The reproductive and developmental toxicity profile of beta-cyclodextrin in rodents

Reprod Toxicol. 1995 Jul-Aug;9(4):389-98. doi: 10.1016/0890-6238(95)00026-7.

Abstract

A 3-generation study with two mating phases per generation and a teratology phase was performed in the rat to assess the reproductive and developmental toxicity of beta-cyclodextrin (beta-CD) in the diet. Transient neonatal growth retardation occurred with 5% beta-CD: a similar, but equivocal, effect was also observed with 2.5%. No permanent defects or other indications of developmental toxicity were found. There was no significant maternal toxicity. The dietary level of 1.25% was found to be a NOAEL for developmental toxicity. Further investigations showed the growth retardation to be specific to dietary administration during lactation: it was not produced by parenteral (i.p.) administration and was not influenced by treatment of the dams or litters during gestation. Slight maternal nutritional deficiency, caused by physico-chemical interactions of beta-CD with nutrients in the gut is proposed as the mechanism of action. No difference in milk composition was found.

MeSH terms

  • Animals
  • Blood Chemical Analysis
  • Body Weight / drug effects
  • Cyclodextrins / pharmacokinetics
  • Cyclodextrins / toxicity*
  • Diet
  • Eating / drug effects
  • Embryo, Mammalian / drug effects
  • Female
  • Food Additives / pharmacokinetics
  • Food Additives / toxicity*
  • Lactation / drug effects
  • Male
  • Maternal Behavior / drug effects
  • Milk / chemistry
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Reproduction / drug effects*
  • Sexual Behavior, Animal / drug effects
  • Teratogens / toxicity*
  • Vitamin A / pharmacology
  • Vitamin D / pharmacology
  • beta-Cyclodextrins*

Substances

  • Cyclodextrins
  • Food Additives
  • Teratogens
  • beta-Cyclodextrins
  • Vitamin A
  • Vitamin D
  • betadex