Inhibition of N-, P/Q- and other types of Ca2+ channels in rat hippocampal nerve terminals by the adenosine A1 receptor

European Journal of Pharmacology

Volumn 340, Issue 2-3, 1997, Pages 301-310

  Ambrósio, António F ^a   Malva, João O ^a,b   Carvalho, Arsélio P ^a   Carvalho, Caetana M ^a  

^a UNIVERSITY OF COIMBRA   (Portugal)

^b UNIVERSITY OF MINHO   (Portugal)

Author keywords

4 Aminopyridine; C2+ concentration ( Ca2+ (i)), intracellular; Glutamate release; N6 Cyclopentyladenosine (CPA)

Indexed keywords

4 AMINOPYRIDINE; 6 N CYCLOPENTYLADENOSINE; 8 CYCLOPENTYL 1,3 DIPROPYLXANTHINE; ADENOSINE A1 RECEPTOR; ADENOSINE RECEPTOR STIMULATING AGENT; CALCIUM CHANNEL; CALCIUM CHANNEL BLOCKING AGENT; GLUTAMIC ACID; OMEGA CONOTOXIN GVIA;

ANIMAL CELL; ARTICLE; CELL MEMBRANE POTENTIAL; HIPPOCAMPUS; NERVE ENDING; NONHUMAN; POTASSIUM CONDUCTANCE; PRIORITY JOURNAL; RAT; SYNAPTOSOME;

ADENINE NUCLEOTIDES; ANIMALS; CALCIUM CHANNEL BLOCKERS; ELECTRODES; EXOCYTOSIS; GLUTAMIC ACID; HIPPOCAMPUS; MALE; MEMBRANE POTENTIALS; NERVE ENDINGS; RATS; RATS, WISTAR; RECEPTORS, PURINERGIC P1; SYNAPTOSOMES;

EID: 0344813710     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-2999(97)01451-9     Document Type: Article

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