Effects of estrogens on cardiovascular structure in uninephrectomized SHRsp rats

被引:14
作者
Gross, ML
Ritz, E
Korsch, M
Adamczak, M
Weckbach, M
Mall, G
Berger, I
Hansen, A
Amann, K
机构
[1] Heidelberg Univ, Dept Pathol, D-69120 Heidelberg, Germany
[2] Dept Pathol, Darmstadt, Germany
[3] Univ Erlangen Nurnberg, Dept Pathol, Erlangen, Germany
[4] Heidelberg Univ, Dept Internal Med, D-6900 Heidelberg, Germany
[5] Heidelberg Univ, Dept Nephrol, D-6900 Heidelberg, Germany
[6] Heidelberg Univ, Dept Cardiol, D-6900 Heidelberg, Germany
[7] Med Univ Silesia, Dept Endocrinol & Metab Dis, Katowice, Poland
关键词
estrogens; left ventricular hypertrophy; heart fibrosis; heart capillaries; SHRsp; moderate renal dysfunction;
D O I
10.1111/j.1523-1755.2005.00149.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. The risk of cardiovascular disease in uremic patients is greater in male than in female patients. Estrogens seem to play a cardioprotective role until menopause. Experimental data on the effect of estrogens on cardiovascular damage are controversial and potential underlying mechanisms especially in renal failure have not been fully clarified. Methods. Three-month-old female uninephrectomized stroke-prone spontaneously hypertensive (SHRsp) rats were sham-operated or ovariectomized. Subsequently, they received either vehicle (sesame oil) or 17-beta-3 benzoate estradiol (E2) (25 mug/day) or estriol (E3) (0.02 mg/day), respectively. After 3 months the animals were sacrified and the organs were harvestel using pressure-con trolled perfusion fixation. Stereologic parameters such as capillary length density (Lv), mean intercapillary distance (MID), and volume density of the interstitial tissue (Vv) were quantitated. Additionally, expression of transforming growth factor-beta (TGF-beta), vascular endothelial growth factor (VEGF), flt-1, endothelial nitric oxide synthase (eNOS), endothelin-1 (ET-1), endothelin A receptor (ETA) receptor, and a estrogen receptor was assessed using immunohistochemistry. Intramyocardial capillaries and the aorta were investigated by morphometric methods. Results. Lv (mm/mm(3)) was significantly lower (2421 +/- 500) and MID (mum) significantly higher (22.2 +/- 2.33) in vehicle-treated uninephrectomized/ovariectomized compared to uninephrectomized/sham-ovariectomized controls (Lv 3629 960, MID 12.7 +/- 2.7) as well as estradiol (L-v 3340 +/- 739, MID 12.1 +/- 4.96) and estriol (L-v 4655 +/- 618, MID 14.2 +/- 2.89) treated uninephrectomized/ovariectomized animals. The volume density of the cardiac interstitium was higher in vehicle-treated uninephrectomized/ovariectomized animals compared to uninephrectomized/sham-ovariectomized, estradiol and estriol treated uninephrectomized/ovariectomized rats. The protein level expression of TGF-beta was higher in vehicle treated uninephrectomized/ovariectomized compared to uninephrectomized/sham and all treatment groups. Conclusion. In ovariectomized SHRsp rats with moderate renal failure cardiac lesions were strikingly less after estradiol or estriol treatment. The results document a beneficial role of estrogens on cardiac abnormalities in a model of moderate renal dysfunction.
引用
收藏
页码:849 / 857
页数:9
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