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高质量肺固定的控制闭环灌注在大型动物模型中的体视学分析。

High-quality lung fixation by controlled closed loop perfusion for stereological analysis in a large animal model.

机构信息

Department of Anesthesiology, University Hospital Berne, University of Berne, Berne, Switzerland.

出版信息

J Surg Res. 2011 Apr;166(2):e97-102. doi: 10.1016/j.jss.2010.12.003. Epub 2010 Dec 31.

Abstract

BACKGROUND

Stereology is an essential method for quantitative analysis of lung structure. Adequate fixation is a prerequisite for stereological analysis to avoid bias in pulmonary tissue, dimensions and structural details. We present a technique for in situ fixation of large animal lungs for stereological analysis, based on closed loop perfusion fixation.

MATERIALS AND METHODS

Twenty anesthetized ventilated pigs (30 ± 3 kg) underwent cannulation of the pulmonary artery and ligation of the right hilus. Following circulatory arrest a continuous positive pressure of 12 mbar was applied to the airways and lung perfusion started with the fixative solution (1.5% paraformaldehyde; 1.5% glutaraldehyde in 0.15 M HEPES). In five animals, a single-pass perfusion technique was performed, in 15 subsequent animals, the closed-loop technique was applied. Afterwards, lungs were removed, externally postfixed in the recycled fixative solution, and stored at 4 °C. Fifteen lung specimens underwent stereological analysis with volume estimation and subsequent systematic uniform random sampling for light and electron microscopic analysis.

RESULTS

Singlepass perfusion did not result in satisfactory fixation. Left lung closed loop perfusion rate was 0.5-0.7 L/min with total median [min-max] perfusion time of 15 min (11-19). Perfusion pressure was 15 mm Hg (9-33). Subsequent lung analysis revealed well-preserved cell and tissue ultrastructure.

CONCLUSION

The closed loop perfusion technique represents a valuable and reproducible fixation method in large animal models. Pressure controlled fixation perfusion results in high-quality preservation of in situ parenchymal architecture of lungs with or without injury, which is ideally suited for quantitative assessment of lung structure by stereology.

摘要

背景

体视学是定量分析肺结构的重要方法。充分固定是进行体视学分析的前提,可避免肺组织、尺寸和结构细节的偏差。我们提出了一种基于闭环灌注固定的大型动物肺原位固定技术,用于体视学分析。

材料和方法

20 只麻醉通气的猪(30±3kg)行肺动脉插管和右肺门结扎。循环停止后,向气道施加 12mbar 的持续正压,开始用固定液(1.5%多聚甲醛;0.15MHEPES 中的 1.5%戊二醛)进行肺灌注。在 5 只动物中,采用单次灌注技术,在随后的 15 只动物中,应用闭环技术。之后,取出肺脏,在外用回收固定液进行后固定,并在 4°C 下储存。15 个肺标本进行体视学分析,进行体积估计,并进行后续的光镜和电镜分析的系统均匀随机抽样。

结果

单次灌注不能达到满意的固定效果。左肺闭环灌注率为 0.5-0.7L/min,总中位数[最小-最大]灌注时间为 15min(11-19)。灌注压力为 15mmHg(9-33)。随后的肺分析显示细胞和组织超微结构保存良好。

结论

闭环灌注技术是大型动物模型中一种有价值且可重复的固定方法。压力控制的固定灌注可实现高质量的原位实质结构保存,无论是否有损伤,非常适合通过体视学对肺结构进行定量评估。

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