Horm Metab Res 1984; 16(9): 471-474
DOI: 10.1055/s-2007-1014822
Basic

© Georg Thieme Verlag, Stuttgart · New York

The Effect of Adrenaline Pretreatment on the In Vitro Generation of 3,5,3′-Triiodothyronine and 3,3′,5′-Triiodothyronine (Reverse T3) in Rat Liver Preparation

A. Nauman1 , S. Porta2 , U. Bardowska1 , K. Fiedorowicz1 , A. Sadjak2 , W. Korsatko2 , J. Nauman1
  • 1Department of Biochemistry, Medical Center of Postgraduate Education, Warsaw, Poland
  • 2Department of Functional Pathology, University of Graz, Austria
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Publication History

1982

1983

Publication Date:
14 March 2008 (online)

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Summary

The effects of adrenaline (A) on liver T3 and rT3 neogenesis from T4 were studied in Wistar rats. The animals were implanted subcutaneously either with A or placebo (P) especially coated tablets which linearly released the hormone. The serum A values 6 hrs after implantation of 7.5, 15.0 and 45.0 mg tablets were 6.5 ± 1.31, 6.8 ± 1.8 and 16.4 ± 1.9 ng/ml, respectively vs 4.4 ± 2.5 ng/ml seen in P pretreated group. The output rates of A were 0.11 (7.5 mg), 0.18 (15 mg) and 0.52 μg/ml (45 mg). The pretreatment with A led to hyperglycemia and the “low T3 syndrome”. Neogenesis of T3 from T4 in medium containing liver microsomes of P pretreated rats was 5.49 ± 0.25 pmol of T3/mg protein/min and decreased in A pretreated rats to 3.82 ± 0.17, 3.12 ± 0.27 and 3.06 ± 0.11 pmol of T3/mg of protein/min. Neogenesis of rT3 from T4 in microsomes from P group was 1.52 ± 0.09 pmol rT3/mg protein/min and increased after A to 2.71 ± 0.11, 2.60 ± 0.21 and 2.21 ± 0.34 pmol of rT3/mg protein/min thus showing no dose dependency. Enrichment of microsomes medium with cytosol either from P or A pretreated rats had no effect on T3 generation thus excluding effect of A on cytosolic cofactor. Although cytosol further increased rT3 neogenesis this was seen regardless of whether cytosol was obtained from A or P implanted rats. It is concluded that A decreases the activity of T4-5′-deiodinase in liver, and possibly increases the activity of T4-5-deiodinase.