. Conclusion:This study reveals the "multi-ingredient,multi-target and multi-pathway" mechanism of SGC against T2DM,which provides a literature basis for the future study of SGC in the treatment of T2DM.

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备注/Memo

备注/Memo:
基金项目: 天津市自然科学基金重点项目(19JCZDJC33500)
作者简介:周新凤(1997-),女,硕士在读,研究方向:临床药理学;通信作者:崔妍,E-mail:cuiyanbio45@163.com; 吴晓辉,E-mail:xiaohuiwu@tmu.edu.cn。
更新日期/Last Update: 2023-02-01