We have been studying the mechanisms whereby pools of motor neurons es
tablish a rostrocaudal bias in the position of their synapses in some
skeletal muscles. The serratus anterior (SA) muscle of the rat display
s a rostrocaudal topographic map before birth, and the topography is r
e-established after denervation. In this report, we explore the potent
ial role of synaptic competition between innervating axons as a means
of generating topographic specificity. We followed the progress of the
reformation of this map in neonatal animals under conditions that enh
anced the likelihood of observing synaptic competition. This was accom
plished by forcing caudal axons to regenerate ahead of rostral axons o
nto a surgically reduced SA muscle. In this way, caudal (C-7) motor ne
urons had unopposed access to vacated synaptic sites on the remaining
rostral half of the SA before the return of the rostral (C-6) axons. I
ntracellular recording revealed that 2 d after the second denervation,
most of the reinnervated end plates contained only axons from the C-7
branch; the remaining reinnervated end plates received input from C-6
only or were multiply innervated by C-6 and C-7 axons. After 6 d, the
pattern was reversed, with most end plates innervated exclusively by
C-6. After 17 d, axons from C-6 were the sole input to reinnervated en
d plates. During the transition from C-7- to C-6-dominated input, at e
nd plates coinnervated by C-6 and C-7 axons, the average quantal conte
nt from C-6 was the same as that from C-7; after 7 d, the quantal cont
ent of C-6 was greater than that of C-7. We have thus developed an exp
erimental situation in which the outcome of synaptic competition is pr
edictable and can be influenced by the positional labels associated wi
th axons from different levels in the spinal cord.