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Endocrinology Vol. 139, No. 2 571-578
Copyright © 1998 by The Endocrine Society


ARTICLES

Thyroxine 5'-Deiodination Mediates Norepinephrine-Induced Lipogenesis in Dispersed Brown Adipocytes1

Antonio C. Bianco, Suzy D. Carvalho, Celso R. F. Carvalho, Rogério Rabelo and Anselmo S. Moriscot

Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil

Address all correspondence and requests for reprints to: Antonio C. Bianco, M.D., Ph.D., Departamento de Fisiologia e Biofísica, ICB-USP, Avenida Prof. Lineu Prestes 1524, 05508–900 Sao Paulo, Sao Paulo, Brazil. E-mail: acbianco{at}usp.br

In euthyroid rats, maximal sympathetic nervous system stimulation (e.g. during cold exposure) results in a 3- to 4-fold increase in brown adipose tissue lipogenesis, a response that is blunted in hypothyroid rats. To further investigate this phenomenon, the role of local type II 5'-deiodinase (5'-DII) was studied in freshly isolated brown adipocytes. In a typical experiment, 1.5 x 106 cells were incubated for up to 48 h in a water-saturated 5% CO2-95% O2 atmosphere. After incubation with medium alone or with different concentrations of T4, T3, and/or norepinephrine (NE), lipogenesis was studied by measuring 1) the rate of fatty acid synthesis as reflected by 3H2O incorporation into lipids and 2) the activity of key rate-limiting enzymes, i.e. acetyl coenzyme A carboxylase and malic enzyme, and the results are reported in terms of DNA content per tube. Lipogenesis decreased progressively over time (~40%) when no additions were made to the incubation medium. T4 or T3 partially prevented that inhibition at physiological concentrations (65 x 10-9 and 0.77 x 10-9 M, respectively), whereas a receptor-saturating concentration of T3 (154 x 10-9 M) doubled the lipogenesis rate. The addition of 10-6 M NE inhibited lipogenesis acutely (~50% by 12 h) and was followed by a progressive stimulation that reached ~2-fold by 48 h, but only in the presence of T4. Furthermore, NE did not attenuate T3 (154 x 10-9 M)-induced lipogenesis. Both the inhibition and the stimulation of lipogenesis caused by NE showed a strong dose-response relationship within the range of 10-11-10-5 M. The role of local 5'-DII was further tested by incubating brown adipocytes with 10-6 M NE and T4 (65 x 10-9 M) in the presence of 100 µM iopanoic acid, a potent inhibitor of 5'-DII. Although iopanoic acid did not affect the T3 stimulation of lipogenesis, it did block the ~2-fold stimulation of lipogenesis triggered by NE in the presence of T4, confirming the mediation of 5'-DII in this process. In conclusion, lipogenesis in brown adipose tissue is under complex hormonal control, with key roles played by NE, thyroid hormones, and local 5'-DII. As in other tissues, NE-generated signals acutely (12 h) inhibited lipogenesis. However, the presence of the 5'-DII generated enough T3 to stimulate lipogenesis and gradually reverse the short-lived NE-induced inhibition, leading to the 2- to 3-fold response observed at later time points.




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