Quercetin administration during chelation therapy protects arsenic-induced oxidative stress in mice

Biological Trace Element Research

Volumn 122, Issue 2, 2008, Pages 137-147

  Mishra, Deepshikha ^a   Flora, S J S ^a  

^a DEFENCE RESEARCH AND DEVELOPMENT ESTABLISHMENT   (India)

Author keywords

Arsenic toxicity; Biochemical and toxicological effects; Chelation; Metal decorporation; MiADMSA; Mouse; Oxidative stress; Quercetin co administration

Indexed keywords

ARSENIC; ARSENITE SODIUM; CHELATING AGENT; DRINKING WATER; GLUTATHIONE; MONOISOAMYL 2,3 DIMERCAPTOSUCCINIC ACID; PORPHOBILINOGEN SYNTHASE; QUERCETIN; REACTIVE OXYGEN METABOLITE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; ANTIOXIDANT; SUCCIMER;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BLOOD; CHELATION THERAPY; CONTROLLED STUDY; DRUG EFFECT; DRUG INHIBITION; DRUG MECHANISM; ERYTHROCYTE COUNT; LEUKOCYTE COUNT; LIVER; MALE; MOUSE; NONHUMAN; OXIDATIVE STRESS; ANIMAL; CHEMICAL STRUCTURE; CHEMISTRY; METABOLISM; METHODOLOGY; TREATMENT OUTCOME;

ANIMALIA; MUS;

ANIMALS; ANTIOXIDANTS; ARSENIC; CHELATION THERAPY; GLUTATHIONE; MALE; MICE; MOLECULAR STRUCTURE; OXIDATIVE STRESS; PORPHOBILINOGEN SYNTHASE; QUERCETIN; REACTIVE OXYGEN SPECIES; SUCCIMER; TREATMENT OUTCOME;

EID: 47049104318     PISSN: 01634984     EISSN: None     Source Type: Journal    
DOI: 10.1007/s12011-007-8064-9     Document Type: Article

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