N. Fares et al., CHARACTERIZATION OF A HYPERPOLARIZATION-ACTIVATED CURRENT IN DEDIFFERENTIATED ADULT-RAT VENTRICULAR CELLS IN PRIMARY CULTURE, Journal of physiology, 506(1), 1998, pp. 73-82
1. The presence of a hyperpolarization-activated pacemaker (I-f)-like
current was tested in dedifferentiated adult rat ventricular myocytes
up to 12 days in primary culture with the whole-cell patch clamp techn
ique. 2. An I-f-like current was found and characterized on freshly is
olated and cultured ventricular cells. Both activation and density of
the current varied in relation to the stage of dedifferentiation. The
current was activated from -92.0 +/- 2.5 and -63.0 +/- 1.0 mV at the b
eginning (4-day-cultured cells) and end of the dedifferentiation proce
ss (12 days), respectively. Its density measured at -170 mV progressiv
ely increased from -2.34 +/- 0.36 to -6.12 +/- 0.64 pA pF(-1) between
the two farthest stages of cellular remodelling. In freshly isolated c
ells the current was activated at -108.0 +/- 1.5 mV and its current de
nsity measured at -170 mV was -1.97 +/- 0.56 pA pF(-1). 3. The current
was blocked by extracellular CsCl (3 mM) in a voltage-dependent manne
r. Modification of reversal potentials obtained at various values of [
K+](o) (5.4 or 25 mill) and [Na+](o) (140 or 30 mM) suggests that the
current was carried by both K+ and Na+ ions. 4. It is concluded that t
he hyperpolarization-activated inward current, recorded in freshly iso
lated and in cultured ventricular cells has characteristics similar to
those of I-f. In adult rat ventricular cells it is activated in a non
-physiological potential range, but can be elicited in a more physiolo
gical range when the cells are remodelled through a dedifferentiated w
ay. It is suggested that such a current could be implicated in ventric
ular arrhythmias developed in pathological events.