IN adult mammals, transection of the hypoglossal nerve results in a dr
amatic loss of choline acetyltransferase (ChAT) in the hypoglossal mot
or neurons without affecting their cell number. This injury-induced re
duction in ChAT is prevented when brain-derived neurotrophic factor (B
DNF) is applied to the proximal end of the transected nerve. In contra
st, application of ciliary neurotrophic factor (CNTF) has no such effe
ct, even though both factors are known to rescue developing motor neur
ons from cell death. These results suggest that BDNF may regulate the
phenotypic expression of ChAT in mature motor neurons, and indicate th
at the sensitivity and response of motor neurons to such neurotrophic
agents change with development.