Alexander J M, Nyby M D, Jasberg K A
J Appl Physiol Respir Environ Exerc Physiol. 1977 Jun;42(6):903-8. doi: 10.1152/jappl.1977.42.6.903.
Hypoxic pulmonary vasoconstriction in blood-perfused isolated dog lungs progressively diminishes with repeated hypoxic challenges. We investigated the role of prostaglandins in effecting the decay of the hypoxic response by using a double perfusion preparation that could separately perfuse the right and left lungs of a single dog. Degeneration of this response was reversed by the addition of prostaglandin (PG) synthesis inhibitors, aspirin, or indomethacin. Various PG's known to be produced by the lung (PGE1, PGE2, and PGF2alpha), were infused, and only PGE1 abolished hypoxic pulmonary vasoconstriction. Since other workers have shown that lungs can synthesize and release PG's in response to various stimuli, we postulate that PGE1 synthesis in isolated lungs may increase and thereby cause the degeneration of the hypoxic response. The addition of aspirin or indomethacin could inhibit the synthesis of PGE1 and thereby restore hypoxic pulmonary vasoconstriction.
在血液灌注的离体犬肺中,反复进行低氧刺激会使低氧性肺血管收缩逐渐减弱。我们使用一种能够分别灌注单只犬左右肺的双灌注制备方法,研究了前列腺素在影响低氧反应衰减中的作用。添加前列腺素(PG)合成抑制剂、阿司匹林或吲哚美辛可逆转这种反应的退化。已知由肺产生的各种PG(PGE1、PGE2和PGF2α)被注入,只有PGE1消除了低氧性肺血管收缩。由于其他研究人员已经表明肺可以响应各种刺激合成并释放PG,我们推测离体肺中PGE1的合成可能增加,从而导致低氧反应的退化。添加阿司匹林或吲哚美辛可抑制PGE1的合成,从而恢复低氧性肺血管收缩。