Literature DB >> 9140825

Effects of exogenous and endogenous nitric oxide on the contractile function of cultured chick embryo ventricular myocytes.

D Ungureanu-Longrois1, Y Bézie, C Perret, S Laurent.   

Abstract

Nitric oxide (NO) has been shown to be a ubiquitous intercellular autacoid in the heart and, in cultured rat ventricular myocytes, to decrease the contractile responsiveness to isoproterenol (ISO). The aim of the present study was to investigate whether exogenous (sodium nitroprusside, SNP) or endogenous nitric oxide generated from L-arginine modulated the response to ISO in cultured chick embryo ventricular myocytes. SNP 1 microM or L-arginine 1 mM had no effect on baseline contractile function. Superfusion with ISO 100 nM significantly increased myocyte amplitude of shortening to 1.31 +/- 0.06 (ratio to baseline amplitude). Initial superfusion with SNP 1 microM or L-arginine 1 mM attenuated the response to ISO to 0.89 +/- 0.05 and 1.09 +/- 0.07 respectively (P < 0.05). Potassium ferrocyanide which is not a NO donor and D-arginine the inactive substrate of NO synthase did not attenuate the response to ISO. Myocyte cGMP content was significantly increased by incubation with SNP 1 microM (31.65 +/- 3 fmol/well) but not by L-arginine 1 mM (11.1 +/- 0.3 fmol/well) as compared to myocytes incubated in control medium (11 +/- 0.9 fmol/well). Preincubation with SNP 1 microM or L-arginine 1 mM significantly attenuated the ISO mediated-increase in cAMP content from 4.33 +/- 0.2 pmol/well (ISO 100 nM alone) to 1.48 +/- 0.36 fmol/well and 1.72 +/- 0.21 pmol/well respectively. Potassium ferrocyanide and D-arginine had no effect on myocyte cGMP or cAMP content. Chick embryo myocytes have measurable and LNMMA-inhibited NO synthase activity as measured by the conversion of [3H] L-arginine to [3H] L-citrulline. In conclusion, these results demonstrate that in cultured chick embryo ventricular myocytes both exogenous and endogenous NO elevate cGMP. This may account for the inhibition of beta-adrenergic agonist-stimulated increases in cAMP and amplitude of shortening via an unidentified intracellular negative coupling.

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Year:  1997        PMID: 9140825     DOI: 10.1006/jmcc.1996.0310

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


  7 in total

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2.  Tetrahydrobiopterin improves diastolic dysfunction by reversing changes in myofilament properties.

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3.  Postanoxic functional recovery of the developing heart is slightly altered by endogenous or exogenous nitric oxide.

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Review 4.  Nitric oxide control of cardiac function: is neuronal nitric oxide synthase a key component?

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6.  Ventricular but not atrial electro-mechanical delay of the embryonic heart is altered by anoxia-reoxygenation and improved by nitric oxide.

Authors:  Philippe Maury; Alexandre Sarre; Jérôme Terrand; Antonio Rosa; Pavel Kucera; Lukas Kappenberger; Eric Raddatz
Journal:  Mol Cell Biochem       Date:  2004-10       Impact factor: 3.396

7.  Sodium nitroprusside induces cell death and cytoskeleton degradation in adult rat cardiomyocytes in vitro: implications for anthracycline-induced cardiotoxicity.

Authors:  M Chiusa; F Timolati; J C Perriard; T M Suter; C Zuppinger
Journal:  Eur J Histochem       Date:  2012-04-16       Impact factor: 3.188

  7 in total

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