GABA-ergic neurons and the neurobiology of schizophrenia and other psychoses

Authors
Citation
Eb. Keverne, GABA-ergic neurons and the neurobiology of schizophrenia and other psychoses, BRAIN RES B, 48(5), 1999, pp. 467-473
Citations number
71
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BRAIN RESEARCH BULLETIN
ISSN journal
03619230 → ACNP
Volume
48
Issue
5
Year of publication
1999
Pages
467 - 473
Database
ISI
SICI code
0361-9230(19990315)48:5<467:GNATNO>2.0.ZU;2-X
Abstract
There are a number of disorders in the Diagnostic and Statistical Manual of Mental Disorders (DSM IV) that are characterised by having psychotic sympt oms as the defining feature [17]. The narrowest definition of psychosis is restricted to delusions or prominent hallucinations, with the hallucination s occurring in the absence of insight into their pathological nature, Schiz ophrenia is the most prevalent form of psychosis, but this may also occur d ue to other medical conditions (e.g,, Prader-Willi syndrome, epilepsy), in the early post-partum period, at menopause, and as a result of drug use. Th is article attempts to draw together an underlying causation across the var ious forms of psychotic disorder and, by integrating this with what is know n about the genetics, neuroanatomy and neuropharmacology of the positive sy mptoms in schizophrenia, produce a broader understanding. At the cellular l evel, gamma-aminobutyric acid (GABA)-ergic interneurons are a common featur e in psychotic states, and are a principal focus for serotonin and dopamine innervations, as well as playing an important role in cortical development . At the systems level, prefrontal and medial temporal cortices are implica ted with activity levels out of synchrony in schizophrenics, How these vast areas of disparately functioning cortical networks are "bound" together to provide coherent conscious experiences is again a function of GABA-ergic i nterneurons. These interneurons have highly divergent inhibitory projection s to large numbers of pyramidal neurons and are themselves synchronised by the ascending dopamine and serotonin innervations. (C) 1999 Elsevier Scienc e Inc.