Published February 2018 | Version v1
Journal article

Maternal exposure to environmental DEHP exacerbated OVA-induced asthmatic responses in rat offspring

  • 1. Division of Pneumoconiosis, School of Public Health, China Medical University, Shenyang (China)

Description

Highlights: • Maternal exposure to DEHP during pregnancy and lactation aggravates pulmonary inflammation of the rat offspring • DEHP maternal exposure increased the OVA-induced Th2 immune response the lung of the rat offspring • DEHP maternal exposure increased OVA-induced Th2 cytokines in lung and promoted the expression of OX40L and GATA3 • These adjuvant effects of DEHP were considered to be closely related to the enhanced TSLP expression and the JAK signals Di (ethylhexyl) phthalate (DEHP) is a commonly used phthalates (PAEs) compound as plasticizer and becomes a severe environmental pollutant worldwide. Studies show that DEHP, as an environmental endocrine disruptor, has potential adverse effects on human. Epidemiologic studies indicate that DEHP is positively correlated to allergic diseases. Maternal exposure to DEHP may contribute to the increasing incidence of allergic diseases in offspring. However, the role of DEHP and its detailed mechanism in allergic disease of the offspring are still unclear. The aim of our study is to investigate whether DEHP maternal exposure could aggravate the allergic responses in offspring and its mechanism. Pregnant Wistar rats were randomly divided into three groups and exposed to different doses of DEHP. Half of the offspring were challenged with OVA after birth. All the pups of each group were sacrificed at postnatal day (PND)14, PND21 and PND28. The number of inflammatory cells in bronchoalveolar lavage was counted, lung pathological changes were observed, Th2 type cytokines expressions were checked, and the expression of TSLP signaling pathway were examined. Our results showed that maternal exposure to DEHP during pregnancy and lactation aggravated the eosinophils accumulation and the pathological inflammatory changes in pups' lung after OVA challenge. And maternal exposure to DEHP during pregnancy and lactation also elevated the levels of typical Th2 cytokines in OVA-challenged rats. What's more, maternal exposure to DEHP during pregnancy and lactation increased the levels of TSLP, TSLPR and IL-7R in the offspring after OVA challenge. Our study suggested that DEHP maternal exposure could aggravate the OVA-induced asthmatic responses in offspring. And this adjuvant effect of DEHP was related with the TSLP/TSLPR/IL-7R and its downstream signal pathways.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.scitotenv.2017.09.276

Additional details

Identifiers

DOI
10.1016/j.scitotenv.2017.09.276;
PII
S0048969717326281;

Publishing Information

Journal Title
Science of the Total Environment
Journal Volume
615
Journal Page Range
p. 253-261
ISSN
0048-9697
CODEN
STENDL

Optional Information

Copyright
Copyright (c) 2017 Published by Elsevier B.V.