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依洛前列素(ZK 36374)可防止离体灌注大鼠肺中血管紧张素I在缺氧情况下的转化。

Iloprost (ZK 36374) prevents angiotensin I conversion in the isolated perfused rat lung against anoxia.

作者信息

Aksulu H E, Türker R K

出版信息

Eur J Pharmacol. 1986 Aug 22;128(1-2):67-72. doi: 10.1016/0014-2999(86)90558-3.

Abstract

The tissue protective effect of iloprost against anoxia was studied in the isolated perfused rat lung. The change in angiotensin converting enzyme activity was taken as a sign of the biochemical activity of pulmonary vascular endothelium and was measured by bioassay of the vasoconstrictor effects of angiotensin I and angiotensin II. A significant decrease in angiotensin converting enzyme activity was observed in the lungs incubated with Krebs alone and exposed to anoxia for 2 h. The decrease in angiotensin converting enzyme activity following anoxia for 2 and 24 h was prevented by prior pretreatment with iloprost. The pulmonary vasoconstrictor effect of angiotensin II was significantly enhanced following anoxia and iloprost prevented this potentiation. The prevention by iloprost of the decrease in angiotensin converting enzyme activity and increase in the pressor response to angiotensin II was attributed to damage of pulmonary vascular endothelium during anoxia. Possible underlying mechanisms are discussed.

摘要

在离体灌注大鼠肺中研究了伊洛前列素的组织缺氧保护作用。以血管紧张素转换酶活性的变化作为肺血管内皮生化活性的指标,并通过生物测定血管紧张素I和血管紧张素II的血管收缩作用来进行测量。在仅用 Krebs 孵育并暴露于缺氧 2 小时的肺中,观察到血管紧张素转换酶活性显著降低。在缺氧 2 小时和 24 小时后血管紧张素转换酶活性的降低可通过预先用伊洛前列素预处理来预防。缺氧后血管紧张素 II 的肺血管收缩作用显著增强,而伊洛前列素可防止这种增强作用。伊洛前列素对血管紧张素转换酶活性降低和对血管紧张素 II 升压反应增加的预防作用归因于缺氧期间肺血管内皮的损伤。文中讨论了可能的潜在机制。

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