“…Lipolytic activity in white adipose tissue was performed as described elsewhere. 87 Briefly, eWAT and iWAT (left side) were isolated in Krebs-Ringer bicarbonate buffer (KRBH) (30 mM HEPES, 120 mM NaCl, 1 mM CaCl 2 , 1 mM MgCl 2 , 10mM NaHCO 3 , 4 mM K 2 HPO 4 ) prewarmed at 37°C. Adipose tissue was divided into 30–50 mg specimens and incubated at 37°C in KRBH buffer supplemented with 2% fatty acid-free BSA (A7030, Sigma) with either vehicle (sterile dH 2 O) or 10 μM isoproterenol (ab146724, Abcam) for 2 h with constant agitation.…”