Adenosine A1 antagonism increases specific synaptic forms of glutamate release during anoxia, revealing a unique source of excitation

Hippocampus

Volumn 6, Issue 3, 1996, Pages 213-224

  Katchman, Alexander N ^a   Hershkowitz, Norman ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

CA1; CA3; Hippocampus; Ischemia; Potassium

Indexed keywords

8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE; ADENOSINE A1 RECEPTOR; ADENOSINE A1 RECEPTOR ANTAGONIST; GLUTAMATE RECEPTOR ANTAGONIST; GLUTAMIC ACID; POTASSIUM CHANNEL; TETRODOTOXIN; 1,3-DIPROPYL-8-CYCLOPENTYLXANTHINE; ADENOSINE RECEPTOR; ION CHANNEL; XANTHINE DERIVATIVE;

ACTION POTENTIAL; ANIMAL TISSUE; ANOXIA; ARTICLE; DEPOLARIZATION; ELECTRODE; EXCITATION; EXCITATORY POSTSYNAPTIC POTENTIAL; HIPPOCAMPUS; HYPERPOLARIZATION; MALE; NONHUMAN; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; RAT; SYNAPSE; VOLTAGE CLAMP; ANIMAL; BRAIN HYPOXIA; CYTOLOGY; DRUG ANTAGONISM; DRUG EFFECT; ELECTROPHYSIOLOGY; IN VITRO STUDY; METABOLISM; PATCH CLAMP; PHYSIOLOGY; SPRAGUE DAWLEY RAT;

ACTION POTENTIALS; ANIMALS; ELECTROPHYSIOLOGY; GLUTAMIC ACID; HIPPOCAMPUS; HYPOXIA, BRAIN; ION CHANNELS; MALE; PATCH-CLAMP TECHNIQUES; PYRAMIDAL CELLS; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, PURINERGIC P1; SYNAPSES; TETRODOTOXIN; XANTHINES;

EID: 0029661917     PISSN: 10509631     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1063(1996)6:3<213::AID-HIPO1>3.0.CO;2-O     Document Type: Article

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