Roberts D C, Koob G F
Pharmacol Biochem Behav. 1982 Nov;17(5):901-4. doi: 10.1016/0091-3057(82)90469-5.
6-Hydroxydopamine-induced destruction of dopaminergic terminals in the nucleus accumbens have been shown previously to disrupt cocaine and amphetamine self-administration. We sought to determine whether lesions of the DA cell bodies in the ventral tegmental area (VTA) which give rise to the DA innervation of the n. accumbens, would also disrupt cocaine self-administration behavior. Rats were trained to self-inject cocaine (0.75 mg/kg) for 4 hr/day. After a stable baseline was established, one group of rats received bilateral injections of 6-OHDA (4 micrograms/l microliter) into the VTA. Control rats received vehicle injections. When retested on the fifth day post-lesion, all of the 6-OHDA treated animals showed a long lasting reduction in cocaine intake. Three animals did not reinitiate cocaine self-administration after the lesion, although each showed stable post-lesion responding for apomorphine. The surgery had no effect on cocaine self-administration in control animals. These data support the hypothesis that dopaminergic mechanisms are necessary for the normal expression of cocaine self-administration.
先前已表明,6-羟基多巴胺诱导的伏隔核中多巴胺能终末的破坏会扰乱可卡因和苯丙胺的自我给药行为。我们试图确定,腹侧被盖区(VTA)中产生伏隔核多巴胺能神经支配的多巴胺能细胞体损伤,是否也会扰乱可卡因自我给药行为。大鼠被训练每天自我注射可卡因(0.75毫克/千克),持续4小时。在建立稳定的基线后,一组大鼠接受双侧向VTA注射6-羟基多巴胺(4微克/1微升)。对照大鼠接受溶剂注射。在损伤后第5天重新测试时,所有接受6-羟基多巴胺治疗的动物可卡因摄入量均出现长期减少。三只动物在损伤后未重新开始可卡因自我给药,尽管每只动物在损伤后对阿扑吗啡的反应均稳定。手术对对照动物的可卡因自我给药没有影响。这些数据支持了多巴胺能机制对于可卡因自我给药正常表达是必需的这一假说。