Santini F, Cortelazzi D, Baggiani A M, Marconi A M, Beck-Peccoz P, Chopra I J
Department of Medicine, University of California, Los Angeles 90024.
J Clin Endocrinol Metab. 1993 Jun;76(6):1583-7. doi: 10.1210/jcem.76.6.8501166.
We have studied T3 sulfate (T3S) levels, blindly, in coded plasma samples from 21 normal and 3 hypothyroid fetuses at different stages of gestation (19-42 weeks). Fetal plasma samples were obtained by cordocentesis. T3S was detectable in all samples studied, with values ranging from 50-294 (mean +/- SD, 130 +/- 62 pmol/L). Plasma T3S was low (< 45 pmol/L) in all 4 normal adult control subjects studied simultaneously; serum T3S ranged from less than 20 to 130 in another set of 18 control subjects (mean +/- SD, 63 +/- 32 pmol/L). Fetal T3S values were positively correlated with gestational age (r = 0.43; P < 0.05), but not with free T4 (FT4), FT3, or TSH values. In the 3 hypothyroid fetuses at 31, 38, and 40 weeks gestation, respectively, plasma TSH was elevated (26, 98, and 24 mU/L, respectively), FT4 was low (10, 6.7, and 7.5 pmol/L, respectively), and FT3 was normal or high (3.2, 8.2, and 2.2 pmol/L, respectively). However, T3S values in hypothyroid fetuses (88, 133, and 252 pmol/L, respectively) were similar to those in normal fetuses at corresponding gestational ages. We conclude that 1) T3S is detectable in fetal circulation from at least 19 weeks gestation, and its concentration increases with fetal-age; 2) plasma T3S concentrations in the fetus at 19-40 weeks gestation are at least comparable to but generally higher than those in the adult; and 3) plasma T3S levels in hypothyroid fetuses are similar to those in normal fetuses. Recent studies demonstrating the ability of some fetal rat tissues (e.g. cerebral cortex) to desulfate T3S to T3 have suggested a possible role of T3S as a source of T3. Normal T3S in fetal hypothyroidism suggests that T3S may contribute to attenuation of the effects of hypothyroidism during intrauterine life.
我们对来自21例正常胎儿和3例甲状腺功能减退胎儿(妊娠19 - 42周不同阶段)的编码血浆样本进行了T3硫酸盐(T3S)水平的盲法研究。胎儿血浆样本通过脐静脉穿刺获取。在所研究的所有样本中均可检测到T3S,其值范围为50 - 294(均值±标准差,130±62 pmol/L)。同时研究的4例正常成年对照受试者的血浆T3S均较低(<45 pmol/L);另一组18例对照受试者的血清T3S范围为小于20至130(均值±标准差,63±32 pmol/L)。胎儿T3S值与胎龄呈正相关(r = 0.43;P < 0.05),但与游离T4(FT4)、FT3或促甲状腺激素(TSH)值无关。在分别处于妊娠31、38和40周的3例甲状腺功能减退胎儿中,血浆TSH升高(分别为26、98和24 mU/L),FT4降低(分别为10、6.7和7.5 pmol/L),FT3正常或升高(分别为3.2、8.2和2.2 pmol/L)。然而,甲状腺功能减退胎儿的T3S值(分别为88、133和252 pmol/L)与相应胎龄的正常胎儿相似。我们得出结论:1)至少从妊娠19周起,胎儿循环中即可检测到T3S,且其浓度随胎龄增加;2)妊娠19 - 40周胎儿的血浆T3S浓度至少与成年人相当,但通常高于成年人;3)甲状腺功能减退胎儿的血浆T3S水平与正常胎儿相似。最近的研究表明,一些胎鼠组织(如大脑皮层)能够将T3S脱硫酸化为T3,这提示T3S可能作为T3的一个来源发挥作用。胎儿甲状腺功能减退时T3S正常表明,T3S可能有助于减轻宫内生活期间甲状腺功能减退的影响。