Literature DB >> 11716799

The cardiovascular actions of omapatrilat in spontaneously hypertensive rats.

Y Dong1, H Zhou, E Shaffer, N Atamas, W C Liao, C Wei.   

Abstract

Omapatrilat is a newly developed vasopeptidase inhibitor that inhibits both angiotensin-converting enzyme (ACE) and neutral endopeptidase and has potent antihypertensive efficacy. However, the specific effect of omapatrilat on cardiac function and left ventricular hypertrophy with hypertension remains controversial. Therefore, we investigated the effect of omapatrilat on blood pressure, cardiac hypertrophy, and cardiac function in spontaneously hypertensive rats (SHR). Studies were performed in SHR that received vehicle (n = 9), omapatrilat (n = 10), or fosinopril (ACE inhibitor, n = 7) by daily gavage for 56 days. Systolic blood pressure (SBP) and mean blood pressure (MBP) were measured by tail plethysmography. Left ventricular fractional shortening and left ventricular mass were measured by echocardiography at day 56. Omapatrilat and fosinopril significantly decreased SBP and MBP from day 1 through day 56, and omapatrilat markedly reduced SBP and MBP compared with fosinopril from day 21 to day 56. Although both omapatrilat and fosinopril decreased left ventricular mass and left ventricular mass-to-body weight ratio with increased LV fractional shortening, omapatrilat had a more potent effect on the reduction of left ventricular mass and improvement of cardiac function. This study shows that in SHR, omapatrilat mediated a potent and stable antihypertensive effect and a reduction in left ventricular mass with improvement of cardiac function, compared with ACE inhibition alone.

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Year:  2001        PMID: 11716799     DOI: 10.1007/s11906-001-0100-0

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


  16 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

Review 2.  Emerging treatments for hypertension: potential role for vasopeptidase inhibition.

Authors:  M Weber
Journal:  Am J Hypertens       Date:  1999-11       Impact factor: 2.689

Review 3.  Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms.

Authors:  N B Schiller; P M Shah; M Crawford; A DeMaria; R Devereux; H Feigenbaum; H Gutgesell; N Reichek; D Sahn; I Schnittger
Journal:  J Am Soc Echocardiogr       Date:  1989 Sep-Oct       Impact factor: 5.251

4.  Bradykinin metabolism in the postinfarcted rat heart: role of ACE and neutral endopeptidase 24.11.

Authors:  R Raut; J L Rouleau; C Blais; H Gosselin; G Molinaro; M G Sirois; Y Lepage; P Crine; A Adam
Journal:  Am J Physiol       Date:  1999-05

5.  The sixth report of the Joint National Committee on prevention, detection, evaluation, and treatment of high blood pressure.

Authors: 
Journal:  Arch Intern Med       Date:  1997-11-24

Review 6.  Vasopeptidase inhibition: a new concept in blood pressure management.

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

7.  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

8.  Cellular mechanisms of altered contractility in the hypertrophied heart: big hearts, big sparks.

Authors:  S R Shorofsky; R Aggarwal; M Corretti; J M Baffa; J M Strum; B A Al-Seikhan; Y M Kobayashi; L R Jones; W G Wier; C W Balke
Journal:  Circ Res       Date:  1999-03-05       Impact factor: 17.367

9.  Angiotensin-converting enzyme inhibition prolongs survival and modifies the transition to heart failure in rats with pressure overload hypertrophy due to ascending aortic stenosis.

Authors:  E O Weinberg; F J Schoen; D George; Y Kagaya; P S Douglas; S E Litwin; H Schunkert; C R Benedict; B H Lorell
Journal:  Circulation       Date:  1994-09       Impact factor: 29.690

10.  Chronic inhibition of endopeptidase 24.11 in essential hypertension: evidence for enhanced atrial natriuretic peptide and angiotensin II.

Authors:  A M Richards; G A Wittert; I G Crozier; E A Espiner; T G Yandle; H Ikram; C Frampton
Journal:  J Hypertens       Date:  1993-04       Impact factor: 4.844

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