先天性肺叶异常突变大鼠的支气管分支异常和肺气肿样变化

H. Aoyama, S. Fujii, S. Teramoto
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引用次数: 2

摘要

本研究旨在研究存活至成年的fpl/fpl突变大鼠:1)支气管分支异常是否是肺叶异常的主要缺陷,如果是这样,2)这些异常是否会导致呼吸功能障碍。对成年fpl/fpl大鼠畸形肺的腐蚀铸型进行检查,发现右侧支气管树出现多种分支异常,如中叶支气管腹侧分支、中叶支气管曲度异常、中叶支气管和中叶支气管第一段支气管位置异常。而在左肺中发现的唯一轻微异常是节段性支气管数量减少。这些结果与我们之前的观察结果一致,即fpl突变的主要表现仅限于右肺叶,并表明该畸形的主要缺陷是支气管分支异常。在这些大鼠中,气管、左右主支气管以及一些大叶支气管和节段支气管的狭窄也可以通过测量其周长而变得明显。老年fpl/fpl大鼠肺组织病理学检查显示肺空间异常扩张,伴肺泡壁破坏和巨噬细胞浸润。这些观察结果表明,fpl/fpl大鼠随着年龄的增长,肺叶异常(符合气管和支气管畸形)会出现肺气肿样呼吸功能障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bronchial Branching Abnormalities and Emphysema‐like Changes in Mutant Rats Having Congenital Lobation Anomalies in the Lung
ABSTRACT The present study aimed at investigating in fpl/fpl mutant rats survived to adulthood 1) whether bronchial branching abnormalities were the primary defects of pulmonary lobation anomalies, and if this was the case, 2) whether these anomalies could lead to respiratory dysfunction. Examination of corrosion casts made from the malformed lungs of adult fpl/fpl rats revealed a variety of branching abnormalities in the right bronchial tree, such as ventral ramification of the middle lobar bronchus, abnormal curvature of the intermediate lobar bronchus, and positional abnormalities of the middle lobar bronchus and first segmental bronchus of the intermediate lobar bronchus, while reduction in the number of segmental bronchi was the only minor abnormality found in the left lung. These results conformed to our previous observations in which the main manifestation of the fpl mutation was restricted to the right lung lobes, and indicated that the primary defect of this malformation was bronchial branching abnormalities. In these rats, stenosis of the trachea, right and left principal bronchi, and some lobar and segmental bronchi also became evident by calipering their circumference. Histopathological examination of the lungs revealed abnormally expanded airspaces accompanied by destruction of alveolar walls and macrophage infiltration in aged fpl/fpl rats. These observations suggest that fpl/fpl rats suffer emphysema‐like respiratory dysfunction with advancing age from pulmonary lobation anomalies conforming to tracheal and bronchial malformations.
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