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首页> 外文期刊>Biological psychiatry >Reduced glutamate decarboxylase 65 protein within primary auditory cortex inhibitory boutons in schizophrenia
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Reduced glutamate decarboxylase 65 protein within primary auditory cortex inhibitory boutons in schizophrenia

机译:在精神分裂症中的原发性听觉皮质抑制方向上减少谷氨酸脱羧酶65蛋白

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摘要

Background: Schizophrenia is associated with perceptual and physiological auditory processing impairments that may result from primary auditory cortex excitatory and inhibitory circuit pathology. High-frequency oscillations are important for auditory function and are often reported to be disrupted in schizophrenia. These oscillations may, in part, depend on upregulation of gamma-aminobutyric acid synthesis by glutamate decarboxylase 65 (GAD65) in response to high interneuron firing rates. It is not known whether levels of GAD65 protein or GAD65-expressing boutons are altered in schizophrenia. Methods: We studied two cohorts of subjects with schizophrenia and matched control subjects, comprising 27 pairs of subjects. Relative fluorescence intensity, density, volume, and number of GAD65-immunoreactive boutons in primary auditory cortex were measured using quantitative confocal microscopy and stereologic sampling methods. Bouton fluorescence intensities were used to compare the relative expression of GAD65 protein within boutons between diagnostic groups. Additionally, we assessed the correlation between previously measured dendritic spine densities and GAD65-immunoreactive bouton fluorescence intensities. Results: GAD65-immunoreactive bouton fluorescence intensity was reduced by 40% in subjects with schizophrenia and was correlated with previously measured reduced spine density. The reduction was greater in subjects who were not living independently at time of death. In contrast, GAD65-immunoreactive bouton density and number were not altered in deep layer 3 of primary auditory cortex of subjects with schizophrenia. Conclusions: Decreased expression of GAD65 protein within inhibitory boutons could contribute to auditory impairments in schizophrenia. The correlated reductions in dendritic spines and GAD65 protein suggest a relationship between inhibitory and excitatory synapse pathology in primary auditory cortex.
机译:背景:精神分裂症与主要听觉皮质兴奋性和抑制电路病理有关的感知和生理听觉处理障碍。高频振荡对于听觉功能很重要,并且通常据报道,在精神分裂症中被扰乱。这些振荡部分可以部分地取决于谷氨酸脱羧酶65(GAD65)的γ-氨基丁酸合成的上调响应于高中性烧制率。尚不清楚是否在精神分裂症中改变了GAD65蛋白或表达GAD65的水平。方法:我们研究了两种患有精神分裂症和匹配的对照受试者的群体,包括27对受试者。使用定量的共聚焦显微镜和立体学取样方法测量主要听觉皮质中的相对荧光强度,密度,体积和GAD65免疫反应性备件。 Bouton荧光强度用于比较诊断基团之间的前置的GAD65蛋白的相对表达。另外,我们评估了先前测量的树突脊柱密度和GAD65-免疫反应性Bouton荧光强度之间的相关性。结果:含有精神分​​裂症的受试者的GAD65-免疫反应性Bouton荧光强度降低了40%,并与先前测量的脊柱密度相关。在死亡时没有独立生活的受试者中减少更大。相反,GAD65-免疫反应性Bouton密度和数量在具有精神分裂症的受试者的主要听觉皮层的深层3中没有改变。结论:降低抑制作油中GAD65蛋白的表达可能导致精神分裂症的听觉障碍。树枝状刺和GAD65蛋白的相关减少表明了主要听觉皮层中抑制和兴奋性突触病理之间的关系。

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