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1.
Circulation ; 100(24): 2443-8, 1999 Dec 14.
Artigo em Inglês | MEDLINE | ID: mdl-10595958

RESUMO

BACKGROUND: Neutral endopeptidase 24.11 (NEP) is a metalloprotease that is localized in the greatest abundance in the kidney and degrades natriuretic peptides, such as atrial natriuretic peptide (ANP). Mild congestive heart failure (CHF) is characterized by increases in circulating ANP without activation of the renin-angiotensin-aldosterone system (RAAS) or sodium retention. In contrast, severe CHF is characterized by sodium retention and coactivation of both ANP and the RAAS. METHODS AND RESULTS: We defined the acute cardiorenal actions of the NEP inhibitor candoxatrilat (8 microg. kg(-1). min(-1)) in 4 groups of anesthetized dogs (normal, n=8; mild CHF, n=6; severe CHF, n=5; and severe CHF with chronic AT(1) receptor antagonism, n=5). Mild CHF was produced by rapid ventricular pacing at 180 bpm for 10 days and severe CHF at 245 bpm for 10 days. In mild CHF, urinary sodium excretion and glomerular filtration rate were greatest in response to acute NEP inhibition compared with the response in either control animals or those with severe CHF. Furthermore, an increase in glomerular filtration rate was observed only in mild CHF in association with increases in renal blood flow and decreases in renal vascular resistance and distal tubular sodium reabsorption. Urinary ANP and cGMP excretion, markers for renal biological actions of ANP, were greatest in mild CHF. The renal actions observed in mild CHF were attenuated in severe CHF and not restored by chronic AT(1) receptor antagonism. CONCLUSIONS: The results of the present study demonstrate that acute NEP inhibition in mild CHF results in marked increases in renal hemodynamics and sodium excretion that exceed that observed in control animals and severe CHF. These studies underscore the potential therapeutic role for NEP inhibition to enhance renal function in mild CHF, an important phase of CHF that is marked by selective activation of endogenous ANP in the absence of an activated RAAS.


Assuntos
Fator Natriurético Atrial/sangue , Insuficiência Cardíaca/metabolismo , Rim/enzimologia , Rim/fisiopatologia , Neprilisina/antagonistas & inibidores , Doença Aguda , Antagonistas de Receptores de Angiotensina , Animais , Modelos Animais de Doenças , Cães , Frequência Cardíaca , Rim/química , Masculino , Neprilisina/metabolismo , Marca-Passo Artificial , Receptor Tipo 1 de Angiotensina , Receptor Tipo 2 de Angiotensina , Função Ventricular
2.
Coron Artery Dis ; 8(8-9): 505-9, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9431478

RESUMO

Congestive heart failure (CHF) is a syndrome in which the kidney plays a fundamental role, as sodium retention is a hallmark of the syndrome. An additional hallmark of CHF is that it affects the elderly disproportionately. This high incidence of CHF in the elderly is complicated by age-related alterations in renal hemodynamics and tubular function. In view of these age-related renal alterations, pharmacologic therapy for CHF in the elderly needs to be closely monitored. In addition, recent understanding of neurohumoral mechanisms of CHF has led to new therapeutic options for the treatment of CHF, which are reviewed here.


Assuntos
Envelhecimento/fisiologia , Fator Natriurético Atrial/efeitos dos fármacos , Fármacos Cardiovasculares/efeitos adversos , Endotelinas/efeitos dos fármacos , Insuficiência Cardíaca/tratamento farmacológico , Sistema Renina-Angiotensina/efeitos dos fármacos , Idoso , Fator Natriurético Atrial/biossíntese , Fármacos Cardiovasculares/uso terapêutico , Endotelinas/biossíntese , Feminino , Insuficiência Cardíaca/etiologia , Insuficiência Cardíaca/fisiopatologia , Humanos , Rim/efeitos dos fármacos , Rim/fisiologia , Testes de Função Renal , Masculino , Valores de Referência , Sistema Renina-Angiotensina/fisiologia
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