Torday J S, Dow K E
Dev Pharmacol Ther. 1984;7(2):133-9. doi: 10.1159/000457153.
It has previously been reported that morphologic and functional indices of fetal lung maturation are delayed in male rabbit fetuses, and these differences cannot be overcome by glucocorticoid treatment. Since thyroid hormone also stimulates surfactant production we have studied the effects of triiodothyronine (T3) and dexamethasone on saturated phosphatidylcholine (SPC) synthesis by day 20 male and female rat lung. Control male lung slices incorporated significantly less 3H-choline into SPC than females; surgery on day 17 markedly stimulated 3H-choline incorporation into SPC by both sexes, but the sex difference persisted. The optimal dose of T3 inhibited SPC synthesis by both sexes while dexamethasone was stimulatory. When T3 and dexamethasone were given together they had a greater effect than that of dexamethasone or T3 alone. Based on these results we conclude that the male deficit in pulmonary surfactant production may be overcome by the synergistic effects of T3 and dexamethasone.
此前有报道称,雄性兔胎儿肺成熟的形态学和功能指标延迟,且这些差异无法通过糖皮质激素治疗来克服。由于甲状腺激素也能刺激表面活性物质的产生,我们研究了三碘甲状腺原氨酸(T3)和地塞米松对20日龄雄性和雌性大鼠肺中饱和磷脂酰胆碱(SPC)合成的影响。对照雄性肺切片中3H-胆碱掺入SPC的量明显低于雌性;17日龄时进行手术显著刺激了两性3H-胆碱掺入SPC,但性别差异仍然存在。T3的最佳剂量抑制了两性的SPC合成,而地塞米松则具有刺激作用。当T3和地塞米松一起使用时,它们的作用比单独使用地塞米松或T3时更大。基于这些结果,我们得出结论,T3和地塞米松的协同作用可能克服雄性在肺表面活性物质产生方面的不足。