Department of Toxicology, Anhui Medical University, Hefei 230032, China; Key Laboratory of Environmental Toxicology of Anhui Higher Education Institutes, Anhui Medical University, Hefei 230032, China; MOE Key Laboratory of Population Health Across Life Cycle, Hefei 230032, Anhui, China.
Department of Toxicology, Anhui Medical University, Hefei 230032, China.
Int Immunopharmacol. 2020 Jun;83:106442. doi: 10.1016/j.intimp.2020.106442. Epub 2020 Apr 2.
The disorder of bile acid metabolism is a common feature during pregnancy, which leads to adverse birth outcomes and maternal damage effects. However, the cause and therapy about the disorder of bile acid metabolism are still poor. Microbial infection often occurs in pregnant women, which can induce the disorder of bile acid metabolism in adult mice. Here, this study observed the acute effect of lipopolysaccharide (LPS) on maternal bile acid of pregnant mice at gestational day 17 and the protective effect of obeticholic acid (OCA) pretreatment, a potent agonist of bile acid receptor farnesoid X receptor (FXR). The results showed LPS significantly increased the level of maternal serum and disordered bile acids components of maternal serum and liver, which were ameliorated by OCA pretreatment with obviously reducing the contents of CA, TCA, DCA, TCDCA, CDCA, GCA and TDCA in maternal serum and DCA, TCA, TDCA, TUDCA, CDCA and TCDCA in maternal liver. Furthermore, we investigated the effects of OCA on LPS-disrupted bile acid metabolism in maternal liver. LPS disrupted maternal bile acid profile by decreasing transport and metabolism with hepatic tight junctions of bile acid in pregnant mice. OCA obviously increased the protein level of nuclear FXR and regulated its target genes involving in the metabolism of bile acid, which was characterized by the lower expression of bile acid synthase CYP7A1, the higher expression of CYP3A and the higher mRNA level of transporter Mdr1a/b. This study provided the evidences that LPS disrupted bile acid metabolism in the late stage of pregnant mice and OCA pretreatment played the protective role on it by activating FXR.
胆汁酸代谢紊乱是妊娠期间的一个常见特征,可导致不良的出生结局和母体损伤效应。然而,胆汁酸代谢紊乱的病因和治疗方法仍不理想。孕妇常发生微生物感染,可诱导成年小鼠胆汁酸代谢紊乱。本研究观察了脂多糖(LPS)在妊娠第 17 天对母体胆汁酸的急性影响,以及胆汁酸受体法尼醇 X 受体(FXR)的强效激动剂奥贝胆酸(OCA)预处理的保护作用。结果表明,LPS 显著增加了母体血清和母体血清及肝脏中胆汁酸成分的水平,而 OCA 预处理可改善这一状况,明显降低了母体血清中 CA、TCA、DCA、TCDCA、CDCA、GCA 和 TDCA 的含量,以及母体肝脏中 DCA、TCA、TDCA、TUDCA、CDCA 和 TCDCA 的含量。此外,我们还研究了 OCA 对 LPS 破坏的母体肝脏胆汁酸代谢的影响。LPS 通过降低妊娠小鼠肝脏中胆汁酸的转运和代谢来破坏母体胆汁酸谱,而 OCA 则明显增加了核 FXR 的蛋白水平,并调节了其参与胆汁酸代谢的靶基因,其特征是胆汁酸合成酶 CYP7A1 的表达降低,CYP3A 的表达升高,以及转运体 Mdr1a/b 的 mRNA 水平升高。本研究提供了证据,表明 LPS 破坏了妊娠晚期小鼠的胆汁酸代谢,而 OCA 预处理通过激活 FXR 发挥了保护作用。