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Neutral endopeptidase is activated in cardiomyocytes in human aortic valve stenosis and heart failure.
Fielitz, Jens; Dendorfer, Andreas; Pregla, Reinhard; Ehler, Elisabeth; Zurbrügg, Heinz R; Bartunek, Jozef; Hetzer, Roland; Regitz-Zagrosek, Vera.
Afiliación
  • Fielitz J; Klinik für Herz-, Gefäss- und Thoraxchirurgie, DHZB (R.P., H.R.Z., R.H., V.R.-Z.), Berlin, Germany.
Circulation ; 105(3): 286-9, 2002 Jan 22.
Article en En | MEDLINE | ID: mdl-11804980
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.
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estenosis de la Válvula Aórtica / Neprilisina / Insuficiencia Cardíaca Límite: Humans Idioma: En Revista: Circulation Año: 2002 Tipo del documento: Article País de afiliación: Alemania
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Estenosis de la Válvula Aórtica / Neprilisina / Insuficiencia Cardíaca Límite: Humans Idioma: En Revista: Circulation Año: 2002 Tipo del documento: Article País de afiliación: Alemania