Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Effect of potential antidotes on the acute toxicity, tissue disposition and elimination of selenium in rats

Journal Article · · Research Communications in Chemical Pathology and Pharmacology; (USA)
OSTI ID:7104291
; ;  [1]
  1. Toxicology Research Unit (Medical Research Council of New Zealand), Dunedin (New Zealand)
Treatment of male Wistar rats with sodium selenate (2.24 mg Se/kg, s.c.) inhibited their body weight gain for 24 hr, after which the animals recovered. Intraperitoneal injections of sodium-2,3-dimercaptopropane-1-sulphonic acid (60 mg/kg), meso-2,3-dimercaptosuccinic acid (50.9 mg/kg) and calcium disodium ethylenediamine-tetraacetate (500 mg/kg) 15 min after Se had no protective effect, while 2,3-dimercaptopropanol (15 mg/kg) inhibited the recovery of the Se-treated animal. Sodium diethyldithiocarbamate (DDTC, 70 mg/kg, i.p.) reduced the Se-induced loss of body weight but had no effect on the tissue disposition of {sup 75}Se when injected 15 min, 3 hr or 6 hr after a s.c. injection of sodium ({sup 75}Se) selenite (50 microCi, 17.4 micrograms Se/kg). The citrate salts of bismuth (2.5 and 5 mg Bi/kg, s.c.), antimony (1.5 and 3 mg Sb/kg, s.c.) and germanium (40 mg Ge/kg, s.c.) also reduced the selenate-induced loss of body weight, while germanium citrate (40 mg Ge/kg) and bis-carboxyethyl germanium sesquioxide (80, 200 and 400 mg Ge/kg) promoted significant dose-related increases in the 24 hr urinary excretion of {sup 75}Se when given 15 min after sodium ({sup 75}Se) selenite (30 microCi, 0.5 mg Se/kg, s.c.).
OSTI ID:
7104291
Journal Information:
Research Communications in Chemical Pathology and Pharmacology; (USA), Journal Name: Research Communications in Chemical Pathology and Pharmacology; (USA) Vol. 66:3; ISSN 0034-5164; ISSN RCOCB
Country of Publication:
United States
Language:
English