Main Title |
Age-Related Changes in Receptor-Mediated Phosphoinositide Hydrolysis in Various Regions of Rat Brain. |
Author |
Mundy, W. ;
Tandon, P. ;
Ali, S. ;
Tilson, H. ;
|
CORP Author |
Health Effects Research Lab., Research Triangle Park, NC. ;National Center for Toxicological Research, Jefferson, AR. |
Publisher |
c1991 |
Year Published |
1991 |
Report Number |
EPA/600/J-91/210; |
Stock Number |
PB91-243014 |
Additional Subjects |
Aging(Biology) ;
Phosphoinositides ;
Brain ;
Rats ;
Hydrolysis ;
Cerebral cortex ;
Corpus striatum ;
Quinuclidinyl benzilate ;
Muscarinic receptors ;
Inositol phosphates ;
Myoinositol ;
Carbachol ;
Norepinephrine ;
Quisqualic acid ;
Choline acetyltransferase ;
Reprints ;
|
Holdings |
Library |
Call Number |
Additional Info |
Location |
Last Modified |
Checkout Status |
NTIS |
PB91-243014 |
Some EPA libraries have a fiche copy filed under the call number shown. |
|
07/26/2022 |
|
Collation |
8p |
Abstract |
The effects of age on cholinergic markers and receptor-stimulated phosphoinositide hydrolysis was examined in the frontal cortex and striatum of male Fischer-344 rats. Choline acetyltransferase activity was decreased 27% in the striatum of aged (24 month) rats compared to young (3 month) controls. Muscarinic receptor density as measured by (3)H-quinuclidinyl benzilate binding showed a similar 26% decrease in the striatum of aged rats. Phosphoinositide hydrolysis was measured by the release of inositol phosphate (IP) from tissue slices prelabeled with (3)H myoinositol in response to carbachol, norepinephrine, and quisqualate. In the cortex, stimulated IP release was significantly greater in slices from aged rats compared to young rats for all three agonists. In contrast, stimulated IP release was significantly decreased in striatal slices from aged rats compared to young for all three agonists. These data indicate a differential effect of age on agonist-stimulated phosphoinositide hydrolysis in the cortex and striatum. The decreased responsiveness in the latter area may result from the age-related loss of postsynaptic receptors. |