The Time-Course of Experience-Dependent Synaptic Potentiation and Depression in Barrel Cortex of Adolescent Rats. Glazewski, Stanislaw and Kevin Fox. Dept. Physiology, 6-255 Millard Hall, University of Minnesota, 435, Delaware St. S.E., Minneapolis MN 55455.
APStracts 2:0308N, 1995.
SUMMARY AND CONCLUSIONS
1.Plasticity could be induced in (S1) barrel cortex of adolescent rats by reducing the complement of vibrissae on one side of the muzzle to a single whisker for a period of 7, 20 or 60 days. The effect of deprivation was assessed quantitatively by measuring cortical responses to stimulation of the spared and regrown, deprived vibrissa. Vibrissae responses were evoked using a standard stimulus generated by an electro-mechanical stimulator and measured using post-stimulus time histogram analysis. 2. Cells located in layers II/III were found to be plastic beyond P28 whereas cells located in layer IV were not. The vibrissae dominance distribution was shifted significantly toward the spared vibrissa after 7, 20 and 60 days of deprivation for cells located in layers II/III of barrel-columns surrounding the D1 column (p<0.0001, 2-factor ANOVA). The vibrissae dominance distribution did not shift significantly for cells located in layer IV of surrounding barrels for any of the durations of deprivation tested (p>0.1). After 7 days of deprivation, 37% of the cells located in layers II/III of deprived vibrissas' columns showed greater responses to the spared vibrissae than to their deprived principal vibrissa, compared with 11% in normally reared adolescent animals and 3% in adults. The percentage of cells dominated by the spared vibrissa was 65% after 20 days of deprivation and 43% after 60 days. 3. 7 days : For cells located in layers II/III, short term deprivation (7 days) caused a decrease in the absolute magnitude of response to stimulation of the deprived vibrissa (reduction to approximately 28% of control levels). However, no change could be detected in the spared (D1) vibrissa input to the same deprived columns. Therefore, the increase in D1 dominance registered in the deprived columns was mainly due to a decrease in principal vibrissa response and no change in the spared D1 vibrissa response. 4. 20 days : The first increase in spared vibrissa response was seen after 20 days of deprivation. The response magnitude cells located in layers II/III increased to 70% above control levels. Responses to deprived vibrissa stimulation were depressed at 20 days of deprivation (reduction to 35% of control) implying that the vibrissae dominance shift at 20 days was due to both an increase in spared vibrissa response and a decrease in deprived vibrissae response. 5. 60 days : The spared vibrissa response was increased after 60 days of deprivation (110% above control) in both near and far halves of the barrel columns surrounding D1. On average, the deprived vibrissa response was depressed at 60 days (84% of control) though less than at 20 or 7 days, due to a recovery of responsiveness in the far half of the deprived barrel column. Layer II/III cells located in the half of the barrel-column furthest from the spared D1 barrel column showed normal levels of deprived vibrissa input, while cells located in the half of the barrel-column closest to the spared D1 barrel column still exhibited depressed levels of deprived vibrissa input (54% of control). 6. Control experiments suggested that depression of the deprived vibrissa response could not be explained by non-specific effects. Depression was not a function of the animal's age, as normally reared P28 and adult animals showed similar principal vibrissa response levels. It was not a result of non-specific depression of cortical responses, as the decreased response only occurred in cells of deprived barrel-columns not spared barrel- columns (recorded in the same animals). Depression was not due to altered vibrissae mechanics as the spared vibrissa response was similarly depressed in animals where the vibrissae had been trimmed rather than removed. Finally, depression was input specific at 7 and 20 days since only the deprived vibrissae responses were depressed, while spared vibrissae responses were either at control levels or at elevated levels for the same cells. 7. Depression occurred in layers II and III but not in layer IV. In penetrations down through deprived columns, poor responses to principal vibrissa stimulation were encountered initially before reaching layer IV, where response levels were normal. In penetrations down through normal columns, response levels were only marginally less in surpragranular layers compared with those in layer IV. This suggests that intracolumnar transmission to layers II/III is depressed after 7 days of deprivation, possibly in the projection from layer IV to layers II/III. 8. In 7 and 20 day deprived animals, the cells located nearest to the spared vibrissa's barrel underwent a greater decrease in response than did cells located in the center of the deprived barrel column or those located at the edge of the barrel column furthest from the spared barrel. Similarly, in 60 day deprived animals, cells in the near half of the deprived barrel column underwent a greater decrease in response than did cells located in the far half of the barrel column One possible explanation is that a heterosynaptic depression of the deprived principal vibrissae input may be produced by the spared vibrissae input. 

Received 10 November 1995; accepted in final form 18 October 1995.
APS Manuscript Number J714-4.
Article publication pending J. Neurophysiol.
ISSN 1080-4757 Copyright 1995 The American Physiological Society.
Published in APStracts on 6 November 95