Bs. Seebach et L. Ziskindconhaim, FORMATION OF TRANSIENT INAPPROPRIATE SENSORIMOTOR SYNAPSES IN DEVELOPING RAT SPINAL-CORDS, The Journal of neuroscience, 14(7), 1994, pp. 4520-4528
The specificity of the convergence of primary afferent projections fro
m ankle muscles onto motoneurons that innervate these muscles was stud
ied in lumbar spinal cords of embryonic and neonatal rats. The connect
ivity pattern was determined for each motoneuron by stimulating nerves
from ankle flexor and extensor muscles and recording the synaptic pot
entials in identified motoneurons. In mature mammals, muscle spindle a
fferents make direct excitatory connections with motoneurons that inne
rvate homonymous and synergistic muscles, and with interneurons that i
nhibit motoneurons innervating antagonistic muscles. Therefore, approp
riate primary afferent-motoneuron connections were identified when sti
mulation of homonymous and synergistic muscle nerves evoked monosynapt
ic EPSPs. Two criteria were used for identification of EPSPs as monosy
naptic potentials: (1) the monosynaptic potentials were evoked at the
shortest latency, and (2) they were more resistant to fatigue by repet
itive nerve stimulation than the longer-latency, polysynaptic potentia
ls. Functionally inappropriate primary afferent-motoneuron contacts we
re identified when stimulation of an antagonistic muscle nerve produce
d monosynaptic EPSPs instead of polysynaptic IPSPs in homonymous moton
eurons. At days 18-21 of gestation, about 30% of motoneurons were inne
rvated by primary afferents off antagonist muscles. Such functionally
inappropriate synapses persisted at birth, but their percentage was si
gnificantly reduced within 3-5 d after birth. The findings suggested t
hat in the developing spinal cord of the rat, a significant percentage
of motoneurons were initially innervated by inappropriate primary aff
erents of antagonistic muscles. The decrease in percentage of such ina
ppropriate connections was correlated temporally with the increase in
the frequency of spontaneous activity and the onset of myelination.