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[邻苯二甲酸酯对孕期及哺乳期暴露子代肺部过敏的影响]

[Effects of phthalate on pulmonary allergy of offspring during intrauterin and lactating exposure].

作者信息

Lü Junfeng, Cheng Xiaoping, Wang Bohan, Liu Yingying, Zhang Yifei

机构信息

Public Health, Jinzhou Medical University, Jinzhou 121000, China.

出版信息

Wei Sheng Yan Jiu. 2019 Jan;48(1):114-143.

Abstract

OBJECTIVE

To investigate the effects of exposure to diethyl phthalate(DEHP) during pregnancy and lactation in respiratory allergy of offspring Wistar rats.

METHODS

To establish the maternal DEHP exposure model: 36 healthy 2-month-old female Wistar rats were divided into three different dose groups. From GD0, each group of pregnant mice were given different concentrations of DEHP(0, 30, 300 mg/(kg·d)) until to the newborn weaning(PND21). After birth, one of offspring was selected from each cage in different dose groups. At PND21 and PND28 the offspring were sensitized by intraperitoneal injection(i. p. ) OVA and continuous nasal sensitization at PND32, PND33, PND34. Bronchoalveolar lavage fluid(BALF) and lung tissue were collected at PND35 with non-sensitized groups. ELISA detected the secretion of Th2 cytokine interleukin(IL)-4, IL-5 and IL-13 in BALF, and the pathological changes of allergic inflammation in lung tissues were observed by HE and PAS staining. Expression of epithelium-derived factor IL-33 detected by immunohistochemistry.

RESULTS

In BALF, compared with the control group, the total number of inflammatory cells and eosinophils in the DEHP0+OVA group increased to(131. 500±25. 548)×104, (32. 000±10. 079)×104(P<0. 05); The total number of inflammatory cells and eosinophils in the DEHP30+OVA group increased to(156. 167±17. 994)×104, (16. 331±6. 667)×104(P<0. 05); and the total number of inflammatory cells and eosinophils in the DEHP300+OVA group increased to(172. 167±19. 994)×104, (55. 000±17. 018)×104(P<0. 05). After adding different doses of DEHP and OVA, compared with the control group, The expression levels of IL-4, IL-5, IL-13 in DEHP0+OVA group increased to(38. 401±6. 594) pg/mL(P>0. 05), (30. 026±2. 756) pg/mL(P<0. 05), (13. 806±4. 355) pg/mL(P<0. 05); The expression levels of IL-4, IL-5 and IL-13 in DEHP30+OVA group increased to(57. 733±7. 293) pg/mL(P<0. 05) and(31. 544±1. 043) pg/mL(P>0. 05), (18. 068±1. 497) pg/mL(P<0. 05); The expression levels of IL-4, IL-5 and IL-13 in DEHP300+OVA group increased to(54. 943±6. 049) pg/mL(P>0. 05) and(32. 377±3. 739)pg/mL(P>0. 05), (20. 168±0. 939) pg/mL(P<0. 05), respectively. The tissue section of all the DEHP+saline groups could be observed that no obvious allergic inflammatory reaction, meanwhile all the DEHP+OVA groups had a relatively obvious allergic reaction and were severe with the increase of DEHP dose. Immunohistochemistry showed no significant increase in the expression of IL-33 in the DEHP+saline groups, while the expression of IL-33 in the DEHP+OVA groups increased with a certain dose response.

CONCLUSION

Exposure to DEHP during pregnancy and lactation will aggravate the sensitization reaction of offspring, the possible mechanism that DEHP increase the Th2 type of immune response may be the overexpression of IL-33 in the epithelial cells.

摘要

目的

探讨孕期及哺乳期暴露于邻苯二甲酸二乙酯(DEHP)对Wistar大鼠子代呼吸道过敏的影响。

方法

建立母鼠DEHP暴露模型:将36只健康的2月龄雌性Wistar大鼠分为三个不同剂量组。从妊娠第0天(GD0)起,每组孕鼠给予不同浓度的DEHP(0、30、300 mg/(kg·d)),直至新生鼠断奶(出生后第21天,PND21)。出生后,从不同剂量组的每个笼子中选取1只子代。在PND21和PND28时,子代通过腹腔注射卵清蛋白(OVA)致敏,并在PND32、PND33、PND34时进行连续鼻腔致敏。在PND35时,对未致敏组收集支气管肺泡灌洗液(BALF)和肺组织。采用酶联免疫吸附测定(ELISA)法检测BALF中Th2细胞因子白细胞介素(IL)-4、IL-5和IL-13的分泌水平,并用苏木精-伊红(HE)染色和过碘酸-雪夫(PAS)染色观察肺组织过敏性炎症的病理变化。采用免疫组织化学法检测上皮源性因子IL-33的表达。

结果

在BALF中,与对照组相比,DEHP0+OVA组炎症细胞总数和嗜酸性粒细胞数分别增加至(131.500±25.548)×10⁴、(32.000±10.079)×10⁴(P<0.05);DEHP30+OVA组炎症细胞总数和嗜酸性粒细胞数分别增加至(156.167±17.994)×10⁴、(16.331±6.667)×10⁴(P<0.05);DEHP300+OVA组炎症细胞总数和嗜酸性粒细胞数分别增加至(172.167±19.994)×10⁴、(55.000±17.018)×10⁴(P<0.05)。加入不同剂量的DEHP和OVA后,与对照组相比,DEHP0+OVA组IL-4、IL-5、IL-13表达水平分别增加至(38.401±6.594)pg/mL(P>0.05)、(30.026±2.756)pg/mL(P<0.05)、(13.806±4.355)pg/mL(P<0.05);DEHP30+OVA组IL-4、IL-5和IL-13表达水平分别增加至(57.733±7.293)pg/mL(P<0.05)、(31.544±1.043)pg/mL(P>0.05)、(18.068±1.497)pg/mL(P<0.05);DEHP300+OVA组IL-4、IL-5和IL-13表达水平分别增加至(54.943±6.049)pg/mL(P>0.05)、(32.377±3.739)pg/mL(P>0.05)、(20.168±0.939)pg/mL(P<0.05)。所有DEHP+生理盐水组的组织切片均未观察到明显的过敏性炎症反应,而所有DEHP+OVA组均有较明显的过敏反应,且随着DEHP剂量的增加而加重。免疫组织化学显示,DEHP+生理盐水组IL-33表达无明显增加,而DEHP+OVA组IL-33表达呈一定剂量反应性增加。

结论

孕期及哺乳期暴露于DEHP会加重子代的致敏反应,DEHP增加Th2型免疫反应的可能机制是上皮细胞中IL-33的过表达。

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