Effects of maternal exposure to di(2-ethylhexyl)phthalate (DEHP) during pregnancy on susceptibility to neonatal asthma

被引:39
作者
Shin, In-Sik [1 ]
Lee, Mee-Young [1 ]
Cho, Eun-Sang [2 ]
Choi, Eun-young [3 ]
Son, Hwa-Young [2 ]
Lee, Kyoung-Youl [3 ]
机构
[1] Korea Inst Oriental Med, Basic Herbal Med Res Grp, Taejon 305811, South Korea
[2] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[3] Kongju Natl Univ, Coll Nursing & Hlth, Chungnam 314701, South Korea
基金
新加坡国家研究基金会;
关键词
Di(2-ethylhexyl)phthalate (DEHP); Maternal exposure; Pregnancy; Offspring; Asthma; DI-(2-ETHYLHEXYL) PHTHALATE; AIRWAY INFLAMMATION; OVALBUMIN; CHILDREN; MICE;
D O I
10.1016/j.taap.2013.12.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Di(2-ethylhexyl) phthalate (DEHP) is used as a plasticizer and is widely dispersed in the environment. In this study, we investigated the effects of maternal exposure to DEHP during pregnancy on neonatal asthma susceptibility using a murine model of asthma induced by ovalbumin (OVA), Pregnant BALB/c mice received DEHP from gestation day 13 to lactation day 21. Their offspring were sensitized on postnatal days (PNDs) 9 and 15 by intraperitoneal injection of 0.5 mu g OVA with 200 mu g aluminum hydroxide. On PNDs 22, 23 and 24, live pups received an airway challenge of OVA for 30 min. Offspring from pregnant mice that received DEHP showed reductions in inflammatory cell count, interleukin (IL)-4, IL-13, and eotaxin in their bronchoalveolar lavage fluid and in total immunoglobulin E and OVA-specific IgE in their plasma compared with offspring from pregnant mice that did not receive DEHP treatment. These results were consistent with histological analysis and immuno-blotting. Maternal exposure to DEHP reduces airway inflammation and mucus production in offspring, with a decrease in inducible nitric oxide synthase (iNOS) in the lung tissue. This study suggests that maternal exposure to DEHP during pregnancy reduces asthmatic responses induced by OVA challenge in offspring. These effects were considered to be closely related to the suppression of Th2 immune responses and iNOS expression. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:402 / 407
页数:6
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