Chertkow Yael, Weinreb Orly, Youdim Moussa B H, Silver Henry
Molecular Neuropsychiatry Unit, Shaar Menashe Brain Behavior Laboratory, Shaar Menashe MHC, and Technion -- Faculty of Medicine, Haifa, Israel.
Prog Neuropsychopharmacol Biol Psychiatry. 2007 Oct 1;31(7):1356-62. doi: 10.1016/j.pnpbp.2007.04.016. Epub 2007 Apr 29.
Antipsychotic treatment combined with Selective Serotonin Reuptake Inhibitor (SSRI) antidepressant can improve negative symptoms in schizophrenic patients that are unresponsive to antipsychotic drugs alone. The mechanism of this therapeutic effect is not clear. The current study examined molecular changes induced by the combined treatment in human peripheral mononuclear cells (PMC) in order to get insight into its mechanism of action. Gene expression profile of PMC from antipsychotic-treated patients was examined before addition of the SSRI fluvoxamine, and 3 and 6 weeks after. Gene expression patterns screened with a cDNA array, comprising 1176 genes, revealed homologous changes in a range of transcripts related to G-protein coupled receptors (GPCR). Genes related to GPCR-family were assayed using customized cDNA array and the results verified by real-time RT-PCR. The mRNA expression of chemokine receptors, IL8RA and CCR1, and of RGS7 was significantly down-regulated following fluvoxamine augmentation. The clinical assessments showed improvement in negative symptoms following the combined treatment. The transcriptional analysis suggests that the therapeutic mechanism of the combined antipsychotic-fluvoxamine treatment may involve genes associated with G-protein coupled receptors (GPCR). Our findings suggest that gene expression changes in PMC may be useful in investigating the mechanism of drug action in schizophrenia.
抗精神病药物治疗联合选择性5-羟色胺再摄取抑制剂(SSRI)类抗抑郁药可改善对单独使用抗精神病药物无反应的精神分裂症患者的阴性症状。这种治疗效果的机制尚不清楚。当前研究检测了联合治疗在人外周血单个核细胞(PMC)中诱导的分子变化,以便深入了解其作用机制。在添加SSRI氟伏沙明之前以及之后3周和6周,检测了接受抗精神病药物治疗患者的PMC的基因表达谱。用包含1176个基因的cDNA阵列筛选的基因表达模式显示,一系列与G蛋白偶联受体(GPCR)相关的转录本发生了同源变化。使用定制的cDNA阵列检测与GPCR家族相关的基因,并通过实时RT-PCR验证结果。氟伏沙明增效后,趋化因子受体IL8RA和CCR1以及RGS7的mRNA表达显著下调。临床评估显示联合治疗后阴性症状有所改善。转录分析表明,抗精神病药物-氟伏沙明联合治疗的作用机制可能涉及与G蛋白偶联受体(GPCR)相关的基因。我们的研究结果表明,PMC中的基因表达变化可能有助于研究精神分裂症的药物作用机制。