Literature DB >> 8427702

A benzodiazepine recognition site associated with the non-NMDA glutamate receptor.

C F Zorumski1, K A Yamada, M T Price, J W Olney.   

Abstract

GYKI 52466 is a benzodiazepine molecule that has muscle relaxant and anticonvulsant properties not attributable to a gamma-aminobutyric acid receptor-mediated mechanism. Here it is shown that GYKI 52466 exerts no blocking action at N-methyl-D-aspartate (NMDA) glutamate receptors, but acts noncompetitively to block ion currents and associated excitotoxicity, including ischemic neuronal degeneration, mediated through non-NMDA glutamate receptors. The inhibition of non-NMDA responses by GYKI 52466 is antagonized by cyclothiazide, hydrochlorothiazide, and diazoxide, benzothiadiazide drugs that inhibit non-NMDA receptor desensitization. These results suggest that non-NMDA receptor-ion channel complexes may contain a novel benzodiazepine recognition site where receptor desensitization is regulated; this postulated site represents a promising new target for rational development of drugs to treat neurological disorders.

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Year:  1993        PMID: 8427702     DOI: 10.1016/0896-6273(93)90242-j

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  25 in total

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4.  AMPA antagonists differ from NMDA antagonists in their effects on operant DRL and delayed matching to position tasks.

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8.  Interactions of 2,3-benzodiazepines and cyclothiazide at AMPA receptors: patch clamp recordings in cultured neurones and area CA1 in hippocampal slices.

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9.  Pharmacological Preconditioning with GYKI 52466: A Prophylactic Approach to Neuroprotection.

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10.  BDNF-TrkB signaling pathway mediates the induction of epileptiform activity induced by a convulsant drug cyclothiazide.

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