...
首页> 外文期刊>Journal of neuroinflammation >Chronic brain inflammation leads to a decline in hippocampal NMDA-R1 receptors
【24h】

Chronic brain inflammation leads to a decline in hippocampal NMDA-R1 receptors

机译:慢性脑部炎症导致海马NMDA-R1受体下降

获取原文

摘要

Background Neuroinflammation plays a prominent role in the progression of Alzheimer's disease and may be responsible for degeneration in vulnerable regions such as the hippocampus. Neuroinflammation is associated with elevated levels of extracellular glutamate and potentially an enhanced stimulation of glutamate N-methyl-D-aspartate receptors. This suggests that neurons that express these glutamate receptors might be at increased risk of degeneration in the presence of chronic neuroinflammation. Methods We have characterized a novel model of chronic brain inflammation using a slow infusion of lipopolysaccharide into the 4th ventricle of rats. This model reproduces many of the behavioral, electrophysiological, neurochemical and neuropathological changes associated with Alzheimer's disease. Results The current study demonstrated that chronic neuroinflammation is associated with the loss of N-methyl-D-aspartate receptors, as determined both qualitatively by immunohistochemistry and quantitatively by in vitro binding studies using [3H]MK-801, within the hippocampus and entorhinal cortex. Conclusion The gradual loss of function of this critical receptor within the temporal lobe region may contribute to some of the cognitive deficits observed in patients with Alzheimer's disease.
机译:背景技术神经炎症在阿尔茨海默氏病的进展中起着重要作用,并且可能导致脆弱区域(如海马体)的变性。神经炎症与细胞外谷氨酸水平升高有关,并可能增强谷氨酸N-甲基-D-天冬氨酸受体的刺激作用。这表明在存在慢性神经炎症的情况下,表达这些谷氨酸受体的神经元的变性风险可能会增加。方法我们已经表征了一种新型的慢性脑炎症模型,该模型使用脂多糖缓慢注入大鼠第四脑室。该模型再现了许多与阿尔茨海默氏病有关的行为,电生理,神经化学和神经病理学变化。结果目前的研究表明,慢性神经炎症与N-甲基-D-天冬氨酸受体的丧失有关,这是通过免疫组织化学定性确定的,并通过使用[3H] MK-801在海马和内嗅皮层中进行的体外结合研究定量确定的。结论该关键受体在颞叶区域逐渐丧失功能可能是阿尔茨海默氏病患者所观察到的某些认知缺陷的原因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号