Literature DB >> 9990539

Sub-antihypertensive doses of ramipril normalize sarcoplasmic reticulum calcium ATPase expression and function following cardiac hypertrophy in rats.

S Y Boateng1, A M Seymour, N S Bhutta, M J Dunn, M H Yacoub, K R Boheler.   

Abstract

We examined the hypothesis that the angiotensin converting enzyme inhibitor ramipril at sub-antihypertensive concentrations could improve sarcoplasmic reticulum (SR) CaATPase expression and function in compensated hypertrophied rat hearts. Five weeks after abdominal aortic constriction, rats received a daily dose (50 micrograms/kg/day) of ramipril or vehicle for 4 weeks. Cardiac angiotensin-converting enzyme (ACE) activity increased with cardiac hypertrophy (CH) but returned to normal following ramipril treatment. SR CaATPase protein levels and activity decreased with CH (P < 0.05) and were normalized following ramipril treatment (P < 0.05 for protein and activity). No change in phospholamban (PLB) protein levels could be demonstrated between any of the groups. In contrast, ramipril treatment specifically increased control SR CaATPase and PLB mRNA levels by > 60% (P < 0.01) and > 30%, respectively. In the hypertrophied group, SR CaATPase increased by 35% (P < 0.05 n = 6) after ramipril treatment. Calsequestrin mRNA levels were unaffected by ramipril administration. In conclusion, ramipril normalizes SR CaATPase protein expression and function in pressure-overloaded and compensated CH. The effects of ramipril are however multifaceted, affecting RNA and protein expression differentially.

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Year:  1998        PMID: 9990539     DOI: 10.1006/jmcc.1998.0830

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  8 in total

1.  The circadian protein Clock localizes to the sarcomeric Z-disk and is a sensor of myofilament cross-bridge activity in cardiac myocytes.

Authors:  Lixin Qi; Samuel Y Boateng
Journal:  Biochem Biophys Res Commun       Date:  2006-11-07       Impact factor: 3.575

2.  Differential induction of cellular proliferation, hypertrophy and apoptosis in H9c2 cardiomyocytes by exogenous tissue factor.

Authors:  G Alkistis Frentzou; Mary E W Collier; Anne-Marie L Seymour; Camille Ettelaie
Journal:  Mol Cell Biochem       Date:  2010-08-22       Impact factor: 3.396

3.  Semiquantitative analysis of collagen types in the hypertrophied left ventricle.

Authors:  K A Linehan; A M Seymour; P E Williams
Journal:  J Anat       Date:  2001-01       Impact factor: 2.610

4.  Compensated cardiac hypertrophy is characterised by a decline in palmitate oxidation.

Authors:  Ashwin Akki; Katie Smith; Anne-Marie L Seymour
Journal:  Mol Cell Biochem       Date:  2008-02-16       Impact factor: 3.396

5.  Myocyte remodeling in response to hypertrophic stimuli requires nucleocytoplasmic shuttling of muscle LIM protein.

Authors:  Samuel Y Boateng; Samuel E Senyo; Lixin Qi; Paul H Goldspink; Brenda Russell
Journal:  J Mol Cell Cardiol       Date:  2009-04-17       Impact factor: 5.000

6.  Lipoma preferred partner is a mechanosensitive protein regulated by nitric oxide in the heart.

Authors:  Charlotte L Hooper; Philip R Dash; Samuel Y Boateng
Journal:  FEBS Open Bio       Date:  2012-06-04       Impact factor: 2.693

7.  Nuclear accumulation of myocyte muscle LIM protein is regulated by heme oxygenase 1 and correlates with cardiac function in the transition to failure.

Authors:  Anju Paudyal; Sukriti Dewan; Cindy Ikie; Benjamin J Whalley; Pieter P de Tombe; Samuel Y Boateng
Journal:  J Physiol       Date:  2016-05-05       Impact factor: 5.182

8.  The exon junction complex senses energetic stress and regulates contractility and cell architecture in cardiac myocytes.

Authors:  Olivier A Pierrat; Anju Paudyal; James Woodruff; Olga Koroleva; Samuel Y Boateng
Journal:  Biosci Rep       Date:  2017-07-07       Impact factor: 3.840

  8 in total

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