Literature DB >> 849983

Extrathyroidal conversion of thyroxine to 3,3',5'-triiodothyronine (reverse-T3) and to 3,5,3'-triiodothyronine (T3) in humans.

L Gavin, J Castle, F McMahon, P Martin, M Hammond, R R Cavalieri.   

Abstract

In order to estimate the relative magnitude of the two alternative pathways of monodeiodination of thyroxine (T4) in adult humans, the metabolic clearance rates (MCR) and production rates (PR) of 3,3',5'-triiodothyronine (reverse-T3,rT3) and of 3,5,3'-triiodothyronine (T3) were determined in six euthyroid control subjects (C) and in five hypothyroid patients (H) receiving L-T4 as replacement therapy (0.15-0.3 mg/day). MCR was computed by a non-compartmental method of analysis from the plasma disappearance of 125I rT3 and 131I T3 during 72 h following simultaneous injection of tracers. PR was calculated from MCR and the serum concentration of rT3 and T3, respectively, determined by radioimmunoassay. In the H subjects, rT3 MCR averaged 97.1 +/- 12.8 (SD) 1/day and rT3 PR, 34.3 +/- 12.8 microng/day; T3 MCR was 28.7 +/- 6.1 1/day and T3 PR, 20.3 +/- 6.6 microng/day (all corrected to 70 kg body weight). These results were not significantly different from those in the control group; rT3 MCR 104 +/- 24 1/day, rT3 PR 33.0 +/- 9.2 microng/day; T3 MCR 24.0 +/- 5.9, T3 PR 24.2 +/- 4.1. The proportionof total triiodothyronine (rT3 averaged 62% in H patients and was similar (57%) in the C group. The results obtained in the H subjects indicate that the production of rT3 is a major route of T4 metabolism, equal to or exceeding that of T3. From the close agreement between the mean values for rT3 PR in the C and H groups it is concluded that most, if not all of the rT3 produced in normal humans is derived by extrathyroidal conversion from T4.

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Year:  1977        PMID: 849983     DOI: 10.1210/jcem-44-4-733

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  12 in total

1.  Hypothyroidism induced by continuous ambulatory peritoneal dialysis.

Authors:  L A Gavin; N F Eitan; R R Cavalieri; W R Schmidt
Journal:  West J Med       Date:  1983-04

2.  3,3'-Diiodothyronine production, a major pathway of peripheral iodothyronine metabolism in man.

Authors:  L A Gavin; M E Hammond; J N Castle; R R Cavalieri
Journal:  J Clin Invest       Date:  1978-05       Impact factor: 14.808

3.  L-triiodothyronine and L-reverse-triiodothyronine generation in the human polymorphonuclear leukocyte.

Authors:  K A Woeber
Journal:  J Clin Invest       Date:  1978-09       Impact factor: 14.808

4.  Thyroid function in patients with acute renal failure.

Authors:  D Bodziony; F Kokot; S Czekalski
Journal:  Int Urol Nephrol       Date:  1981       Impact factor: 2.370

5.  Peripheral tissue mechanism for maintenance of serum triiodothyronine values in a thyroxine-deficient state in man.

Authors:  S M Lum; J T Nicoloff; C A Spencer; E M Kaptein
Journal:  J Clin Invest       Date:  1984-02       Impact factor: 14.808

6.  The importance of reverse triiodothyronine in hypothyroid children on replacement treatment.

Authors:  M Desai; A J Irani; K Patil; C S Pandya
Journal:  Arch Dis Child       Date:  1984-01       Impact factor: 3.791

7.  Low serum 3, 5, 3'-triiodothyronine (T3) and raised 3, 3', 5'-triidothyronine (reverse T3 or RT3) in diabetes mellitus: normalization on improvement in hyperglycemia.

Authors:  U M Kabadi; B N Premachandra; M Maayan
Journal:  Acta Diabetol Lat       Date:  1982 Jul-Sep

8.  Dietary modification of thyroxine deiodination in rat liver is not mediated by hepatic sulfhydryls.

Authors:  L A Gavin; F A McMahon; M Moeller
Journal:  J Clin Invest       Date:  1980-04       Impact factor: 14.808

9.  Isomeric discrimination and quantification of thyroid hormones, T3 and rT3, by the single ratio kinetic method using electrospray ionization mass spectrometry.

Authors:  Avvaru Praveen Kumar; Hua Jin; Sung-Chan Jo; Changdae Kim; Sang-Ho Nam; Yong-Ill Lee
Journal:  J Am Soc Mass Spectrom       Date:  2009-07-14       Impact factor: 3.109

10.  Ether link cleavage is the major pathway of iodothyronine metabolism in the phagocytosing human leukocyte and also occurs in vivo in the rat.

Authors:  A G Burger; D Engler; U Buergi; M Weissel; G Steiger; S H Ingbar; R E Rosin; B M Babior
Journal:  J Clin Invest       Date:  1983-04       Impact factor: 14.808

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