Comparison between dopamine transporter affinity and self-administration potency of local anesthetics in rhesus monkeys

被引:44
|
作者
Wilcox, KM [1 ]
Paul, IA [1 ]
Woolverton, WL [1 ]
机构
[1] Univ Mississippi, Med Ctr, Dept Psychiat & Human Behav, Jackson, MS 39216 USA
关键词
local anesthetic; dopamine transporter; self-administration; radioligand binding; (rhesus monkey);
D O I
10.1016/S0014-2999(98)00967-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Local anesthetics bind to dopamine transporters and inhibit dopamine uptake in rodent brain. Additionally, local anesthetics are self-administered in rhesus monkeys. The present study determined binding affinities of cocaine and five local anesthetics at dopamine transporters in rhesus monkey brain, and compared binding affinities to published self-administration potencies in rhesus monkeys. The affinity order at dopamine transporters was cocaine > dimethocaine > tetracaine > procaine greater than or equal to chloroprocaine > lidocaine. The correlation between dopamine transporter affinities and self-administration potencies was significant. Binding affinities were also determined at sodium (Na2+) channels in rhesus monkey brain. There was not a significant correlation between Na2+ channel affinities and self-administration potencies Local anesthetics with high dopamine transporter and low Na2+ channel affinities were self-administered, whereas those with either high or low affinity at both sites were not consistently self-administered. These data suggest that affinity at dopamine transporters is related to the reinforcing effects of local anesthetics in rhesus monkeys, and Na2+ channel effects may interfere with the reinforcing effect of these drugs. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:175 / 181
页数:7
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