Memory Effects of Benzodiazepines: Memory Stages and Types Versus Binding-Site Subtypes

Author:

Savic Miroslav M.12,Obradovic Dragan I.3,Ugrešic Nenad D.1,Bokonjic Dubravko R.4

Affiliation:

1. Department of Pharmacology, Faculty of Pharmacy, University of Belgrade, Belgrade 11000, Serbia and Montenegro

2. Department of Pharmacology, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, Belgrade 11221, Serbia and Montenegro

3. Department of Pharmacology, Medical Faculty, University of Belgrade, Belgrade 11000, Serbia and Montenegro

4. National Poison Center, Military Medical Academy, Crnotravska 17, Belgrade 11000, Serbia and Montenegro

Abstract

Benzodiazepines are well established as inhibitory modulators of memory processing. This effect is especially prominent when applied before the acquisition phase of a memory task. This minireview concentrates on the putative subtype selectivity of the acquisition-impairing action of benzodiazepines. Namely, recent genetic studies and standard behavioral tests employing subtype-selective ligands pointed to the predominant involvement of two subtypes of benzodiazepine binding sites in memory modulation. Explicit memory learning seems to be affected through theGABAAreceptors containing theα1andα5subunits, whereas the effects on procedural memory can be mainly mediated by theα1subunit. The pervading involvement of theα1subunit in memory modulation is not at all unexpected because this subunit is the major subtype, present in 60% of allGABAAreceptors. On the other hand, the role ofα5subunits, mainly expressed in the hippocampus, in modulating distinct forms of memory gives promise of selective pharmacological coping with certain memory deficit states.

Publisher

Hindawi Limited

Subject

Clinical Neurology,Neurology

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