Literature DB >> 11716802

Effects of omapatrilat on pharmacodynamic biomarkers of neutral endopeptidase and Angiotensin-converting enzyme activity in humans.

O Vesterqvist1, R A Reeves.   

Abstract

Vasopeptidase inhibition is a new concept in blood pressure management. A single molecule simultaneously inhibits two enzymes that regulate cardiovascular function: neutral endopeptidase (NEP) and angiotensin-converting enzyme (ACE)[1]. Development of vasopeptidase inhibitors stemmed from the need for new and more efficacious antihypertensive agents that not only reduce blood pressure but also treat hypertension as part of a larger syndrome involving endothelial dysfunction [2]. By inhibiting NEP and ACE, vasopeptidase inhibitors enhance the natriuretic peptide and kallikrein-kinin systems and inhibit the renin-angiotensin-aldosterone system. This article outlines the pharmacodynamic effects of the vasopeptidase inhibitor omapatrilat on biomarkers of NEP and ACE activity in humans.

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Year:  2001        PMID: 11716802     DOI: 10.1007/s11906-001-0103-x

Source DB:  PubMed          Journal:  Curr Hypertens Rep        ISSN: 1522-6417            Impact factor:   5.369


  30 in total

Review 1.  Vasopeptidase inhibition: a new direction in cardiovascular treatment.

Authors:  J R Asher; A J Naftilan
Journal:  Curr Hypertens Rep       Date:  2000-08       Impact factor: 5.369

2.  Pharmacodynamic effects of dual neutral endopeptidase-angiotensin-converting enzyme inhibition versus angiotensin-converting enzyme inhibition in humans.

Authors:  C Massien; M Azizi; T T Guyene; O Vesterqvist; B Mangold; J Ménard
Journal:  Clin Pharmacol Ther       Date:  1999-04       Impact factor: 6.875

3.  Vasopeptidase inhibition exhibits endothelial protection in salt-induced hypertension.

Authors:  T Quaschning; L V d'Uscio; S Shaw; T F Lüscher
Journal:  Hypertension       Date:  2001-04       Impact factor: 10.190

4.  Comparison of the short-term effects of candoxatril, an orally active neutral endopeptidase inhibitor, and frusemide in the treatment of patients with chronic heart failure.

Authors:  D B Northridge; D E Newby; E Rooney; J Norrie; H J Dargie
Journal:  Am Heart J       Date:  1999-12       Impact factor: 4.749

Review 5.  Atrial natriuretic peptide and its potential role in pharmacotherapy.

Authors:  A Deutsch; W H Frishman; D Sukenik; B G Somer; A Youssri
Journal:  J Clin Pharmacol       Date:  1994-12       Impact factor: 3.126

6.  Endopeptidase 24.11 inhibition by SCH 42495 in essential hypertension.

Authors:  A M Richards; I G Crozier; T Kosoglou; M Rallings; E A Espiner; M G Nicholls; T G Yandle; H Ikram; C Frampton
Journal:  Hypertension       Date:  1993-07       Impact factor: 10.190

Review 7.  Vasopeptidase inhibition: a new concept in blood pressure management.

Authors:  J C Burnett
Journal:  J Hypertens Suppl       Date:  1999-02

8.  Comparison of vasopeptidase inhibitor, omapatrilat, and lisinopril on exercise tolerance and morbidity in patients with heart failure: IMPRESS randomised trial.

Authors:  J L Rouleau; M A Pfeffer; D J Stewart; D Isaac; F Sestier; E K Kerut; C B Porter; G Proulx; C Qian; A J Block
Journal:  Lancet       Date:  2000-08-19       Impact factor: 79.321

9.  Metabolic clearance rate and plasma half life of alpha-human atrial natriuretic peptide in man.

Authors:  T G Yandle; A M Richards; M G Nicholls; R Cuneo; E A Espiner; J H Livesey
Journal:  Life Sci       Date:  1986-05-19       Impact factor: 5.037

10.  Relationship of increased plasma atrial natriuretic factor and renal sodium handling during immersion-induced central hypervolemia in normal humans.

Authors:  M Epstein; R Loutzenhiser; E Friedland; R M Aceto; M J Camargo; S A Atlas
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

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