Maternal Disononyl Phthalate Exposure Activates Allergic Airway Inflammation via Stimulating the Phosphoinositide 3-kinase/Akt Pathway in Rat Pups

Biomed Environ Sci. 2015 Mar;28(3):190-8. doi: 10.3967/bes2015.025.

Abstract

Objective: To evaluate the effect of diisononyl phthalate (DINP) exposure during gestation and lacta- tion on allergic response in pups and to explore the role of phosphoinositide 3-kinase/Akt pathway on it.

Methods: Female Wistar rats were treated with DINP at different dosages (0, 5, 50, and 500 mg/kg of body weight per day). The pups were sensitized and challenged by ovalbumin (OVA). The airway response was assessed; the airway histological studies were performed by hematoxylin and eosin (HE) staining; and the relative cytokines in phosphoinositide 3-kinase (PI3K)/Akt pathway were measured by enzyme-linked immunosorbent assay (ELISA) and western blot analysis.

Results: There was no significant difference in DINP's effect on airway hyperresponsiveness (AHR) between male pups and female pups. In the 50 mg/(kg·d) DINP-treated group, airway response to OVA significantly increased and pups showed dramatically enhanced pulmonary resistance (RI) compared with those from controls (P<0.05). Enhanced Akt phosphorylation and NF-κB translocation, and Th2 cytokines expression were observed in pups of 50 mg/(kg·d) DINP-treated group. However, in the 5 and 500 mg/(kg·d) DINP-treated pups, no significant effects were observed.

Conclusion: There was an adjuvant effect of DINP on allergic airway inflammation in pups. Maternal DINP exposure could promote OVA-induced allergic airway response in pups in part by upregulation of PI3K/Akt pathway.

Keywords: Allergic airway inflammation; Asthma; DINP; Maternal exposure; PI3K/Akt.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Bronchitis / chemically induced*
  • Bronchoalveolar Lavage Fluid
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Hypersensitivity / etiology*
  • Male
  • Maternal Exposure*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation
  • Phthalic Acids / toxicity*
  • Pregnancy
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Phthalic Acids
  • phthalic acid
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt