Agonists that increase cAMP stimulate both lipolysis and AMPK
activation. L1 adipocytes were treated with the phosphodiesterase
inhibitor IBMX (0.5 mm), the β-agonist isoproterenol
(Iso, 10 μm), or the adenylyl cyclase activator
forskolin (FKN, 20 μm) for 1 h, following a 4-h
preincubation period in serum-free DMEM containing 0.5% fatty acid-free BSA.
Ctrl, control. A, activation of AMPK as assessed from
immunoblots of phospho-AMPK Thr-172 and P-ACC Ser-79. IB, immunoblot.
B, lipolysis was quantified on the basis of glycerol release into the
incubation media. Results for glycerol release are means ± S.E.
(n = 9) and were obtained in three independent experiments.
Immunoblots shown are representative of those obtained in a total of nine
lysates. Significantly different from control group: ***,
p < 0.001.