Abstract
Veratridine (50 microM), an agent known to activate voltage-dependent Na+ channels, induced a strong release of [3H]dopamine from the rabbit carotid body in vitro. The effect of veratridine was dependent on the presence of both Na+ and Ca2+ in the extracellular medium and was abolished by 1 microM tetrodotoxin. These results suggest that chemoreceptor type I cells have voltage-dependent Na+ channels, which could be involved in the depolarization of the cell membrane and activation of voltage-dependent Ca2+ channels.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Calcium / pharmacology
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Carotid Body / cytology
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Carotid Body / metabolism*
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Dopamine / metabolism*
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Dopamine Antagonists
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In Vitro Techniques
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Rabbits
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Sodium / pharmacology
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Sodium Channels / drug effects
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Sodium Channels / metabolism*
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Sodium Channels / physiology
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Tetrodotoxin / pharmacology
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Veratridine / pharmacology*
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Veratrine / analogs & derivatives*
Substances
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Dopamine Antagonists
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Sodium Channels
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Tetrodotoxin
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Veratridine
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Sodium
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Veratrine
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Calcium
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Dopamine