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Network pharmacology and molecular docking analysis on molecular targets: Mechanisms of baicalin and baicalein against hyperuricemic nephropathy

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成果类型:
期刊论文
作者:
Xiang, Huilong;Lei, Huan;Liu, Ziyuan;Liu, Yongjie;Li, Yang;...
通讯作者:
Xu, Lingyun
作者机构:
[Xu, Lingyun; Li, Yang; Xiang, Huilong; Liu, Yongjie; Lei, Huan; Liu, Ziyuan] Wuhan Polytech Univ, Coll Life Sci & Technol, Xuefu South Rd 68, Wuhan 430023, Peoples R China.
[Qiu, Yinsheng] Wuhan Polytech Univ, Sch Anim Sci & Nutr Engn, Wuhan 430023, Peoples R China.
通讯机构:
[Xu, Lingyun] C
College of Life Science and Technology, Wuhan Polytechnic University, Wuhan 430023, China. Electronic address:
语种:
英文
关键词:
Baicalein;Baicalin;Hyperuricemic nephropathy;Molecular docking.;Network pharmacology;Xanthine oxidase
期刊:
Toxicology and Applied Pharmacology
ISSN:
0041-008X
年:
2021
卷:
424
期:
2
页码:
115594
基金类别:
Open Project of Hubei Key Laboratory of Animal Nutrition and Feed Science [201912]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [31572572]
机构署名:
本校为第一机构
院系归属:
生命科学与技术学院
动物科学与营养工程学院
摘要:
Oxidative stress and inflammation in kidney are the main causes for hyperuricemic nephropathy (HN). Baicalin and baicalein, two flavonoids, have anti-inflammatory and anti-oxidative effects and they are interconvertible in the body. In this study, both baicalin and baicalein were administered by intragastric administration (i.g.) or intraperitoneal injection (i.p.) at the dose of 50 mg kg(-1), once a day for 15 consecutive days to HN mice, a model established by i.g. of yeast extract combined with i.p. of potassium oxonate. In HN mice, baical...

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