In addition to skeletal muscle paralysis, type A botulinum toxin commo
nly causes sprouting of motor axons in various experimental whole-anim
al systems. The use of type A botulinum toxin in clinical treatment of
muscle spasm disorders is becoming increasingly popular. The eventual
, unwanted return of involuntary activity in the treated muscles may b
e a consequence of such axon sprouting. We have developed a coculture
model allowing the quantification of botulinum toxin-induced sprouting
that shows promise for future studies on its mechanism and control. C
hick embryo ciliary ganglion motor neurons were cocultured with chick
leg muscle cells. The presence of type A botulinum toxin in the cocult
ure medium was correlated with significantly increased branching frequ
ency of neurites. Toxin-increased branching frequency occurred even wh
en the neurons and muscle cells were separated from each other on the
culture dishes, suggesting a presynaptic effect of toxin. Cocultures i
ncubated in the presence of curare, a post-synaptic blocker, had contr
ol levels of neurite branching, ruling out the possibility that simple
synaptic blockade causes sprouting but again supporting the hypothesi
s of a pre-synaptic activity of botulinum toxin.