Li X, Lu W C, Zhu Y J
Peking Union Medical College Hospital, Beijing.
Zhonghua Nei Ke Za Zhi. 1990 Jan;29(1):8-10, 59.
In order to observe the effect of acute hypoxia on release of vasoactive intestinal peptide (VIP), the plasma VIP content was determined in anesthetized dogs by a specific radioimmunoassay technique during acute hypoxia. Blood gases and hemodynamics were monitored simultaneously. After inhalation of 10% oxygen. the plasma VIP levels elevated along with decrease in PaO2 and increase in pulmonary artery pressure. The plasma concentration of VIP in the portal vein increased significantly from 106 +/- 21 pg/ml before hypoxia to 173 +/- 36 pg/ml 15 minutes after the onset of hypoxia (P less than 0.01). The difference of arterio-venous VIP content increased from -3 +/- 6 pg/ml before hypoxia to +9 +/- 7 pg/ml after inhalation of 10% oxygen for 30 minutes. The results suggested that VIP was released from the gastrointestinal tract as well as from the lung in case of hypoxia and pulmonary hypertension. It is considered that the release of VIP may be an adaptive and compensatory response, promoting vasodilation and perfusion in vital organs.
为观察急性缺氧对血管活性肠肽(VIP)释放的影响,采用特异性放射免疫测定技术,在急性缺氧过程中测定麻醉犬的血浆VIP含量。同时监测血气和血流动力学。吸入10%氧气后,血浆VIP水平随PaO₂降低和肺动脉压升高而升高。门静脉血浆VIP浓度从缺氧前的106±21 pg/ml显著升高至缺氧开始后15分钟的173±36 pg/ml(P<0.01)。动静脉VIP含量差值从缺氧前的-3±6 pg/ml增加至吸入10%氧气30分钟后的+9±7 pg/ml。结果提示,在缺氧和肺动脉高压情况下,VIP可从胃肠道以及肺释放。认为VIP的释放可能是一种适应性和代偿性反应,促进重要器官的血管舒张和灌注。