Bj. Corrette et al., AN INACTIVATING INWARD-RECTIFYING K-CURRENT PRESENT IN PROLACTIN CELLS FROM THE PITUITARY OF LACTATING RATS, The Journal of membrane biology, 150(2), 1996, pp. 185-195
Primary cultures containing a high percentage of lactotrophs were obta
ined by dissociating the pituitary of rats following 14-18 days of lac
tation. Lactotrophs with a distinctive appearance were recorded after
1-35 days in vitro and identified by immunocytochemical staining for p
rolactin. Whole-cell voltage clamp measurements in isotonic KCl soluti
on from a holding potential of -40 mV revealed the presence of inward-
rectifying K currents with a time-dependent, Nat independent inactivat
ion at potentials negative to -60 mV. The time for complete inactivati
on was strikingly different between lactotrophs, varying between 1 sec
and more than 5 sec at -120 mV, and was not related to time in cultur
e. The reversal potential shifted 59 mV (25 degrees C) for a tenfold c
hange in external K+ concentration, demonstrating the selectivity of t
he channel for K+ over Na+ The inward-rectifying K current was blocked
by 5 mM Ba2+ and partially blocked by 10 mM TEA. Chloramine-T (1 and
2 mM) produced a total block of the inward-rectifying K current in lac
totrophs. Thyrotropin-releasing hormone (500 mM) significantly reduced
the inward-rectifying K current in about half of the lactotrophs. Thi
s current is similar to the inward-rectifying K current previously cha
racterized in clonal somatomam-motrophic pituitary cells (GH(3)B(6)).
The variability of the rate of inactivation of this current in lactotr
ophs and its responsiveness to TRH is discussed.