| 注册
首页|期刊导航|烟台大学学报(自然科学与工程版)|丹酚酸A通过抗炎抗氧化发挥对急性肾损伤大鼠的保护作用

丹酚酸A通过抗炎抗氧化发挥对急性肾损伤大鼠的保护作用

张作凯 王学凯 高振芳 田霄 杨明艳 范华英

烟台大学学报(自然科学与工程版)2017,Vol.30Issue(2):124-130,7.
烟台大学学报(自然科学与工程版)2017,Vol.30Issue(2):124-130,7.DOI:10.13951/j.cnki.37-1213/n.2017.02.008

丹酚酸A通过抗炎抗氧化发挥对急性肾损伤大鼠的保护作用

Salvianolic Acid A Protects against Acute Kidney Injury inRats through Anti-inflammation and Antioxidation

张作凯 1王学凯 1高振芳 1田霄 1杨明艳 1范华英1

作者信息

  • 1. 烟台大学新型制剂与生物技术药物研究山东省高校协同创新中心、分子药理和药物评价教育部重点实验室(烟台大学),山东 烟台 264005
  • 折叠

摘要

Abstract

To study the effect of salvianolic acid A (SAA) on acute kidney injury (AKI) induced by ischemia-reperfusion (I/R) in rats, male SD rats are randomly divided into control group, sham operation group, I/R group and SAA (2.5 mg/kg, 5 mg/kg, 10 mg/kg) groups.The model of AKI in rats is made by clipping bilateral renal pedicles for 60 min, and then reperfusion for 24 hours.Twenty-four hours after reperfusion, the levels of serum creatinine (Scr), blood urea nitrogen (BUN) and renal injury factor1 (KIM-1) are determined, and morphological changes of renal tissues are also recorded.Furthermore, the serum interleukin-6 (IL-6), interleukin-10 (IL-10), malondialdehyde (MDA) concentrations, and superoxide dismutase (SOD) activity are tested.Experimental results show that treatment with SAA significantly reduces the serum levels of Scr, BUN and urine KIM-1, and alleviates the degree of tubular necrosis compared with those of the I/R group.SAA also decreases the production of IL-6 and MDA, elevates the level of IL-10, and enhances the activity of SOD.Thus, SAA can prevent AKI induced by I/R in rats, which may be related to its anti-inflammation and antioxidation features.

关键词

丹酚酸A/急性肾损伤/缺血再灌注/抗炎/抗氧化

Key words

salvianolic acid A/acute kidney injury/ischemia/reperfusion/anti-inflammation antioxidation

分类

医药卫生

引用本文复制引用

张作凯,王学凯,高振芳,田霄,杨明艳,范华英..丹酚酸A通过抗炎抗氧化发挥对急性肾损伤大鼠的保护作用[J].烟台大学学报(自然科学与工程版),2017,30(2):124-130,7.

基金项目

国家自然科学基金资助项目(81303259) (81303259)

山东省优秀中青年科学家科研奖励基金资助项目(BS2013YY046). (BS2013YY046)

烟台大学学报(自然科学与工程版)

1004-8820

访问量0
|
下载量0
段落导航相关论文