REGIONAL PATTERNS OF CHOLINERGIC AND GLUTAMATE ACTIVITY IN THE DEVELOPING AND AGING HUMAN BRAIN

Citation
Ja. Court et al., REGIONAL PATTERNS OF CHOLINERGIC AND GLUTAMATE ACTIVITY IN THE DEVELOPING AND AGING HUMAN BRAIN, Developmental brain research, 74(1), 1993, pp. 73-82
Citations number
57
Categorie Soggetti
Neurosciences
ISSN journal
01653806
Volume
74
Issue
1
Year of publication
1993
Pages
73 - 82
Database
ISI
SICI code
0165-3806(1993)74:1<73:RPOCAG>2.0.ZU;2-J
Abstract
The levels of choline acetyltransferase (ChAT) and the binding activit y of N-methyl-D-aspartate (NMDA) and non-NMDA receptors have been meas ured in the hippocampus, entorhinal cortex, frontal cortex and cerebel lum, in a series of human brains from 24 weeks gestation to 100 years. The patterns of ChAT and glutamate receptor activity during aging and development were strikingly different in the different brain areas. I n the hippocampus and associated cortex, ChAT activity did not reach a peak until middle age, when it almost immediately started to decline by 50-60% to the 10th decade, whereas in the frontal cortex ChAT peake d transiently in the infant and then stayed constant during aging. In the cerebellum ChAT activity was very high in the foetus and fell in t he neonate to maintain a constant level more in line with the concentr ations found in the other brain areas through the rest of life. The hi gh levels of ChAT in the foetal cerebellum were not associated with hi gh acetylcholinesterase (AChE) content, which tended to increase durin g development, and was present initially in Purkinje cells (foetus and neonate) and the molecular layer in the adult. In the hippocampus and entorhinal cortex, autoradiographic [H-3]MK-801 binding was relativel y constant throughout life, however, [H-3]CNQX binding rose from the p erinatal period up to a peak in the lst or 2nd decade and then tended to fall with age. In the cerebellum, autoradiographic binding of both ligands rose from the foetal period to reach a plateau by the age of 1 0 years and there was no apparent further change during aging. These d ata on cholinergic and glutamatergic phenotypic changes during develop ment and senescence reflect marked variations in regional plasticity a nd aging within and between the two transmitter systems and are likely to contribute to our understanding of their role in the different bra in areas investigated.