DECREASED PERIPHERAL 3,5,3'-TRIIODOTHYRONINE (T-3) PRODUCTION FROM THYROXINE (T-4) - A SYNDROME OF IMPAIRED THYROID-HORMONE ACTIVATION DUE TO TRANSPORT INHIBITION OF T-4-PRODUCING INTO T-3-PRODUCING TISSUES

Citation
G. Hennemann et al., DECREASED PERIPHERAL 3,5,3'-TRIIODOTHYRONINE (T-3) PRODUCTION FROM THYROXINE (T-4) - A SYNDROME OF IMPAIRED THYROID-HORMONE ACTIVATION DUE TO TRANSPORT INHIBITION OF T-4-PRODUCING INTO T-3-PRODUCING TISSUES, The Journal of clinical endocrinology and metabolism, 77(5), 1993, pp. 1431-1435
Citations number
15
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
0021972X
Volume
77
Issue
5
Year of publication
1993
Pages
1431 - 1435
Database
ISI
SICI code
0021-972X(1993)77:5<1431:DP3(PF>2.0.ZU;2-Z
Abstract
T-4, rT(3), and T-3 kinetic studies have been performed in a T-4-subst ituted female who showed an increased serum T-4/T-3 ratio and substant ially increased rT(3) serum levels in the presence of normal serum thy roid hormone binding properties. The kinetic studies were performed to discriminate between T-4 transport inhibition into plasma T-3-produci ng tissues and inhibition of extrathyroidal T-4 to T-3 conversion. The principal findings were that both T-4 and rT(3) transport were inhibi ted into the rapid equilibrating pool (REP), which mainly consists of the liver. The plasma T-3 production rate was decreased. Despite an el evated serum free T-4 level, serum TSH was elevated, pointing to T-4 t ransport inhibition at the level of the thyrotroph as well. Transport of T-4 and rT(3) was normal to the slowly equilibrating pool, whereas no transport inhibition of T-3 was found to either pool. Because T-4 i nto T-3 conversion efficiency in the REP (the main source of plasma T- 3 production) was normal, it was concluded that the lowered T-3 produc tion in the subject was caused by transport inhibition of T-4 into the liver. Although the occurrence of the syndrome is rare, its significa nce is of general importance, in that it shows that transport of thyro id hormone may vary at the tissue level. Furthermore, as T-3 is the pr incipal biologically active thyroid hormone, regulation of transport o f T-4 into the REP may play a (patho)physiological role in the ultimat e determination of thyroid hormone activity in the tissues.