Pv. Ayyagari et al., UNCOUPLING OF MUSCARINIC CHOLINERGIC PHOSPHOINOSITIDE SIGNALS IN SENESCENT CEREBRAL CORTICAL AND HIPPOCAMPAL MEMBRANES, Neurochemistry international, 32(1), 1998, pp. 107-115
Muscarinic-cholinergic signals in brain are mediated in part through t
he hydrolysis of phosphoinositides (PtdIns) by phospholipase C (PLC).
To test the hypothesis that muscarinic PtdIns signals change during ag
ing, membranes were prepared from the cerebral cortex and hippocampus
of young (4-6 months old), middle aged (8-10 months old) and senescent
(24-26 months old) Fisher 344 rats. Carbachol dose-dependently increa
sed [H-3]-PtdIns hydrolysis in both brain regions in all three age gro
ups, however, in senescent rats the maximal response was decreased to
69.26 +/- 4.33% (p<0.01) in cortex and to 48.29 +/- 2.55% (p<0.01) in
hippocampus of young rat values. In contrast to the decrease in carbac
hol-stimulated phosphoinositide hydrolysis, calcium-stimulated phospho
inositide hydrolysis was not altered. GTP gamma S also dose-dependentl
y increased [H-3]-PtdIns hydrolysis in membranes from all three age gr
oups through G-protein-PLC activation. Similar to carbachol, GTP gamma
S-activated [H-3]-PtdIns hydrolysis was reduced approximately 40% in
senescent rats membranes. Muscarinic receptor (mAChR) density, as dete
rmined by [H-3]-QNB binding decreased slightly in cortical membranes,
but not in hippocampal membranes. These data suggest that muscarinic s
timulated [H-3]-PtdIns responses are decreased in senescent brain prim
arily due to an uncoupling of the receptor-G-protein and/or G-protein-
PLC link, although decreases in receptor density may also contribute t
o reduced muscarinic [H-3]-PtdIns signaling. (C) 1998 Elsevier Science
Ltd. All rights reserved.