Journal of Neuroscience, Vol 12, 4447-4459, Copyright © 1992 by Society for Neuroscience
Hormonal regulation of motor unit size and synaptic strength during synapse elimination in the rat levator ani muscle
CL Jordan, PA Pawson, AP Arnold and AD Grinnell
Department of Psychology, University of California, Los Angeles 90024.
Previous anatomical studies suggest that androgen regulates synapse
elimination in the androgen-sensitive levator ani(LA) muscle of the rat.
Androgen treatment beginning on postnatal day 7 (P7) prevents some of the
normal loss of multiaxonal innervation in this muscle. The present study
used physiological techniques to measure the number and size of LA motor
units during the synapse elimination period in muscles from normals, and
castrates treated with either testosterone propionate or oil. The number of
increments in LA twitch tension as nerve stimulation intensity increased, a
measure of the number of motor units, was the same at the end (P28) of
synapse elimination as near the beginning (P7) of this process. This result
indicates that motoneuronal cell death does not contribute to synapse
elimination in the LA. Moreover, androgen during this period did not
influence the number of LA motor units. In contrast, between P7 and P28,
there was a dramatic decline in the size of LA motor units, as indicated by
a decrease in the percentage of twitch or tetanus tension of individual
motor units relative to the maximal twitch or tetanus tension of the whole
muscle. In addition, androgen treatment of castrated males during this
period prevented some of the normal decline in the size of LA motor units.
Estimates of the number of inputs per LA muscle fiber derived from the
number of LA motor units and their average size indicate that androgen
maintains polyneuronal innervation in the LA muscle. This finding supports
previous anatomical studies suggesting that androgen can prevent synapse
elimination in this muscle. The strength of LA synapses was also examined
by measuring the tetanus: twitch ratio of individual motor units and by
measuring the safety margin of LA synapses. Both measurements indicated
that the average strength of LA synapses increases during synapse
elimination. Moreover, androgen appeared to spare synapses from elimination
without increasing their strength, since androgen-treated muscles generally
had larger motor units but the same mean tetanus:twitch ratio and safety
margins as untreated LA muscles except at P28, when synapses in
androgen-treated LA muscles had appreciably lower safety margins than
normal. These results suggest that androgen regulates synapse elimination
through a mechanism(s) independent of synaptic strength.