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聚磷酸根皮苷对豚鼠回肠中前列腺素E1和F2α收缩作用的拮抗特性。

The character of the antagonism by polyphloretin phosphate of contractions to prostaglandins E1 and F 2alpha in guinea-pig ileum.

作者信息

Petkov V, Radomirov R, Petkov O, Todorov S

出版信息

J Pharm Pharmacol. 1978 Aug;30(8):491-4. doi: 10.1111/j.2042-7158.1978.tb13300.x.

Abstract

Polyphloretin phosphate (PPP) produced a dose-dependent decrease in the tone and reduction of the spontaneous phasic contactions of the longitudinal muscle of guinea-pig isolated ileum. PPP (100 microgram ml-1) after a 2 min contact with the ileum decreased the contractile effects of PGE1 0.1 micron by 40.6 +/- 7.4%, of PGE1 0.01 micron by 86.7 +/- 3.3% and of PGE2alpha 0.1 micron by 62.2 +/- 8.6%. After 10 min contact of PPP the contractile effect of PGE1 0.1 micron was decreased by 47.7 +/- 4.7% and that of PGE2alpha 0.1 micron by 89.6 +/- 1.7%. When the contact was longer, PPP showed a pronounced after-effect in respect to the effects of PGE1 and particularly of PGF2alpha. PPP signicantly reduced contractions to 5-HT and BaCL2, but not to acetylcholine, histamine or substance P. The type of antagonism of PGE1 by PPP was examined using cumulative concentration-effect curves for PGE1 in the presence of increasing concentrations of PPP. We conclude that on guinea-pig ileum PPP acts as a non-competitive antagonist of PGE1 and PGF2alpha.

摘要

聚磷酸根皮苷(PPP)使豚鼠离体回肠纵肌的张力呈剂量依赖性降低,并减少其自发的阶段性收缩。PPP(100微克/毫升)与回肠接触2分钟后,使0.1微摩尔PGE1的收缩效应降低40.6±7.4%,使0.01微摩尔PGE1的收缩效应降低86.7±3.3%,使0.1微摩尔PGE2α的收缩效应降低62.2±8.6%。PPP接触10分钟后,0.1微摩尔PGE1的收缩效应降低47.7±4.7%,0.1微摩尔PGE2α的收缩效应降低89.6±1.7%。当接触时间更长时,PPP对PGE1尤其是PGF2α的效应显示出明显的后效应。PPP显著降低对5-羟色胺和氯化钡的收缩反应,但对乙酰胆碱、组胺或P物质的收缩反应无影响。使用在PPP浓度增加时PGE1的累积浓度-效应曲线研究了PPP对PGE1的拮抗类型。我们得出结论,在豚鼠回肠上,PPP作为PGE1和PGF2α的非竞争性拮抗剂起作用。

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