Kashimura M, Okuno M, Himeno S, Kuroshima T, Kawamoto H, Shinomura Y, Tarui S
Second Department of Internal Medicine, Osaka University Medical School, Japan.
Prostaglandins. 1988 Apr;35(4):583-95. doi: 10.1016/0090-6980(88)90033-0.
The effect of Prostaglandin D2 (PGD2) on ion transport was investigated in the rat colon in vitro. Ion transport across the intestinal mucosa was estimated by transmucosal potential difference (PD) and short circuit current (Isc) in the Ussing chamber. PGD2 added to the serosal reservoir induced a sustained reduction in PD and Isc at the concentration of higher than 10(-7)M, producing the maximal decrease at 10(-5)M. PGD2 at 10(-5)M completely blocked the increase in PD elicited by prostaglandin E1 (PGE1), theophylline, dibutyryl cAMP or serotonin. Adenylate cyclase activity was determined in the colonic mucosal homogenates after addition of PGD2 and PGE1. Treatment with PGD2 or PGE1 caused a significant increase in the enzyme activity. Combined treatment with both prostaglandins induced no more increase than that elicited by PGE1 alone. These results suggest that PGD2 has an anti-secretory effect on the rat colon and it may regulate the ion transport process through other mechanism than the modification of cyclic AMP concentration in mucosal cells.
在体外对大鼠结肠研究了前列腺素D2(PGD2)对离子转运的影响。通过Ussing小室中的跨粘膜电位差(PD)和短路电流(Isc)评估离子跨肠粘膜的转运。添加到浆膜储库中的PGD2在高于10(-7)M的浓度下可使PD和Isc持续降低,在10(-5)M时产生最大降幅。10(-5)M的PGD2完全阻断了前列腺素E1(PGE1)、茶碱、二丁酰环磷腺苷或5-羟色胺引起的PD升高。在添加PGD2和PGE1后,测定结肠粘膜匀浆中的腺苷酸环化酶活性。用PGD2或PGE1处理导致酶活性显著增加。两种前列腺素联合处理引起的增加不超过单独使用PGE1引起的增加。这些结果表明,PGD2对大鼠结肠有抗分泌作用,并且它可能通过不同于改变粘膜细胞中环磷酸腺苷浓度的其他机制来调节离子转运过程。