Inhibition of willardiine-induced currents through rat GluR6/KA-2 kainate receptor channels by Zinc and other divalent cations

Neuroscience Letters

Volumn 349, Issue 2, 2003, Pages 107-110

  Fukushima, Teruyuki ^a   Shingai, Ryuzo ^a   Ogurusu, Tarou ^a   Ichinose, Mitsuyuki ^a  

^a IWATE UNIVERSITY   (Japan)

Author keywords

Divalent cations; Glutamate receptors; HEK 293 cell; Kainate receptor GluR6 KA 2; Willardiine

Indexed keywords

BARIUM CHLORIDE; CALCIUM CHLORIDE; DIVALENT CATION; KAINIC ACID RECEPTOR; MAGNESIUM CHLORIDE; WILLARDIINE; ZINC CHLORIDE; ALANINE; BARIUM; CALCIUM; DRUG DERIVATIVE; GLUR6 KAINATE RECEPTOR; MAGNESIUM; PYRIMIDINONE DERIVATIVE; URACIL; ZINC;

ARTICLE; BINDING SITE; CELL LINE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; ELECTRIC CURRENT; ELECTRIC POTENTIAL; EMBRYO; HUMAN; HUMAN CELL; IC 50; INHIBITION KINETICS; PRIORITY JOURNAL; PROTEIN EXPRESSION; ANIMAL; BINDING COMPETITION; CELL MEMBRANE POTENTIAL; DOSE RESPONSE; DRUG EFFECT; METABOLISM; PATCH CLAMP; RAT;

ALANINE; ANIMALS; BARIUM; BINDING, COMPETITIVE; CALCIUM; CATIONS, DIVALENT; CELL LINE, TRANSFORMED; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; MAGNESIUM; MEMBRANE POTENTIALS; PATCH-CLAMP TECHNIQUES; PYRIMIDINONES; RATS; RECEPTORS, KAINIC ACID; URACIL; ZINC;

EID: 0142089847     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(03)00805-X     Document Type: Article

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