Leptin, the product of the ob gene, is secreted front white adipocytes and
regulates food intake and whole-body energy metabolism. In rodents and huma
ns, leptin gene expression is under complex endocrine and metabolic control
, and is strongly influenced by energy balance. Growth hormone (GH) has myr
iad effects on adipose tissue metabolism. The primary aim of this study was
to determine the ability of GH to regulate leptin mRNA expression in bovin
e adipose tissue in vitro and in vivo. Incubation of subcutaneous adipose t
issue explants for 24 h with GH alone had no effect on bovine leptin gene e
xpression, whereas high concentrations of insulin or dexamethasone (DEX) po
tently stimulated bovine leptin mRNA abundance. GH, ill combination with hi
gh concentrations of insulin, DEX, or both, attenuated the ability of insul
in or DEX to stimulate leptin expression in vitro. These data indicate that
GH can indirectly regulate leptin expression in vitro by altering the adip
ose tissue response to insulin or DEX. We extended these: studies to examin
e the ability of GH to regulate leptin expression in vivo, using young cast
rate male cattle treated with no hormone (control) or GH (200 mu g/kg body
weight per day) for 3 days. GH increased plasma GH and insulin concentratio
ns, but not those of cortisol or non-esterified fatty acid (NEFA) concentra
tions. GH treatment increased adipose tissue leptin and IGF-1 mRNA concentr
ations (n=9, P>0.001). In addition, leptin abundance was highly correlated
with adipose tissue IGF-1 mRNA in GH-treated animals (P>0.001). The timing
of GH-induced changes in leptin gene expression preceded measurable GH effe
cts on adiposity.