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前列腺素E1、E2和F2α对豚鼠离体胆囊液体转运的三相效应。

Triphasic effect of prostaglandins E1, E2 and F2alpha on the fluid transport of isolated gall-bladder of guinea-pigs.

作者信息

Heintze K, Leinesser W, Petersen K U, Heidenreich O

出版信息

Prostaglandins. 1975 Feb;9(2):309-22. doi: 10.1016/0090-6980(75)90035-0.

Abstract

Prostaglandins (PGs) F2alpha, E1 and E2 exerted a triphasic influence on the fluid transport of isolated guinea-pig gall-bladders, when applied to the serosal side. PGE1 and PGE2 produced these effects in lower concentrations than F2alpha. Directly after PG addition to the serosal side a short stimulation of fluid transport to between 200 and 400% was observed. The stimulatory effect of PGs was most distinct in gall-bladders from female guinea-pigs, less pronounced in male and nearly absent in pregnant animals. Since PGs increased intraluminal hydrostatic pressure in gall-bladders by contraction of the smooth muscle, experiments were performed in which hydrostatic pressure was increased by different procedures. These included the addition of imidazole (10- minus 2 M), raising of K+ in the bathing solution and an increase in intraluminal pressure by addition of Ringer's solution into the lumen. All three procedures stimulated fluid reabsorption temporarily in the same way as PGs, hence increase of intraluminal pressure is thought to be the reason for the observed temporary stimulation of fluid transport. Direct evidence for this thesis was obtained when the gall-bladder was mounted as a flat sheet over a chamber; in this preparation no stimulation of fluid transport was obtained. The second phase of the PG influence was characterized by a concentration-related inhibition of fluid reabsorption followed by a significant but small reverse of fluid transport (secretion of fluid). When PGs were applied to the mucosal side, only an inhibition of fluid transport was observed, which was much weaker compared to the addition to the serosal side.

摘要

当将前列腺素(PGs)F2α、E1和E2应用于分离的豚鼠胆囊浆膜侧时,它们对胆囊的液体转运产生了三相影响。PGE1和PGE2产生这些效应的浓度低于F2α。在将PG添加到浆膜侧后,立即观察到液体转运短暂刺激至200%至400%之间。PGs的刺激作用在雌性豚鼠的胆囊中最为明显,在雄性豚鼠中较不明显,而在怀孕动物中几乎不存在。由于PGs通过平滑肌收缩增加了胆囊内的静水压力,因此进行了通过不同程序增加静水压力的实验。这些程序包括添加咪唑(10⁻²M)、提高浴液中的K⁺浓度以及通过向腔内添加林格氏液来增加腔内压力。所有这三个程序都以与PGs相同的方式暂时刺激了液体重吸收,因此腔内压力的增加被认为是观察到的液体转运暂时刺激的原因。当将胆囊作为平片安装在腔室上时,获得了这一论点的直接证据;在这种制备中未观察到液体转运的刺激。PG影响的第二阶段的特征是与浓度相关的液体重吸收抑制,随后是液体转运的显著但较小的逆转(液体分泌)。当将PG应用于粘膜侧时,仅观察到液体转运的抑制,与添加到浆膜侧相比,这种抑制要弱得多。

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