Pharmaceuticals 2010, 3(10), 3240-3257; doi:10.3390/ph3103240

Allosteric Inhibitors of NMDA Receptor Functions

Department of Biochemistry, University at Buffalo, SUNY/3435 Main Street, Buffalo NY 14214, USA
* Author to whom correspondence should be addressed.
Received: 10 August 2010; in revised form: 9 October 2010 / Accepted: 12 October 2010 / Published: 14 October 2010
(This article belongs to the Special Issue Allosteric Modulation)
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Abstract: NMDA receptors are glutamate-activated ion-channels involved in many essential brain functions including learning, memory, cognition, and behavior. Given this broad range of function it is not surprising that the initial attempts to correct NMDA receptor-mediated pathologies with en-mass receptor blockade were derailed by unacceptable side effects. Recent successes with milder or more targeted pharmaceuticals and increasing knowledge of how these receptors operate offer new incentives for rational development of effective NMDA receptor-targeted therapies. In this article we review evidence that L-alanine, a glycine-site partial agonist and pregnanolone sulfate, a use-dependent allosteric inhibitor, while attenuating NMDA receptor activity to similar levels elicit remarkably dissimilar functional outcomes. We suggest that detailed understanding of NMDA receptor activation mechanisms and of structural correlates of function will help better match modulator with function and neurological condition and may unleash the yet untapped potential of NMDA receptor pharmaceutics.
Keywords: NMDA receptor; allosteric modulation; gating modifiers

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MDPI and ACS Style

Popescu, G.K.; Murthy, S.; Borschel, W.F. Allosteric Inhibitors of NMDA Receptor Functions. Pharmaceuticals 2010, 3, 3240-3257.

AMA Style

Popescu GK, Murthy S, Borschel WF. Allosteric Inhibitors of NMDA Receptor Functions. Pharmaceuticals. 2010; 3(10):3240-3257.

Chicago/Turabian Style

Popescu, Gabriela K.; Murthy, Swetha; Borschel, William F. 2010. "Allosteric Inhibitors of NMDA Receptor Functions." Pharmaceuticals 3, no. 10: 3240-3257.

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