Saverymuttu S H, Wood J R, Morton I K
Eur J Pharmacol. 1979 Nov 23;60(1):7-14. doi: 10.1016/0014-2999(79)90046-3.
Prostaglandin (PG) A, E and F compounds applied serosally inhibited net fluid absorption and increased intraluminal pressure in guinea-pig isolated gallbladder. The inhibition was dose-dependent for a given animal body weight but sensitivity varied inversely with animal body weight; relative potencies were PGE2 greater than F2alpha greater than A1. In heavier animals the inhibition was preceded by an apparent increase in fluid absorption, due to fluid extrusion following muscle contraction. Net fluid secretion was observed at higher concentrations of PGE2 or F2alpha in lighter animals. Mucosally applied PGs less potently inhibited absorption, with relative potencies of PGE2 greater than A1 greater than F2beta greater than F2alpha. The spasmogenic effect was estimated by measuring intraluminal pressure (PGE2 greater than F2alpha greater than A1).
经浆膜面应用的前列腺素(PG)A、E和F类化合物可抑制豚鼠离体胆囊的净液体吸收,并增加腔内压力。对于给定的动物体重,这种抑制作用呈剂量依赖性,但敏感性与动物体重呈反比;相对效力为PGE2大于F2α大于A1。在较重的动物中,在抑制作用之前会出现液体吸收明显增加的情况,这是由于肌肉收缩后液体挤出所致。在较轻的动物中,当PGE2或F2α浓度较高时可观察到净液体分泌。经黏膜应用的PG对吸收的抑制作用较弱,相对效力为PGE2大于A1大于F2β大于F2α。通过测量腔内压力来评估致痉作用(PGE2大于F2α大于A1)。