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一种新的出生时脊柱和胸壁畸形的绵羊模型,伴有呼吸系统力学和肺发育的改变:一项可行性研究。

A new ovine model of spine and chest wall deformity at birth with alteration of respiratory system mechanics and lung development: a feasibility study.

机构信息

Department of Surgery, Centre de recherche du CHU Sainte-Justine, 3175 Côte-Sainte Catherine, Montreal, H3T 1C5, QC, Canada.

University of Montreal, Montreal, QC, Canada.

出版信息

Eur Spine J. 2019 Jan;28(1):114-120. doi: 10.1007/s00586-018-5818-3. Epub 2018 Nov 29.

DOI:10.1007/s00586-018-5818-3
PMID:30498959
Abstract

PURPOSE

To develop an animal model of spine and chest wall deformity (CWD) at birth and to evaluate its effects on respiratory system mechanics and lung development.

METHODS

A spine and CWD was created in utero between 70 and 75 days of gestation in six ovine fetuses by resection of the seventh and eighth left ribs. Two days after birth, respiratory system mechanics was assessed in anesthetized lambs using the flexiVent apparatus, followed by postmortem measurement of lung mechanics as well as histological lung analysis.

RESULTS

A range of severity of CWD was found (Cobb angle from 0° to 48°) with a mean decrease in compliance of 47% and in inspiratory capacity of 39% compared to control lambs. Proof-of-concept histological analysis in one lamb showed marked lung hypoplasia.

CONCLUSION

Our ovine model represents a pilot proof-of-concept study evaluating the impact of a spine and CWD present at birth on lung respiratory mechanics and development. This study lays down the groundwork for future studies evaluating the impact of these deformities on lung development and potential treatments. These slides can be retrieved under Electronic Supplementary Material.

摘要

目的

建立一种出生时脊柱和胸廓畸形(CWD)的动物模型,并评估其对呼吸系统力学和肺发育的影响。

方法

在 6 只绵羊胎儿妊娠 70-75 天时,通过切除第 7 和第 8 对左侧肋骨,在子宫内创建脊柱和 CWD。出生后 2 天,使用 flexiVent 仪器对麻醉羔羊进行呼吸系统力学评估,然后进行肺力学的死后测量以及组织学肺分析。

结果

发现 CWD 的严重程度范围很广(Cobb 角为 0°至 48°),与对照组羔羊相比,顺应性降低了 47%,吸气量降低了 39%。对一只羔羊进行的概念验证组织学分析显示,肺部明显发育不良。

结论

我们的绵羊模型代表了一项初步的概念验证研究,评估了出生时存在的脊柱和 CWD 对肺呼吸力学和发育的影响。这项研究为未来评估这些畸形对肺发育和潜在治疗的影响的研究奠定了基础。这些幻灯片可在电子补充材料中检索。

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引用本文的文献

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Ovine model of congenital chest wall and spine deformity: From birth to 3 months follow-up.先天性胸壁和脊柱畸形的绵羊模型:从出生到3个月随访
JOR Spine. 2023 Oct 18;7(1):e1295. doi: 10.1002/jsp2.1295. eCollection 2024 Mar.

本文引用的文献

1
Long-term Outcome of Early Fusions for Congenital Scoliosis.先天性脊柱侧弯早期融合术的长期疗效
Spine Deform. 2018 Sep-Oct;6(5):552-559. doi: 10.1016/j.jspd.2018.02.003.
2
Expansion Thoracoplasty in Rabbit Model: Effect of Timing on Preserving Pulmonary Growth and Correcting Spine Deformity.兔模型中胸廓扩张成形术:时机对维持肺生长和矫正脊柱畸形的影响。
Spine (Phila Pa 1976). 2018 Aug 1;43(15):E877-E884. doi: 10.1097/BRS.0000000000002573.
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An official research policy statement of the American Thoracic Society/European Respiratory Society: standards for quantitative assessment of lung structure.
美国胸科学会/欧洲呼吸学会官方研究政策声明:肺结构定量评估标准
Am J Respir Crit Care Med. 2010 Feb 15;181(4):394-418. doi: 10.1164/rccm.200809-1522ST.
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Expansion thoracoplasty improves respiratory function in a rabbit model of postnatal pulmonary hypoplasia: a pilot study.胸廓扩张成形术改善了一种新生后肺发育不全兔模型的呼吸功能:一项初步研究。
Spine (Phila Pa 1976). 2010 Jan 15;35(2):153-61. doi: 10.1097/BRS.0b013e3181c4b8c7.
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The reciprocal relationship between thoracic and spinal deformity and its effect on pulmonary function in a rabbit model: a pilot study.兔模型中胸廓与脊柱畸形的相互关系及其对肺功能的影响:一项初步研究。
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AN ANALYSIS OF PRESSURE-VOLUME CHARACTERISTICS OF THE LUNGS.肺压力-容积特性分析
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