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Evaluation of developmental toxicity of 1-butanol given to rats in drinking water throughout pregnancy.

Abstract
The objective of this study was to evaluate the developmental toxicity of 1-butanol in rats. Pregnant rats were given drinking water containing 1-butanol at 0.2%, 1.0% or 5.0% (316, 1454 or 5654 mg/kg/day) on days 0-20 of pregnancy. A significant decrease in maternal body weight gain accompanied by reduced food and water consumption was found at 5.0%. No significant increase in the incidence of pre- and postimplantation embryonic loss was observed in any groups treated with 1-butanol. Fetal weight was significantly lowered at 5.0%. Although a significant increase in the incidence of fetuses with skeletal variations and decreased degree of ossification was found at 5.0%, no increase in the incidence of fetuses with external, skeletal and internal abnormalities was detected in any groups treated with 1-butanol. The data demonstrate that 1-butanol is developmental toxic only at maternal toxic doses. No evidence for teratogenicity of 1-butanol was noted in rats. Based on the significant decreases in maternal body weight gain and fetal weight, it is concluded that the no observed adverse effect levels (NOAELs) of 1-butanol for both dams and fetuses are 1.0% (1454 mg/kg/day) in rats.
AuthorsM Ema, H Hara, M Matsumoto, A Hirose, E Kamata
JournalFood and chemical toxicology : an international journal published for the British Industrial Biological Research Association (Food Chem Toxicol) Vol. 43 Issue 2 Pg. 325-31 (Feb 2005) ISSN: 0278-6915 [Print] England
PMID15621345 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Teratogens
  • 1-Butanol
Topics
  • 1-Butanol (toxicity)
  • Abnormalities, Drug-Induced (epidemiology, etiology)
  • Administration, Oral
  • Animals
  • Bone Development (drug effects)
  • Dose-Response Relationship, Drug
  • Drinking
  • Drug Evaluation, Preclinical
  • Female
  • Fetal Development (drug effects)
  • Fetal Weight (drug effects)
  • Male
  • Maternal Exposure
  • No-Observed-Adverse-Effect Level
  • Pregnancy
  • Rats
  • Teratogens (toxicity)
  • Time Factors
  • Weight Gain (drug effects)

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