Electrophysiologic properties of lidocaine, cocaine, and n-3 fatty-acids block of cardiac Na+ channels

European Journal of Pharmacology

Volumn 485, Issue 1-3, 2004, Pages 31-41

  Xiao, Yong Fu ^a,b,c   Ke, Qingen ^a,b   Wang, Sho Ya ^d   Yang, Yinke ^a,b   Chen, Yu ^a,b   Wang, Ging Kuo ^a,e   Morgan, James P ^a,b   Cox, Benjamin ^c   Leaf, Alexander ^a,c  

^a HARVARD MEDICAL SCHOOL   (United States)

^b BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d STATE UNIVERSITY OF NEW YORK   (United States)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Adrenoceptor agonists; Arrhythmias; Docosahexaenoic acid; Eicosapentaenoic acid; Fish oil; Polyunsaturated fatty acid

Indexed keywords

ALPHA 1 ADRENERGIC RECEPTOR STIMULATING AGENT; ANESTHETIC AGENT; ANTIARRHYTHMIC AGENT; COCAINE; LIDOCAINE; OMEGA 3 FATTY ACID; PHENYLEPHRINE; POLYUNSATURATED FATTY ACID; VOLTAGE GATED SODIUM CHANNEL;

ANIMAL CELL; ANTIARRHYTHMIC ACTIVITY; ARTICLE; CELL CULTURE; CONTROLLED STUDY; DRUG EFFECT; DRUG POTENCY; ELECTRIC POTENTIAL; ELECTROPHYSIOLOGY; HEART; HEART ARRHYTHMIA; HEART MUSCLE CELL; HUMAN; HUMAN CELL; HYPERPOLARIZATION; NEWBORN; NONHUMAN; PRIORITY JOURNAL; RAT; STEADY STATE; TACHYCARDIA;

EID: 1642497592     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejphar.2003.11.042     Document Type: Article

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