1. The effects of high-frequency (5-50 Hz) stimulation of dorsal root
afferents on monosynaptic excitation of a motoneurons was studied in t
he in vitro spinal cord preparation of the neonatal rat, using sharp-e
lectrode intracellular recordings. 2. Double pulse stimulation of dors
al root afferents induced severe depression of testing excitatory post
synaptic potentials (EPSPs) at each of the tested interstimulus interv
als (15 ms-5 s). After perfusion of the preparation with low-calcium,
high-magnesium Krebs saline, the amplitude of the conditioning EPSPs w
as markedly decreased and the testing EPSPs exhibited substantial faci
litation that was maximal at the 20-ms interval and that was accompani
ed by depression at intervals greater-than-or-equal-to 60-100 ms. 3. S
hort-duration stimulus trains applied to dorsal root afferents normall
y induced tetanic depression of the intracellularly recorded monosynap
tic EPSPs. Switching the bathing solution to low-calcium, high-magnesi
um saline decreased the control EPSP and induced facilitation and then
tetanic potentiation (TP) of the EPSPs within the applied train. The
magnitude of potentiation (% potentiation) of these EPSPs depended on
the interpulse interval of the short stimulus train and on the degree
of attenuation of the unpotentiated control EPSP after the solution wa
s changed from normal- to low-calcium Krebs solution. 4. Long-duration
stimulus trains applied to dorsal root afferents at 5-10 Hz induced m
arked depression of monosynaptic EPSPs during the train. The depressio
n was alleviated after cessation of the tetanic stimulation and was fo
llowed in some cases by slight posttetanic potentiation. Perfusion of
the preparation with low-calcium, high-magnesium solution reduced the
amplitude of the pretetanic EPSPs and induced moderate potentiation or
slight depression during the tetanic train. After the tetanic train,
EPSPs exhibited posttetanic potentiation (PTP) that lasted less-than-o
r-equal-to 10 min. 5. On the basis of these results, it is suggested t
hat monosynaptic EPSPs produced by dorsal root afferents in the neonat
al rat spinal cord are modulated simultaneously (as in the adult spina
l cord) by processes acting to increase the EPSP amplitude (facilitati
on, TP, and PTP) and to decrease it (depression). Unlike the adult spi
nal cord, the immature transmitter release machinery of the developing
spinal cord imposes, under normal conditions, a prolonged synaptic de
pression that masks facilitation and TP but allows occasionally the ex
pression of moderate PTP. Substantial expression of facilitation TP an
d PTP is revealed only by conditions that decrease calcium influx to p
resynaptic terminals, and, concomitantly, transmitter release. The lon
g duration of PTP in low-calcium solution in the neonatal rat may be a
ttributed to slower kinetics of processes involved in extrusion and in
traterminal buffering of calcium in the developing mammalian spinal co
rd.