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R-type Ca2+ currents evoke transmitter release at a rat central synapse

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Wu,  Ling-Gang
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Borst,  J. Gerard G.
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Sakmann,  Bert
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Zitation

Wu, L.-G., Borst, J. G. G., & Sakmann, B. (1998). R-type Ca2+ currents evoke transmitter release at a rat central synapse. Proceedings of the National Academy of Sciences of the United States of America, 95(8), 4720-4725. Retrieved from http://www.pnas.org/content/95/8/4720.abstract.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002B-9B10-9
Zusammenfassung
Voltage-dependent Ca2+ currents evoke synaptic transmitter release. Of six types of Ca2+ channels, L-, N-, P-, Q-, R-, and T-type, only N- and P/Q-type channels have been pharmacologically identified to mediate action-potential-evoked transmitter release in the mammalian central nervous system. We tested whether Ca2+ channels other than N- and P/Q-type control transmitter release in a calyx-type synapse of the rat medial nucleus of the trapezoid body. Simultaneous recordings of presynaptic Ca2+ influx and the excitatory postsynaptic current evoked by a single action potential were made at single synapses. The R-type channel, a high-voltage-activated Ca2+ channel resistant to L-, N-, and P/Q-type channel blockers, contributed 26% of the total Ca2+ influx during a presynaptic action potential. This Ca2+ current evoked transmitter release sufficiently large to initiate an action potential in the postsynaptic neuron. The R-type current controlled release with a lower efficacy than other types of Ca2+ currents. Activation of metabotropic glutamate receptors and γ-aminobutyric acid type B receptors inhibited the R-type current. Because a significant fraction of presynaptic Ca2+ channels remains unidentified in many other central synapses, the R-type current also could contribute to evoked transmitter release in these synapses.