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β淀粉样蛋白通过升高ROS水平上调晚期糖基化终末产物受体的表达

孔卫娜 张佳 高维娟 刘清涛 周利明 柴锡庆

南方医科大学学报2013,Vol.33Issue(8):1132-1136,5.
南方医科大学学报2013,Vol.33Issue(8):1132-1136,5.DOI:10.3969/j.issn.1673-4254.2013.08.07

β淀粉样蛋白通过升高ROS水平上调晚期糖基化终末产物受体的表达

β-amyloid protein up-regulates the expression of the receptor for advanced glycation end products by increasing ROS production

孔卫娜 1张佳 1高维娟 2刘清涛 1周利明 1柴锡庆1

作者信息

  • 1. 河北化工医药职业技术学院∥河北省高校生物反应器与蛋白类药物开发应用技术研发中心,河北石家庄050026
  • 2. 河北医科大学第一附属医院神经内科,河北石家庄050017
  • 折叠

摘要

Abstract

Objective To investigate the mechanism of β-amyloid protein (Aβ) in regulating the expression of the receptor for advanced glycation end products (RAGE).Methods Aβ1~40 was injected into the bilateral hippocampus of rats,and 3 weeks later,the levels of reactive oxygen species (ROS) production were detected by flow cytometry.The expressions of RAGE,reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (gp91phox and p47phox),nuclear factor-κB (NF-κB),and inhibitor of κB (IκB) were measured by Western blotting.Results Injection of A1~40 caused a significant increase in the expressions of RAGE,gp91phox,p47phox,phospho-p47phox,phospho-IκBα,NF-κB and phospho-NF-κB in rat hippocampus but decreased the level of IκBα.Aβ1~40 injection also resulted in a significantly increased content of ROS in the hippocampus of the rats.Conclusion Aβ up-regulates the expression of RAGE in rat hippocampus via NADPH/ROS/NF-κB signaling pathway.

关键词

阿尔茨海默病/晚期糖基化终末产物受体/β淀粉样蛋白/活性氧/还原型烟酰胺腺嘌呤二核苷酸氧化酶/核因子-κb/NF-κB抑制蛋白

Key words

Alzheimer's disease/receptor for advanced glycation end products/β-amyloid protein/reactive oxygen species/reduced nicotinamide adenine dinucleotide phosphate oxidases/nuclear factor-κB/inhibitor of κB

引用本文复制引用

孔卫娜,张佳,高维娟,刘清涛,周利明,柴锡庆..β淀粉样蛋白通过升高ROS水平上调晚期糖基化终末产物受体的表达[J].南方医科大学学报,2013,33(8):1132-1136,5.

基金项目

国家自然科学基金(81273983) (81273983)

河北省自然科学基金(C2010001471) (C2010001471)

河北省高等学校科学技术研究青年基金(Q2012036)Supported by National Natural Science Foundation of China (81273983). (Q2012036)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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