Cardiac contractility modulation by non-excitatory currents: studies in isolated cardiac muscle.

Abstract:

BACKGROUND:Myocardial contractility can be altered using voltage clamp techniques by modulating amplitude and duration of the action potential resulting in enhanced calcium entry in the cell of isolated muscle strips (Non-Excitatory Currents; NEC). Extracellular electrical stimuli delivered during the absolute refractory period (Cardiac Contractility Modulation; CCM) have recently been shown to produce inotropic effects in-vivo. AIM:Understanding the cellular mechanism, underlying the CCM effect, is essential for evaluating its clinical potential. We tested the hypothesis that NEC and CCM modulate contractility via similar cellular mechanisms. METHODS:Square wave electric currents were applied in the organ bath to isometrically contracting rabbit RV papillary muscle and human failing trabecular muscle during the absolute refractory period (ARP). RESULTS:These currents, which did not initiate new action potentials or contractions, modulated action potential duration (shortened or lengthened) and contractility (enhanced or depressed) in a manner that depended upon their amplitude, duration and delay from the pacing stimulus. The contractility modulation effect in the rabbit RV papillary muscle was markedly blunted after exposure to ryanodine, indicating that the sarcoplasmic reticulum plays an important role in the contractility modulation. CONCLUSION:Like voltage clamping, extracellular currents applied during the ARP can similarly modulate action potential duration in-vitro and modulate myocardial contractility by similar intracellular mechanisms. This concept provides the potential of a therapeutic strategy in patients with heart failure to enhance contractility.

journal_name

Eur J Heart Fail

authors

Brunckhorst CB,Shemer I,Mika Y,Ben-Haim SA,Burkhoff D

doi

10.1016/j.ejheart.2005.05.011

keywords:

subject

Has Abstract

pub_date

2006-01-01 00:00:00

pages

7-15

issue

1

eissn

1388-9842

issn

1879-0844

pii

S1388-9842(05)00134-0

journal_volume

8

pub_type

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