Angiotensin receptor type 1 mRNA in human right ventricular endomyocardial biopsies: Downregulation in heart failure

被引:27
作者
RegitzZagrosek, V
Fielitz, J
Dreysse, R
Hildebrandt, AG
Fleck, E
机构
[1] DEUTSCH HERZZENTRUM,D-13353 BERLIN,GERMANY
[2] BUNDESINST ARZNEIMITTEL,BERLIN,GERMANY
关键词
human; angiotensin receptor; mRNA; RT-PCR;
D O I
10.1016/S0008-6363(97)00089-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Atrial angiotensin II receptors type 1 (AT(1)) are downregulated in end-stage human heart failure at mRNA and protein level. The present study investigated whether AT(1) ventricular mRNA content was reduced in myocardial biopsies from heart failure patients. Methods: AT(1) mRNA was quantitated in right ventricular endomyocardial biopsies from 16 patients with decreased left ventricular function (LVEF 36 +/- 3%) due to dilated cardiomyopathy (DCM) and in biopsies from 12 patients with suspected myocardial disease but normal cardiac function (LVEF 62 +/- 2%). Two biopsies per patient were pooled, RNA was extracted and reverse-transcribed after addition of an AT(1) cRNA standard. AT(1) standard and wild-type RNA were amplified with the same primers in the same PCR tube. The PCR products were hybridized to a microtiter plate and detected and quantitated by an ELISA system. Glyceraldehyde phosphate dehydrogenase (GAPDH) mRNA was determined in the same samples as AT(1) mRNA. Results: In the biopsies from 16 patients with heart failure, a 68% decrease in AT(1) mRNA content was found in comparison with 12 controls (heart failure 94 +/- 15 AT(1) mRNA copies/ng RNA; controls 297 +/- 45; P < 0.001). Relating AT(1) mRNA content to GAPDH mRNA confirmed the specific decrease in AT(1) mRNA (AT(1)/GAPDH: heart failure 1.3 +/- 0.15; controls 3.4 +/- 0.5; P < 0.002). The best correlation between AT(1) mRNA content and clinical parameters was found for right ventricular ejection fraction (r = 0.59, P < 0.01). Conclusions: The quantitative RT-PCR procedure indicated a loss of ventricular AT(1) mRNA in human heart failure which corresponds to the loss of AT(1) protein described previously. It may underlie the decrease in AT(1) protein expression in human heart failure.
引用
收藏
页码:99 / 105
页数:7
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