Literature DB >> 14498755

Dual ACE and neutral endopeptidase inhibitors: novel therapy for patients with cardiovascular disorders.

Reza Tabrizchi1.   

Abstract

Elevated blood pressure is a risk factor for a variety of cardiovascular disorders, including coronary heart disease, peripheral vascular disease, cardiac failure and cerebrovascular disease. The prevailing view is that an elevated systolic rather than diastolic blood pressure is the major contributor in mortality and morbidity attributed to cardiovascular disorders. Isolated high systolic blood pressure, especially in the elderly, is a major risk factor and should undoubtedly be a target for drug treatment. In the general population, systolic and diastolic blood pressure are highly correlated, and thus it is difficult to dissociate the effects of these two components of the blood pressure and specifically ascribe cardiovascular risk factors to just elevated systolic blood pressure. Therefore, the goal in therapy of an individual with hypertension must be to reduce elevated systolic and diastolic blood pressure in order to reduce mortality and morbidity. ACE and neutral peptidase inhibitors are a new class of drugs that may be beneficial in the treatment of patients with hypertension and heart failure. They may also be useful in the treatment of diabetic patients with hypertension and/or heart failure. Drugs of this class are dual inhibitors of ACE and neutral endopeptidase, and are capable of affecting vascular tone and fluid balance. They are capable of producing vasodilatation by virtue of inhibiting the production of angiotensin II, degradation of natriuretic peptides and bradykinin. They also appear to promote natriuresis and diuresis by amplifying the actions of natriuretic peptidase and reducing aldosterone effects. In addition, they should also attenuate trophogenic actions of the renin angiotensin system and the sympathetic nervous system. Omapatrilat is one drug that appears to be at the advanced stages of clinical development. This drug has been shown to be quite effective in the treatment of hypertension. Evidence also seems to indicate that treatment with omapatrilat results in a higher tendency towards preventing death and worsening heart failure when compared with treatment with a pure ACE inhibitor in patients with advanced heart failure. Overall safety with omapatrilat appears to be good, but like other ACE inhibitors the incidence of cough is higher when compared with placebo. Other common adverse effects noted are headaches, facial flushing/warm sensation, dizziness, nausea and dyspnoea. Of greater concern is the occurrence of angio-oedema, the true incidence of which remains to be fully established as part of the published medical literature.

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Year:  2003        PMID: 14498755     DOI: 10.2165/00003495-200363200-00003

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  76 in total

1.  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

2.  Reduced cardiovascular morbidity and mortality in hypertensive diabetic patients on first-line therapy with an ACE inhibitor compared with a diuretic/beta-blocker-based treatment regimen: a subanalysis of the Captopril Prevention Project.

Authors:  L Niskanen; T Hedner; L Hansson; J Lanke; A Niklason
Journal:  Diabetes Care       Date:  2001-12       Impact factor: 19.112

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Journal:  Circulation       Date:  1980-06       Impact factor: 29.690

4.  The effect of irbesartan on the development of diabetic nephropathy in patients with type 2 diabetes.

Authors:  H H Parving; H Lehnert; J Bröchner-Mortensen; R Gomis; S Andersen; P Arner
Journal:  N Engl J Med       Date:  2001-09-20       Impact factor: 91.245

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Authors: 
Journal:  JAMA       Date:  1991-06-26       Impact factor: 56.272

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

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Journal:  Lancet       Date:  2000-08-19       Impact factor: 79.321

7.  Metabolism of [(14)C]omapatrilat, a sulfhydryl-containing vasopeptidase inhibitor in humans.

Authors:  R A Iyer; J Mitroka; B Malhotra; S Bonacorsi; S C Waller; J K Rinehart; V A Roongta; K Kripalani
Journal:  Drug Metab Dispos       Date:  2001-01       Impact factor: 3.922

8.  Combined inhibition of neutral endopeptidase and angiotensin-converting enzyme by sampatrilat in essential hypertension.

Authors:  E J Wallis; L E Ramsay; J Hettiarachchi
Journal:  Clin Pharmacol Ther       Date:  1998-10       Impact factor: 6.875

9.  Dual inhibition of angiotensin-converting enzyme and neutral endopeptidase by the orally active inhibitor mixanpril: a potential therapeutic approach in hypertension.

Authors:  M C Fournié-Zaluski; W Gonzalez; S Turcaud; I Pham; B P Roques; J B Michel
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

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Authors:  A Sagie; M G Larson; D Levy
Journal:  N Engl J Med       Date:  1993-12-23       Impact factor: 91.245

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  3 in total

1.  Is omapatrilat a novel therapy of the past rather than the future?

Authors:  Tsung O Cheng
Journal:  Drugs       Date:  2004       Impact factor: 9.546

Review 2.  Atrial natriuretic peptide and renal dopaminergic system: a positive friendly relationship?

Authors:  Marcelo Roberto Choi; Natalia Lucía Rukavina Mikusic; Nicolás Martín Kouyoumdzian; María Cecilia Kravetz; Belisario Enrique Fernández
Journal:  Biomed Res Int       Date:  2014-06-12       Impact factor: 3.411

3.  The role of sacubitril/valsartan in the treatment of chronic heart failure with reduced ejection fraction in hypertensive patients with comorbidities: From clinical trials to real-world settings.

Authors:  Alberto Mazza; Danyelle M Townsend; Gioia Torin; Laura Schiavon; Alessandro Camerotto; Gianluca Rigatelli; Stefano Cuppini; Pietro Minuz; Domenico Rubello
Journal:  Biomed Pharmacother       Date:  2020-08-21       Impact factor: 6.529

  3 in total

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