Serotonin 5-HT2C receptors in nucleus accumbens regulate expression of the hyperlocomotive and discriminative stimulus effects of cocaine

被引:86
作者
Filip, M
Cunningham, KA [1 ]
机构
[1] Univ Texas, Med Branch, Dept Pharmacol & Toxicol, Galveston, TX 77555 USA
[2] Polish Acad Sci, Inst Pharmacol, PL-31343 Krakow, Poland
关键词
5-HT2C receptors; behavior; cocaine; drug discrimination; MK; 212; RO; 60-0175; RS; 102221; serotonin;
D O I
10.1016/S0091-3057(01)00741-9
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The serotonin 5-HT2C receptor (5-HT2CR) is abundant in the nucleus accumbens (NAc) shell and is considered an important target for 5-HT to modulate the dopamine (DA) mesoaccumbens circuit, which plays a prominent role in the behavioral effects of cocaine. The present study analyzed the ability of intra-NAc shell infusions of the 5-HT2CR agonists, MK 212 and RO 60-0175, or the 5-HT2CR antagonist, RS 10222 1, to alter either spontaneous or cocaine-evoked activity as well as the discriminative stimulus properties of cocaine. In male Sprague-Dawley rats implanted with bilateral cannulae aimed at the NAc shell, locally injected MK 212 (0.05-0.5 mug/side) or RO 60-0175 (0.5-5 mug/side) did not alter spontaneous activity, but dose-dependently enhanced hyperactivity evoked by cocaine (10 mg/kg ip). In rats trained to discriminate cocaine (10 mg/kg ip) from saline (ip) in a two-lever, water-reinforced FR 20 task, intra-NAc microinfusion of MK 212 (0.05 mug/side) or RO 60-0175 (0.5 mug/side) evoked 37% or 48% cocaine lever responding, respectively. Both MK 212 (0.05 mug/side) and RO 60-0175 (0,5 mug/side) enhanced the discriminability of submaximal doses of cocaine (0.625-2.5 mg/kg). Moreover, intra-NAc infusion of RS 102221 (0.05-1.5 mug/side) dose-dependently attenuated the stimulus effects of cocaine. These data reinforce the hypothesis that 5-HT2CR plays a role in the regulatory neurochemistry of the NAc shell that is important to the full expression of the behaviors evoked by cocaine. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:745 / 756
页数:12
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