C. Chouabe et al., REDUCTION OF I-CA,I-L AND I(TO1)DENSITY IN HYPERTROPHIED RIGHT-VENTRICULAR CELLS BY SIMULATED HIGH-ALTITUDE IN ADULT-RATS, Journal of Molecular and Cellular Cardiology, 29(1), 1997, pp. 193-206
The present paper describes the effect of a simulated hypobaric condit
ion (at the altitude of 4500 m) on morphological characteristics and o
n some ionic currents in ventricular cells of adult rats. According to
current data, chronic high-altitude exposure led to mild right ventri
cular hypertrophy. Increase in right ventricular weight appeared to be
due wholly or partly to an enlargement of myocytes. The whole-cell pa
tch-clamp technique was used and this confirmed, by cell capacitance m
easurement, that chronic high-altitude exposure induced an increase in
the size of the right Ventricular cells. Hypertrophied cells showed p
rolongation of action potential (AP). Four ionic currents, playing a r
ole along with many others in the precise balance of inward and outwar
d currents that control the duration of cardiac AP, were investigated.
We report a significant decrease in the transient outward (I-to1) and
in the L-type calcium current (I-CaL) densities while there was no si
gnificant difference in the delayed rectifier current (I-K) or in the
inward rectifier current (I-Kl) densities in hypertrophied right ventr
icular cells compared to control cells. At a given potential the decre
ase in I-to1 density was relatively more important than the decrease i
n I-CaL density. In both cell types, all the currents displayed the sa
me voltage dependence. The inactivation kinetics of I-to1 and I-CaL or
the steady-state activation and inactivation relationships were not s
ignificantly modified by chronic high-altitude exposure. We conclude t
hat chronic high-altitude exposure induced true right ventricular myoc
yte hypertrophy and that the decrease ih I-to1 density might account f
or the lengthened action potential, or have a partial effect. (C) 1997
Academic Press Limited.