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

被引:10
作者
Bracco, D
Morin, O
Liang, H
Jequier, E
Burger, AG
Schutz, Y
机构
[1] UNIV LAUSANNE,FAC MED,INST PHYSIOL,CH-1011 LAUSANNE,SWITZERLAND
[2] UNIV HOSP GENEVA,DIV ENDOCRINE,THYROID UNIT,GENEVA,SWITZERLAND
来源
OBESITY RESEARCH | 1996年 / 4卷 / 03期
关键词
thyroid hormones; thyroxin; obesity; indirect calorimetry; urinary nitrogen;
D O I
10.1002/j.1550-8528.1996.tb00539.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 mu g 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.
引用
收藏
页码:213 / 219
页数:7
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