ROLE OF PASSIVE ELECTRICAL-PROPERTIES DURING ACTION-POTENTIAL RESTITUTION IN INTACT HEART

Citation
Kr. Laurita et al., ROLE OF PASSIVE ELECTRICAL-PROPERTIES DURING ACTION-POTENTIAL RESTITUTION IN INTACT HEART, American journal of physiology. Heart and circulatory physiology, 42(3), 1997, pp. 1205-1214
Citations number
46
Categorie Soggetti
Physiology
ISSN journal
03636135
Volume
42
Issue
3
Year of publication
1997
Pages
1205 - 1214
Database
ISI
SICI code
0363-6135(1997)42:3<1205:ROPEDA>2.0.ZU;2-O
Abstract
Action potential duration (APD) restitution is classically attributed to membrane ionic currents; however, the role of cell-to-cell coupling in restitution is poorly understood. To test the hypothesis that pass ive electrical properties of multicellular preparations influence rest itution, spatial gradients of transmembrane voltage were measured with high spatial (0.83 mm), voltage (1 mV), and temporal (0.5 ms) resolut ions using voltage-sensitive dye in Langendorff-perfused guinea pig ve ntricle. At short premature coupling intervals, APD failed to shorten in cells located near (<3 mm) the site of pacing corresponding to the site of earliest repolarization, deviating from classical restitution. In contrast, APD shortened exponentially with increasing stimulus pre maturity when pacing was remote from the identical recording site. The mechanism responsible for nonexponential restitution was investigated in a one-dimensional propagation model using the dynamic Luo-Rudy for mulation of the ventricular cell and was found to be attributable to d epolarizing axial current present in regions of steep repolarization g radients. Moreover, axial current loading attenuated spatial gradients of repolarization that were prominent in the absence of cell-to-cell coupling. These data demonstrate that 1) in contrast to restitution in isolated cells, restitution in multicellular tissue is influenced by axial current from neighboring cells, and 2) in normal myocardium, axi al current between cells attenuates dispersion of repolarization durin g premature stimulation of the heart.