Priming threshold: a novel quantitative measure of the reinstatement of cocaine self-administration

被引:50
作者
Norman, AB
Norman, MK
Hall, JF
Tsibulsky, VL
机构
[1] Univ Cincinnati, Coll Med, Dept Psychiat, Div Neurosci, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Coll Med, Dept Pharmacol, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Coll Med, Dept Physiol, Cincinnati, OH 45267 USA
[4] Univ Cincinnati, Coll Med, Dept Cell Biol, Cincinnati, OH 45267 USA
关键词
addiction; drug abuse; relapse; medications development; psychomotor stimulant;
D O I
10.1016/S0006-8993(99)01423-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The intravenous injection of cocaine has been reported to reliably reinstate (prime) the self-administration of cocaine in animals. We report herein that there is a cocaine priming threshold in rats trained to self-administer cocaine. The cocaine priming threshold is defined as the minimum level of cocaine in the body that will reinstate maintained cocaine self-administration. The mean cocaine priming threshold in rats was calculated to be approximately 186 to 212 mu g kg(-1). Therefore, any injection, series of injections or continuous infusion that result in a level of cocaine equivalent to that produced by a single intravenous injection of this range of doses, will reinstate cocaine self-administration. The priming threshold was significantly increased by the D-1 dopamine receptor antagonist SCH23390 (10 mu g kg(-1), i.v.), indicating a role for dopaminergic neurotransmission. The priming threshold, but not the inter-injection interval of maintained self-administration, was increased following withdrawal from a 7-day infusion of D-amphetamine. In addition, there was no correlation between the cocaine priming threshold and the inter-injection intervals of maintained cocaine self-administration. Therefore, the mechanisms underlying the reinstatement of cocaine self-administration are distinct from the mechanisms underlying the maintenance of cocaine self-administration and they are differentially regulated. It is possible that the priming threshold may represent a distinct target for medications development. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:165 / 174
页数:10
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