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甲状腺激素在脑早期发育过程中的作用。

Role of thyroid hormone during early brain development.

作者信息

Morreale de Escobar Gabriella, Obregon María Jesús, Escobar del Rey Francisco

机构信息

Instituto de Investigaciones Biomedicas Alberto Sols, Consejo Superior de Investigaciones Cientificas (CSIC) y Universidad Autonoma de Madrid (UAM), Arturo Duperier, 4, 28029-Madrid, Spain.

出版信息

Eur J Endocrinol. 2004 Nov;151 Suppl 3:U25-37. doi: 10.1530/eje.0.151u025.

Abstract

The present comments are restricted to the role of maternal thyroid hormone on early brain development, and are based mostly on information presently available for the human fetal brain. It emphasizes that maternal hypothyroxinemia - defined as thyroxine (T4) concentrations that are low for the stage of pregnancy - is potentially damaging for neurodevelopment of the fetus throughout pregnancy, but especially so before midgestation, as the mother is then the only source of T4 for the developing brain. Despite a highly efficient uterine-placental 'barrier' to their transfer, very small amounts of T4 and triiodothyronine (T3) of maternal origin are present in the fetal compartment by 4 weeks after conception, with T4 increasing steadily thereafter. A major proportion of T4 in fetal fluids is not protein-bound: the 'free' T4 (FT4) available to fetal tissues is determined by the maternal serum T4, and reaches concentrations known to be of biological significance in adults. Despite very low T3 and 'free' T3 (FT3) in fetal fluids, the T3 generated locally from T4 in the cerebral cortex reaches adult concentrations by midgestation, and is partly bound to its nuclear receptor. Experimental results in the rat strongly support the conclusion that thyroid hormone is already required for normal corticogenesis very early in pregnancy. The first trimester surge of maternal FT4 is proposed as a biologically relevant event controlled by the conceptus to ensure its developing cerebral cortex is provided with the necessary amounts of substrate for the local generation of adequate amounts of T3 for binding to its nuclear receptor. Women unable to increase their production of T4 early in pregnancy would constitute a population at risk for neurological disabilities in their children. As mild-moderate iodine deficiency is still the most widespread cause of maternal hypothyroxinemia in Western societies, the birth of many children with learning disabilities may already be preventable by advising women to take iodine supplements as soon as pregnancy starts, or earlier if possible.

摘要

本评论仅限于母体甲状腺激素在早期脑发育中的作用,且主要基于目前人类胎儿大脑的现有信息。它强调,母体甲状腺素血症(定义为孕期甲状腺素(T4)浓度低于相应孕周水平)在整个孕期对胎儿神经发育都有潜在损害,尤其是在妊娠中期之前,因为此时母亲是发育中大脑唯一的T4来源。尽管存在高效的子宫 - 胎盘“屏障”阻止其转移,但受孕后4周时,胎儿体内就已存在极少量母体来源的T4和三碘甲状腺原氨酸(T3),此后T4稳步增加。胎儿体液中大部分T4未与蛋白质结合:胎儿组织可利用的“游离”T4(FT4)由母体血清T4决定,并达到已知对成年人具有生物学意义的浓度。尽管胎儿体液中T3和“游离”T3(FT3)含量极低,但大脑皮质中由T4局部生成的T3在妊娠中期达到成人浓度,并部分与其核受体结合。大鼠实验结果有力支持了这样的结论:甲状腺激素在妊娠早期就已对正常皮质发生是必需的。有人提出,妊娠早期母体FT4的激增是由受精卵控制的一个生物学相关事件,以确保其发育中的大脑皮质获得足够的底物,用于局部生成足够量的T3以与其核受体结合。孕期无法在早期增加T4分泌的女性,其子女有患神经功能障碍的风险。由于轻度至中度碘缺乏仍是西方社会母体甲状腺素血症最普遍的原因,通过建议女性一旦怀孕就开始补充碘,若可能则更早补充,许多有学习障碍儿童的出生或许已经可以预防。

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