Abstract
The present study investigates the electrophysiological actions of BmK M1, an alpha-like toxin purified from the venom of the scorpion Buthus martensi Karsch, on voltage-gated Na+ channels. Using the voltage clamp technique, we assessed the BmK M1 activity on the cardiac Na+ channel (hH1) functionally expressed in Xenopus oocytes. The main actions of the toxin are a concentration-dependent slowing of the inactivation process and a hyperpolarizing shift of the steady-state inactivation. This work is the first electrophysiological characterization of BmK M1 on a cloned Na+ channel, demonstrating that this toxin belongs to the class of scorpion alpha-toxins. Our results also show that BmK M1 can be considered as a cardiotoxin.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Dose-Response Relationship, Drug
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Gene Expression
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Humans
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Insect Proteins
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Membrane Potentials / drug effects
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Microinjections
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Molecular Sequence Data
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Neurotoxins / pharmacology
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Oocytes / cytology
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Oocytes / drug effects
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Oocytes / metabolism
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Patch-Clamp Techniques
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RNA, Complementary / administration & dosage
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RNA, Complementary / genetics
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RNA, Complementary / metabolism
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Scorpion Venoms / pharmacology*
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Scorpions
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Sequence Homology, Amino Acid
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Sodium Channel Blockers
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Sodium Channels / genetics
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Sodium Channels / metabolism
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Xenopus
Substances
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BmK M1 neurotoxin
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Insect Proteins
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Neurotoxins
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RNA, Complementary
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Scorpion Venoms
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Sodium Channel Blockers
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Sodium Channels