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大鼠肺气肿饥饿模型与弹性蛋白酶模型的比较。

A comparison of starvation and elastase models of emphysema in the rat.

作者信息

Harkema J R, Mauderly J L, Gregory R E, Pickrell J A

出版信息

Am Rev Respir Dis. 1984 Apr;129(4):584-91.

PMID:6561948
Abstract

Starvation and elastase-induced changes in rat lung structure, biochemistry, and function were compared as models of human pulmonary emphysema. Ten-week-old male rats were instilled intratracheally with either porcine pancreatic elastase in saline (E) or with saline alone. A group of the saline-instilled rats were fed one third of their normal food intake until a 45% loss of body weight occurred (S). The remaining saline-instilled rats served as control animals (C). Post-treatment evaluations included in vivo respiratory function, lung histopathologic and morphometric analyses, lung tissue proteinolytic activity, and lung collagen. The E rats had in vivo respiratory function changes more similar to human emphysema than those of S rats. All lung volume subdivisions were decreased in S rats and increased in E rats. The volume-pressure curve of S rats was shifted to the right of the C curve, whereas that of E rats was shifted to the left. Forced expiratory flow rates of E rats were decreased at all lung volumes, but those of S rats were not. Both E and S rats had larger terminal air spaces and less alveolar surface area than did C rats. The S rats had more collagen per gram lung and higher proteinolytic activity than did C or E rats. These results show that, although starvation induces some changes characteristic of human emphysema, elastase-treatment provides a model more similar to the human disease.

摘要

将饥饿和弹性蛋白酶诱导的大鼠肺结构、生物化学及功能变化作为人类肺气肿模型进行比较。给10周龄雄性大鼠经气管内滴注生理盐水配制的猪胰弹性蛋白酶(E组)或仅滴注生理盐水。一组滴注生理盐水的大鼠喂食正常食量的三分之一,直至体重减轻45%(S组)。其余滴注生理盐水的大鼠作为对照动物(C组)。治疗后评估包括体内呼吸功能、肺组织病理学和形态计量学分析、肺组织蛋白水解活性及肺胶原蛋白。与S组大鼠相比,E组大鼠体内呼吸功能变化更类似于人类肺气肿。S组大鼠所有肺容积细分均减小,E组大鼠则增大。S组大鼠的容积 - 压力曲线向C组曲线右侧偏移,而E组大鼠的则向左侧偏移。E组大鼠在所有肺容积下的用力呼气流速均降低,但S组大鼠未降低。与C组大鼠相比,E组和S组大鼠的终末气腔更大,肺泡表面积更小。S组大鼠每克肺中的胶原蛋白更多,蛋白水解活性高于C组或E组大鼠。这些结果表明,尽管饥饿会诱导一些人类肺气肿的特征性变化,但弹性蛋白酶处理提供了一个更类似于人类疾病的模型。

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