Cyclothiazide potently inhibits γ-aminobutyric acid type A receptors in addition to enhancing glutamate responses

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue 22, 2003, Pages 13025-13029

  Deng, Lunbin ^a   Chen, Gong ^a  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; 6 CYANO 7 NITRO 2,3 QUINOXALINEDIONE; AMPA RECEPTOR; BICUCULLINE; CYCLOTHIAZIDE; GLUTAMIC ACID; TETRODOTOXIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DRUG EFFECT; DRUG MECHANISM; DRUG POTENCY; DRUG RECEPTOR BINDING; EXCITATORY POSTSYNAPTIC POTENTIAL; INHIBITORY POSTSYNAPTIC POTENTIAL; INTRACELLULAR RECORDING; MEMBRANE CURRENT; MOLECULAR DYNAMICS; NEUROLOGIC DISEASE; NEUROTRANSMISSION; NEWBORN; NONHUMAN; PATCH CLAMP; PRIORITY JOURNAL; RAT; RECEPTOR DOWN REGULATION;

ANIMALS; BENZOTHIADIAZINES; EVOKED POTENTIALS; EXCITATORY POSTSYNAPTIC POTENTIALS; GABA ANTAGONISTS; GAMMA-AMINOBUTYRIC ACID; GLUTAMIC ACID; HIPPOCAMPUS; MALE; MEMBRANE POTENTIALS; PATCH-CLAMP TECHNIQUES; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, GABA-A; SYNAPSES;

ANIMALIA;

EID: 0242363125     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.2133370100     Document Type: Article

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