In vivo effects of CGP-12177 on the expression of leptin and uncoupling protein genes in mouse brown and white adipose tissues

OBJECTIVE: To assess the effect of chronic treatment with CGP-12177 a beta( 3)-adrenergic receptor (AR) agonist with beta(2)/beta(1)-AR antagonist acti on, on the expression of the leptin gene and of genes coding for uncoupling proteins (ucp1, ucp2 and ucp3) in brown and white adipose tissues. DESIGN: NMRI mice received a daily subcutaneous injection of CGP-12177 at a dose of 0.05, 0.2, 0.5 or 1 mg/kg for 15 days. The specific levels of the mRNAs of interest were analysed in interscapular brown adipose tissue (BAT) and in two white adipose tissue (WAT) depots, inguinal (IWAT) and epididym al (EWAT). RESULTS: No changes in food intake or body weight were detected at any dose of CGP-12177. In the two WAT depots, the treatment led to enhanced express ion of ucp1 and ucp3. but not: of ucp2. In BAT, low doses (0.05 and 0.2 mg/ kg) led to a decreased expression of the three ucp genes, whereas a slight stimulatory effect on the three ucp genes was elicited with a high dose (1 mg/kg). Treated animals displayed increased expression of leptin in BAT and , to a lesser extent, in IWAT. but not in EWAT. CONCLUSION: The results reveal that simultaneous stimulation of the express ion of certain ucp genes and the leptin gene can be achieved, and suggest t hat adrenergic regulation of the leptin gene and of genes of the ucp family in adipose tissues is the result of complex interactions between the diffe rent beta-AR pathways.