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Improvement in verbal memory following SSRI augmentation of antipsychotic treatment is associated with changes in the expression of mRNA encoding for the GABA-A receptor and BDNF in PMC of schizophrenic patients

机译:SSRI增强抗精神病药物治疗后语言记忆的改善与精神分裂症患者PMC中编码GABA-A受体和BDNF的mRNA表达的变化有关

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Verbal memory impairment in schizophrenia is associated with abnormalities in gamma-aminobutyric acid (GABA)-ergic and brain-derived neurotrophic factor (BDNF) systems. Recent evidence from animal and clinical studies that adding fluvoxamine to antipsychotics alters the expression of transcripts encoding for the GABA-A receptor and BDNF led us to postulate that fluvoxamine augmentation may improve memory in schizophrenia. To test this, we examined the effect of add-on fluvoxamine on verbal memory and other cognitive functions and related it to the expression of mRNA coding for the GABA-A receptor and BDNF in peripheral mononuclear cells (PMC) of schizophrenic patients. Twenty-nine patients completed a 6-week study in which fluvoxamine (100 mg/day) was added to ongoing antipsychotic treatment. Verbal memory, abstraction working memory, object and face recognition, and psychomotor speed and clinical symptoms were assessed at baseline and after 3 and 6 weeks of treatment. Blood samples were taken at baseline and weeks 1, 3, and 6 and PMC was assayed for the GABA-A beta3 receptor and BDNF mRNA by quantitative real-time reverse transcription-PCR. Associative and logical verbal memory improved significantly and showed a significant correlation with changes in PMC BDNF and GABA-A beta3 receptor mRNA, which increased during treatment. Abstraction and object recognition improved, but this did not correlate with PMC measures. Negative and positive symptoms improved significantly; the latter showed significant correlations with changes in PMC measures. Addition of fluvoxamine to antipsychotics improves verbal memory. It is postulated that the mechanism involves enhanced GABA-A receptor/BDNF-dependent synaptic plasticity in the hippocampus. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
机译:精神分裂症的语言记忆障碍与γ-氨基丁酸(GABA)-能动和脑源性神经营养因子(BDNF)系统异常有关。来自动物和临床研究的最新证据表明,在抗精神病药中添加氟伏沙明会改变编码GABA-A受体和BDNF的转录本的表达,这使我们推测氟伏沙明的增强可改善精神分裂症的记忆。为了测试这一点,我们检查了氟伏沙明对言语记忆和其他认知功能的影响,并将其与精神分裂症患者外周单核细胞(PMC)中编码GABA-A受体和BDNF的mRNA表达相关。 29名患者完成了为期6周的研究,其中在正在进行的抗精神病药物治疗中加入了氟伏沙明(100毫克/天)。在基线以及治疗3周和6周后评估言语记忆,抽象工作记忆,对象和面部识别以及心理运动速度和临床症状。在基线,第1、3和6周采集血样,并通过定量实时逆转录PCR检测PMC的GABA-A beta3受体和BDNF mRNA。联想和逻辑口头记忆显着改善,并与治疗期间增加的PMC BDNF和GABA-A beta3受体mRNA的变化显着相关。抽象和对象识别得到改善,但这与PMC措施无关。阴性和阳性症状明显改善;后者显示与PMC措施的变化具有显着的相关性。在抗精神病药中加入氟伏沙明可改善言语记忆。推测该机制涉及海马中增强的GABA-A受体/ BDNF依赖性突触可塑性。版权所有(C)2015 Wolters Kluwer Health,Inc.保留所有权利。

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