Differential effect of losartan in female and male spontaneously hypertensive rats

被引:12
作者
Rodrigues, SFD [1 ]
dos Santos, RA [1 ]
Silva-Antonialli, MM [1 ]
Scavone, C [1 ]
Nigro, D [1 ]
Carvalho, MHC [1 ]
Tostes, RD [1 ]
Fortes, ZB [1 ]
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Pharmacol, Lab Hypertens, BR-05508900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
vascular reactivity; SHR; losartan; angiotensin AT2 receptor; nitric-oxide synthase; angiotensin AT1 receptor;
D O I
10.1016/j.lfs.2005.09.049
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We demonstrated that the decreased response to acetylcholine observed in aorta of male and female spontaneously hypertensive rats is corrected after sustained (15 days) reduction of blood pressure levels by losartan. In order to verify if the same occurs in resistance vessels, vascular diameter changes induced by topical application of acetylcholine and bradykinin (endothelium-dependent vasodilators) and sodium nitroprusside (endothelium-independent vasodilator) to mesenteric arterioles studied in vivo, in situ were determined in rats treated with losartan for 24 h (acute) or 15 days (chronic). Rats that presented similar reduction (in %) of the blood pressure levels after losartan treatment were chosen. Sodium nitroprusside induced similar responses in losartan-treated and untreated male or female SHR. Whereas in female SHR, losartan corrected the diminished arteriolar response to endothelium-dependent vasodilators after acute and chronic treatment, in male SHR this correction only occurred after chronic treatment. Thus, losartan corrected the endothelial dysfunction more easily in female than in male SHR and independently of the normalization or the magnitude of the reduction of the blood pressure levels. In an attempt to explain the difference, we evaluated the losartan effect on nitric-oxide synthase (NOS) activity and angiotensin II AT1 and AT2 receptor gene expression in these animals. In male and female SHR, NOS activity and AT1 receptor expression were not altered by acute or chronic treatment. On the other hand, AT2 receptor expression was augmented only in female SHR by these treatments. Therefore, augmented AT2 receptor expression, but not alteration of NOS activity or AT I receptor expression, might explain the difference observed. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2280 / 2285
页数:6
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