Neutral endopeptidase is activated in cardiomyocytes in human aortic valve stenosis and heart failure

被引:60
作者
Fielitz, J
Dendorfer, A
Pregla, R
Ehler, E
Zurbrügg, HR
Bartunek, J
Hetzer, R
Regitz-Zagrosek, V
机构
[1] DHZB, Klin Herz Gefass & Thoraxchirurg, D-13353 Berlin, Germany
[2] Franz Volhard Klin, Charite, Berlin, Germany
[3] Med Univ Phrmacol & Toxicol, Lubeck, Germany
[4] ETH Zurich, Inst Zellbiol, CH-8093 Zurich, Switzerland
[5] Ctr Cardiovasc, Aalst, Belgium
关键词
hypertrophy; cardiomyopathy; heart failure; metalloproteinases;
D O I
10.1161/hc0302.103593
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background-The regulation of the cardiac neutral endopeptidase (EC 24.10, NEP) that degrades bradykinin and natriuretic peptides has been investigated in human cardiac hypertrophy and heart failure. Methods and Results-NEP mRNA was quantitated by real-time polymerase chain reaction (PCR) in left ventricular biopsies from patients with aortic valve stenosis (AS, n=19) and heart failure due to dilated cardiomyopathy (DCM, n=14), and control subjects with normal systolic function (CON, n=14). Left ventricular NEP mRNA content was increased 3-fold in AS (P<0.005) and 4.1-fold in DCM (P<0.002). The increase in NEP mRNA was related to the increase in end diastolic pressure in AS and DCM. In a second series, myocardial NEP enzymatic activity was determined. It increased 3.6-fold in AS (P<0.02) and 4-fold in DCM (P<0.002). NEP was localized in the myocardium by immunofluorescence microscopy and in situ PCR to myocytes and nonmyocyte areas and cells. Conclusions-Elevated cardiac NEP activity in pressure loaded and failing human hearts may increase the local degradation of bradykinin and natriuretic peptides.
引用
收藏
页码:286 / 289
页数:4
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