Rats can readily be trained to jump a gap of around 16 cm in the dark and a
considerably larger gap in the light for a food reward. In the light, they
use vision to estimate the distance to be jumped. In the dark, they use th
eir vibrissae at the farthest distances. Bilateral whisker shaving or barre
l field lesions reduce the gap crossed in the dark by about 2 cm. Informati
on from the barrel fields reaches motor areas via cortico-cortical, basal g
anglia, or cerebellar pathways. The cells of origin of the ponto-cerebellar
pathway are segregated in layer Vb of the barrel field. Efferent axons of
Vb cells occupy a central position within the basis pedunculi and terminate
on cells in the pontine nuclei. Pontine cells, in turn, project to the cer
ebellar cortex as mossy fibers. We trained normal rats to cross a gap in th
e light and in a dark alley that was illuminated with an infra-red source.
When the performance was stable, we made unilateral lesions in the central
region of the basis pedunculi, which interrupted connections from the barre
l field to the pons while leaving cortico-cortical and basal ganglia pathwa
ys intact. Whisking was not affected on either side by the lesion, and the
rats with unilateral peduncle lesions crossed gaps of the same distance as
they did pre-operatively. Shaving the whiskers on the side of the face that
retains its input to the pontine nuclei reduced the maximal gap jumped in
the dark by the same amount as bilateral whisker shaving. Performance in th
e light was not affected. Regrowth of the shaved whiskers was associated wi
th the recovery of the maximum distance crossed in the dark. In control cas
es, shaving the whiskers on the other side of the face did not reduce the d
istance jumped in the dark or in the light. These results suggest that the
cerebellum must receive whisker information from the barrel fields for whis
ker-guided jumps.