Previous work on normal adult rat showed that the vibrissae project, t
hrough the climbing fiber (CF) system, onto the Purkinje cells (PCs) o
f the contralateral cerebellar hemivermis of lobule VII. The highly el
aborated CF projections from a given row of vibrissae delimit a narrow
parasagittal zone which can be regarded as a functional olive-cerebel
lar microzone. Interestingly, the adult one-to-one relationship betwee
n PCs and CFs is preceded by a transient phase during which each PC re
ceives synaptic inputs from several CF collaterals which will be elimi
nated but one, when granule cells begin to establish synapses on PCs.
Therefore, the question arose as to whether this synaptic elimination
process could participate in the refinement of the topographical organ
ization of CF projections and could contribute to the formation of suc
h precise peripheral maps onto the cerebellum. In the present study, t
he topographical map of the CF-mediated projection of mystacial vibris
sae onto the vermal PCs of lobule VII was determined in adult rats who
se cerebellar PCs remain polyinnervated by olivary CFs due to degranul
ation by postnatal X-irradiation. Using intracellular recordings, we e
xamined the responsiveness of PCs in lobule VII during mechanical stim
ulation of the 3rd row of contralateral vibrissae, and positioned cell
s responding to the stimulation on an averaged planar map of lobule VI
I. Comparison of the results to those obtained in our previous work on
normal rats showed that the activated cells were more numerous and mo
re diffusely distributed. PCs exhibiting the best characteristics of r
esponse were distributed evenly from the midline to 700 mu m lateral i
n the contralateral hemivermis and not gathered in a parasagittal micr
ozone centered on the plane 200 mu m as in normal rats. These results
strongly suggest that synaptic elimination in the olive-cerebellar sys
tem participates in the segregation of CF-mediated inputs into functio
nal microzones on the cerebellar cortex.