Antihistamine terfenadine inhibits calcium influx, cGMP formation, and NMDA receptor-dependent neurotoxicity following activation of L-type voltage sensitive calcium channels

Neurotoxicity Research

Volumn 4, Issue 1, 2002, Pages 15-23

  Diaz Trelles R ^a   Fernandez Sanchez M T ^a   Marini, A M ^b   Novelli, A ^c  

^a UNIVERSIDAD DE OVIEDO   (Spain)

^b Uniformed Services University of the Health Sciences and the Walter Reed National Military Medical Center   (United States)

^c NONE

Author keywords

cGMP; Cultured cerebellar neurons; Excitotoxicity; Terfenadine; Voltage sensitive calcium channels

Indexed keywords

1,4 DIHYDRO 2,6 DIMETHYL 5 NITRO 4 [2 (TRIFLUOROMETHYL)PHENYL] 3 PYRIDINECARBOXYLIC ACID METHYL ESTER; CALCIUM CHANNEL L TYPE; CALCIUM ION; CYCLIC GMP; GLUTAMIC ACID; HISTAMINE H1 RECEPTOR ANTAGONIST; N METHYL DEXTRO ASPARTIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR STIMULATING AGENT; TERFENADINE;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; CELL CULTURE; CELL GROWTH; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG EFFECT; NEUROPROTECTION; NEUROTOXICITY; NONHUMAN; NUCLEOTIDE METABOLISM; PRIORITY JOURNAL; RAT; STEADY STATE;

ANIMALIA;

EID: 0036205609     PISSN: 10298428     EISSN: None     Source Type: Journal    
DOI: 10.1080/10298420290007583     Document Type: Article

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