| Literature DB >> 21812515 |
L F Nurullin1, A R Mukhitov, A N Tsentsevytsky, N V Petrova, D V Samigullin, A I Malomouzh, E A Bukharaeva, F Vyskočil, E E Nikolsky.
Abstract
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 alpha1A 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 omega-agatoxin IVA (20 nM) reduced the action potential-induced 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.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21812515 DOI: 10.33549/physiolres.932219
Source DB: PubMed Journal: Physiol Res ISSN: 0862-8408 Impact factor: 1.881