CHRONIC ADMINISTRATION OF THE SELECTIVE DOPAMINE UPTAKE INHIBITOR GBR-12909, BUT NOT COCAINE, PRODUCES MARKED DECREASES IN DOPAMINE TRANSPORTER DENSITY

The chronic continuous infusion of cocaine produces partial behavioral tolerance to cocaine and tolerance to the inhibition of dopamine upta ke by cocaine, without changing dopamine transporter binding. In order to examine more closely the dopaminergic contribution to this effect, the selective dopamine uptake inhibitor GBR 12909 (30 mg/kg/day), coc aine (50 mg/kg/day), or vehicle, were continuously infused via osmotic minipump, and their effects on the dopamine transporter ex amined. Dr ug and vehicle pumps were implanted into male Sprague-Dawley rats and removed after seven days. [H-3]WIN 35,428 binding and [H-3]dopamine up take were measured in caudate putamen and nucleus accumbens at varying intervals after pump removal. The B-max for [H-3]MN 35,428 binding wa s decreased by approximately 75% in the caudate putamen and by 40% in the nucleus accumbens of GBR 12909-treated rats both 1 and 4 days afte r pump removal, and was still significantly decreased after 10 days, b ut had returned to normal by 20 days post-treatment. In contrast, coca ine did not significantly alter [H-3]WIN 35,428 binding. GBR 12909 pro duced both tolerance to the inhibition of [H-3]dopamine uptake by coca ine, and a decrease in total uptake of dopamine, in the caudate putame n, with no change in the nucleus accumbens. The persistent reduction o f [H-3]WIN 35,428 binding following continuous GBR 12909 does not appe ar to result from residual drug binding. These findings suggest that G BR 12909 and cocaine may bind to and regulate the dopamine transporter in different ways.