Zha Xiaomeng, Fang Man, Zhong Wen, Chen Liang, Feng Hui, Zhang Min, Wang Hui, Zhang Yuanzhen
Department of Obstetrics and Gynaecology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Department of Obstetrics and Gynaecology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China; Hubei Provincial Key Laboratory of Developmentally Originated Diseases, Wuhan 430071, China; Hubei Clinical Research Center for Prenatal Diagnosis and Birth Health, Wuhan 430071, China.
Toxicol Lett. 2024 Dec;402:68-80. doi: 10.1016/j.toxlet.2024.11.005. Epub 2024 Nov 22.
Prednisone, a synthetic glucocorticoid, is commonly used to treat autoimmune diseases in pregnant women. However, some studies suggest that the use of prednisone during pregnancy may lead to adverse pregnancy outcomes. In this study, we established PPE mouse models at different doses (0.25, 0.5, 1.0 mg/kg·d) and different stages (whole pregnancy, early pregnancy and middle-late pregnancy) and determined outcomes on the placenta and fetus. The results of our study indicated that at the highest dose of 1 mg/kg PPE using a GD 0-18 dosing regime, PPE caused placental morphological changes measured as a decrease in placental weight relative to controls and a decrease in the placenta junctional zone (JZ)/labyrinth zone (LZ) ratio. No changes were observed on the fetuses for number of live, stillborn, and absorbed fetuses between the experimental groups and the control group. In the placentas at some doses, there were decreases in cell proliferation markers measured at the RNA and protein level by Western blot and increased apoptosis. Measures of gene expression at the mRNA level showed altered nutrients (including glucose, amino acid, and cholesterol) transport gene expressions with the most significant change associated with the male placentas at high-dose and whole pregnancy PPE group. It was further found that PPE led to the inhibition of the insulin-like growth factor 2 (IGF2)/insulin-like growth factor 1 receptor (IGF1R) signaling pathway, which was well correlated with the indicators of cell proliferation, syncytialization and nutrient (glucose and amino acid) transport indices. In conclusion, PPE can alter placental morphology and nutrient transport function, with differences in effect related to dose, stage and gender. Differential gene expressions measured for genes of the IGF2/IGF1R signaling pathway suggested this pathway may be involved in the effects seen with PPE. This study provides a theoretical and experimental basis for enhancing the understanding of the effects of prednisone use on placenta during human pregnancy but does not currently raise concerns for human use as effects were not seen on the fetuses and while the effects on cell proliferation are informative they were inconsistent and the differential effects on female and male placentas unexplained suggesting that further work is required to elucidate if these findings have relevance for human use of PPE during pregnancy.
泼尼松是一种合成糖皮质激素,常用于治疗孕妇的自身免疫性疾病。然而,一些研究表明,孕期使用泼尼松可能会导致不良妊娠结局。在本研究中,我们建立了不同剂量(0.25、0.5、1.0毫克/千克·天)和不同阶段(整个孕期、孕早期和孕中晚期)的泼尼松暴露(PPE)小鼠模型,并测定了胎盘和胎儿的相关结局。我们的研究结果表明,在使用1毫克/千克PPE且给药方案为妊娠第0至18天的最高剂量下,PPE导致胎盘形态发生变化,表现为相对于对照组胎盘重量减轻以及胎盘交界区(JZ)/迷路区(LZ)比值降低。实验组和对照组之间,活胎、死胎和吸收胎的数量在胎儿方面未观察到变化。在某些剂量下的胎盘组织中,通过蛋白质印迹法在RNA和蛋白质水平检测到细胞增殖标志物减少,且细胞凋亡增加。在mRNA水平的基因表达检测显示,营养物质(包括葡萄糖、氨基酸和胆固醇)转运基因表达发生改变,其中变化最显著的是高剂量且整个孕期PPE组的雄性胎盘。进一步发现,PPE导致胰岛素样生长因子2(IGF2)/胰岛素样生长因子1受体(IGF1R)信号通路受到抑制,这与细胞增殖、合体化以及营养物质(葡萄糖和氨基酸)转运指标密切相关。总之,PPE可改变胎盘形态和营养物质转运功能,其效应存在剂量、阶段和性别的差异。对IGF2/IGF1R信号通路基因的差异基因表达检测表明,该信号通路可能参与了PPE所产生的效应。本研究为增进对孕期人类使用泼尼松对胎盘影响的理解提供了理论和实验依据,但目前并不引发对人类使用的担忧,因为在胎儿方面未观察到影响,虽然对细胞增殖的影响具有参考价值,但并不一致,且对雌性和雄性胎盘的差异影响无法解释,这表明需要进一步开展工作以阐明这些发现是否与孕期人类使用PPE相关。