“…Addition of spermidine (sigma), spermine (Calbiochem) or putrescine (Merck) to the medium was done at zero time. At the end of the incubations, fat pads were quickly removed, homogenized in 0.25 M sucrose (pH 8.1) containing heparin (2 IU/ml) and the heparin eluted lipoprotein lipase activity determined using Intralipid (Vitrum) as substrate, following the experimental conditions previously described [7]. The amount of free fatty acids (FFA) released during 60 rain in each assay (carried out in duplicate) was determined according to Dole and Meinertz [8] and taken as a measure of lipoprotein lipase activity, which was expressed as micromoles of FFA released per hour and per g adipose tissue wet weight.…”