Maternal exposure to triclosan causes fetal development restriction, deregulation of the oestrous cycle, and alters uterine tissue in rat offspring

Environ Toxicol. 2019 Oct;34(10):1105-1113. doi: 10.1002/tox.22812. Epub 2019 Jun 25.

Abstract

The aim of the present study was to evaluate the effects of maternal exposure to triclosan (TCS) during pregnancy and lactation on the uterine morphology of rat offspring. For this, 32 Wistar rat dams were distributed into four dose groups (eight mothers per group), and gavage daily, throughout pregnancy and lactation, as follows: Group I-control (GI): corn oil; Group II (GII): TCS diluted in corn oil at a dose of 75 mg/kg/d; Group III (GIII): TCS diluted in corn oil at a dose of 150 mg/kg/d; Group IV (GIV): TCS diluted in corn oil at a dose of 300 mg/kg/d. A female pup of each mother was selected, and at 90 days the pups were euthanized for weighing and collection of the uterus for histomorphometric analysis. The results showed that the mean litter weight was minor in all the groups treated with TCS, when compared with control. The levels thyroid hormones thyroxine (T4) and triiodothyronine (T3) in TCS mother rats were reduced; however the levels of thyroid stimulating hormone (TSH) were increases. The offspring of all groups exposed to TCS presented deregulation of the estrous cycle, compared with control. Analysis of the uterine histological structure demonstrated that all layers of the uterus were affected by the administration of TCS, and the morphometric analysis showed increased uterine layers thickness in the treated groups. We concluded that maternal exposure to TCS during pregnancy and lactation causes intrauterine development restriction, deregulation of the oestrous cycle, and alters uterine tissue in rat offspring.

Keywords: endocrine disrupters; rats; triclosan; uterus.

MeSH terms

  • Animals
  • Anti-Infective Agents, Local / adverse effects*
  • Estrous Cycle / drug effects
  • Female
  • Fetal Development / drug effects
  • Fetal Growth Retardation / etiology*
  • Fetal Growth Retardation / physiopathology
  • Humans
  • Lactation / drug effects
  • Male
  • Maternal Exposure / adverse effects*
  • Pregnancy
  • Prenatal Exposure Delayed Effects / etiology
  • Prenatal Exposure Delayed Effects / physiopathology*
  • Rats
  • Rats, Wistar
  • Thyroid Hormones / metabolism
  • Triclosan / adverse effects*
  • Uterus / drug effects
  • Uterus / growth & development*
  • Uterus / physiology

Substances

  • Anti-Infective Agents, Local
  • Thyroid Hormones
  • Triclosan

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