Regulation of leptin by thyroid hormone in humans: Studies in vivo and in vitro

The influence of thyroid hormones on human adipose tissue leptin production and leptin gene expression was investigated in vitro and in vivo. Twelve women received 60 mu g triiodothyronine (T-3) per day for 7 days, which increased total T-3 by 195% (1.78 +/- 0.07 to 5.25 +/- 0.39 mU/L. P <.001), significantly decreased thyrotropin ([TSH] 1.57 +/- 0.40 to 0.03 +/- 0.01 mU/L, P <.01), and increased energy expenditure (1,602 +/- 32 to 1.754 +/- 34 kca1/24 h, P <.05). However, serum leptin did not change (9.36 +/- 1.6 v 8.90 +/- 1.3 mu g/L. nonsignificant). Human subcutaneous adipose tissue biopsies from eight healthy women were incubated in vitro as small fragments with T-3 in concentrations from 1 to 50 nmol/L. Leptin production was inhibited dose-dependently. After 24 hours of incubation, a T-3 concentration of 50 nmol/L reduced basal leptin production by 42% (P <.05) and the stimulated leptin production (dexamethasone 10 nmol/L) by 52% (P <.05). Leptin mRNA expression was measured by a semiquantitative multiplex reverse transcriptase-polymerase chain reaction (RT-PCR) method. Fifty nanomolars T-3 decreased basal leptin mRNA expression by 47% compared with controls (P <.001), and the stimulated leptin mRNA expression was reduced to a similar degree (53%). In conclusion, in human adipose tissue, T-3 (>20 nmol/L) inhibited leptin production and leptin gene expression in vitro, whereas an elevation of T3 corresponding to a moderate thyrotoxic state (T-3 5.25 +/- 0.39 nmol/L) was without any impact on serum leptin levels in vivo. Copyright (C) 1999 by W.B. Saunders Company.