Papantoniou N E, Papapetrou P D, Antsaklis A J, Kontoleon P E, Mesogitis S A, Aravantinos D
First Department of Obstetrics and Gynecology, Alexandra State and University Maternity Hospital, Athens, Greece.
Eur J Endocrinol. 1996 Apr;134(4):437-42. doi: 10.1530/eje.0.1340437.
Undetectable or extremely low levels of circulating immunoreactive parathyroid hormone (PTH) have been reported in human newborns while PTH bioactivity was high. This prompted the hypothesis that the fetal calcemic hormone might be PTH-related protein. The purpose of this study was to measure circulating immunoreactive PTH-related protein in human fetuses and newborns in order to investigate this hypothesis. Parathyroid hormone-related protein (PTHrP(1-86) and intact PTH were measured using two-site immunoradiometric assays in plasma obtained by cordocentesis from 23 fetuses (19-33 weeks of gestation), from 17 newborns at term (38-41 weeks), from their mothers and from 22 normal women of reproductive age. Plasma PTHrP was detectable in all but one of the fetuses and newborns and in all the mothers and the controls. The mean level was similar among fetuses (19-33 weeks) (0.43 +/- 0.18 pmol/l), newborns (0.48 +/- 0.12), mothers (0.48 +/- 0.14) and normal controls (0.46 +/- 0.09). Plasma PTH was found to be significantly higher in fetuses at midgestation (1.0 +/- 0.99 pmol/l) than in the newborns (0.22 +/- 0.21) (p < 0.0025); maternal PTH was significantly higher compared to fetal level at mid-gestation (2.1 +/- 1.0, p < 0.01) as well as at term (2.69 +/- 1.40, p < 0.001). In the control women PTH was 3.07 +/- 1.25 pmol/l. These results showed that plasma amino-terminal PTHrP-(1-86) is detectable during the second half of human fetal life and its level remains unchanged during this period of time, in contrast to changing levels of fetal plasma PTH. The relatively low PTHrP-(1-86) level that we found in the newborns is not responsible for the high PTH-like bioactivity found by some investigators in cord blood at term.
据报道,人类新生儿循环中的免疫反应性甲状旁腺激素(PTH)水平检测不到或极低,而PTH生物活性却很高。这引发了一个假说,即胎儿血钙调节激素可能是甲状旁腺激素相关蛋白(PTHrP)。本研究的目的是测量人类胎儿和新生儿循环中的免疫反应性PTHrP,以验证这一假说。采用双位点免疫放射分析方法,对23例胎儿(妊娠19 - 33周)、17例足月新生儿(38 - 41周)、他们的母亲以及22例正常育龄妇女经脐静脉穿刺获取的血浆中的甲状旁腺激素相关蛋白(PTHrP(1 - 86))和完整PTH进行检测。除1例胎儿外,所有胎儿、新生儿以及所有母亲和对照组的血浆PTHrP均可检测到。胎儿(19 - 33周)(0.43±0.18 pmol/L)、新生儿(0.48±0.12)、母亲(0.48±0.14)和正常对照组(0.46±0.09)的平均水平相似。发现妊娠中期胎儿的血浆PTH(1.0±0.99 pmol/L)显著高于新生儿(0.22±0.21)(p < 0.0025);母亲的PTH在妊娠中期(2.1±1.0,p < 0.01)以及足月时(2.69±1.40,p < 0.001)均显著高于胎儿水平。对照组女性的PTH为3.07±1.25 pmol/L。这些结果表明,在人类胎儿生命的后半期可检测到血浆氨基端PTHrP-(1 - 86),且在此期间其水平保持不变,这与胎儿血浆PTH水平的变化形成对比。我们在新生儿中发现的相对较低的PTHrP-(1 - 86)水平并非一些研究者在足月脐血中发现的高PTH样生物活性的原因。