Literature DB >> 1423430

The L type calcium current in single hypertrophied cardiomyocytes isolated from the right ventricle of ferret heart.

A Bouron1, D Potreau, G Raymond.   

Abstract

OBJECTIVE: The aim was to study L type calcium current alterations in relation to the action potential lengthening induced by hypertrophy in isolated cardiomyocytes from the right ventricle of ferret.
METHODS: Chronic pulmonary artery constriction was established in adult male ferrets under anaesthesia. Sham operated animals were used as controls. Four to six weeks later the heart was excised and treated with a mixed collagenase-elastase solution to isolate the right ventricular myocytes. The calcium current was investigated in control and hypertrophied cells with the whole cell configuration of the patch clamp technique. The validity of the model was tested by analysis of the structural and passive electrical characteristics of the cells, which were enzymatically isolated from right ventricles previously overloaded (4 to 6 weeks) by clipping the pulmonary artery.
RESULTS: Isolated cells from right ventricles submitted to a chronic pressure overload had well preserved cellular integrity suggesting the absence of myocardial failure. This compensated form of hypertrophy was characterised by a dilated transverse tubular system, which could explain the increased membrane capacity. Such cells developed a prolonged action potential with a less pronounced fast repolarisation phase inducing a higher plateau phase. When studied in physiological Tyrode solution the density and kinetics of the L type calcium current were not apparently modified, but a significant decrease in density was unmasked when sodium and potassium currents were suppressed by external and internal substitution of sodium and potassium by tetraethyl ammonium.
CONCLUSIONS: The decrease in L type calcium current cannot be involved in the lengthening of action potential observed on hypertrophied myocytes, but it could account for the depressed contractile activity. A noticeable decrease of the transient outward current is suggested to explain the action potential alterations.

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Year:  1992        PMID: 1423430     DOI: 10.1093/cvr/26.7.662

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  5 in total

1.  Relationship between K+ channel down-regulation and [Ca2+]i in rat ventricular myocytes following myocardial infarction.

Authors:  R Kaprielian; A D Wickenden; Z Kassiri; T G Parker; P P Liu; P H Backx
Journal:  J Physiol       Date:  1999-05-15       Impact factor: 5.182

2.  Regulation of L-type inward calcium channel activity by captopril and angiotensin II via the phosphatidyl inositol 3-kinase pathway in cardiomyocytes from volume-overload hypertrophied rat hearts.

Authors:  Zikiar Alvin; Graham G Laurence; Bernell R Coleman; Aiqiu Zhao; Majd Hajj-Moussa; Georges E Haddad
Journal:  Can J Physiol Pharmacol       Date:  2011-03       Impact factor: 2.273

3.  Cellular distribution of calcium current is unaltered during compensated hypertrophy in the spontaneously hypertensive rat.

Authors:  Mark R Fowler; Clive H Orchard; Simon M Harrison
Journal:  Pflugers Arch       Date:  2006-10-26       Impact factor: 3.657

4.  Overexpression of nerve growth factor in the heart alters ion channel activity and beta-adrenergic signalling in an adult transgenic mouse.

Authors:  B M Heath; J Xia; E Dong; R H An; A Brooks; C Liang; H J Federoff; R S Kass
Journal:  J Physiol       Date:  1998-11-01       Impact factor: 5.182

Review 5.  The cardiac ventricular myocyte as a substrate for sudden death. The regional lecture in Bath 1993.

Authors:  G Hart
Journal:  J R Coll Physicians Lond       Date:  1993-10
  5 in total

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