Uncoupling proteins (UCPs) are considered to be major determinants of energ
y expenditure in mammals. During development in rodents, the expression of
the UCP genes occurs sequentially. UCP2 mRNA is expressed long before birth
. UCP1 mRNA expression in brown adipose tissue (BAT) starts in the late fet
al period, and the expression of UCP3 mRNA begins immediately after birth i
n BAT and skeletal muscle. The postnatal induction of UCP1 gene expression
is due mainly to cold stimuli, whereas the switch-on of UCP3 mRNA expressio
n after birth requires the stimulus of food intake, specifically of lipids
in the mother's milk. However, UCP3 mRNA expression after birth is also hig
hly sensitive to leptin, and administration of a single injection of leptin
to neonatal mice that were not allowed to suckle partly mimicked the natur
al induction of UCP3 gene expression in BAT and skeletal muscle. The speed
of the effects of leptin on UCP3 mRNA expression suggests a direct action o
n skeletal muscle and BAT. The injection of leptin produced minor effects o
n UCP1 mRNA expression, and no effects were observed on UCP2 mRNA. In summa
ry, leptin appears to contribute to the regulation of UCP3 gene expression
in the perinatal period. Whatever the mechanism of action of leptin in BAT
and skeletal muscle, it is already functional at birth.