Vasopressin inhibits sarcolemmal ATP-sensitive K+ channels via V1 receptors activation in the guinea pig heart

Circulation Journal

Volumn 66, Issue 3, 2002, Pages 277-282

  Tsuchiya, Masago ^a   Tsuchiya, Kunihiko ^a   Maruyama, Rumi ^a   Takemura, Genzou ^a   Minatoguchi, Shinya ^a   Fujiwara, Hisayoshi ^a  

^a GIFU UNIVERSITY   (Japan)

Author keywords

Sarcolemmal KATP channels; V1 receptor; Vasopressin

Indexed keywords

ADENOSINE TRIPHOSPHATE; MOZAVAPTAN; PINACIDIL; POTASSIUM CHANNEL; POTASSIUM ION; STREPTOLYSIN O; VASOPRESSIN; VASOPRESSIN RECEPTOR ANTAGONIST; VASOPRESSIN V1 RECEPTOR; POTASSIUM CHANNEL BLOCKING AGENT; VASOPRESSIN DERIVATIVE; VASOPRESSIN RECEPTOR;

ANIMAL TISSUE; ARTICLE; CELL ADHESION; CHANNEL GATING; CONCENTRATION RESPONSE; CONTROLLED STUDY; GLYCOLYSIS; GUINEA PIG; HEART MUSCLE CELL; HORMONE ACTION; IC 50; MALE; NONHUMAN; OXIDATION; PATCH CLAMP; RECEPTOR INTRINSIC ACTIVITY; SARCOLEMMA; ANIMAL; CHEMISTRY; CYTOLOGY; DRUG EFFECT; HEART; HEART VENTRICLE; PHYSIOLOGY; ULTRASTRUCTURE;

ADENOSINE TRIPHOSPHATE; ANIMALS; GUINEA PIGS; HEART; HEART VENTRICLES; INHIBITORY CONCENTRATION 50; MALE; PATCH-CLAMP TECHNIQUES; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; RECEPTORS, VASOPRESSIN; SARCOLEMMA; VASOPRESSINS;

EID: 0036236267     PISSN: 13469843     EISSN: None     Source Type: Journal    
DOI: 10.1253/circj.66.277     Document Type: Article

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