Bruch H P, Schmidt E, Laven R, Kehrer G, Wasner K H
Acta Hepatogastroenterol (Stuttg). 1978 Aug;25(4):303-7.
Prostaglandines (PG) of the E and F series cause peristaltic activity in isolated longitudinal muscle strips of the human colon. As this phasic motor reaction can be varied by acetyl choline and adrenaline it was supposed, that prostaglandines contribute to peristalsis. The role of PG E and F in the human colon was studied by inhibiting the prostaglandine synthesis and by antagonizing the prostaglandine-effects. Indomethacin proved to be a suitable inhibitor. HR 546 was found a powerful antagonist. The effect of Pentagastrin and Cholecystokinin (CCK) on peristaltic activity were suppressed by Indomethacin and HR 546. The inhibition of peristalsis by Indomethacin and HR 546 was removed by high doses of PG E and F. On the basis of these results the role of PG for the motility of the gut is discussed.
E 系列和 F 系列前列腺素可引起人结肠离体纵行肌条的蠕动活动。由于这种阶段性运动反应可被乙酰胆碱和肾上腺素改变,因此推测前列腺素参与了蠕动。通过抑制前列腺素合成和拮抗前列腺素效应,研究了前列腺素 E 和 F 在人结肠中的作用。吲哚美辛被证明是一种合适的抑制剂。发现 HR 546 是一种强效拮抗剂。吲哚美辛和 HR 546 可抑制五肽胃泌素和胆囊收缩素(CCK)对蠕动活动的影响。高剂量的前列腺素 E 和 F 可消除吲哚美辛和 HR 546 对蠕动的抑制作用。基于这些结果,讨论了前列腺素在肠道运动中的作用。