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The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
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Long-term Behavioral and Reproductive Consequences of Embryonic Exposure to Low-dose Toxicants
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Multiple Endocrine Disrupting Effects in Rats Perinatally Exposed to Butylparaben.

J Boberg1, M Axelstad2, T Svingen2

  • 1National Food Institute, Technical University of Denmark, Søborg, Denmark jubo@food.dtu.dk.

Toxicological Sciences : an Official Journal of the Society of Toxicology
|April 29, 2016
PubMed
Summary

Butylparaben, a common preservative, disrupts endocrine systems in developing rats, affecting reproductive development and sperm counts even at low doses. This study highlights its potential risks for both male and female offspring.

Keywords:
breastendocrine disruptionparabenprostatereproductionsexual developmenttestis

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Area of Science:

  • Endocrinology
  • Developmental Toxicology
  • Environmental Health

Background:

  • Parabens are widely used preservatives in consumer products.
  • Butylparaben exhibits estrogenic and antiandrogenic properties.
  • Previous studies linked butylparaben to reduced sperm counts in male rats.

Purpose of the Study:

  • To investigate the effects of perinatal butylparaben exposure on endocrine-sensitive endpoints in Wistar rats.
  • To determine if butylparaben affects reproductive development and steroidogenesis in offspring.

Main Methods:

  • Oral exposure of time-mated Wistar rats to butylparaben (0, 10, 100, 500 mg/kg bw/d) from gestation day 7 to pup day 22.
  • Evaluation of endocrine-sensitive endpoints including anogenital distance, ovary weight, mammary gland outgrowth, sperm count, and gene expression (CYP19a1, Nr5a1).
  • Histological examination of prostate tissue and measurement of prostate weight.

Main Results:

  • Reduced anogenital distance in both male and female offspring at higher doses.
  • Decreased ovary weights and increased mammary gland outgrowth in prepubertal females.
  • Significant reduction in sperm count in males at all tested doses (≥10 mg/kg bw/d).
  • Altered testicular CYP19a1 expression in prepubertal rats and reduced Nr5a1 expression in adult testes.
  • Prostate histology alterations and reduced adult prostate weight in the high-dose group.

Conclusions:

  • Perinatal butylparaben exposure exerts adverse endocrine-disrupting effects on both male and female rat offspring.
  • The lowest observed adverse effect level for developmental toxicity on sperm count is 10 mg/kg bw/d.
  • Findings are significant for risk assessment of butylparaben exposure during development.