Abstract
The double sucrose gap and patch-clamp studies revealed that phencyclidine blocked the ATP-sensitive K+ channel in isolated cardiac cells (half-maximal inhibition at approximately 20 microM; Hill coefficient approximately 1). 10 microM phencyclidine increased the inward Ca2+ current and blocked the outward K+ current in the frog auricle trabeculae. The phencyclidine effects on the frog auricle trabeculae and the isolated cardiac cells proved to be quite reversible.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Action Potentials
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Adenosine Triphosphate / pharmacology*
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Animals
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Calcium Channels / drug effects
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Calcium Channels / physiology
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Electric Conductivity
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Heart / drug effects
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Heart / physiology*
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Phencyclidine / pharmacology*
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Potassium Channel Blockers*
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Potassium Channels / physiology
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Rana ridibunda
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Rats
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Rats, Wistar
Substances
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Calcium Channels
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Potassium Channel Blockers
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Potassium Channels
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Adenosine Triphosphate
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Phencyclidine