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缺氧诱导的肺动脉高压早期发育过程中大鼠肺动脉干细胞增殖和蛋白质合成的放射自显影分析

Autoradiographic analysis of cell proliferation and protein synthesis in the pulmonary trunk of rats during the early development of hypoxia-induced pulmonary hypertension.

作者信息

McKenzie J C, Clancy J, Klein R M

出版信息

Blood Vessels. 1984;21(2):80-9.

PMID:6230123
Abstract

The results of this study indicate that both cell proliferation and increased synthesis of extracellular matrix protein contribute to hypertrophy of the rat pulmonary trunk during the early development of hypoxia-induced pulmonary hypertension. As determined by autoradiography after 3H-thymidine injection, pulmonary hypertension results in increased labelling in all cell compartments of the pulmonary trunk wall, the most dramatic response occurring in the adventitia following 3 days' hypoxic exposure. Autoradiography also demonstrated differences in the degree of incorporation of 3H-proline into extracellular protein between hypoxic (3 and 21 days) and control rats. The major focus of 3H-proline incorporation shifted from the adventitia at 3 days to the tunica media at 21 days, although incorporation was significantly higher at 3 compared to 21 days in all wall compartments. The patterns of hyperplasia and matrix protein synthesis in the extrapulmonary arteries of the rat, as reported here, are distinctly different from those seen in many large elastic arteries during development of systemic hypertension. For example, the hyperplastic response of arterial vessels follows a similar temporal sequence in pulmonary and systemic hypertension. However, the adventitia is the region of the pulmonary trunk with highest cell proliferation in pulmonary hypertension while the media is most affected by systemic hypertension. The relevance of the changing patterns of cell proliferation and protein synthesis in the wall of the pulmonary trunk of chronically hypoxic rats to the structural and biochemical properties of this vessel during the early development of pulmonary hypertension is discussed.

摘要

本研究结果表明,在缺氧诱导的肺动脉高压早期发展过程中,细胞增殖和细胞外基质蛋白合成增加均有助于大鼠肺动脉干肥大。通过注射3H-胸腺嘧啶核苷后的放射自显影测定,肺动脉高压导致肺动脉干壁所有细胞区室的标记增加,在缺氧暴露3天后,外膜出现最显著的反应。放射自显影还显示,缺氧(3天和21天)大鼠与对照大鼠相比,3H-脯氨酸掺入细胞外蛋白的程度存在差异。3H-脯氨酸掺入的主要焦点从3天时的外膜转移到21天时的中膜,尽管在所有壁层中,3天时的掺入量均显著高于21天。本文报道的大鼠肺外动脉增生和基质蛋白合成模式与许多大弹性动脉在系统性高血压发展过程中所见的模式明显不同。例如,动脉血管的增生反应在肺动脉高压和系统性高血压中遵循相似的时间顺序。然而,外膜是肺动脉高压时肺动脉干细胞增殖最高的区域,而中膜在系统性高血压中受影响最大。文中讨论了慢性缺氧大鼠肺动脉干壁细胞增殖和蛋白质合成模式的变化与肺动脉高压早期发展过程中该血管结构和生化特性的相关性。

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