Pollard I, Murray J F, Hiller R, Scaramuzzi R J, Wilson C A
School of Biological Sciences, Macquarie University, Sydney, New South Wales, Australia.
J Matern Fetal Med. 1999 Sep-Oct;8(5):220-4. doi: 10.1002/(SICI)1520-6661(199909/10)8:5<220::AID-MFM4>3.0.CO;2-W.
A previous study demonstrated for the first time that a drug such as caffeine, administered prior to ovulation and genomic activation, causes a quantitative difference in growth-promoting energy utilization in a proportion of 5-day-old blastocysts. The objective of the present study was to investigate whether developmental changes induced by caffeine administered throughout the estrus cycle prior to fertilization are sustained throughout pregnancy and after birth.
Caffeine was administered to rats throughout the estrus cycle prior to fertilization, with control and experimental groups subdivided into preimplantation and postimplantation categories. Preimplantation fertilization rate was assessed on day 4 of pregnancy by a pregnancy-induced elevation in maternal plasma progesterone concentration, or by flushing each uterine horn on day 5 of pregnancy to determine the presence or absence of a litter. Postimplantation fetuses were collected on gestational day 12 or allowed to go to term.
Preconceptual caffeine exposure significantly reduced maternal fertility by the failure of a proportion of the litters to implant, rather than curtailing preimplantation development or postimplantation losses. Postnatal mortality between weeks 0 and 1 was elevated and the weekly incremental growth rate of the pups from week 3 through week 7 was significantly reduced in the preconceptually caffeine-treated offspring. Experimental females reached puberty at the same age as the controls but at a significantly lower body weight. Gestation length, hirthweight, litter size, sex ratio, and anogenital distance (a measure of prenatal androgenization) were not affected by preconceptual caffeine treatment.
It was concluded that the reduced fertility rate in preconceptually caffeine-exposed rats was due to the failure of litters to implant rather than to a reduced fertilization rate, which was normal. It was further concluded that the growth rate over the neonatal and prepubertal periods of surviving pups in the caffeine-treated group was subnormal.
先前的一项研究首次表明,在排卵和基因组激活之前给予咖啡因等药物,会使一部分5日龄囊胚在促进生长的能量利用上产生数量差异。本研究的目的是调查在受精前整个发情周期给予咖啡因所诱导的发育变化在整个孕期及出生后是否持续存在。
在受精前的整个发情周期给大鼠施用咖啡因,将对照组和实验组再细分为植入前和植入后类别。通过妊娠诱导的母体血浆孕酮浓度升高来评估妊娠第4天的植入前受精率,或者在妊娠第5天冲洗每个子宫角以确定是否有一窝幼崽。在妊娠第12天收集植入后的胎儿,或者让其足月出生。
受孕前接触咖啡因会显著降低母体生育力,原因是一部分幼崽未能着床,而非抑制植入前发育或植入后损失。在受孕前接受咖啡因处理的后代中,0至1周龄的产后死亡率升高,3至7周龄幼崽的每周生长增量率显著降低。实验雌性大鼠与对照组在相同年龄达到青春期,但体重显著较低。受孕前咖啡因处理对妊娠期长度、出生体重、窝仔数、性别比例和肛门生殖器距离(产前雄激素化的一种度量)没有影响。
得出的结论是,受孕前接触咖啡因的大鼠生育率降低是由于幼崽未能着床,而非受精率降低,受精率是正常的。进一步得出的结论是,咖啡因处理组中存活幼崽在新生儿期和青春期前的生长速度低于正常水平。