The International Journal of Neuropsychopharmacology



The effect of chronic co-administration of fluvoxamine and haloperidol compared to clozapine on the GABA system in the rat frontal cortex


Yael Chertkow a1a2, Orly Weinreb a2, Moussa B. H. Youdim a2 and Henry Silver a1
a1 Molecular Neuropsychiatry Unit, Shaar Menashe Brain Behavior Laboratory, Shaar Menashe MHC, and Technion – Faculty of Medicine, Haifa, Israel
a2 Eve Topf and National Parkinson Foundation Centers of Excellence for Neurodegenerative Diseases Research, Department of Pharmacology, Technion – Faculty of Medicine, Haifa, Israel

Article author query
chertkow y   [PubMed][Google Scholar] 
weinreb o   [PubMed][Google Scholar] 
youdim mb   [PubMed][Google Scholar] 
silver h   [PubMed][Google Scholar] 

Abstract

Clinical studies in schizophrenia patients have shown that adding a selective serotonin reuptake inhibitor (SSRI) to antipsychotics can ameliorate negative symptoms that frequently resist standard treatments. It has been proposed that this combined treatment produces a ‘net effect’, different from that of the individual drugs and possibly common to that of the atypical antipsychotic, clozapine, which also ameliorates negative symptoms. The present study was initiated to determine the molecular events in the rat frontal cortex resulting from combined treatment of fluvoxamine and haloperidol compared to clozapine. Rats were allocated to five groups and received a daily intraperitoneal injection with one of the following: haloperidol (1 mg/kg), fluvoxamine (11 mg/kg), clozapine (11 mg/kg), haloperidol (1 mg/kg) plus fluvoxamine (11 mg/kg), or vehicle for 30 d. cDNA arrays were used to screen a broad range of genes in the frontal cortex. Several of the most prominent alterations were taken for analysis in real-time RT–PCR and their related proteins were examined by the Western-blotting technique. The gene expression profile of the combined fluvoxamine plus haloperidol treatment was different from that of the individual drugs. Moreover, clozapine showed some degree of homology with the dual treatment. The protein expression changes, specific to the combined treatment, included glutamic acid decarboxylase (GAD67) and protein kinase Cβ (PKCβ). The latter showed a similar trend following clozapine treatment. The present findings support the existence of a unique mechanism for SSRI–antipsychotic combination, different from that of the individual drugs and suggest that it may involve modification of the gamma aminobutyric acid (GABA) system.

(Received February 15 2005)
(Reviewed March 21 2005)
(Revised March 27 2005)
(Accepted April 9 2005)
(Published Online June 21 2005)


Key Words: Antipsychotics; GABA; negative symptoms; schizophrenia; SSRI.

Correspondence:
c1 Shaar Menashe Brain Behavior Laboratory, Shaar Menashe MHC, Mobile post Hefer 38814, Israel. Tel.: 972-4-6278100 Fax: 972-4-6278004 E-mail: mdsilver@tx.technion.ac.il


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