Aortic Cell Apoptosis in Rat Primary Aldosteronism Model
10.1007/s11596-010-0362-3
- Author:
YAN YONGJI
1
,
2
;
OUYANG JINZHI
;
WANG CHAO
;
WU ZHUN
;
MA XIN
;
LI HONGZHAO
;
XU HUA
;
HU ZHENG
;
LI JUN
;
WANG BAOJUN
;
SHI TAOPING
;
GONG DAOJING
;
NI DONG
;
ZHANG XU
Author Information
1. Department of Urology,Tongji Hospital,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China
2. Department of Urology,Chinese People's Liberation Army General Hospital,Military Postgraduate Medical College,Beijing 100853,China
- Keywords:
aldosteronism;
apoptosis;
mineralocorticoid receptor;
aorta
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2010;30(3):385-390
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to determine whether aldosterone could induce vascular cell apoptosis in vivo.Thirty-two male rats were randomly divided into 4 groups: vehicle(control),aldosterone,aldosterone plus eplerenone or hydralazine.They were then implanted with an osmotic mini-pump that infused either aldosterone or the vehicle.Systolic blood pressure(SBP)was measured weekly by the tail-cuff method.After 8 weeks,plasma aldosterone concentration(PAC)and renin activity(PRA)were determined by radioimmunoassay.Aortic apoptosis was examined by TUNEL assay.The levels of cytochrome c and caspase-3 were determined by Western blotting and the expression of Bax and Bcl-2 was detected by immnuohistochemistry and Western blotting.The results showed that as compared with control group,aldosterone-infused rats exhibited:(1)an increase in SBP;(2)significantly elevated PAC with depressed PRA;(3)elevated aortic vascular cell apoptosis accompanied with higher levels ofcytochrome c and activated caspase-3; and(4)significantly up-regulated Bax protein with down-regulated Bcl-2.These effects of aldosterone were significantly inhibited after co-administration with eplerenone but not with hydralazine.It was concluded that aldosterone inducedvascular cell apoptosis by its direct effect on the aorta via mineralocorticoid receptors and independently of blood pressure,which may contribute to aldosterone-mediated vascular injury.
