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A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neurones

Abstract

Calcium channels in excitable membranes are essential for many cellular functions. Recent analyses of the burst-firing mode of some vertebrate neurones1–3 suggest that changes in their functional state are controlled by a Ca conductance that is largely inactivated at resting membrane potentials (−50 to −60 mV), but becomes activated following a conditioning hyperpolarization of the cell membrane. Here, using chick and rat sensory neurones, we present evidence for a new type of Ca channel with time- and voltage-dependent properties which is probably responsible for the inactivation behaviour of the Ca conductance. At membrane potentials between −50 and +10 mV, openings of this channel last 3–6 ms and tend to occur in rapid succession. Inactivation of this channel is indicated by prolonged and eventually complete closures brought about by long-lasting depolarizing voltage steps. This channel coexists in isolated membrane patches with the more common Ca channel4 which is less sensitive to changes in holding potential and shows a considerably shorter average life time and smaller currents.

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Carbone, E., Lux, H. A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neurones. Nature 310, 501–502 (1984). https://doi.org/10.1038/310501a0

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