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人妊娠期间雌三醇的生物合成:潜在途径。

Biosynthesis of estetrol in human pregnancy: Potential pathways.

机构信息

Department of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.

Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, VA, United States.

出版信息

J Steroid Biochem Mol Biol. 2023 Sep;232:106359. doi: 10.1016/j.jsbmb.2023.106359. Epub 2023 Jun 28.

Abstract

Estetrol (E) has emerged as a novel and highly promising estrogen for therapeutic use. E is a weak natural estrogen produced only in pregnancy. Because of its novelty, there is considerable interest by clinicians in how it is produced in pregnancy. Although the fetal liver plays a key role in its production, the placenta is also involved. A current view is that estradiol (E) formed in the placenta enters the fetal compartment and is then rapidly sulfated. E sulfate then undergoes 15α-/16α-hydroxylation in the fetal liver thereby forming E sulfate (phenolic pathway). However, another pathway involving 15α,16α-dihydroxy-DHEAS formed in the fetal liver and converted to E in the placenta also plays a significant role (neutral pathway). It is not known which pathway predominates, but both pathways appear to be important in E biosynthesis. In this commentary, we summarize the well-established pathways in the formation of estrogens in the nonpregnant and pregnant female. We then review what is known about the biosynthesis of E and describe the 2 proposed pathways involving the fetus and placenta.

摘要

雌三醇(E)作为一种新型且极具应用前景的雌激素药物正在出现。E 是一种在妊娠期间产生的弱天然雌激素。由于其新颖性,临床医生对其在妊娠期间的产生方式非常感兴趣。尽管胎儿肝脏在其产生过程中发挥着关键作用,但胎盘也参与其中。目前的观点认为,胎盘内形成的雌二醇(E)进入胎儿隔室,然后迅速硫酸化。E 硫酸盐随后在胎儿肝脏中进行 15α-/16α-羟化,从而形成 E 硫酸盐(酚途径)。然而,另一条涉及胎儿肝脏中形成的 15α,16α-二羟基-DHEAS 并在胎盘内转化为 E 的途径也起着重要作用(中性途径)。目前尚不清楚哪种途径占主导地位,但这两种途径在 E 的生物合成中似乎都很重要。在这篇评论中,我们总结了非妊娠和妊娠女性体内雌激素形成的既定途径。然后,我们回顾了已知的 E 生物合成,并描述了涉及胎儿和胎盘的 2 种拟议途径。

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