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Neurosci Lett. 2009 Feb 13;451(1):29-33. doi: 10.1016/j.neulet.2008.12.036. Epub 2008 Dec 24.

Blockade of NMDA receptor channels by 9-aminoacridine and its derivatives.

Author information

1
I.M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.

Abstract

9-Aminoacridine is known as "foot-in-the-door" NMDA receptor channel blocker because its binding prevents channel closure. Structural determinants of this mechanism of block were studied using a series of 9-aminoacridine derivatives. Experiments were performed on native NMDA receptors of hippocampal pyramidal neurons, isolated from rat brain slices. The use-dependence of block and kinetics of recovery from block were used to characterize mechanism of block produced by the compounds. Modifications, which preserve the flat structure of the tricyclic 9-aminoacridine moiety, affect blocking activity and kinetics but not the foot-in-the-door mechanism. On the contrary, disruption of the flat structure changes the mechanism of block to trapping. It is concluded that flat aromatic structure is one of the critical determinants of the action mechanism of 9-aminoacridine.

PMID:
19111901
DOI:
10.1016/j.neulet.2008.12.036
[Indexed for MEDLINE]

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