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[支气管肺发育不良动物模型的建立方法及其评价]

[Methods for establishing animal model of bronchopulmonary dysplasia and their evaluation].

作者信息

Xiong Zeng, Zhou Xia, Yue Shao-Jie

机构信息

Department of Radiology, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jan;19(1):121-125. doi: 10.7499/j.issn.1008-8830.2017.01.020.

DOI:10.7499/j.issn.1008-8830.2017.01.020
PMID:28100335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7390119/
Abstract

With the development of treatment, the survival rate of premature infants has significantly increased, especially extremely premature infants and very low birth weight infants. This has led to an increase in incidence of bronchopulmonary dysplasia (BPD) year by year. BPD has been one of the most common respiratory system diseases in premature infants, especially the small premature infants. Arrested alveolar development is an important cause of BPD. Therefore, the mechanism of arrested alveolar development and the intervention measures for promoting alveolar development are the focuses of research on BPD. Selecting the appropriate animal model of BPD is the key to obtaining meaningful results in the basic research on BPD. Based on above, several common methods for establishing an animal model of BPD and the corresponding changes in pathophysiology are summarized and evaluated in order to provide a reference for selecting the appropriate animal model in studies on the pathogenesis, pathophysiology, and prevention and control strategies of BPD.

摘要

随着治疗手段的发展,早产儿尤其是极早产儿和极低出生体重儿的存活率显著提高。这导致支气管肺发育不良(BPD)的发病率逐年上升。BPD一直是早产儿尤其是小早产儿最常见的呼吸系统疾病之一。肺泡发育停滞是BPD的重要病因。因此,肺泡发育停滞的机制以及促进肺泡发育的干预措施是BPD研究的重点。选择合适的BPD动物模型是在BPD基础研究中获得有意义结果的关键。基于此,总结并评估了几种建立BPD动物模型的常用方法及其相应的病理生理变化,以便为BPD的发病机制、病理生理学以及防控策略研究中选择合适的动物模型提供参考。

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[Methods for establishing animal model of bronchopulmonary dysplasia and their evaluation].[支气管肺发育不良动物模型的建立方法及其评价]
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Int J Biochem Cell Biol. 2024 Jul;172:106587. doi: 10.1016/j.biocel.2024.106587. Epub 2024 May 11.
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引用本文的文献

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An Innovative Model of Bronchopulmonary Dysplasia in Premature Infants.一种早产儿支气管肺发育不良的创新模型。
Front Pediatr. 2020 May 27;8:271. doi: 10.3389/fped.2020.00271. eCollection 2020.
2
The expression of miR-125b in Nrf2-silenced A549 cells exposed to hyperoxia and its relationship with apoptosis.Nrf2 沉默的 A549 细胞在高氧暴露下 miR-125b 的表达及其与细胞凋亡的关系。
J Cell Mol Med. 2020 Jan;24(1):965-972. doi: 10.1111/jcmm.14808. Epub 2019 Nov 12.
3
[Preventive effect of caffeine on bronchopulmonary dysplasia in preterm infants].咖啡因对早产儿支气管肺发育不良的预防作用
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Jul;20(7):598-602. doi: 10.7499/j.issn.1008-8830.2018.07.017.

本文引用的文献

1
Animal models of bronchopulmonary dysplasia. The term mouse models.支气管肺发育不良的动物模型。术语“鼠模型”。
Am J Physiol Lung Cell Mol Physiol. 2014 Dec 15;307(12):L936-47. doi: 10.1152/ajplung.00159.2014. Epub 2014 Oct 10.
2
MicroRNA expression profile in intrauterine hypoxia-induced pulmonary hypoplasia in rats.大鼠宫内缺氧诱导肺发育不全中的微小RNA表达谱
Exp Ther Med. 2014 Sep;8(3):747-753. doi: 10.3892/etm.2014.1796. Epub 2014 Jun 20.
3
Epithelial-mesenchymal transitions in bronchopulmonary dysplasia of newborn rats.新生大鼠支气管肺发育不良中的上皮-间质转化
Pediatr Pulmonol. 2014 Nov;49(11):1112-23. doi: 10.1002/ppul.22969. Epub 2014 Apr 11.
4
Altered lung development in bronchopulmonary dysplasia.支气管肺发育不良中肺发育的改变。
Birth Defects Res A Clin Mol Teratol. 2014 Mar;100(3):158-67. doi: 10.1002/bdra.23237. Epub 2014 Mar 17.
5
Bronchopulmonary dysplasia - trends over three decades.支气管肺发育不良——三十年的发展趋势
Paediatr Child Health. 2013 Feb;18(2):86-90. doi: 10.1093/pch/18.2.86.
6
Ventilator-induced lung injury.呼吸机相关性肺损伤
N Engl J Med. 2013 Nov 28;369(22):2126-36. doi: 10.1056/NEJMra1208707.
7
Human umbilical cord blood mononuclear cells in a double-hit model of bronchopulmonary dysplasia in neonatal mice.人脐带血单个核细胞在新生鼠支气管肺发育不良双重打击模型中的作用。
PLoS One. 2013 Sep 19;8(9):e74740. doi: 10.1371/journal.pone.0074740. eCollection 2013.
8
Histologic evidence of intrapulmonary anastomoses by three-dimensional reconstruction in severe bronchopulmonary dysplasia.严重支气管肺发育不良中三维重建的肺内吻合的组织学证据。
Ann Am Thorac Soc. 2013 Oct;10(5):474-81. doi: 10.1513/AnnalsATS.201305-124OC.
9
Interleukin-1 receptor antagonist prevents murine bronchopulmonary dysplasia induced by perinatal inflammation and hyperoxia.白细胞介素-1 受体拮抗剂可预防围生期炎症和高氧诱导的小鼠支气管肺发育不良。
Proc Natl Acad Sci U S A. 2013 Aug 27;110(35):14384-9. doi: 10.1073/pnas.1306859110. Epub 2013 Aug 14.
10
Bronchopulmonary dysplasia: the earliest and perhaps the longest lasting obstructive lung disease in humans.支气管肺发育不良:人类最早且可能持续时间最长的阻塞性肺部疾病。
Early Hum Dev. 2013 Oct;89 Suppl 3:S3-5. doi: 10.1016/j.earlhumdev.2013.07.015. Epub 2013 Aug 7.