实用医学杂志 ›› 2021, Vol. 37 ›› Issue (10): 1235-1239.doi: 10.3969/j.issn.1006⁃5725.2021.10.001

• 基础研究 •    下一篇

G蛋白偶联雌激素受体通过减轻大鼠肾小管上皮细胞凋亡保护肾脏缺血再灌注损伤

闫林轩, 梅霄阳, 章林明, 常越辰,马克涛, 李丽,王勤章, 李应龙   

  1. 1 石河子大学医学院(新疆石河子 832000);2 石河子大学医学院第一附属医院(新疆石河子 832000);3 成都中医药大学附属第五人民医院(成都 610000)

  • 出版日期:2021-05-25 发布日期:2021-05-25
  • 通讯作者: 李应龙 E⁃mail:lyl0993@sina.com
  • 基金资助:
    国家自然科学基金资助项目(编号:81960188)

GPER protects renal ischemia⁃reperfusion injury by reducing the apoptosis of renal tubular epithelial cells in rats 

YAN Linxuan,MEI Xiaoyang,ZHANG Linming,CHANG Yuechen,MA Ketao,LI Li,WANG Qin⁃ zhang,LI Yinglong.    

  1. Shihezi University Medical SchoolShihezi 832000China 
  • Online:2021-05-25 Published:2021-05-25
  • Contact: LI Yinglong E⁃mail:lyl0993@sina.com

摘要:

目的 探讨G 蛋白偶联雌激素受体(G protein⁃coupled estrogen receptor,GPER)能否减轻肾小管上皮细胞凋亡,从而保护肾脏缺血再灌注(ischemia⁃reperfusion,I/R)损伤。方法 雌性去卵巢(ovariec⁃ tomized,OVX)大鼠随机分为 OVX 组、OVX+I/R 组、OVX+I/R+G1(GPER 激动剂)组、OVX+I/R+G15(GPER 断剂)+G1 组。检测各组大鼠肾功能,HE 染色、Paller 评分评价肾组织损伤程度,观察肾组织凋亡相关蛋白 的表达位置及表达水平。结果  OVX 组相比,OVX+I/R 组肾功能损伤明显(P < 0.01),Paller 评分升高 P < 0.01),Bcl⁃2 蛋白在肾小管上皮细胞阳性表达及肾组织的表达均减少,Caspase⁃3 蛋白在肾小管上皮细 胞阳性表达及肾组织的表达均增加(P < 0.01);G1 干预后肾功能损害减轻(P < 0.01),Paller 评分降低(P < 0.01),Bcl⁃2 蛋白的表达上升,Caspase⁃3 蛋白的表达下降(P < 0.01);G15 组可部分逆转 G1 激活 GPER 后的保护作用(均 P < 0.01)。结论 激活 GPER 可以减轻肾脏 I/R 损伤,其机制可能是通过调控凋亡通路实现的。

关键词:

G 蛋白偶联雌激素受体, 肾脏缺血再灌注损伤, 肾小管上皮细胞, 细胞凋亡

Abstract:

Objective To investigate the effect of G protein ⁃ coupled estrogen receptor (GPER)on ischemia ⁃ reperfusion(I/R)injury. Methods Female ovariectomized(OVX)rats were randomly divided into OVX group,OVX + I/R group,OVX + I/R +G1(GPER agonist)group,OVX + I/R +G15(GPER blocker)+ G1 group. The renal function of rats in each group was detected,HE staining and Paller score were used to evaluate the degree of renal tissue damage ,and the expression position and expression level of renal tissue apoptosis⁃ related proteins were observed. Results Compared with the OVX group,the renal function of the OVX+I/R group was significantly damaged(P < 0.01),Paller score increased(P < 0.01),and the positive expression of Bcl⁃2 protein in renal tubular epithelial cells and the expression of renal tissue were reduced. The positive expression of Caspase⁃3 protein in renal tubular epithelial cells and the expression of renal tissue increased(P < 0.01). The renal function damage was significantly reduced after G1 intervention (P < 0.01),Paller score significantly decreased(P < 0.01),the expression of Bcl⁃2 significantly increased,and the expression of Caspase⁃3 protein significantly decreased (P < 0.01). The protective effect of G1 activated GPER G15 group was partially reversed (all P < 0.01). Conclusion Activated GPER can alleviate renal I/R injury,and its mechanism may be achieved by regulating the apoptosis pathway.

Key words:

G protein ?coupled estrogen receptor, renal ischemia ? reperfusion injury, renal tubular epithelial cells, apoptosis