Increased postsynaptic density protein-95 expression in the frontal cortex of aged cognitively impaired rats

Author:

Preissmann Delphine12,Leuba Geneviève13,Savary Christine4,Vernay André1,Kraftsik Rudolf4,Riederer IrèNe Monika14,Schenk Françoise12,Riederer Béat Michel14,Savioz Armand56

Affiliation:

1. Center for Psychiatric Neuroscience, Department of Psychiatry, CHUV, 1008 Prilly;

2. Institute of Psychology, University of Lausanne, 1015 Lausanne;

3. Service of Old Age Psychiatry, Department of Psychiatry, CHUV, 1008 Prilly;

4. Department of Cell Biology and Morphology, University of Lausanne, 1005 Lausanne;

5. Department of Psychiatry, HUG, 1225 Geneva;

6. Geneva Neuroscience Center, University of Geneva, 1225 Geneva, Switzerland

Abstract

In the present work we studied synaptic protein concentrations in relation to behavioral performance. Long-Evans rats, aged 22-23 months, were classified for individual expression of place memory in the Morris water maze, in reference to young adults. Two main subgroups of aged rats were established: the Aged cognitively Unimpaired (AU) had search accuracy within the range (percent of time in training sector within mean+2 SEM) of young rats and the Aged cognitively Impaired (AI) rats had search accuracy below this range. Samples from the hippocampus and frontal cortex of all the AI, AU and young rats were analyzed for the expression of postsynaptic protein PSD-95 by Image J analysis of immunohistochemical data and by Western blots. PSD-95 expression was unchanged in the hippocampus, but, together with synaptophysin, was significantly increased in the frontal cortex of the AI rats. A significant correlation between individual accuracy (time spent in the training zone) and PSD-95 expression was observed in the aged group. No significant effect of age or PSD-95 expression was observed in the learning of a new position. All together, these data suggest that increased expression of PSD-95 in the frontal cortex of aged rats co-occurs with cognitive impairment that might be linked to functional alterations extending over frontal networks.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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