Differential vulnerability of hippocampus, basal ganglia, and prefrontal cortex to long-term NMDA excitotoxicity

Citation
F. Bernal et al., Differential vulnerability of hippocampus, basal ganglia, and prefrontal cortex to long-term NMDA excitotoxicity, EXP NEUROL, 161(2), 2000, pp. 686-695
Citations number
58
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EXPERIMENTAL NEUROLOGY
ISSN journal
00144886 → ACNP
Volume
161
Issue
2
Year of publication
2000
Pages
686 - 695
Database
ISI
SICI code
0014-4886(200002)161:2<686:DVOHBG>2.0.ZU;2-X
Abstract
In human brain, nonartherosclerotic calcification is associated with normal aging and several pathological conditions without any clear significance. In all situations, calcification appears predominantly in the basal ganglia , but is also frequent in the hippocampus and cerebral cortex, alpha-Amino- (3-hydroxi-5-methyl-4-isoxazol-4-il)-propionic acid-induced lesion of the g lobus pallidus is associated in rats with the formation of calcium deposits similar to those observed in the human brain. To determine whether direct neuronal activation may induce calcification, N-methyl-D-aspartate (NMDA) w as microinjected in rat hippocampus, globus pallidus, and lateral prefronta l cortex. Two months later, neuronal death was associated with calcium depo sits that were characterized in terms of distribution and size. A unique po pulation of deposits was present in the hippocampus and prefrontal cortex, whereas in the globus pallidus two main groups could be differentiated. Cal cification was always associated with a significant microglial reaction as shown by the peripheral benzodiazepine receptor autoradiography. Monoamine oxidase B autoradiography, reflecting the astroglial reaction, was also sig nificantly increased. Our results provide evidence that acute NMDA neuronal activation leads with time to calcification associated with a glial reacti on and indicate that nonartherosclerotic calcification in the human brain m ay develop from an acute NMDA receptor activation. A key role of the metabo tropic mGluR1 receptor is also suggested. (C) 2000 Academic Press.