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September 1, 1995Cardiovascular Research42 citations

Depressed transient outward current in single hypertrophied cardiomyocytes isolated from the right ventricle of ferret heart

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DPDaniel PotreauJGJean‐Pierre GomezNFNassim Farès

Structured PICO

Does pressure-overload right ventricular hypertrophy alter the transient outward potassium current in ferret cardiomyocytes?

P
Population
Adult male ferrets with right ventricular hypertrophy induced by chronic pulmonary artery constriction and sham-operated controls
I
Intervention
Chronic pulmonary artery constriction (banding) to induce right ventricular hypertrophy
C
Comparator
Sham-operated (control) animals
O
Outcome
Transient outward potassium current (Ito) changes (density, kinetics, and recovery from inactivation)surrogate

Alterations in the transient outward potassium current, including reduced density and altered kinetics, explain the prolongation of the action potential in pressure-overload hypertrophied ferret hearts.

Abstract

OBJECTIVE: The aim of this study was to investigate transient outward potassium current (Ito) changes as a basis for the prolongation of the action potential associated with cardiac hypertrophy. METHODS: Right ventricular hypertrophy was induced by chronic pulmonary artery constriction in adult male ferrets. After 4-6 weeks, hearts were excised and single myocytes were isolated from the right ventricles of banded and sham-operated (control) animals by enzymatic dissociation. Ito was recorded by means of the whole cell patch clamp technique. RESULTS: Heart weight:body weight ratio and cell membrane capacitance, as indications of hypertrophy, were increased by 17% (P < 0.05) and 32% (P < 0.01) respectively in the banded group. Analysis of Ito showed that in hypertrophied myocytes compared to normal controls: (1) the density of current was significantly reduced; (2) both the time to peak and the time constant of inactivation were increased; (3) the voltage-dependent steady-state availability was not changed, with similar potentials for half activation (30.4 +/- 6.8 mV in control and 33.9 +/- 8.5 mV in hypertrophied cells) and half inactivation (-12.3 +/- 3.3 mV in control and -11.4 +/- 2.7 mV in hypertrophied cells); (4) the time constant for recovery from inactivation was significantly increased regardless of the holding potentials (-50 mV, -70 mV or -90 mV). CONCLUSIONS: Alterations of the transient outward potassium current with respect to its density, kinetics and recovery from inactivation can explain the prolongation of the action potential in myocytes isolated from pressure-overload hypertrophied heart and may thus be an important step in such cardiac adaptation.

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Potreau et al. (1995) studied this question.

synapsesocial.com/papers/6a215bf7e06b4fc4c1ab9a6chttps://doi.org/10.1016/s0008-6363(95)00073-9
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