| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
ARTICLES |
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, 05508900 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.
This article has been cited by other articles:
![]() |
M. A. Christoffolete, C. C.G. Linardi, L. de Jesus, K. N. Ebina, S. D. Carvalho, M. O. Ribeiro, R. Rabelo, C. Curcio, L. Martins, E. T. Kimura, et al. Mice with Targeted Disruption of the Dio2 Gene Have Cold-Induced Overexpression of the Uncoupling Protein 1 Gene but Fail to Increase Brown Adipose Tissue Lipogenesis and Adaptive Thermogenesis Diabetes, March 1, 2004; 53(3): 577 - 584. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. Bianco, D. Salvatore, B. Gereben, M. J. Berry, and P. R. Larsen Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases Endocr. Rev., February 1, 2002; 23(1): 38 - 89. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Curcio, A. M. Lopes, M. O. Ribeiro, O. A. Francoso Jr., S. D. Carvalho, F. B. Lima, J. E. Bicudo, and A. C. Bianco Development of Compensatory Thermogenesis in Response to Overfeeding in Hypothyroid Rats Endocrinology, August 1, 1999; 140(8): 3438 - 3443. [Abstract] [Full Text] |
||||
![]() |
D. Salvatore, T. Bartha, and P. R. Larsen The Guanosine Monophosphate Reductase Gene Is Conserved in Rats and Its Expression Increases Rapidly in Brown Adipose Tissue during Cold Exposure J. Biol. Chem., November 20, 1998; 273(47): 31092 - 31096. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |