Differential response to acrylonitrile toxicity in rat primary astrocytes and microglia

NeuroToxicology

Volumn 37, Issue , 2013, Pages 93-99

  Caito, Samuel ^a   Yu, Yingchun ^a   Aschner, Michael ^a,b  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Acrylonitrile; Astrocytes; Glutathione; Microglia; Oxidative stress

Indexed keywords

ACRYLONITRILE; GLUTATHIONE; ISOPROSTANE DERIVATIVE; TRANSCRIPTION FACTOR NRF2;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; ASTROCYTE; BIOACCUMULATION; CELL VIABILITY; CONTROLLED STUDY; CYTOTOXICITY; EXPOSURE; LIPID PEROXIDATION; MICROGLIA; NEUROTOXICITY; NEWBORN; NONHUMAN; OXIDATIVE STRESS; PRIMARY CELL CULTURE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; UPREGULATION;

ACETONITRILES; ANIMALS; ANIMALS, NEWBORN; ASTROCYTES; CELL SURVIVAL; CELLS, CULTURED; DOSE-RESPONSE RELATIONSHIP, DRUG; F2-ISOPROSTANES; GLUTATHIONE; LIPID PEROXIDATION; MICROGLIA; NF-E2-RELATED FACTOR 2; OXIDATIVE STRESS; PRIMARY CELL CULTURE; RATS; RATS, SPRAGUE-DAWLEY;

EID: 84877906664     PISSN: 0161813X     EISSN: 18729711     Source Type: Journal    
DOI: 10.1016/j.neuro.2013.04.007     Document Type: Article

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