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局部缺血会打开神经元间隙连接半通道。

Ischemia opens neuronal gap junction hemichannels.

作者信息

Thompson Roger J, Zhou Ning, MacVicar Brian A

机构信息

Department of Psychiatry and Brain Research Centre, University of British Columbia, Vancouver, British Columbia V6T 2B5, Canada.

出版信息

Science. 2006 May 12;312(5775):924-7. doi: 10.1126/science.1126241.

Abstract

Neuronal excitotoxicity during stroke is caused by activation of unidentified large-conductance channels, leading to swelling and calcium dysregulation. We show that ischemic-like conditions [O(2)/glucose deprivation (OGD)] open hemichannels, or half gap junctions, in neurons. Hemichannel opening was indicated by a large linear current and flux across the membrane of small fluorescent molecules. Single-channel openings of hemichannels (530 picosiemens) were observed in OGD. Both the current and dye flux were blocked by inhibitors of hemichannels. Therefore, hemichannel opening contributes to the profound ionic dysregulation during stroke and may be a ubiquitous component of ischemic neuronal death.

摘要

中风期间的神经元兴奋毒性是由未明确的大电导通道激活引起的,导致肿胀和钙调节异常。我们发现,类似缺血的条件[氧/葡萄糖剥夺(OGD)]会使神经元中的半通道(即半缝隙连接)开放。大的线性电流以及小荧光分子跨膜通量表明半通道已开放。在OGD条件下观察到了半通道的单通道开放(530皮西门子)。半通道的电流和染料通量均被半通道抑制剂阻断。因此,半通道开放促成了中风期间严重的离子调节异常,可能是缺血性神经元死亡的一个普遍因素。

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