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顽固性癫痫患者大脑中白蛋白启动子结合蛋白D位点的上调。

Upregulation of D site of albumin promoter binding protein in the brain of patients with intractable epilepsy.

作者信息

Yuan Jinxian, Guo Jing, Zhang Melin, Wang Qian, Huang Hao, Chen Yangmei

机构信息

Department of Neurology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, P.R. China.

出版信息

Mol Med Rep. 2015 Apr;11(4):2486-92. doi: 10.3892/mmr.2014.3065. Epub 2014 Dec 9.

Abstract

The mechanisms that underlie the pathogenesis of intractable epilepsy (IE) remain to be elucidated. The present study aimed to investigate the expression of D site of albumin promoter binding protein (DBP) and mitogen‑activated protein kinases (MAPKs) in the temporal lobes of patients with IE, in order to examine the possible roles of DBP in the pathogenesis of IE. The expression of DBP and MAPK was detected by immunohistochemistry and double‑label immunofluorescence staining against DBP/MAPK in 35 patients with IE, and the data were compared with those of the 15 controls. The results demonstrated that DBP expression in IE group (0.31±0.03) was significantly higher compared with that in the controls (0.18±0.02; P<0.05) and MAPK expression in the IE group (0.19±0.03) was also higher compared with that in the controls (0.12±0.02; P<0.05). DBP and MAPK were mainly expressed in the cytoplasm of neurons and the double‑label immunofluorescence staining demonstrated that DBP and MAPK expression occurred in the same neurons. Therefore, the expression of DBP and MAPK in epilepsy patients was upregulated, suggesting a possible pathogenetic role in IE.

摘要

难治性癫痫(IE)发病机制仍有待阐明。本研究旨在调查IE患者颞叶中白蛋白启动子结合蛋白(DBP)和丝裂原活化蛋白激酶(MAPK)的表达,以检验DBP在IE发病机制中的可能作用。采用免疫组织化学和针对DBP/MAPK的双标免疫荧光染色检测35例IE患者中DBP和MAPK的表达,并将数据与15例对照者的数据进行比较。结果表明,IE组中DBP表达(0.31±0.03)显著高于对照组(0.18±0.02;P<0.05),IE组中MAPK表达(0.19±0.03)也高于对照组(0.12±0.02;P<0.05)。DBP和MAPK主要表达于神经元细胞质中,双标免疫荧光染色表明DBP和MAPK表达于同一神经元中。因此,癫痫患者中DBP和MAPK的表达上调,提示其在IE发病机制中可能具有致病作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c25/4337482/c2e87dda4217/MMR-11-04-2486-g00.jpg

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