PSYCHOPHARMACOLOGY OF BENZODIAZEPINES - AN UPDATE

Citation
Al. Malizia et Dj. Nutt, PSYCHOPHARMACOLOGY OF BENZODIAZEPINES - AN UPDATE, Human psychopharmacology, 10, 1995, pp. 1-14
Citations number
148
Categorie Soggetti
Psychology,Psychology,"Pharmacology & Pharmacy",Neurosciences
Journal title
ISSN journal
08856222
Volume
10
Year of publication
1995
Supplement
1
Pages
1 - 14
Database
ISI
SICI code
0885-6222(1995)10:<1:POB-AU>2.0.ZU;2-G
Abstract
Benzodiazepines are one of the classes of compounds which bind at the benzodiazepine site in the central nervous system. The benzodiazepine site is phylogenetically new and modulates allosterically the GABA-chl oride ionophore. This complex is a pentamer surrounding the chloride c hannel and is made up of various combinations of alpha, beta and gamma subunits. The anatomical distribution of these subunits is diverse an d underlies the differential binding of a number of benzodiazepine mod ulators in the brain. Other compounds which act at this complex includ e bicuculline, musicmol, ethanol and neurosteroids. Modulation at the benzodiazepine site is bidirectional. The net result of positive modul ation is facilitation of conductance and thus hyperpolarisation i.e. a n inhibitory effect, while negative modulation has the inverse effects . There is considerable receptor reserve at this complex, in addition since modulators depend on the presence of GABA for their effects, sup raphysiological stimulation does not occur. These factors account for the extreme safety of benzodiazepines and explain the lack of selectiv ity of action of full agonists, since small increases in fractional oc cupancy are enough to produce the full gamut of effects. The same howe ver does not apply to partial agonists which manifest the different ac tions at well separated receptor occupation. Endogenous ligands have n ot yet been found for these sites, although benzodiazepines have been found in brains collected prior to their pharmaceutic marketing-these probably originate from vegetable foodstuffs and gut bacteria. Changes in this site can be induced by stress, convulsions and repeated admin istration of modulators and animals bred for different sensitivity at the benzodiazepine site manifest consistent behavioural differences. T hese observations have instigated a search for potential endogenous in verse agonists in human anxiety disorders and epilepsy and for endogen ous agonists in metabolic encephalopathies. While thus far this has no t been successful the putative isolation of endozapines in the rare co ndition of idiopathic recurrent stupor indicate that this may be a use ful line of research. In addition the emergence of partial agonists at these sites which have fewer side effects is likely to rekindle inter est in the clinical use of such compounds in a variety of neurological and psychiatric syndromes.