Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Reviewing the role of the genes G72 and DAAO in glutamate neurotransmission in schizophrenia

Boks, M. P.M. ; Rietkerk, T. ; van de Beek, M. H. ; Sommer, I. E. ; de Koning, T. J. LU and Kahn, R. S. (2007) In European Neuropsychopharmacology 17(9). p.567-572
Abstract

We review the role of two susceptibility genes; G72 and DAAO in glutamate neurotransmission and the aetiology of schizophrenia. The gene product of G72 is an activator of DAAO (D-amino acid oxidase), which is the only enzyme oxidising D-serine. D-serine is an important co-agonist for the NMDA glutamate receptor and plays a role in neuronal migration and cell death. Studies of D-serine revealed lower serum levels in schizophrenia patients as compared to healthy controls. Furthermore, administration of D-serine as add-on medication reduced the symptoms of schizophrenia. The underlying mechanism of the involvement of G72 and DAAO in schizophrenia is probably based on decreased levels of D-serine and decreased NMDA receptor functioning in... (More)

We review the role of two susceptibility genes; G72 and DAAO in glutamate neurotransmission and the aetiology of schizophrenia. The gene product of G72 is an activator of DAAO (D-amino acid oxidase), which is the only enzyme oxidising D-serine. D-serine is an important co-agonist for the NMDA glutamate receptor and plays a role in neuronal migration and cell death. Studies of D-serine revealed lower serum levels in schizophrenia patients as compared to healthy controls. Furthermore, administration of D-serine as add-on medication reduced the symptoms of schizophrenia. The underlying mechanism of the involvement of G72 and DAAO in schizophrenia is probably based on decreased levels of D-serine and decreased NMDA receptor functioning in patients. The involvement of this gene is therefore indirect support for the glutamate dysfunction hypothesis in schizophrenia.

(Less)
Please use this url to cite or link to this publication:
author
; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
subject
keywords
D-Serine, DAAO;, G72;, Glutamate;, Schizophrenia;
in
European Neuropsychopharmacology
volume
17
issue
9
pages
6 pages
publisher
Elsevier
external identifiers
  • scopus:34447550448
  • pmid:17250995
ISSN
0924-977X
DOI
10.1016/j.euroneuro.2006.12.003
language
English
LU publication?
no
id
760bf859-a0ac-4180-a3a1-c0780648f0ec
date added to LUP
2020-02-28 13:57:22
date last changed
2024-05-29 10:17:38
@article{760bf859-a0ac-4180-a3a1-c0780648f0ec,
  abstract     = {{<p>We review the role of two susceptibility genes; G72 and DAAO in glutamate neurotransmission and the aetiology of schizophrenia. The gene product of G72 is an activator of DAAO (D-amino acid oxidase), which is the only enzyme oxidising D-serine. D-serine is an important co-agonist for the NMDA glutamate receptor and plays a role in neuronal migration and cell death. Studies of D-serine revealed lower serum levels in schizophrenia patients as compared to healthy controls. Furthermore, administration of D-serine as add-on medication reduced the symptoms of schizophrenia. The underlying mechanism of the involvement of G72 and DAAO in schizophrenia is probably based on decreased levels of D-serine and decreased NMDA receptor functioning in patients. The involvement of this gene is therefore indirect support for the glutamate dysfunction hypothesis in schizophrenia.</p>}},
  author       = {{Boks, M. P.M. and Rietkerk, T. and van de Beek, M. H. and Sommer, I. E. and de Koning, T. J. and Kahn, R. S.}},
  issn         = {{0924-977X}},
  keywords     = {{D-Serine; DAAO;; G72;; Glutamate;; Schizophrenia;}},
  language     = {{eng}},
  month        = {{09}},
  number       = {{9}},
  pages        = {{567--572}},
  publisher    = {{Elsevier}},
  series       = {{European Neuropsychopharmacology}},
  title        = {{Reviewing the role of the genes G72 and DAAO in glutamate neurotransmission in schizophrenia}},
  url          = {{http://dx.doi.org/10.1016/j.euroneuro.2006.12.003}},
  doi          = {{10.1016/j.euroneuro.2006.12.003}},
  volume       = {{17}},
  year         = {{2007}},
}