Goerg K J, Wanitschke R, Diener M, Rummel W
I. Medizinische Klinik, Johannes Gutenberg University, Mainz, Germany.
Gastroenterology. 1992 Sep;103(3):781-8. doi: 10.1016/0016-5085(92)90006-k.
The effect of prostaglandin D2 (PGD2) on ion transport across the mucosa of the descending colon was studied in rats. PGD2 dose-dependently decreased baseline short-circuit current of mucosa-submucosal preparations mounted either in the Ussing chamber or mounted as an everted sac. However, with the everted sac technique, the tissue was about 1000 times more sensitive to PGD2. Concomitant with the decrease in short-circuit current, PGD2 increased the mucosal-to-serosal fluxes of sodium and chloride and decreased the serosal-to-mucosal flux of chloride. PGD2 inhibited the secretory action of the PGI2 analogue iloprost, PGD2 alpha, and neurotensin. The action of these secretagogues was dependent on the presence of the submucosal plexus. In contrast, PGD2 had no effect on the increase in short-circuit current caused by PGD2, substance P, or serotonin, the actions of which were not dependent on the presence of the submucosal plexus. The results indicate that the action site of the antisecretory mechanism of PGD2 is localized in the secretomotor neurons.
研究了前列腺素D2(PGD2)对大鼠降结肠黏膜离子转运的影响。PGD2剂量依赖性地降低了安装在尤斯灌流室或外翻肠囊中的黏膜-黏膜下层制剂的基线短路电流。然而,采用外翻肠囊技术时,组织对PGD2的敏感性约高1000倍。伴随短路电流的降低,PGD2增加了钠和氯从黏膜到浆膜的通量,并降低了氯从浆膜到黏膜的通量。PGD2抑制了前列环素类似物伊洛前列素、PGD2α和神经降压素的分泌作用。这些促分泌剂的作用取决于黏膜下神经丛的存在。相反,PGD2对由PGD2、P物质或5-羟色胺引起的短路电流增加没有影响,这些物质的作用不依赖于黏膜下神经丛的存在。结果表明,PGD2抗分泌机制的作用位点定位于分泌运动神经元。