Promising targets of cell death signaling of NR2B receptor subunit in stroke pathogenesis.

IF 2
Regenerative Medicine Research Pub Date : 2014-07-23 eCollection Date: 2014-12-01 DOI:10.1186/2050-490X-2-8
Shu Shu, Lei Pei, Youming Lu
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引用次数: 21

Abstract

Stroke is an acute cerebrovascular disease caused by acute brain artery bursting or cerebral embolism that leads to neuronal death and severe dysfunction of synaptic transmission. Neuronal damage after stroke remains a major cause of morbidity and mortality worldwide and affects 795 000 of lives every year in United States. However, effective treatments remain lacking, which makes the identification of new therapeutic targets a matter of great importance. N-methyl-D-aspartate glutamate (NMDA) receptor is important both in the normal synaptic transmission and in the neuronal death after stroke. Accumulated evidences show NMDA receptor downstream effectors, such as PSD-95, DAPK1, and ERK, had been revealed to be linked with neuronal damage. Based on our recent studies, we review the promising targets of the NMDA receptor downstream signaling involved in stroke treatment. This review will provide the concept of NR2B downstream signaling in neuronal death after stroke and provide evidences for developing better NMDAR-based therapeutics by targeting downstream proteins.

Abstract Image

Abstract Image

NR2B受体亚基细胞死亡信号在脑卒中发病中的潜在靶点。
脑卒中是由急性脑动脉破裂或脑栓塞引起的急性脑血管疾病,可导致神经元死亡和突触传递严重功能障碍。中风后的神经元损伤仍然是世界范围内发病率和死亡率的主要原因,在美国每年影响79.5万人的生命。然而,有效的治疗方法仍然缺乏,这使得确定新的治疗靶点变得非常重要。n -甲基- d -天冬氨酸(NMDA)受体在正常突触传递和脑卒中后神经元死亡中都起重要作用。越来越多的证据表明,NMDA受体下游效应物,如PSD-95、DAPK1和ERK,已被发现与神经元损伤有关。基于我们最近的研究,我们回顾了NMDA受体下游信号参与脑卒中治疗的有希望的靶点。本综述将提供NR2B下游信号在脑卒中后神经元死亡中的概念,并为开发更好的基于nmda的靶向下游蛋白的治疗方法提供证据。
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来源期刊
Regenerative Medicine Research
Regenerative Medicine Research MEDICINE, RESEARCH & EXPERIMENTAL-
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