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Hyperpolarization-activated Na(+)-K+ current (Ih) in neocortical neurons is blocked by external proteolysis and internal TEA
Journal article   Peer reviewed

Hyperpolarization-activated Na(+)-K+ current (Ih) in neocortical neurons is blocked by external proteolysis and internal TEA

T Budde, John A White and A R Kay
Journal of neurophysiology, Vol.72(6), pp.2737-2742
12/1994
DOI: 10.1152/jn.1994.72.6.2737
PMID: 7534826

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Abstract

1. After 1 day in culture, neurons derived from the neonatal cerebral cortex of the rat exhibited a slowly activating current gated by hyperpolarizing voltage clamp pulses. The current was blocked by extracellular Cs+ and unaffected by extracellular Ba2+, and was permeable to both Na+ and K+ (PNa/PK = 0.29). Its form and pharmacology are consistent with a current termed Ih in other preparations. 2. Ih was absent from cells acutely dissociated from both the neonatal and mature cerebral cortex, despite the use of low enzyme concentrations. The sensitivity of Ih to extracellular proteolysis was demonstrated by superfusing the cells with trypsin (1 mg/ml) while monitoring the presence of Ih in the whole cell mode of recording. Ih was rapidly abolished (t1/2 approximately 5 min at 22 degrees C) by proteolysis and exhibited no shifts in its range of activation or changes in its activation kinetics during the course of the digestion. 3. Intracellular tetraethylammonium (TEA), at a concentration of < 15 mM was shown to block Ih completely, while extracellular TEA had no effect on the current. This suggests that the inner vestibule of Ih may be structurally related to that of potassium channels.
Electrophysiology Cells, Cultured Rats Ion Channels - drug effects Sodium Channels - drug effects Potassium Channels - drug effects Cerebral Cortex - cytology Cerebral Cortex - metabolism Tetraethylammonium Compounds - pharmacology Potassium Channels - metabolism Patch-Clamp Techniques Animals Trypsin - pharmacology Ion Channels - metabolism Sodium Channels - metabolism Neurons - metabolism Ion Channel Gating - drug effects

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