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壁内前列腺素E2与胎羊动脉导管产前通畅的关系。

Involvement of intramural prostaglandin E2 in prenatal patency of the lamb ductus arteriosus.

作者信息

Coceani F, Huhtanen D, Hamilton N C, Bishai I, Olley P M

出版信息

Can J Physiol Pharmacol. 1986 Jun;64(6):737-44. doi: 10.1139/y86-124.

Abstract

Release of prostaglandin E2 (PGE2) was studied in isolated ductus arteriosus preparations from immature (103 or 104 days gestation; term, 147 days) and near-term fetal lambs. Mature preparations produced measurable amounts of the compound in most cases and the release rate was 19 +/- 2 pg/(100 mg wet weight X min) at a PO2 of 3-8 Torr (1 Torr = 133.3 Pa). PGE2 release increased with the PO2 of the medium, peak values (about 125 pg/(100 mg X min)) being attained at 106-276 Torr when the oxygen-induced contraction was still submaximal. Experiments in which tissues were either contracted with excess potassium or relaxed with CO proved that PGE2 formation is independent from the contractile state. PGE2 was also released from ductus preparations lacking the adventitia, the intima, or both; however, release values were maximal when the adventitia was preserved. The magnitude of the intrinsic tone in these stripped preparations was inversely related to the rate of PGE2 formation. Reduced glutathione increased PGE2 release from the mature ductus, whole or stripped, and also relaxed hypoxic preparations; both effects were reversed by concomitant treatment with indomethacin. PGE2 synthesis tended to be greater in the immature than the mature ductus, maximal values (115 +/- 27 pg/(100 mg X min)) being observed at 6-8 Torr. We conclude that the ductus arteriosus is endowed with an enzyme system for the synthesis of PGE2 whose function accords with an effector role of the compound in the regulation of tone. These findings, together with the potent relaxation exerted by PGE2 at low PO2, indicate that the locally generated prostaglandin is well suited for keeping the ductus patent in the fetus.

摘要

在未成熟(妊娠103或104天;足月为147天)和接近足月的胎羊的离体动脉导管标本中研究了前列腺素E2(PGE2)的释放情况。在大多数情况下,成熟标本能产生可测量量的该化合物,在3 - 8托(1托 = 133.3帕)的氧分压下,释放速率为19±2皮克/(100毫克湿重×分钟)。PGE2释放量随培养基氧分压的升高而增加,当氧诱导的收缩仍未达到最大值时,在106 - 276托时达到峰值(约125皮克/(100毫克×分钟))。用过量钾使组织收缩或用一氧化碳使其舒张的实验证明,PGE2的形成与收缩状态无关。PGE2也从缺乏外膜、内膜或两者的动脉导管标本中释放;然而,当保留外膜时,释放值最大。这些剥脱标本中的内在张力大小与PGE2形成速率呈负相关。还原型谷胱甘肽增加了成熟动脉导管(完整或剥脱的)中PGE2的释放,并且也使缺氧标本舒张;吲哚美辛同时处理可逆转这两种作用。未成熟动脉导管中的PGE2合成往往比成熟动脉导管中的更大,在6 - 8托时观察到最大值(115±27皮克/(100毫克×分钟))。我们得出结论,动脉导管具有合成PGE2的酶系统,其功能符合该化合物在调节张力中的效应器作用。这些发现,连同PGE2在低氧分压下发挥的有效舒张作用,表明局部产生的前列腺素非常适合使胎儿的动脉导管保持开放。

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