[1]张婷,尹哲,杨阳,等.柏薏颗粒对高尿酸血症大鼠的初步药效学分析[J].华侨大学学报(自然科学版),2020,41(6):791-796.[doi:10.11830/ISSN.1000-5013.202006021]
 ZHANG Ting,YIN Zhe,YANG Yang,et al.Preliminary Pharmacodynamic Analysis of Baiyi Granules on Hyperuricemia Rats[J].Journal of Huaqiao University(Natural Science),2020,41(6):791-796.[doi:10.11830/ISSN.1000-5013.202006021]
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柏薏颗粒对高尿酸血症大鼠的初步药效学分析()
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《华侨大学学报(自然科学版)》[ISSN:1000-5013/CN:35-1079/N]

卷:
第41卷
期数:
2020年第6期
页码:
791-796
栏目:
出版日期:
2020-11-20

文章信息/Info

Title:
Preliminary Pharmacodynamic Analysis of Baiyi Granules on Hyperuricemia Rats
文章编号:
1000-5013(2020)06-0791-06
作者:
张婷1 尹哲1 杨阳1 吴振2 王立强1
1. 华侨大学 医学院, 福建 泉州 362021;2. 厦门大学 药学院, 福建 厦门 361102
Author(s):
ZHANG Ting1 YIN Zhe1 YANG Yang1 WU Zhen2 WANG Liqiang1
1. School of Medicine, Huaqiao University, Quanzhou 362021, China; 2. School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China
关键词:
柏薏颗粒 高尿酸血症 黄嘌呤氧化酶 药效学
Keywords:
Baiyi granule hyperuricemia xanthine oxidase pharmacodynamics
分类号:
R971.1;R285.5
DOI:
10.11830/ISSN.1000-5013.202006021
文献标志码:
A
摘要:
针对高尿酸血症大鼠模型开展柏薏颗粒的初步药效学研究,探究其作用机制.将72只雄性大鼠随机分为空白组、模型组、柏薏颗粒高、中、低剂量组及非布司他阳性对照组,采用氧嗪酸钾灌胃给药法建立高尿酸血症大鼠模型,连续给药治疗14 d,每天1次.采用酶联免疫吸附剂测定(ELISA)试剂盒测定血清尿酸(SUA)、肌酐(Cr)、尿素氮(BUN)水平及肝脏黄嘌呤氧化酶(XOD)活性,并用免疫印迹法测定肾脏中有机阴离子转运体1(OAT1)及葡萄糖转运体9(GLUT9)的表达.结果表明:与模型组相比,柏薏颗粒可剂量依赖性地降低SUA水平、肝脏XOD活性及GLUT9蛋白表达,并上调OAT1蛋白表达,且高剂量组与非布司他作用相当(P>0.05);柏薏颗粒组与空白组大鼠血清中Cr和BUN浓度无显著性差异,表明柏薏颗粒无肾损伤;柏薏颗粒具有明显的降血尿酸作用,其机制可能与抑制XOD活性和肾脏GLUT9蛋白表达,并上调OAT1蛋白表达有关.
Abstract:
Based on the rat model of hyperuricemia, a preliminary study on the pharmacodynamics of Baiyi granule was carried out and its mechanism was explored. 72 male rats were randomly divided into control group, model group, Baiyi granule high, medium and low dose groups and febuxostat positive control group. The rats were induced hyperuricemia through intragastric administration of oxonic aid potassium salt, and then administrated drugs by gavage, once a day for 14 consecutive days. The levels of uric acid(SUA), serum creatinine(Cr), urea nitrogen(BUN)and the xanthine oxidase(XOD)activity in liver were determined by enzyme linked immunosorbent assay(ELISA)kits, and the organic anion transporter 1(OAT1)and glucose transporter 9(GLUT9)proteins expressions in kidney were determined by western blot. Compared with themodel group, Baiyi granules can reduce the SUA level and liver XOD activity as well as GLUT9 protein expression in a dose-dependent manner, and up-regulate the OAT1 protein expression, and the high-dose group has the same effect as febuxostat(P>0.05). There is no significant difference in the contents of Cr and BUN in serum between Baiyi granule groups and control group, which indicates that Baiyi granule has no renal injury. In addition, Baiyi granules have obvious effect on reducing SUA, and its mechanism may be related to the inhibition of XOD activity and the expression of GLUT9 protein in kidney, and the up-regulation of OAT1 protein expression.

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备注/Memo

备注/Memo:
收稿日期: 2020-06-12
通信作者: 王立强(1970-),男,教授,博士,主要从事药剂学与创新药物的研究.E-mail:wlq1599@163.com.
基金项目: 国家重点研发计划项目(2016YFE0101700); 福建省高校产学合作重大项目(2019Y4007); 华侨大学研究生科研创新基金资助项目(18014071025)http://www.hdxb.hqu.edu.cn
更新日期/Last Update: 2020-11-20