Prior to the inception of inspiratory synaptic drive transmission from medu
llary respiratory centers, rat phrenic motoneurons (PMNs) have action poten
tial and repetitive firing characteristics typical of immature embryonic mo
toneurons. During the period spanning from when respiratory bulbospinal and
segmental afferent synaptic connections are formed at embryonic day 17 (E1
7) through to birth (gestational period is similar to 21 days), a pronounce
d transformation of PMN electrophysiological properties occurs. In this stu
dy, we test the hypothesis that the elaboration of action potential afterpo
tentials and the resulting changes in repetitive firing properties are due
in large part to developmental changes in PMN potassium conductances. Ionic
conductances were measured via whole cell patch recordings using a cervica
l slice-phrenic nerve preparation isolated from perinatal rats. Voltage- an
d current-clamp recordings revealed that PMNs expressed outward rectifier (
I-KV) and A-type potassium currents that regulated PMN action potential and
repetitive firing properties throughout the perinatal period. There was an
age-dependent leftward shift in the activation voltage and a decrease in t
he time-to-peak of I-KV during the period from E16 through to birth. The mo
st dramatic change during the perinatal period was the increase in calcium-
activated potassium currents after the inception of inspiratory drive trans
mission at E17. Block of the maxi-type calcium-dependent potassium conducta
nce caused a significant increase in action potential duration and a suppre
ssion of the fast afterhyperpolarizing potential. Block of the small conduc
tance calcium-dependent potassium channels resulted in a marked suppression
of the medium afterhyperpolarizing potential and an increase in the repeti
tive firing frequency. In conclusion, the increase in calcium-mediated pota
ssium conductances are in large part responsible for the marked transformat
ion in action potential shape and firing properties of PMNs from the time b
etween the inception of fetal respiratory drive transmission and birth.