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首页> 外文期刊>American journal of psychiatry >Altered expression of genes involved in GABAergic transmission and neuromodulation of granule cell activity in the cerebellum of schizophrenia patients.
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Altered expression of genes involved in GABAergic transmission and neuromodulation of granule cell activity in the cerebellum of schizophrenia patients.

机译:精神分裂症患者小脑中参与GABA能传递和颗粒细胞活性神经调节的基因表达改变。

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OBJECTIVE: Deficits in gamma-aminobutyric acid (GABA) signaling have been described in the prefrontal cortex, limbic system, and cerebellum in individuals with schizophrenia. The purpose of the present study was to further investigate cerebellar gene expression alterations as they relate to decreases in GABAergic transmission by examining the expression of GABAergic markers, N-methyl-d-aspartic-acid (NMDA) receptor subunits, and cerebellum neuromodulators in individuals with schizophrenia. METHOD: Subjects were postmortem men with a diagnosis of schizophrenia (N=13) and a postmortem interval-matched non-psychiatric male comparison group (N=13). The authors utilized real-time-quantitative polymerase chain reaction (PCR) to measure mRNA levels of the following GABAergic markers: glutamic acid decarboxylase (GAD) 65 and 67; GABA plasma membrane transporter-1 (GAT-1); GABA type A (GABA(A)) receptor subunits alpha(6), beta(3), and delta; and parvalbumin. In addition, real-time-quantitative PCR was utilized to assess mRNA levels of the NMDA receptor (NR) subunits NR1, NR2-A, NR2-B, NR2-C, and NR2-D as well as the cerebellar neuromodulators glutamate receptor (GluR)-6, kainate-preferring glutamate receptor subunit-2 (KA2), metabotropic glutamate receptor (mGluR)-2 and mGluR3, and neuronal nitric oxide synthase. Measurements for mRNA levels were determined using lateral cerebellar hemisphere tissue from both schizophrenia and comparison subjects. RESULTS: Schizophrenia subjects showed significant decreases in mRNA levels of GAD(67), GAD(65), GAT-1, mGluR2, and neuronal nitric oxide synthase. Increases in GABA(A)-alpha(6 )and GABA(A)-delta as well as GluR6 and KA2 were also observed. Medication effects on the expression of the same genes were examined in rats treated with either haloperidol (Sprague-Dawley rats [N=16]) or clozapine (Long-Evans rats [N=20]). Both haloperidol and clozapine increased the levels of GAD(67) in the cerebellum and altered the expression of other cerebellar mRNAs. CONCLUSIONS: These findings suggest that GABA transmission is decreased in the cerebellar cortices in individuals with schizophrenia and additional gene expression changes may reflect an attempt to increase GABA neurotransmission at the cerebellar glomerulus.
机译:目的:精神分裂症患者的前额叶皮层,边缘系统和小脑中存在γ-氨基丁酸(GABA)信号转导的缺陷。本研究的目的是通过检查个体中的GABA能标志物,N-甲基-d-天冬氨酸(NMDA)受体亚基和小脑神经调节因子的表达,进一步研究小脑基因表达变化与GABA能传递减少的关系与精神分裂症。方法:受试者为诊断为精神分裂症的死后男性(N = 13)和死后间隔匹配的非精神病男性比较组(N = 13)。作者利用实时定量聚合酶链反应(PCR)来测量以下GABA能标记的mRNA水平:谷氨酸脱羧酶(GAD)65和67;谷氨酸脱羧酶(GAD)65和67。 GABA质膜转运蛋白1(GAT-1); GABA A型(GABA(A))受体亚基alpha(6),beta(3)和delta;和小白蛋白。此外,实时定量PCR还用于评估NMDA受体(NR)NR1,NR2-A,NR2-B,NR2-C和NR2-D亚基以及小脑神经调节剂谷氨酸受体( GluR)-6,首选海藻酸盐的谷氨酸受体亚基2(KA2),代谢型谷氨酸受体(mGluR)-2和mGluR3,以及神经元一氧化氮合酶。使用来自精神分裂症和比较对象的小脑半球外侧组织测定mRNA水平。结果:精神分裂症患者的GAD(67),GAD(65),GAT-1,mGluR2和神经元一氧化氮合酶的mRNA水平显着降低。还观察到GABA(A)-alpha(6)和GABA(A)-δ以及GluR6和KA2的增加。在用氟哌啶醇(Sprague-Dawley大鼠[N = 16])或氯氮平(Long-Evans大鼠[N = 20])治疗的大鼠中检查了对相同基因表达的药物作用。氟哌啶醇和氯氮平均会增加小脑中GAD(67)的水平,并改变其他小脑mRNA的表达。结论:这些发现表明,精神分裂症患者小脑皮质中的GABA传递减少,另外的基因表达变化可能反映了增加小脑小球GABA神经传递的尝试。

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