Type II and type III deiodinase activity in human placenta as a function of gestational age

被引:118
作者
KoopdonkKool, JM
deVijlder, JJM
Veenboer, GJM
RisStalpers, C
Kok, JH
Vulsma, T
Boer, K
Visser, TJ
机构
[1] UNIV AMSTERDAM, ACAD MED CTR, DEPT PEDIAT & NEONATOL, 1100 DE AMSTERDAM, NETHERLANDS
[2] UNIV AMSTERDAM, ACAD MED CTR, DEPT EXPT PEDIAT ENDOCRINOL, 1100 DE AMSTERDAM, NETHERLANDS
[3] UNIV AMSTERDAM, ACAD MED CTR, DEPT OBSTET & GYNECOL, 1100 DE AMSTERDAM, NETHERLANDS
[4] ERASMUS UNIV ROTTERDAM, SCH MED, DEPT INTERNAL MED 3, 3000 DR ROTTERDAM, NETHERLANDS
关键词
D O I
10.1210/jc.81.6.2154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thyroid hormones are essential for fetal development. T-4 can be activated by type I (ID-I) and type II (ID-II) iodothyronine deiodinase or inactivated by type III deiodinase (ID-III). The influence of placental ID-II and ID-III on the regulation of fetal thyroid hormone levels was investigated. Using [I-125]T-4 and [I-125]T-3, respectively, ID-II and ID-III activities were measured in homogenates of normal human placentas from 6-43 weeks gestational age and in placentas from five term neonates with a total thyroid hormone synthesis defect; ID-II and ID-III activities related to protein or DNA concentration decreased and total placental ID-III activity increased significantly during pregnancy, whereas the increase in total placental ID-II activity was not significant. Absolute placental ID-Il activity was approximately 200 times lower than ID-III activity at all gestational ages. Therefore, fluctuations in ID-II activity were not likely to have a significant influence on Fetal thyroid hormone concentrations, but may play a role in the regulation of intraplacental T-3 generation. The high ID-III activity most likely influences the thyroid hormone economy of the fetus. Severely hypothyroid newborns showed strongly decreased serum T-4 levels, but serum T-3 and placental ID-III activities were similar to those in euthyroid newborns. These results suggest that placental ID-ID activity is regulated by serum T-3, but not by serum T-3.
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页码:2154 / 2158
页数:5
相关论文
共 45 条
[1]  
ASHITAKA Y, 1988, ENDOCRINOL JAPON, V35, P197
[2]   CONVERSION OF THYROXINE TO TRIIODOTHYRONINE AND REVERSE TRIIODOTHYRONINE IN HUMAN-PLACENTA AND FETAL MEMBRANES [J].
BANOVAC, K ;
BZIK, L ;
TISLARIC, D ;
SEKSO, M .
HORMONE RESEARCH, 1980, 12 (05) :253-259
[3]   THE IODOTHYRONINE DEIODINASES AND 5'-DEIODINATION [J].
BECKETT, GJ ;
ARTHUR, JR .
BAILLIERES CLINICAL ENDOCRINOLOGY AND METABOLISM, 1994, 8 (02) :285-304
[4]   IDENTIFICATION OF 5 NOVEL INACTIVATING MUTATIONS IN THE HUMAN THYROID PEROXIDASE GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS [J].
BIKKER, H ;
VULSMA, T ;
BAAS, F ;
DEVIJLDER, JJM .
HUMAN MUTATION, 1995, 6 (01) :9-16
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]  
BRZEZINSKASLEBODZINSKA E, 1989, J DEV PHYSIOL, V11, P351
[7]  
BURROW GN, 1994, NEW ENGL J MED, V331, P1072
[9]   SELENIUM DEFICIENCY AND TYPE-II 5'-DEIODINASE REGULATION IN THE EUTHYROID AND HYPOTHYROID RAT - EVIDENCE OF A DIRECT EFFECT OF THYROXINE [J].
CHANOINE, JP ;
SAFRAN, M ;
FARWELL, AP ;
TRANTER, P ;
EKENBARGER, DM ;
DUBORD, S ;
ALEX, S ;
ARTHUR, JR ;
BECKETT, GJ ;
BRAVERMAN, LE ;
LEONARD, JL .
ENDOCRINOLOGY, 1992, 131 (01) :479-484
[10]   THYROID-HORMONES IN TISSUES FROM HUMAN EMBRYOS AND FETUSES [J].
COSTA, A ;
ARISIO, R ;
BENEDETTO, C ;
BERTINO, E ;
FABRIS, C ;
GIRAUDI, G ;
MAROZIO, L ;
MAULA, V ;
PAGLIANO, M ;
TESTORI, O ;
ZOPPETTI, G .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1991, 14 (07) :559-568