1 The present study examined the e ect of dopamine on rat jejunal electrolyte transport (rheogenic transport and Na + , K + -ATPase activity) in adult (60-day old) and young (20-day old) animals. 2 In young rats, dopamine, in the presence of phentolamine, produced an increase in jejunal I sc , this being completely abolished by SKF 83566, and not changed by S-sulpiride. SKF 38393, but not quinerolane, also increased I sc ; this e ect was abolished by SKF 83566 and ouabain, but not by furosemide. In adult rats, dopamine in the presence of phentolamine (0.2 mM) decreased I sc . 3 Na + , K + -ATPase activity in isolated jejunal epithelial cells from adult rats was 2.4 fold that in young rats. In the presence of phentolamine, both dopamine and SKF 38393, but not quinerolane, signi®cantly decreased jejunal Na + , K + -ATPase activity in young animals but not in adult animals. 4 Binding [ 3 H]-Sch 23390 to membranes of jejunal mucosa revealed the presence of a single class of receptors in both young and adult rats, with similar K D and B max values. 5 GTPgS and cholera toxin inhibited jejunal Na + , K + -ATPase activity in young, but not in adult rats. Co-incubation of pertussis toxin with dopamine was found to potentiate the inhibitory e ects of dopamine upon the enzyme in both young and adult rats. 6 Regulation of Na + , K + -ATPase activity by cholera toxin-sensitive G proteins is absent in adult animals, and such di erence may explain the failure of dopamine to inhibit intestinal Na + , K + -ATPase activity in adult rats.