CHARACTERIZATION OF TRANSIENT OUTWARD CURRENT IN YOUNG HUMAN ATRIAL MYOCYTES

Citation
Gj. Gross et al., CHARACTERIZATION OF TRANSIENT OUTWARD CURRENT IN YOUNG HUMAN ATRIAL MYOCYTES, Cardiovascular Research, 29(1), 1995, pp. 112-117
Citations number
27
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
ISSN journal
00086363
Volume
29
Issue
1
Year of publication
1995
Pages
112 - 117
Database
ISI
SICI code
0008-6363(1995)29:1<112:COTOCI>2.0.ZU;2-7
Abstract
Objective: The aim was to characterise the development of the transien t outward current (I-to) in atrial myocytes of infants and children. M ethods: Whole cell voltage clamp was used to study outward currents in enzymatically isolated atrial myocytes from infants and children rang ing in age from 3 days to 13.2 years. Results: A transient inactivatin g current characteristic of I-to was observed in 71 myocytes from 22 p atients aged 3 days to 13.2 years, including a 10 day old infant born prematurely at 33 weeks gestation. There was no discernible developmen tal trend in I-to current density [10.74(SEM 0.65) pA.pF(-1) at +40 mV , n=71 cells from 22 patients] or voltage dependence of inactivation, newborn values being similar to those in older children, and in adults reported elsewhere. A developmental reduction in total outward curren t density was attributable entirely to diminution of the non-inactivat ing steady state current component. The I-to time course of inactivati on showed an apparent maturational evolution, with the youngest infant s having slightly but significantly slower inactivation kinetics. The kinetics of I-to recovery from inactivation were well described by a s ingle exponential model with no appreciable developmental trend in tim e course. Conclusions: I-to is expressed in human atrial myocytes from early infancy and does not show significant developmental changes in current density. The relative contribution of I-to to myocyte repolari sation might increase with age as a result of diminution in the non-in activating current component. There is an apparent slight maturational acceleration in the time course of I-to inactivation but not in recov ery from inactivation, perhaps excluding the latter as a mechanism for the previously reported functional unavailability of I-to in young hu man atrial muscle.