CYTOPROTECTIVE EFFECT OF NMDA RECEPTOR ANTAGONISTS ON PRION PROTEIN (PRION(SC))-INDUCED TOXICITY IN RAT CORTICAL CELL-CULTURES

Citation
Weg. Muller et al., CYTOPROTECTIVE EFFECT OF NMDA RECEPTOR ANTAGONISTS ON PRION PROTEIN (PRION(SC))-INDUCED TOXICITY IN RAT CORTICAL CELL-CULTURES, European journal of pharmacology. Molecular pharmacology section, 246(3), 1993, pp. 261-267
Citations number
43
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
09224106
Volume
246
Issue
3
Year of publication
1993
Pages
261 - 267
Database
ISI
SICI code
0922-4106(1993)246:3<261:CEONRA>2.0.ZU;2-V
Abstract
Rat cortical cells were incubated with the Scrapie prion protein, Prio n(Sc). At concentrations of 3 ng/ml of Prion(Sc) and higher, the viabi lity of the cells decreased significantly after a 12-h incubation peri od. Simultaneously, the degree of DNA fragmentation increased. In cont rol experiments with antibodies against Prion(Sc), Prions' lost its de leterious effect on neurons. Prion(Sc) did not affect the viability of astrocytes. Drugs known to block NMDA receptor channels, such as mema ntine (1-amino-3,5-dimethyladamantane) (Mem), its analogue 1-N-methyla mino-3,5-dimethyl-adamantane as well as ,11-dihydro-5H-di-benzo[a,d]cy clohepten-5,10-imine maleate (MK-801) prevented the effect of Prion(Sc ). Production of Prion(Sc) in the Scrapie prion-infected subclone of N 2a cells (ScN2a cells) was not affected by memantine. We conclude that antagonists of the NMDA receptor-channel complex (i) abolish the Prio n(Sc)-induced neuronal injury in vitro, and (ii) display no influence on the synthesis and/or the processing of Prion(Sc).