The teratogenicity and behavioral teratogenicity of di(2-ethylhexyl) phthalate (DEHP) and di-butyl Phthalate (DBP) in a chick model

Safa Abdul-Ghani, Joseph Yanai, Rula Abdul-Ghani, Adi Pinkas, Ziad Abdeen

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Phthalates are industrial chemicals widely used in consumer products, plastics and children toys, and the risk of exposure to phthalates, especially prenatal exposure, is a growing concern justifying the development of an animal model to better understand their effect. The present study was designed to evaluate the suitability of a chick model for phthalate DEHP teratogenicity and neurobehavioral teratogenicity, a model which is simple and devoid of potential confounding factors such as maternal toxicity, maternal-fetal unit and maternal-neonatal interactions; major findings were confirmed in the DBP study. Prehatch exposure to DEHP in doses ranging from 20 to 100. mg/kg, reduced the percent hatching from 80% in control eggs to 65%, and increased late hatchings from 12.5% in control eggs to 29.4%. In addition it induced developmental defects characterized by an opening or weakening of abdominal muscles allowing internal organs to protrude externally with or without a sac, omphalocele or gastroschisis, respectively. The effect was dose dependent ranging from 8% with DEHP (20. mg/kg) to 22% (100. mg/kg). Similar treatment with DBP 100. mg/kg has reduced percentage hatching to 57% and increased late hatching to 37.5%, with a 14% increase in gastroschisis. Biochemical evaluation revealed elevated levels of alkaline phosphatase, which reflects non-specific toxicity of DEHP at such a high dose. Behavioral evaluation using an imprinting test and locomotor activity on chicks pretreated with DEHP (100. mg/kg) has shown an abolishment of imprinting performance from the control (0.65) preference ratio. DNA damage measurements of the metabolite 8-hydroxydeoxyguanosine (8-OH-dG) in blood samples showed an increase of 39.7% after prehatch exposure to phthalates. This was statistically significant for DEHP and indicates genetic toxicity, since part of the teratogenic activity is associated with oxidative stress and DNA damage.

Original languageEnglish (US)
Pages (from-to)56-62
Number of pages7
JournalNeurotoxicology and Teratology
Volume34
Issue number1
DOIs
StatePublished - Jan 1 2012
Externally publishedYes

Fingerprint

Dibutyl Phthalate
Gastroschisis
Toxicity
Mothers
Eggs
DNA Damage
phthalic acid
Industrial chemicals
Abdominal Muscles
Umbilical Hernia
Play and Playthings
Oxidative stress
Consumer products
DNA
Locomotion
Metabolites
Plastics
Alkaline Phosphatase
Muscle
Animals

Keywords

  • DNA damage
  • Embryonic development
  • Gastroschisis
  • Neurobehavioral teratogenicity
  • Omphalocele
  • Phthalates

ASJC Scopus subject areas

  • Toxicology
  • Developmental Neuroscience
  • Cellular and Molecular Neuroscience

Cite this

The teratogenicity and behavioral teratogenicity of di(2-ethylhexyl) phthalate (DEHP) and di-butyl Phthalate (DBP) in a chick model. / Abdul-Ghani, Safa; Yanai, Joseph; Abdul-Ghani, Rula; Pinkas, Adi; Abdeen, Ziad.

In: Neurotoxicology and Teratology, Vol. 34, No. 1, 01.01.2012, p. 56-62.

Research output: Contribution to journalArticle

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