首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Sequence of structural changes and elastin peptide release during vascular remodelling in sheep with chronic pulmonary hypertension induced by air embolization.
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Sequence of structural changes and elastin peptide release during vascular remodelling in sheep with chronic pulmonary hypertension induced by air embolization.

机译:空气栓塞诱发的慢性肺动脉高压绵羊的血管重构过程中的结构变化和弹性蛋白肽释放序列。

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摘要

The progression of structural changes in the pulmonary arterial bed were followed in a model of chronic pulmonary hypertension. Chronically instrumented awake sheep received continuous air embolization for 0 (controls), 1, 4, 8, or 12 days (n = 5-6/group). After the period of embolization, the lungs were removed, the pulmonary arteries were distended with barium-gelatin, and the lungs were fixed via the airways with formal-saline. Quantitative techniques were applied to sections from random blocks from the lungs of each animal. One day of embolization resulted in granulocyte sequestration in the lung interstitium and in small vessels; additionally, intraalveolar and perivascular edema was present. By 4 days, increased medial thickness, appearance of muscle in smaller arteries than normal (e.g., muscular arteries at alveolar duct level: control = 1.2 +/- 1.2%; day 4 = 22.7 +/- 7.7) and reduction in number of barium-filled intraacinar arteries was found. The arterial changes progressed in severity to day 8 and were similar at day 12. Since arterial remodelling involves increased elastin deposition, the concentration of elastin peptides was measured in lung lymph. Increased flux of elastin peptides was apparent from day 2 of embolization and continued to increase to a level 20 x baseline by day 12 (baseline 351 +/- 86 micrograms/15 min; day 12 = 6338 +/- 2999). Comparison of the onset of the structural changes with previous findings shows that the arterial remodelling parallels the onset of sustained pulmonary hypertension. The increase in lung-lymph elastin peptides by day 2 provides evidence that vascular remodelling is initiated before day 4 of embolization. The early sequestration of granulocytes and appearance of edema suggest that these may be part of the trigger to the development of the structural changes.
机译:在慢性肺动脉高压模型中追踪肺动脉床结构变化的进程。长期使用器械清醒的绵羊接受连续0天(对照组),1、4、8或12天(n = 5-6 /组)的空气栓塞。栓塞期过后,取出肺,用明胶钡剂使肺动脉扩张,并用正规盐水经气道固定肺。将定量技术应用于来自每只动物肺的随机块的切片。栓塞的一天导致肺间质和小血管中的粒细胞隔离。另外,还存在肺泡内和血管周围水肿。到第4天,内侧厚度增加,比正常小动脉的肌肉出现(例如,在肺泡管水平的肌肉动脉:对照= 1.2 +/- 1.2%;第4天= 22.7 +/- 7.7)并且钡的数量减少发现充满了髋臼的动脉。严重程度的动脉病变进展至第8天,第12天相似。由于动脉重塑涉及增加的弹性蛋白沉积,因此测量了肺淋巴中弹性蛋白肽的浓度。从栓塞的第2天开始,弹性蛋白肽的通量增加,并且在第12天时继续增加至基线水平的20倍(基线351 +/- 86微克/ 15分钟;第12天= 6338 +/- 2999)。结构变化的发作与先前发现的比较表明,动脉重构与持续性肺动脉高压的发作平行。到第2天肺淋巴弹性蛋白肽的增加提供了证据,表明在栓塞形成的第4天之前就开始了血管重塑。粒细胞的早期隔离和浮肿的出现表明,这些可能是结构改变发展的触发因素。

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