Brown J A, Zipser R D
Gastroenterology. 1987 Jan;92(1):54-9. doi: 10.1016/0016-5085(87)90839-0.
Human and experimental colitis are associated with release of both vasoconstrictor and vasodilator eicosanoids. To determine the pattern of colonic blood flow in vivo and the role of prostaglandins and thromboxanes, immune complex-mediated colitis and delayed hypersensitivity-mediated colitis were induced in rabbits. Organ blood flow was determined in conscious animals by radiolabeled microspheres before and after cyclooxygenase or thromboxane synthetase inhibition. Colonic blood flow was twofold higher in colitis than in control animals. Thromboxane synthetase inhibition with dazoxiben caused a slight further increase of colon perfusion in animals with colitis, but thromboxane receptor blockade had no effect. Prostaglandin inhibition with indomethacin and ibuprofen did not affect blood flow in controls, but in animals with colitis these drugs markedly reduced colonic blood flow to the level of control animals. The data demonstrate that vasodilatory prostaglandins enhance colonic blood flow in acute colon inflammation.
人类和实验性结肠炎都与血管收缩性和血管舒张性类花生酸的释放有关。为了确定体内结肠血流模式以及前列腺素和血栓素的作用,在兔中诱导了免疫复合物介导的结肠炎和迟发型超敏反应介导的结肠炎。在环氧化酶或血栓素合成酶抑制前后,通过放射性标记微球在清醒动物中测定器官血流。结肠炎动物的结肠血流比对照动物高两倍。用达唑氧苯抑制血栓素合成酶导致结肠炎动物的结肠灌注略有进一步增加,但血栓素受体阻断没有效果。用吲哚美辛和布洛芬抑制前列腺素对对照动物的血流没有影响,但在结肠炎动物中,这些药物显著降低结肠血流至对照动物水平。数据表明,血管舒张性前列腺素在急性结肠炎症中增强结肠血流。