Trans-Placental Transfer of Thirteen Perfluorinated Compounds and Relations with Fetal Thyroid Hormones

2011 ◽  
Vol 45 (17) ◽  
pp. 7465-7472 ◽  
Author(s):  
Sunmi Kim ◽  
Kyungho Choi ◽  
Kyunghee Ji ◽  
Jihyeon Seo ◽  
Younglim Kho ◽  
...  
Cancers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 2693
Author(s):  
Gabriella Schiera ◽  
Carlo Maria Di Liegro ◽  
Italia Di Liegro

The development and maturation of the mammalian brain are regulated by thyroid hormones (THs). Both hypothyroidism and hyperthyroidism cause serious anomalies in the organization and function of the nervous system. Most importantly, brain development is sensitive to TH supply well before the onset of the fetal thyroid function, and thus depends on the trans-placental transfer of maternal THs during pregnancy. Although the mechanism of action of THs mainly involves direct regulation of gene expression (genomic effects), mediated by nuclear receptors (THRs), it is now clear that THs can elicit cell responses also by binding to plasma membrane sites (non-genomic effects). Genomic and non-genomic effects of THs cooperate in modeling chromatin organization and function, thus controlling proliferation, maturation, and metabolism of the nervous system. However, the complex interplay of THs with their targets has also been suggested to impact cancer proliferation as well as metastatic processes. Herein, after discussing the general mechanisms of action of THs and their physiological effects on the nervous system, we will summarize a collection of data showing that thyroid hormone levels might influence cancer proliferation and invasion.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Lin Yang ◽  
Jingguang Li ◽  
Jianqiang Lai ◽  
Hemi Luan ◽  
Zongwei Cai ◽  
...  

PEDIATRICS ◽  
1965 ◽  
Vol 35 (5) ◽  
pp. 743-752
Author(s):  
Marvin A. Schultz ◽  
Jean B. Forsander ◽  
Ronald A. Chez ◽  
Donald L. Hutchinson

The placental transfer of I131-labeled triiodothyronine has been studied in Rhesus monkeys. The majority of maternal to fetal placental transfer of radioactivity was in the form of iodide and a chemically unrecognized compound on chromatograms. Only traces of triiodothyronine or thyroxine were detected. In the fetal to maternal transfer studies, triiodothyronine was more readily transferred into the maternal circulation with small amounts of iodide and a similar unknown compound appearing. This substance may be sulfate conjugated triiodothyronine. There was a considerably higher concentration gradient used in the fetal to maternal transfers than in the reverse direction. The implications of this gradient difference are discussed. The data from this study add further evidence to the clinical experience that maternal thyroid hormones are not readily available to meet all of the fetal needs during the latter part of pregnancy.


PEDIATRICS ◽  
1975 ◽  
Vol 55 (4) ◽  
pp. 497-499
Author(s):  
Richard M. Cowett ◽  
Leo Stern

In order to establish whether maternal thyroid hormones cross the placenta and produce surfactant in the fetus, possibly reducing the incidence of respiratory distress syndrome (RDS), a retrospective analysis of low-birthweight infants was undertaken. Results indicate that maternal thyroid hormones play a negligible role and that any thyroid mediation would result from fetal thyroid activity.


2012 ◽  
Vol 215 (2) ◽  
pp. 216-219 ◽  
Author(s):  
Kristine Bjerve Gützkow ◽  
Line Småstuen Haug ◽  
Cathrine Thomsen ◽  
Azemira Sabaredzovic ◽  
Georg Becher ◽  
...  

1997 ◽  
Vol 82 (9) ◽  
pp. 3099-3102 ◽  
Author(s):  
R. H. Mortimer ◽  
G. R. Cannell ◽  
R. S. Addison ◽  
L. P. Johnson ◽  
M. S. Roberts ◽  
...  

Abstract Propylthiouracil (PTU) is widely believed to cross the placenta less freely than methimazole (MMI) and is therefore regarded as the preferred drug for treatment of hyperthyroidism in pregnancy. Clinical studies comparing the two drugs show, however, no differences in maternal or fetal thyroid function. We investigated transfer from the maternal to the fetal circuit in the isolated perfused term human placental lobule of low and high doses of PTU (4 μg/mL and 40μ g/mL) and MMI (1.5 μg/mL and 15 μg/mL) in protein-free perfusate and low doses of both drugs with addition of 40 g/L of bovine albumin. Both drugs readily crossed the placenta, reaching equilibrium in all experiments in about 2 h. Drug concentrations in the two circuits fitted a two compartmental model. Transfer kinetics for the two drugs were similar, nonsaturable, and unaffected by addition of albumin. Clearances (mL·min−1·g−1, means ± sd) of PTU from maternal to fetal circuits were: 0.229± 0.110, 0.216 ± 0.065, and 0.170 ± 0.032; and for transfer of MMI: 0.165 ± 0.025, 0.232 ± 0.153, and 0.174 ± 0.009 (for low doses without, low doses with, and high doses without albumin, respectively). Clearances of PTU from fetal to maternal circuits were: 0.147 ± 0.072, 0.109 ± 0.014, and 0.116 ± 0.028; and for transfer of MMI: 0.095 ± 0.029, 0.122 ± 0.088, and 0.12 ± 0.005 (in the same experiments). There was no significant difference between drugs or drug doses and no effect of addition of albumin. We conclude that PTU and MMI have similar placental transfer kinetics.


PEDIATRICS ◽  
1962 ◽  
Vol 29 (6) ◽  
pp. 961-967
Author(s):  
R. W. Chandler ◽  
M. A. Kyle ◽  
W. Hung ◽  
Robert M. Blizzard

Studies were undertaken to determine whether cretinism could be produced in rabbits born to immunized does with autoimmune thyroditis. Although anti-thyroid antibodies crossed the placenta of the rabbit and disappeared from the serum of the neonates by 7 weeks of age, the growth curves and thyroid histology of the newborns were normal. Passive immunization of normal does at 20 and 21 days of gestation was not associated with placental transfer of antibodies although transfer occurred at 30 days gestation. The possibility that the short time interval of exposure of the fetal thyroid to antibodies accounted for the failure of thyroid damage to occur was investigated. The role of cellular antibodies was also investigated by injecting lymphoid cells from immunized adult rabbits into newborns. No thyroid damage or serum antibodies were produced. The possible explanations for failure to obtain thyroid damage by circulating antibodies in newborn rabbits are discussed.


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