Pawlik W W, Gustaw P, Sendur R, Czarnobilski K, Konturek S J, Beck G, Jendralla M
Institute of Physiology, Academy of Medicine, Kraków, Poland.
Hepatogastroenterology. 1988 Apr;35(2):87-90.
The effects of intra-arterial administration of leukotrienes (LT) C4 and D4 upon total intestinal and mucosal blood flow, intestinal oxygen consumption and motor activity were measured in anesthetized dogs. Blood flow to a segment of distal ileum was measured with an electromagnetic blood flow meter, and arteriovenous oxygen difference (AVO2) was determined spectrophotometrically. Oxygen consumption was calculated as the product of AVO2 and total blood flow. Intestinal mucosal blood flow was determined by a local H2-gas clearance technique. Motor activity was monitored on the basis of changes in intraluminal pressure. LTC4 and LTD4 induced a dose-related decrease in total intestinal blood flow, mucosal blood flow and in oxygen consumption, and an increase in intestinal motor activity. Both LT produced a redistribution of blood flow into the muscular compartment of the intestinal circulation. The results of these studies indicate that LTC4 and LTD4 are potent vasoconstrictors in the intestinal microcirculation, and that endogenous LT may contribute to the microvascular changes leading to the intestinal damage.
在麻醉犬身上测量了动脉内给予白三烯(LT)C4和D4对肠道总血流量和黏膜血流量、肠道氧耗量以及运动活性的影响。用电磁血流仪测量一段回肠远端的血流量,并用分光光度法测定动静脉氧差(AVO2)。氧耗量通过AVO2与总血流量的乘积计算得出。肠道黏膜血流量采用局部氢气清除技术测定。根据腔内压力变化监测运动活性。LTC4和LTD4引起肠道总血流量、黏膜血流量和氧耗量呈剂量相关的减少,以及肠道运动活性增加。两种LT均导致血流重新分布到肠道循环的肌肉部分。这些研究结果表明,LTC4和LTD4是肠道微循环中的强效血管收缩剂,内源性LT可能促成导致肠道损伤的微血管变化。