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PMID: 8997624 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Study of potency, kinetics of block and toxicity of NMDA receptor antagonists using fura-2.

European journal of pharmacology ·Vol. 317 ·No. 2-3 ·1996-12-19 ·Pages 377-81

Black M, Lanthorn T, Small D, Mealing G, Lam V, Morley P

Abstract

NMDA receptor antagonists reduced NMDA-triggered increases in [Ca2+]i measured by fura-2 and showed qualitative differences in the potency and kinetics of block. High potency antagonists produced a slow block which allowed an initial increase in [Ca2+]i that was greater than the steady-state level, while compounds with moderate to low potency produced a rapid block that was at steady-state from the first measurement. The more potent antagonists showed the slowest unblocking rates. Using this simple method, novel NMDA antagonists can be screened to ascertain potency, kinetics of block and relative toxicity, prior to animal testing.

MeSH Terms
Animals Calcium/metabolism Cells, Cultured Cerebral Cortex/drug effects,metabolism Chelating Agents Excitatory Amino Acid Antagonists/pharmacology Fura-2 Indicators and Reagents Kinetics Neurons/drug effects,metabolism Rats Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors
Chemicals
Chelating Agents Excitatory Amino Acid Antagonists Indicators and Reagents Receptors, N-Methyl-D-Aspartate Calcium Fura-2
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Black M
Institute for Biological Sciences, National Research Council of Canada, Ottawa, Ontario, Canada.
Lanthorn T
Small D
Mealing G
Lam V
Morley P
Article Info
Journal
European journal of pharmacology
Abbr.
Eur J Pharmacol
ISSN
0014-2999
Published
1996-12-19
Pages
377-81
Language
English
Region
Netherlands
NLM ID
1254354
Subset
IM
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