Changes in sleeping and basal energy expenditure and substrate oxidation induced by short term thyroxin administration in man.

Details

Serval ID
serval:BIB_B538E192DD04
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Changes in sleeping and basal energy expenditure and substrate oxidation induced by short term thyroxin administration in man.
Journal
Obesity Research
Author(s)
Bracco D., Morin O., Liang H., Jéquier E., Burger A.G., Schutz Y.
ISSN
1071-7323 (Print)
ISSN-L
1071-7323
Publication state
Published
Issued date
05/1996
Volume
4
Number
3
Pages
213-219
Language
english
Notes
Publication types: Clinical Trial ; Journal Article
Publication Status: ppublish
Abstract
The present study was designed to explore the thermogenic effect of thyroid hormone administration and the resulting changes in nitrogen homeostasis. Normal male volunteers (n = 7) received thyroxin during 6 weeks. The first 3-week period served to suppress endogenous thyroid secretion (180 micrograms T4/day). This dose was doubled for the next 3 weeks. Sleeping energy expenditure (respiratory chamber) and BMR (hood) were measured by indirect calorimetry, under standardized conditions. Sleeping heart rate was continuously recorded and urine was collected during this 12-hour period to assess nitrogen excretion. The changes in energy expenditure, heart rate and nitrogen balance were then related to the excess thyroxin administered. After 3 weeks of treatment, serum TSH level fell to 0.15 mU/L, indicating an almost complete inhibition of the pituitary-thyroid axis. During this phase of treatment there was an increase in sleeping EE and sleeping heart rate, which increased further by doubling the T4 dose (delta EE: +8.5 +/- 2.3%, delta heart rate +16.1 +/- 2.2%). The T4 dose, which is currently used as a substitutive dose, lead to a borderline hyperthyroid state, with an increase in EE and heart rate. Exogenous T4 administration provoked a significant increase in urinary nitrogen excretion averaging 40%. It is concluded that T4 provokes an important stimulation of EE, which is mostly mediated by an excess protein oxidation.
Keywords
Adult, Body Composition/physiology, Calorimetry, Indirect, Carbohydrate Metabolism, Dose-Response Relationship, Drug, Energy Metabolism/drug effects, Energy Metabolism/physiology, Heart Rate/drug effects, Heart Rate/physiology, Homeostasis/drug effects, Homeostasis/physiology, Humans, Hypothalamo-Hypophyseal System/drug effects, Hypothalamo-Hypophyseal System/physiology, Lipid Metabolism, Male, Nitrogen/metabolism, Nitrogen/urine, Oxidation-Reduction, Sleep/drug effects, Sleep/physiology, Thyroid Gland/drug effects, Thyroid Gland/physiology, Thyrotropin/blood, Thyroxine/administration & dosage, Thyroxine/blood, Time Factors, Triiodothyronine/blood
Pubmed
Web of science
Create date
21/01/2008 14:07
Last modification date
20/08/2019 16:23
Usage data