σ receptor activation blocks potassium channels and depresses neuroexcitability in rat intracardiac neurons

Journal of Pharmacology and Experimental Therapeutics

Volumn 313, Issue 3, 2005, Pages 1387-1396

  Zhang, Hongling ^a   Cuevas, Javier ^a  

^a UNIVERSITY OF SOUTH FLORIDA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BIS(2 METHYLPHENYL)GUANIDINE; 5' O (2 THIODIPHOSPHATE)TRILITHIUM; CALCIUM ION; HALOPERIDOL; IBOGAINE; LINOPIRDINE; LITHIUM DERIVATIVE; METAPHIT; N ALLYLNORMETAZOCINE; PENTAZOCINE; POTASSIUM CHANNEL; POTASSIUM ION; RECEPTOR PROTEIN; SIGMA 1 OPIATE RECEPTOR; UNCLASSIFIED DRUG; VOLTAGE GATED POTASSIUM CHANNEL;

ANIMAL CELL; ARTICLE; CARDIOVASCULAR SYSTEM; CELL FUNCTION; CONTROLLED STUDY; DEPOLARIZATION; DRUG POTENCY; DRUG RECEPTOR BINDING; NERVE CELL; NERVE CELL EXCITABILITY; NEWBORN; NONHUMAN; OUTWARDLY RECTIFYING POTASSIUM CHANNEL; PARASYMPATHETIC NERVE; PATCH CLAMP; POTASSIUM TRANSPORT; PRIORITY JOURNAL; RAT; SIGNAL TRANSDUCTION; WHOLE CELL;

ACTION POTENTIALS; ANIMALS; CALCIUM; DOSE-RESPONSE RELATIONSHIP, DRUG; GUANIDINES; GUANOSINE DIPHOSPHATE; GUANOSINE TRIPHOSPHATE; HEART; NEURONS; PHENCYCLIDINE; POTASSIUM CHANNELS; RATS; RECEPTORS, SIGMA; THIONUCLEOTIDES;

EID: 19344376717     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: 10.1124/jpet.105.084152     Document Type: Article

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