Using in situ patch-clamp techniques, we have studied K current expres
sion in rat telencephalon from embryonic day 12 to 21. For cells recor
ded in the ventricular zone, the K current consisted of a delayed rect
ifier and a large-conductance calcium-activated component, and display
ed little variation from embryonic day 12 to 21. Cells recorded in pia
l regions could be separated into two classes: radially oriented, puta
tively migrating cells, and cells tangentially oriented in layer I, wh
ich were assumed to be Cajal-Retzius cells. When using a voltage-clamp
protocol that included a prepulse to -120 mV, Cajal-Retzius cells dis
played a larger density of total K current than radial cells, and both
types revealed an inactivating component (I-A). The proportion of thi
s component increased from embryonic day 18 to 21 in both cell types,
although the amplitude of total K current, in the respective cell type
, did not vary. This suggested a concomitant decrease in delayed recti
fier current, which was verified directly with an appropriate protocol
. The activation rate of the delayed rectifier current was slower for
ventricular zone cells than for radial or Cajal-Retzius cells. I-A was
studied in Cajal-Retzius cells and displayed a strikingly negative (s
imilar to -100 mV) voltage of half-maximal steady-state inactivation.
Tetraethylammonium ions only blocked the non-inactivating component(s)
of K current whereas 4-aminopyridine appeared to decrease both inacti
vating and non-inactivating components. The quantitative changes in K
current expression are likely to underlie the overall increase in exci
tability of differentiating cells. On the other hand, the observation
of qualitative differences among channel properties opens an interesti
ng area of investigation into their physiological significance. (C) 19
97 IBRO. Published by Elsevier Science Ltd.