Department of Pharmacology, Basic Medical School of Wuhan University, Wuhan 430071, China; Department of Obstetrics and Gynaecology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Department of Pharmacology, Basic Medical School of Wuhan University, Wuhan 430071, China; Hubei Provincial Key Laboratory of Developmentally Originated Diseases, Wuhan 430071, China.
Ecotoxicol Environ Saf. 2024 Sep 15;283:116929. doi: 10.1016/j.ecoenv.2024.116929. Epub 2024 Aug 29.
During pregnancy, the maternal body undergoes a series of adaptative physiological changes, leading to a slight increase in serum bile acid (BA) levels. Although the fetal liver can synthesize BAs since the first trimester through the alternative pathway, the BA metabolic system is immature in the fetus. Compared to adults, the fetus has a distinct composition of BA pool and limited expression of BA synthesis enzymes and transporters. Besides, the "enterohepatic circulation" of BAs is absent in fetus. Thus, fetal BAs need to be transported to the mother through the placenta for further metabolism and excretion, and maternal BAs can also be transported to the fetus. That is what we call the "fetal-placental-maternal BA circulation". Various BA transporters and nuclear receptors are essential for maintaining the balance of this BA circulation to ensure normal fetal development. However, prenatal adverse environments can alter fetal BA metabolism, resulting in intrauterine developmental abnormalities and susceptibility to a variety of adult chronic diseases. This review summarizes the current understanding of the fetal-placental-maternal BA circulation and discusses the effects of prenatal adverse environments on this particular BA circulation, aiming to provide a theoretical basis for exploring early prevention and treatment strategies for BA metabolism-associated adverse pregnancy outcomes and long-term impairments.
在妊娠期间,母体经历一系列适应性生理变化,导致血清胆汁酸(BA)水平略有升高。虽然胎儿的肝脏在妊娠早期可以通过替代途径合成 BA,但胎儿的 BA 代谢系统尚未成熟。与成人相比,胎儿的 BA 池组成明显不同,合成酶和转运体的表达有限。此外,胎儿中不存在 BA 的“肠肝循环”。因此,胎儿的 BA 需要通过胎盘转运到母体进行进一步代谢和排泄,而母体的 BA 也可以转运到胎儿。这就是我们所说的“胎儿-胎盘-母体 BA 循环”。各种 BA 转运体和核受体对于维持这种 BA 循环的平衡以确保正常的胎儿发育至关重要。然而,产前不良环境可以改变胎儿的 BA 代谢,导致宫内发育异常和易患多种成人慢性疾病。本综述总结了目前对胎儿-胎盘-母体 BA 循环的理解,并讨论了产前不良环境对这种特定 BA 循环的影响,旨在为探索与 BA 代谢相关的不良妊娠结局和长期损害的早期预防和治疗策略提供理论依据。