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Journal of Neuroscience
Article . 2007 . Peer-reviewed
License: CC BY NC SA
Data sources: Crossref
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Neurovascular Coupling Is Not Mediated by Potassium Siphoning from Glial Cells

Authors: Monica R, Metea; Paulo, Kofuji; Eric A, Newman;

Neurovascular Coupling Is Not Mediated by Potassium Siphoning from Glial Cells

Abstract

Neuronal activity evokes localized changes in blood flow, a response termed neurovascular coupling. One widely recognized hypothesis of neurovascular coupling holds that glial cell depolarization evoked by neuronal activity leads to the release of K+onto blood vessels (K+siphoning) and to vessel relaxation. We now present two direct tests of this glial cell-K+siphoning hypothesis of neurovascular coupling. Potassium efflux was evoked from glial cells in the rat retina by applying depolarizing current pulses to individual cells. Glial depolarizations as large as 100 mV produced no change in the diameter of adjacent arterioles. We also monitored light-evoked vascular responses in Kir4.1 knock-out mice, where functional Kir K+channels are absent from retinal glial cells. The magnitude of light-evoked vasodilations was identical in Kir4.1 knock-out and wild-type animals. Contrary to the hypothesis, the results demonstrate that glial K+siphoning in the retina does not contribute significantly to neurovascular coupling.

Related Organizations
Keywords

Male, Mice, Knockout, Light, Retinal Vessels, In Vitro Techniques, Retina, Rats, Electrophysiology, Vasodilation, Vasomotor System, Arterioles, Mice, Regional Blood Flow, Kcnj10 Channel, Potassium, Animals, Nervous System Physiological Phenomena, Rats, Long-Evans, Potassium Channels, Inwardly Rectifying, Neuroglia

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    81
    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.
    Top 10%
    influence
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citations
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!
81
Top 10%
Top 10%
Top 10%
hybrid