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引用本文:Ѧ����,����,������,���,����,������,���.��������ҩ��ѧ̽�ָ�����ǻ��Գɷּ����û��Ƶ��о�[J].中国药学杂志,2018,53(20):1748-1754.
作者姓名:Ѧ����  ����  ������  ���  ����  ������  ���
作者单位:1. ??????????, ???? ???? 453002;
2. ???????????????, ???? ???? 453003
摘    要:

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Hypoglycemic Bioactive Components and Mechanism of Puerariae Lobatae Radix by Network Pharmacology
XUE Jin-tao,HUANG Ning,KONG Wen-yan,LI Chun-yan,JING Yun,ZHANG Ming-xiang,LI Peng.Hypoglycemic Bioactive Components and Mechanism of Puerariae Lobatae Radix by Network Pharmacology[J].Chinese Pharmaceutical Journal,2018,53(20):1748-1754.
Authors:XUE Jin-tao  HUANG Ning  KONG Wen-yan  LI Chun-yan  JING Yun  ZHANG Ming-xiang  LI Peng
Institution:1. School of Pharmacy, Xinxiang Medical University, Xinxiang 453002, China;
2.School of Pharmacy, Sanquan Medical College, Xinxiang Medical University, Xinxiang 453003, China
Abstract:??OBJECTIVE To predict the action targets of the hypoglycemic bioactive components of Gegen (Puerariae Lobatae Radix), and investigate the ??multi-components, multi-targets and multi-pathways?? mechanism. METHODS Based on the network pharmacology, the reported 27 active ingredients in Gegen were used to predict the action target and reveal the action mechanism via reversed pharmacophore matching method, database mining, and some other methods. The PharmMapper database and DrugBank database were applied to screen the hypoglycemic drug targets approved by FDA. Additionlly, the information of these targets and their intentions were revealed by the String database. At last the ingredients-targets-pathways network was constructed via the Cytoscape software. RESULTS Studies found that Gegen contained hypoglycemic components, such as:puerarin, 3'-hydroxypuerarin, 3'-methoxypuerarin, daidzein and so on. Their actions involved in 9 potential targets and 25 energy metabolism or signal transmutation relevant biological processes, e.g. insulin receptor, angiotensin-converting enzyme 2 (ACE2), and peroxisome proliferator-activated receptor ?? (PPAR??). While the mainly metabolism and signal transmutation pathways were HIF-1 signaling pathway, renin-angiotensin system, FoxO signaling pathway, AMPK signaling pathway and so on. CONCLUSION From the view of molecular network, this study applied provides network pharmacology methods and technologies to clarify the multi-components, multi-targets and multi-pathways of Gegen on the hypoglycemic effect, and it provides a theoretical basis and a clue for further exploration of the hypoglycemic mechanism of Gegen.
Keywords:
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