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Voltage-dependent P/Q-type calcium channels at the frog neuromuscular junction
L. F. Nurullin, A. R. Mukhitov, A. N. Tsentsevytsky, N. V. Petrova, D. V. Samigullin, A. I. Malomouzh, E. A. Bukharaeva, F. Vyskočil, E. E. Nikolsky
Language English Country Czech Republic
Document type Research Support, Non-U.S. Gov't
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- MeSH
- Ion Channel Gating physiology MeSH
- Membrane Potentials physiology MeSH
- Neuromuscular Junction physiology MeSH
- Synaptic Transmission physiology MeSH
- Rana ridibunda MeSH
- Calcium metabolism MeSH
- Calcium Signaling physiology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Research Support, Non-U.S. Gov't MeSH
It is well known that antagonists of N-type voltage-gated calcium channels inhibit the evoked quantal release of acetylcholine in amphibian neuromuscular synapses. This, however, does not exclude the functional expression of other types of voltage-gated calcium channels in these nerve terminals. Using immunocytochemistry, we detected the expression of the α1A subunit of P/Q-type calcium channels (that is otherwise typical of mammalian motor nerve endings) in the frog neuromuscular junction. In addition, we demonstrated that the P/Q-type channel blocker ω-agatoxin IVA (20 nM) reduced the action potentialinduced calcium transient and significantly decreased both spontaneous and evoked mediator release. Our data indicates the functional expression of P/Q-type calcium channels in the frog motor nerve ending which participate in acetylcholine release.
Department of Animal Physiology Faculty of Sciences Charles University Prague
Institute of Physiology Academy of Sciences of the Czech Republic Prague
Kazan Institute of Biochemistry and Biophysics Russian Academy of Sciences Kazan Russia
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- $a It is well known that antagonists of N-type voltage-gated calcium channels inhibit the evoked quantal release of acetylcholine in amphibian neuromuscular synapses. This, however, does not exclude the functional expression of other types of voltage-gated calcium channels in these nerve terminals. Using immunocytochemistry, we detected the expression of the α1A subunit of P/Q-type calcium channels (that is otherwise typical of mammalian motor nerve endings) in the frog neuromuscular junction. In addition, we demonstrated that the P/Q-type channel blocker ω-agatoxin IVA (20 nM) reduced the action potentialinduced calcium transient and significantly decreased both spontaneous and evoked mediator release. Our data indicates the functional expression of P/Q-type calcium channels in the frog motor nerve ending which participate in acetylcholine release.
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