Differential effects of aging on binding sites of the activated NMDA receptor complex in mice.

TitleDifferential effects of aging on binding sites of the activated NMDA receptor complex in mice.
Publication TypeJournal Article
Year of Publication1995
AuthorsMagnusson KR
JournalMechanisms of ageing and development
Volume84
Issue3
Pagination227-43
Date Published1995 Oct 27
ISSN0047-6374
KeywordsAging, Analysis of Variance, Animals, Autoradiography, Binding Sites, Brain, Mice, Mice, Inbred C57BL, Radioligand Assay, Receptors, AMPA, Receptors, Glycine, Receptors, N-Methyl-D-Aspartate
Abstract

The NMDA receptor site has been shown to be vulnerable to the effects of aging. Decreases in binding to the receptor site of up to 50% have been reported in aged animals. The present study was designed to quantitate and compare the effects of aging on multiple binding sites of the NMDA receptor complex in various brain regions. Autoradiography with [3H]glutamate, [3H]CPP, [3H]glycine, [3H]MK801 and [3H]TCP was performed on brain sections from 3, 10 and 28-30 month old C57B1/6 mice. The percent declines between 3 and 28-30 months of age in [3H]-glutamate (15-35% declines) and [3H]CPP (20-42% declines) binding were similar within most cortical regions and the caudate nucleus but [3H]glutamate binding showed less change (0-11% declines) than [3H]CPP (13-27% declines) in the occipital/temporal cortex and hippocampal regions. [3H]MK801 and [3H]TCP binding, stimulated by 10 microM glutamate, exhibited intermediate aging changes between the glycine and NMDA sites, both in percent decline (3-28% and 0-26%, respectively) and in the number of brain regions involved. [3H]Glycine binding, stimulated by 10 microM glutamate, showed no significant overall effect of age (declines ranged from 0-34%). [3H]CPP binding was significantly more affected than [3H]glycine binding in many regions. These results suggest that aging has heterogeneous effects on different sites on the NMDA receptor complex throughout the brain and on NMDA receptor agonist versus antagonist binding in selected brain regions.

Alternate JournalMech. Ageing Dev.