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EGR1/zif268(一种神经活性标志物)在精神分裂症患者和其动物模型的听觉皮层中的升高。

Elevation of EGR1/zif268, a Neural Activity Marker, in the Auditory Cortex of Patients with Schizophrenia and its Animal Model.

机构信息

Department of Molecular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.

Department of Brain Tumor Biology, Brain Research Institute, Niigata University, 1-757 Asahimachi-Dori, Chuo-ku, Niigata City, Niigata, 951-8585, Japan.

出版信息

Neurochem Res. 2022 Sep;47(9):2715-2727. doi: 10.1007/s11064-022-03599-9. Epub 2022 Apr 25.

Abstract

The family of epidermal growth factor (EGF) including neuregulin-1 are implicated in the neuropathology of schizophrenia. We established a rat model of schizophrenia by exposing perinatal rats to EGF and reported that the auditory pathophysiological traits of this model such as prepulse inhibition, auditory steady-state response, and mismatch negativity are relevant to those of schizophrenia. We assessed the activation status of the auditory cortex in this model, as well as that in patients with schizophrenia, by monitoring the three neural activity-induced proteins: EGR1 (zif268), c-fos, and Arc. Among the activity markers, protein levels of EGR1 were significantly higher at the adult stage in EGF model rats than those in control rats. The group difference was observed despite an EGF model rat and a control rat being housed together, ruling out the contribution of rat vocalization effects. These changes in EGR1 levels were seen to be specific to the auditory cortex of this model. The increase in EGR1 levels were detectable at the juvenile stage and continued until old ages but displayed a peak immediately after puberty, whereas c-fos and Arc levels were nearly indistinguishable between groups at all ages with an exception of Arc decrease at the juvenile stage. A similar increase in EGR1 levels was observed in the postmortem superior temporal cortex of patients with schizophrenia. The commonality of the EGR1 increase indicates that the EGR1 elevation in the auditory cortex might be one of the molecular signatures of this animal model and schizophrenia associating with hallucination.

摘要

表皮生长因子(EGF)家族包括神经调节素-1,与精神分裂症的神经病理学有关。我们通过在围产期暴露于 EGF 建立了精神分裂症大鼠模型,并报告说该模型的听觉病理生理学特征,如前脉冲抑制、听觉稳态反应和失匹配负波,与精神分裂症的特征相关。我们通过监测三种神经活性诱导蛋白:早期生长反应基因 1(zif268)、c-fos 和 Arc,评估了该模型以及精神分裂症患者的听觉皮层的激活状态。在活性标志物中,EGF 模型大鼠在成年期的 EGR1 蛋白水平明显高于对照组大鼠。尽管 EGF 模型大鼠和对照大鼠被安置在一起,但观察到组间差异,排除了大鼠发声效应的影响。这种 EGR1 水平的变化被认为是该模型听觉皮层特有的。EGR1 水平的增加在幼年期即可检测到,并持续到老年期,但在青春期后立即达到峰值,而 c-fos 和 Arc 水平在所有年龄段均几乎无差异,仅在幼年期出现 Arc 下降。在精神分裂症患者的死后颞上皮质中也观察到类似的 EGR1 水平增加。EGR1 水平升高的共同性表明,听觉皮层中 EGR1 的升高可能是该动物模型和与幻觉相关的精神分裂症的分子特征之一。

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