Adrenergic activation of triiodothyronine production in brown adipose tissue

doi:doi:10.1038/305712a0

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Nature 305, 712 - 713 (20 October 1983); doi:10.1038/305712a0

Adrenergic activation of triiodothyronine production in brown adipose tissue

J. E. Silva & P. R. Larsen

Howard Hughes Medical Institute Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA

There are several mechanisms by which homeothermic animals increase heat production, including shivering, sympathetic nervous system activation and stimulation of thyroid hormone secretion. Studies in rats have shown that increased sympathetic activity causes increased heat production in brown adipose tissue (BAT) after cold exposure or food ingestion¹⁻³. Acute cold exposure also increases circulating thyroid hormones⁴ which in turn stimulate cellular metabolism through induction⁵ of various enzymes. Most metabolic effects of thyroxine (T₄) are thought to be due to the triiodothyronine (T₃) which is produced from T₄ by a process of 5' monodeiodination. There are two enzymes responsible for this reaction⁶⁻⁸: type I, or propylthiouracil (PTU)-sensitive iodothyronine deiodinase (5'D-I), which is reduced in hypothyroidism, stimulated in hyperthyroidism and probably provides most of the circulating T₃ in the adult rat⁹. Type II 5'-deiodinase (5'D-II) is characteristic of brain and pituitary, is increased by thyroidectomy, is not inhibited by PTU and provides 50−80% of the intraceUular T₃ in these two tissues. Recently, 5'D-II activity was identified in interscapular BAT¹⁰. As the sympathetic nervous system influences the metabolic activation of BAT, we have studied the effects of noradrenaline and acute cold exposure on BAT 5'D-II. We report here that both noradrenaline and cold exposure increase BAT 5'D-II through ₁-adrenergic receptors, whereas depletion of catecholamines with -methyl-p-tyrosine (MPT) prevents the effect of cold but not that of noradrenaline. These results suggest that the sympathetic nervous system may increase T₃ production in rats by stimulating BAT 5'D-II. By increasing metabolic rate, this rise in T₃ would enhance the thermogenic response to sympathetic stimulation.