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Prog Neuropsychopharmacol Biol Psychiatry. 2013 Apr 5;42:146-53. doi: 10.1016/j.pnpbp.2012.11.008. Epub 2012 Nov 23.

Anti-inflammatory treatment in schizophrenia.

Author information

1
Department of Psychiatry and Psychotherapy, Ludwig Maximilian University, Munich, Germany. Norbert.Mueller@med.uni-muenchen.de

Abstract

Antipsychotics, which act predominantly as dopamine D2 receptor antagonists, have several shortcomings. The exact pathophysiological mechanism leading to dopaminergic dysfunction in schizophrenia is still unclear, but inflammation has been postulated to be a key player in the pathophysiology of the disorder. A dysfunction in activation of the type 1 immune response seems to be associated with an imbalance in tryptophan/kynurenine metabolism; the degrading enzymes involved in this metabolism are regulated by cytokines. Kynurenic acid (KYNA), an N-methyl-d-aspartate antagonist, was found to be increased in critical regions of the central nervous system (CNS) in schizophrenia, resulting in reduced glutamatergic neurotransmission. The differential activation of microglial cells and astrocytes as functional carriers of the immune system in the CNS may also contribute to this imbalance. The immunological effects of many existing antipsychotics, however, rebalance in part the immune imbalance and overproduction of KYNA. The immunological imbalance results in an inflammatory state combined with increased prostaglandin E(2) production and increased cyclo-oxygenase-2 (COX-2) expression. Growing evidence from clinical studies with COX-2 inhibitors points to favorable effects of anti-inflammatory therapy in schizophrenia, in particular in an early stage of the disorder. Further options for immunomodulating therapies in schizophrenia will be discussed.

PMID:
23178230
DOI:
10.1016/j.pnpbp.2012.11.008
[Indexed for MEDLINE]

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