The β1 sodium channel subunit modifies the interactions of neurotoxins and local anesthetics with the rat brain IIA α sodium channel in isolated membranes but not in intact cells

Neuropharmacology

Volumn 35, Issue 5, 1996, Pages 605-613

  Bonhaus, Douglas W ^a   Herman, Ronald C ^a   Brown, Christine M ^a   Cao, Zhen ^a   Chang, Li Feng ^a   Loury, Dana N ^a   Sze, Ping ^a   Zhang, Li ^a   Hunter, John C ^a  

^a ROCHE BIOSCIENCE   (United States)

Author keywords

CHO; Sodium channel; Stable expression; 14C guanidinium; 3H Batrachotoxinin; 1 sodium channel subunit

Indexed keywords

AMITRIPTYLINE; BATRACHOTOXININ A 20ALPHA BENZOATE; BREVETOXIN; DESIPRAMINE; FLUNARIZINE; GUANIDINE; LIDOCAINE; LOCAL ANESTHETIC AGENT; MEXILETINE; MORACIZINE; N [3 (2,6 DIMETHYL 1 PIPERIDINYL)PROPYL] ALPHA PHENYLBENZENEACETAMIDE; NEUROTOXIN; PRENYLAMINE; PROTEIN SUBUNIT; RADIOISOTOPE; RU 39568; SCORPION VENOM; SODIUM CHANNEL; SODIUM CHANNEL BLOCKING AGENT; TETRACAINE; UNCLASSIFIED DRUG; VERATRIDINE;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; CELL LINE; CELL MEMBRANE; CHO CELL; CONTROLLED STUDY; DRUG TRANSPORT; GENE EXPRESSION; HUMAN; MOLECULAR CLONING; NONHUMAN; PRIORITY JOURNAL; PROTEIN CONFORMATION; RAT;

EID: 0030152116     PISSN: 00283908     EISSN: None     Source Type: Journal    
DOI: 10.1016/0028-3908(96)84631-4     Document Type: Article

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