The progression of photoreceptor degeneration in retinally degenerate
(rd) mice commences early in postnatal development resulting in the co
mplete loss of rods by 60-70 days of age followed by the more protract
ed loss of cones. We have previously shown that rd mice 80 days of age
are capable of phase shifting their circadian locomotor rhythms in re
sponse to brief pulses of light and these animals show the same sensit
ivity as wild-type (+/+) controls. If surviving cones mediate these ci
rcadian responses, then one would expect the sensitivity of the circad
ian system in rd mice to decline with age and parallel the loss of con
es. We demonstrate that aging rd mice (80-767 days of age) remain capa
ble of photically regulating circadian locomotor rhythms in a manner i
ndistinguishable from +/+ mice. Circadian responses to light do not pa
rallel cone cell degeneration in rd mice. In contrast to the circadian
responses to light, old (> 210 days of age) rd mice show no visually-
evoked behavioral or electroretinogram (ERG) responses.