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Ischemia Opens Neuronal Gap Junction Hemichannels

Authors: Roger J, Thompson; Ning, Zhou; Brian A, MacVicar;

Ischemia Opens Neuronal Gap Junction Hemichannels

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.

Related Organizations
Keywords

Neurons, Cell Membrane Permeability, Patch-Clamp Techniques, Gap Junctions, Nerve Tissue Proteins, In Vitro Techniques, Fluoresceins, Hippocampus, Cell Hypoxia, Connexins, Ion Channels, Brain Ischemia, Membrane Potentials, Mice, Necrosis, Adenosine Triphosphate, Glucose, Lanthanum, Carbenoxolone, Animals

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
505
Top 1%
Top 1%
Top 1%
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