DEMONSTRATION OF IN-VIVO METABOLIC EFFECTS OF 3,5-DI-IODOTHYRONINE

Citation
M. Cimmino et al., DEMONSTRATION OF IN-VIVO METABOLIC EFFECTS OF 3,5-DI-IODOTHYRONINE, Journal of Endocrinology, 149(2), 1996, pp. 319-325
Citations number
24
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00220795
Volume
149
Issue
2
Year of publication
1996
Pages
319 - 325
Database
ISI
SICI code
0022-0795(1996)149:2<319:DOIMEO>2.0.ZU;2-8
Abstract
The objective of the present study was to test in vivo the metabolic e ffects of 3,5-di-iodothyronine (3,5-T-2) in unanesthetized and unrestr ained male Sprague-Dawley rats. Amino acid and lipid metabolisms were investigated by breath tests using as tracers the C-13-carboxyl-labele d molecules of leucine, alpha-ketoisocaproic acid (KIC) and octanoic a cid, in four different groups of rats: hypothyroid animals (receiving propylthiouracil (PTU) and iopanoic acid), hypothyroid animals treated with either a daily i.p. injection of 3,5-T-2 (25 mu g/100 g body wei ght), or tri-iodothyronine (T-3) (1 mu g/100 g body weight), and contr ol euthyroid animals receiving equivalent volumes of the vehicle solut ions. Energy expenditure was measured by continuous monitoring of O-2 consumption and CO2 production in these different groups. Daily energy expenditure was decreased by 30% in PTU-treated rats. The chronic tre atments with 3,5-T-2 and T-3 restored daily energy expenditure to the control level. (CO2)-C-13 recovered in breath following the i.v. injec tion of octanoic acid-[1-C-13] was decreased in hypothyroid animals co mpared with control animals (P<0.05) and restored to control values by T-3 and 3,5-T-2 treatments. The (CO2)-C-13 recovered in breath after i.v. injection of leucine-[1-C-13] was increased in PTU-treated compar ed with control animals (P<0.05). Chronic treatment with either 3,5-T- 2 or T-3 restored 13CO(2) to control values. Excretion of (CO2)-C-13 r ecovered in breath following the i.v. injection of KIC-[1-C-13] was in creased in PTU-treated compared with control animals. Chronic treatmen ts with either 3,5-T-2 or Tg did not restore KIC decarboxylation. Thes e results suggest that 3,5-T-2 exerts metabolic effects on energy expe nditure, on both lipid beta-oxidation and leucine metabolism in hypoth yroid rats. We conclude that 3,5-T-2 is a metabolically active iodothy ronine.