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前列环素(PGI2)对大鼠妊娠子宫的双重作用。

Dual actions of prostacyclin (PGI2) on the rat pregnant uterus.

作者信息

Williams K I, El-Tahir K E, Marcinkiewicz E

出版信息

Prostaglandins. 1979 May;17(5):667-72. doi: 10.1016/s0090-6980(79)80039-8.

Abstract

Using strips of rat pregnant uterus, treated with indomethacin to suppress spontaneous contractility, the oxytocic activity of prostacyclin was compared with other prostaglandins. A prostacyclin concentration of 32 ng/ml elicited uterine contractions in all experiments. In this respect prostacyclin was 80 times more active than 6-oxo-PGF1 alpha but less active than PGE2 or PGF2 alpha. Apart from a direct stimulant effect, prostacyclin also exhibited an indirect potentiating action. In threshold concentrations prostacyclin caused a 3-fold potentiation of threshold doses of oxytocin. A lesser 1.5-fold potentiation of PGE2 alpha was also observed. The implications of these findings in relation to prostacyclin playing a role in parturition are discussed.

摘要

使用经吲哚美辛处理以抑制自发收缩性的大鼠妊娠子宫条,将前列环素的催产活性与其他前列腺素进行比较。在所有实验中,32 ng/ml的前列环素浓度均可引起子宫收缩。在这方面,前列环素的活性比6-氧代-PGF1α高80倍,但比PGE2或PGF2α低。除直接刺激作用外,前列环素还表现出间接增强作用。在阈浓度下,前列环素使催产素阈剂量增强3倍。还观察到PGE2α有较小的1.5倍增强作用。讨论了这些发现与前列环素在分娩中发挥作用的关系。

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