Journal of Animal Science · 1990 · 59 citations · 0 references
Life SciencesBiochemistryPharmacologyBiochemical PharmacologyLipid BiochemistryMetabolic RegulationAdipose TissueFatty Acid BiosynthesisFatty Acid MetabolismFatty Acid SynthesisLipid MetabolismAdipose Tissue Lipid MetabolismAdipose Tissue LipogenesisAdipose Tissue LipolysisAdrenergic Receptor AgonistsDirect EffectsFatty AcidsLipid Metabolism EffectsLipolytic Activity
The effects of the beta-adrenergic agonists isoproterenol, cimaterol, ractopamine and clenbuterol on lipolysis (release of glycerol and free fatty acids) and lipogenesis (incorporation of 14C into fatty acids from [14C]glucose) was examined in porcine adipose tissue explants in vitro. Lipolysis was stimulated by isoproterenol, cimaterol or ractopamine but not by clenbuterol. Insulin reduced the lipolytic effects of the beta-adrenergic agonists (isoproterenol, cimaterol and ractopamine). Lipogenesis was inhibited by all beta-adrenergic agonists tested (isoproterenol, cimaterol, ractopamine and clenbuterol). The antilipogenic effect of the beta-adrenergic agonists was reduced by the presence of insulin in the incubation. Although effects of the different beta-adrenergic agonists varied, all had some direct effects that could be expected to reduce adipose accretion. Effects of beta-adrenergic agonists in the pig are due in part to direct effects on adipose tissue.