Involvement of three mechanisms in the alteration of cytokine responses by sodium methyldithiocarbamate

Toxicology and Applied Pharmacology

Volumn 213, Issue 2, 2006, Pages 172-178

  Pruett, Stephen B ^a   Fan, Ruping ^a   Zheng, Qiang ^a  

^a LOUISIANA STATE UNIVERSITY HEALTH SCIENCES CENTER   (United States)

Author keywords

IL 10; IL 12; Lipopolysaccharide; Macrophage; Metam sodium

Indexed keywords

ACETYLCYSTEINE; CATECHOLAMINE; CHELATING AGENT; COPPER; CORTICOSTERONE; CXCL9 CHEMOKINE; CYTOKINE; GLUTATHIONE; INTERLEUKIN 10; INTERLEUKIN 12; LIPOPOLYSACCHARIDE; MIFEPRISTONE; NADOLOL; SCAVENGER; SODIUM METHYLDITHIOCARBAMATE; TOLL LIKE RECEPTOR 4; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; CORTICOSTERONE BLOOD LEVEL; CYTOKINE PRODUCTION; DRUG MECHANISM; DRUG POTENTIATION; FEMALE; MOUSE; NEUROENDOCRINOLOGY; NONHUMAN; OXIDATION; OXIDATION REDUCTION REACTION; PERITONEAL FLUID; PROTEIN BLOOD LEVEL; PROTEIN DEPLETION; STRESS;

ANIMALS; CHELATING AGENTS; COPPER; CORTICOSTERONE; CROSSES, GENETIC; CYTOKINES; FEMALE; FREE RADICAL SCAVENGERS; INTERLEUKIN-10; INTERLEUKIN-12; LIPOPOLYSACCHARIDES; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; OXIDATION-REDUCTION; PESTICIDES; STATISTICS, NONPARAMETRIC; THIOCARBAMATES;

EID: 33646585398     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2005.10.004     Document Type: Article

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