Cumberland A L, Palliser H K, Hirst J J
1 School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia.
J Dev Orig Health Dis. 2014 Apr;5(2):74-8. doi: 10.1017/S2040174413000573.
Placental 5α-reductase (5αR) is influenced by in utero compromises and has a role in regulating neuroactive steroid concentrations in the fetus. The objective of this study was to determine if changes in placental 5αR were associated with neonatal outcome after birth. Guinea pigs were delivered by cesarean section at term (GA69, n=22) or preterm (GA62, n=36) and the placenta collected. Preterm neonates were maintained for 24 h unless their condition deteriorated before this time. Enzyme mRNA expression of 5αR type-1 and 5αR type-2 were determined using real-time PCR. All preterm neonates had significantly higher 5αR2 expression in their placenta compared with placentae from term neonates (P<0.0001). Expression was also markedly higher in the placentae from neonates that did not survive until 24 h, compared with surviving preterm neonates (P=0.04). These findings suggest differences of in utero neurosteroidogenic capacity between surviving and non-surviving preterm guinea pig neonates. The increased 5αR2 mRNA expression in the placenta of non-survivors suggests an induction of the neurosteroid pathway due to prior exposure to an in utero compromise, with such exposure possibly a predisposing factor that contributed to their poor ex utero outcome.
胎盘5α-还原酶(5αR)受子宫内不良因素影响,在调节胎儿神经活性甾体浓度方面发挥作用。本研究的目的是确定胎盘5αR的变化是否与出生后的新生儿结局相关。豚鼠在足月(孕龄69天,n = 22)或早产(孕龄62天,n = 36)时通过剖宫产分娩,并收集胎盘。早产新生儿维持24小时,除非在此之前病情恶化。使用实时PCR测定5αR 1型和5αR 2型的酶mRNA表达。与足月新生儿的胎盘相比,所有早产新生儿胎盘的5αR2表达均显著更高(P<0.0001)。与存活的早产新生儿相比,未存活至24小时的新生儿胎盘的表达也明显更高(P = 0.04)。这些发现表明存活和未存活的早产豚鼠新生儿在子宫内神经甾体生成能力方面存在差异。未存活者胎盘5αR2 mRNA表达增加表明由于先前暴露于子宫内不良因素而诱导了神经甾体途径,这种暴露可能是导致其宫外不良结局的一个易感因素。