Stewart J D, Gonzalez C L, Christensen H D, Rayburn W F
Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City 73190, USA.
Am J Obstet Gynecol. 1997 Nov;177(5):1138-44. doi: 10.1016/s0002-9378(97)70030-9.
Our purpose was to determine in a randomized, placebo-controlled manner whether multiple antenatal doses of betamethasone affect long-term growth and development of exposed mouse offspring.
Sixty pregnant CD-1 mice received either two, four, or eight antepartum doses of 0.1 mg betamethasone or placebo. Perinatal outcomes, growth, and development of the offspring were compared in a blinded manner. Variables were compared by analysis of variance or chi 2 testing.
Betamethasone-exposed subjects gained less weight during pregnancy and were delivered of fewer live pups, with fewer male survivors and lower birth weights. These trends were dose related. Growth measurements were similar after the neonatal period. No differences in functional development and physical maturation in the offspring were noted. The reproductive capability, perinatal outcomes, and growth and development of the second-generation offspring were unaffected by betamethasone exposure.
Multiple antenatal dosings of betamethasone, reaching toxic levels, did not have an impact on the long-term growth and development of the surviving mouse offspring.
我们旨在以随机、安慰剂对照的方式确定产前多次给予倍他米松是否会影响暴露的小鼠后代的长期生长和发育。
60只怀孕的CD-1小鼠接受了0.1毫克倍他米松或安慰剂的两次、四次或八次产前剂量。以盲法比较后代的围产期结局、生长和发育情况。通过方差分析或卡方检验比较变量。
暴露于倍他米松的小鼠在怀孕期间体重增加较少,活产幼崽数量较少,雄性存活者较少且出生体重较低。这些趋势与剂量相关。新生儿期后生长测量结果相似。未观察到后代功能发育和身体成熟的差异。倍他米松暴露对第二代后代的生殖能力、围产期结局以及生长和发育没有影响。
产前多次给予达到中毒水平的倍他米松对存活的小鼠后代的长期生长和发育没有影响。