b2-Agonist ritodrine, unlike natural catecholamines, activates thermogenesis prematurely in fetal sheep

Bassett, John M., and Michael E. Symonds. b2-Agonist ritodrine, unlike natural catecholamines, activates thermogenesis prematurely in fetal sheep. Am. J. Physiol. 275 (Regulatory Integrative Comp. Physiol. 44): R112–R119, 1998.— Prolonged administration of the b2-adrenergic agonist ritodrine to fetal sheep increases nonesterified fatty acid mobilization. To investigate whether changes in fetal growth or functional development of brown adipose tissue (BAT) also occur, ritodrine was infused at 5 μg/min iv into eight fetal sheep (6 twins and 2 singletons at 125–128 days of gestation) for 5 days and then at twice this rate for a further 7–11 days. Fetal growth was reduced significantly (P , 0.02) during ritodrine infusion relative to controls (5.8 6 17.5 vs. 79.7 6 10.3 g/day), with growth of skeletal muscles ceasing. Ritodrine reduced perirenal BAT weight by 50% from 18.6 6 1.89 to 9.3 6 0.60 g (P , 0.01) and its lipid content by .70% from 6.5 6 0.96 to 1.9 6 0.45 g (P , 0.01). Mitochondrial protein in BAT was also less (P , 0.002), but GDP binding to uncoupling protein increased (P , 0.05). In similar experiments, epinephrine and norepinephrine increased plasma nonesterified fatty acid initially, but neither altered perirenal BAT composition. The b2-adrenergic agonist ritodrine appears able to promote lipid mobilization and thermogenesis in utero.