
Toxins that block voltage-dependent K+ channels and those that modify Na+ channel gating exhibit positive inotropic effect on skeletal muscle. We compared the effect of the venom of Tityus cambridgei (Tc) and Tityus serrulatus (Ts) scorpions on mouse diaphragm force, in vitro. In indirect and direct (using D-tubocurarine 7.3 microM) stimulation, Tc, 10microg/mL, increased the contractile force, an effect prevented by tetrodotoxin (TTX) while Ts, 0.5 microg/mL, potentiated only indirectly stimulated diaphragm, thus indicating its activity is mainly mediated through acetylcholine release from nerve terminal. This effect is prevented by TTX and attenuated by the K+ channel opener cromakalim. In conclusion, our data show that while the positive inotropic effect of both venoms appears associated to the activity of Na+ and K+ channels, only Tc venom acts also directly on skeletal muscle. This finding call for further studies on Tc venom to identify the toxin responsible for its direct inotropic activity as it may have clinical applications.
Male, Cromakalim, Potassium Channels, Time Factors, Diaphragm, 590, 610, Scorpion Venoms, Tetrodotoxin, In Vitro Techniques, Acetylcholine, Electric Stimulation, Sodium Channels, Phrenic Nerve, Mice, Potassium Channel Blockers, Animals, Muscle Strength, Ion Channel Gating, Muscle Contraction, Neuromuscular Nondepolarizing Agents, Sodium Channel Blockers
Male, Cromakalim, Potassium Channels, Time Factors, Diaphragm, 590, 610, Scorpion Venoms, Tetrodotoxin, In Vitro Techniques, Acetylcholine, Electric Stimulation, Sodium Channels, Phrenic Nerve, Mice, Potassium Channel Blockers, Animals, Muscle Strength, Ion Channel Gating, Muscle Contraction, Neuromuscular Nondepolarizing Agents, Sodium Channel Blockers
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