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本文引用的文献

1
P2X7 signaling promotes microsphere embolism-triggered microglia activation by maintaining elevation of Fas ligand.P2X7 信号通过维持 Fas 配体的升高促进微球栓塞触发的小胶质细胞激活。
J Neuroinflammation. 2012 Jul 12;9:172. doi: 10.1186/1742-2094-9-172.
2
Inhibition of P2X7 receptor ameliorates transient global cerebral ischemia/reperfusion injury via modulating inflammatory responses in the rat hippocampus.P2X7 受体抑制剂通过调节大鼠海马区炎症反应改善短暂性全脑缺血/再灌注损伤。
J Neuroinflammation. 2012 Apr 18;9:69. doi: 10.1186/1742-2094-9-69.
3
P2X7 receptor modulation of the viability of radial glial clone L2.3 cells during hypoxic-ischemic brain injury.P2X7 受体对缺氧缺血性脑损伤中放射状胶质克隆 L2.3 细胞活力的调节作用。
Mol Med Rep. 2012 May;5(5):1357-61. doi: 10.3892/mmr.2012.816. Epub 2012 Feb 29.
4
P2X7 receptor blockade prevents ATP excitotoxicity in neurons and reduces brain damage after ischemia.P2X7 受体阻断可防止神经元中的 ATP 兴奋性毒性,并减少缺血后的脑损伤。
Neurobiol Dis. 2012 Mar;45(3):954-61. doi: 10.1016/j.nbd.2011.12.014. Epub 2011 Dec 11.
5
Microglial cells contribute to endogenous brain defenses after acute neonatal focal stroke.小胶质细胞在急性新生儿局灶性脑卒中后有助于内源性脑防御。
J Neurosci. 2011 Sep 7;31(36):12992-3001. doi: 10.1523/JNEUROSCI.2102-11.2011.
6
The activation of P2X7 receptor induces cathepsin D-dependent production of a 20-kDa form of IL-1β under acidic extracellular pH in LPS-primed microglial cells.P2X7 受体的激活在 LPS 预处理的小胶质细胞中,在外源 pH 值偏酸性的条件下,诱导组织蛋白酶 D 依赖性产生 20kDa 形式的白细胞介素-1β。
J Neurochem. 2011 May;117(4):712-23. doi: 10.1111/j.1471-4159.2011.07240.x. Epub 2011 Mar 28.
7
Glutamate and ATP signalling in white matter pathology.谷氨酸和三磷酸腺苷信号在脑白质病变中的作用。
J Anat. 2011 Jul;219(1):53-64. doi: 10.1111/j.1469-7580.2010.01339.x. Epub 2011 Jan 20.
8
Functional significance of the negative-feedback regulation of ATP release via pannexin-1 hemichannels under ischemic stress in astrocytes.在缺血应激下星形胶质细胞中通过连接蛋白-1 半通道的 ATP 释放的负反馈调节的功能意义。
Neurochem Int. 2011 Feb;58(3):376-84. doi: 10.1016/j.neuint.2010.12.013. Epub 2010 Dec 24.
9
Ion channels on microglia: therapeutic targets for neuroprotection.小胶质细胞上的离子通道:神经保护的治疗靶点。
CNS Neurol Disord Drug Targets. 2011 Feb;10(1):44-56. doi: 10.2174/187152711794488638.
10
Microglia: proliferation and activation driven by the P2X7 receptor.小胶质细胞:P2X7 受体驱动的增殖和激活。
Int J Biochem Cell Biol. 2010 Nov;42(11):1753-6. doi: 10.1016/j.biocel.2010.06.021. Epub 2010 Jul 3.

脑缺血中的 P2X(7)受体。

P2X(7) receptors in cerebral ischemia.

机构信息

Department of Physiology, Dalian Medical University, Dalian, 116044, China.

出版信息

Neurosci Bull. 2013 Jun;29(3):390-8. doi: 10.1007/s12264-013-1338-7. Epub 2013 May 3.

DOI:10.1007/s12264-013-1338-7
PMID:23640286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561845/
Abstract

Cerebral ischemia is one of the most common diseases resulting in death and disability in aged people. It leads immediately to rapid energy failure, ATP depletion, and ionic imbalance, which increase extracellular ATP levels and accordingly activate P2X7 receptors. These receptors are ATP-gated cation channels and widely distributed in nerve cells, especially in the immunocompetent cells of the brain. Currently, interest in the roles of P2X7 receptors in ischemic brain injury is growing. In this review, we discuss recent research progress on the actions of P2X7 receptors, their possible mechanisms in cerebral ischemia, and the potential therapeutic value of P2X7 receptor antagonists which may provide a new target both for clinical and for research purposes.

摘要

脑缺血是导致老年人死亡和残疾的最常见疾病之一。它会导致能量迅速衰竭、三磷酸腺苷(ATP)耗竭和离子失衡,从而增加细胞外 ATP 水平,并相应地激活 P2X7 受体。这些受体是 ATP 门控阳离子通道,广泛分布于神经细胞中,特别是在大脑的免疫活性细胞中。目前,人们对 P2X7 受体在脑缺血损伤中的作用越来越感兴趣。在这篇综述中,我们讨论了 P2X7 受体作用的最新研究进展,以及它们在脑缺血中的可能机制,以及 P2X7 受体拮抗剂的潜在治疗价值,这可能为临床和研究目的提供一个新的靶点。