Vanilloid (subtype 1) receptor-modulatory drugs inhibit [ 3H]batrachotoxinin-A 20-α-benzoate binding to Na+ channels

Basic and Clinical Pharmacology and Toxicology

Volumn 100, Issue 2, 2007, Pages 91-95

  Duan, Yin ^a   Zheng, Jian ^b   Nicholson, Russell A ^a  

^a SIMON FRASER UNIVERSITY   (Canada)

^b CHONGQING MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; ASPARTIC ACID; BATRACHOTOXININ A 20ALPHA BENZOATE; CAPSAICIN; CAPSAZEPINE; CENTRAL DEPRESSANT AGENT; GLUTAMIC ACID; NEUROTRANSMITTER; OLVANIL; POTASSIUM CHLORIDE; RADIOLIGAND; SODIUM CHANNEL; TRITIUM; VANILLOID RECEPTOR 1; VERATRIDINE; VOLTAGE GATED SODIUM CHANNEL;

ARTICLE; BINDING AFFINITY; BINDING ASSAY; BINDING SITE; CONTROLLED STUDY; DEPOLARIZATION; DRUG EFFECT; DRUG RECEPTOR BINDING; MALE; MOUSE; NEUROTRANSMISSION; NEUROTRANSMITTER RELEASE; NONHUMAN; PRIORITY JOURNAL; SYNAPTOSOME;

ANIMALS; ASPARTIC ACID; BATRACHOTOXINS; BRAIN; CAPSAICIN; GAMMA-AMINOBUTYRIC ACID; GLUTAMIC ACID; MALE; MICE; MICE, INBRED STRAINS; POTASSIUM CHLORIDE; SODIUM CHANNELS; SYNAPTOSOMES; TRITIUM; TRPV CATION CHANNELS; VERATRIDINE;

MAMMALIA;

EID: 33846428075     PISSN: 17427835     EISSN: 17427843     Source Type: Journal    
DOI: 10.1111/j.1742-7843.2006.00010.x     Document Type: Article

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