Abstract

Electrically-induced twitch responses of the prostatic segment of vas deferens (0.1 Hz, 65 V, 1 ms) are mainly due to the transient presynaptic release of ATP, which acts postsynaptically on non-adrenergic receptors to contract smooth muscle cells. These responses were fully blocked by nanomolar concentrations of the ω-conotoxins GVIA, MVIIA, and MVIIC, most likely by inhibiting Ca 2+ entry through presynaptic N-type Ca 2+ channels controlling the release of ATP. Repeated washout of the toxins allowed the recovery of contractions, except for ω-conotoxin GVIA, whose inhibitory effects remained unchanged for at least 60 min. In addition, micromolar concentrations of ω-conotoxin MVIIC were unable to protect against the irreversible inhibition of twitch contractions induced by nanomolar concentrations of ω-conotoxin GVIA. At low extracellular Ca 2+ concentrations (1.5 mM), 20 nM of ω-conotoxin GVIA or MVIIA inhibited completely the twitch contractions in about 10 min. In 5 mM Ca 2+ the blockade of twitch contractions after 10 min was 70% for both toxins. In 1.5 mM Ca 2+ ω-conotoxin MVIIC (1 μM) inhibited completely the twitch contraction after 10 min. In 5 mM Ca 2+ blockade developed very slowly and was very poor after 30 min, ω-conotoxin MVIIC depressed the response by only 20%. These results are compatible with the idea that the three ω-conotoxins block the purinergic neurotransmission of the vas deferens by acting on presynaptic N-type voltage-dependent Ca 2+ channels. However, ω-conotoxin MVIIC seems to bind to sites different from those recognised by ω-conotoxin GVIA and MVIIA, which are markedly differentiated by their Ca 2+ requirements for binding to their receptors.

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