Effect of substance P on the release of acetylcholine at the frog neuromuscular junction

1985 ◽  
Vol 13 (1) ◽  
pp. 167-167 ◽  
Author(s):  
F. A. WALI
Neuroscience ◽  
1990 ◽  
Vol 37 (1) ◽  
pp. 271-275 ◽  
Author(s):  
M. Matteoli ◽  
C. Haimann ◽  
P. De Camilli

2011 ◽  
pp. 815-823 ◽  
Author(s):  
L. F. NURULLIN ◽  
A. R. MUKHITOV ◽  
A. N. TSENTSEVYTSKY ◽  
N. V. PETROVA ◽  
D. V. SAMIGULLIN ◽  
...  

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 1A 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 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.


1992 ◽  
Vol 23 (4) ◽  
pp. 318-322 ◽  
Author(s):  
R. A. Giniatullin ◽  
A. L. Zefirov ◽  
L. G. Magazanik ◽  
S. F. Oshchepkova

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