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. 2013 Oct 1;7:159. doi: 10.3389/fncel.2013.00159

Figure 3.

Figure 3

High potassium permeability of glial cells is mediated by Kir4.1 channels. (A) Schematic illustration of simultaneous recordings of extracellular K+ concentration (K+) and glial membrane potential (INTRA). (B) In vivo simultaneous recordings of extracellular K+ concentrations and glial membrane potential fluctuations during long lasting stimulations (10 Hz, 30 s). Glial membranes behave as K+ electrodes, reflecting their high K+ permeability. Abbreviation for Nernst equation: R, universal gas constant; T, temperature; F, Faraday constant; EK, K+ equilibrium potential; Vm, membrane potential; [K+]o, extracellular K+ concentration; [K+]i, intracellular K+ concentration. (C) Similar protocol applied in a Kir4.1 knockout animal. Glial membrane potential does not follow K+ fluctuations, indicating a strong loss of K+ conductances. A small and delayed depolarization, which is not associated with K+ increase, could, however, be observed in response to long lasting stimulations only. Adapted, with permission, from Chever et al. (2010) (B,C).