Pyridoxine inhibits depolarization-evoked glutamate release in nerve terminals from rat cerebral cortex: A possible neuroprotective mechanism?

Journal of Pharmacology and Experimental Therapeutics

Volumn 331, Issue 1, 2009, Pages 244-254

  Yang, Tsung Tair ^a   Wang, Su Jane ^b  

^a CARDINAL TIEN HOSPITAL   (Taiwan)

^b FU JEN CATHOLIC UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

2 [1 (3 AMIDINOTHIOPROPYL) 1H INDOL 3 YL] 3 (1 METHYL 1H INDOL 3 YL)MALEIMIDE; 2 [1 (3 DIMETHYLAMINOPROPYL) 3 INDOLYL] 3 (3 INDOLYL)MALEIMIDE; BAFILOMYCIN A1; CALCIUM CHANNEL; CALCIUM ION; GLUTAMIC ACID; PROTEIN KINASE C; PYRIDOXINE; SODIUM CHANNEL;

ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; CALCIUM TRANSPORT; CYTOSOL; DEPOLARIZATION; DRUG MECHANISM; MALE; MEMBRANE POTENTIAL; NERVE ENDING; NEUROPROTECTION; NONHUMAN; PRIORITY JOURNAL; RAT; SYNAPTOSOME;

ANIMALS; CEREBRAL CORTEX; GLUTAMIC ACID; MALE; MEMBRANE POTENTIALS; NEUROPROTECTIVE AGENTS; PRESYNAPTIC TERMINALS; PYRIDOXINE; RATS; RATS, SPRAGUE-DAWLEY; SIGNAL TRANSDUCTION; SYNAPTOSOMES;

EID: 70349338805     PISSN: 00223565     EISSN: 15210103     Source Type: Journal    
DOI: 10.1124/jpet.109.155176     Document Type: Article

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