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The Journal of Neurophysiology Vol. 88 No. 4 October 2002, pp. 1933-1940
Copyright ©2002 by the American Physiological Society
Department of Ophthalmology and Visual Sciences, Yale University Medical School, New Haven, Connecticut 06520-8061
Beaver, Chris J.,
Quentin S. Fischer,
Qinghua Ji, and
Nigel
W. Daw.
Orientation Selectivity Is Reduced by Monocular Deprivation in
Combination With PKA Inhibitors. J. Neurophysiol. 88: 1933-1940, 2002. We have previously shown that
the protein kinase A (PKA) inhibitor,
8-chloroadenosine-3',5'-monophosphorothioate (Rp-8-Cl-cAMPS), abolishes ocular dominance plasticity in the cat visual cortex. Here we
investigate the effect of this inhibitor on orientation selectivity.
The inhibitor reduces orientation selectivity in monocularly deprived
animals but not in normal animals. In other words, PKA inhibitors by
themselves do not affect orientation selectivity, nor does monocular
deprivation by itself, but monocular deprivation in combination with a
PKA inhibitor does affect orientation selectivity. This result is found
for the receptive fields in both deprived and nondeprived eyes.
Although there is a tendency for the orientation selectivity in the
nondeprived eye to be higher than the orientation selectivity in the
deprived eye, the orientation selectivity in both eyes is considerably
less than normal. The result is striking in animals at 4 wk of age. The
effect of the monocular deprivation on orientation selectivity is
reduced at 6 wk of age and absent at 9 wk of age, while the effect on
ocular dominance shifts is less changed in agreement with previous
results showing that the critical period for orientation/direction
selectivity ends earlier than the critical period for ocular dominance.
We conclude that closure of one eye in combination with inhibition of
PKA reduces orientation selectivity during the period that orientation
selectivity is still mutable and that the reduction in orientation
selectivity is transferred to the nondeprived eye.
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