Robledo P, Koob G F
Scripps Research Institute, Department of Neuropharmacology, La Jolla, CA 92037.
Behav Brain Res. 1993 Jun 30;55(2):159-66. doi: 10.1016/0166-4328(93)90112-4.
The region of the nucleus accumbens and its connections have been implicated in the reinforcing actions of cocaine as measured by intravenous self-administration. Our previous work has demonstrated that ibotenic acid lesions of one of the output regions of the nucleus accumbens, the sublenticular region of the extended amygdala (SEA), resulted in significant decreases in the highest ratio obtained in rats self-administering cocaine. In the present study, the importance of another nucleus accumbens output, the subcommissural ventral pallidum (SVP), in mediating the self-administration of cocaine in the rat was explored. Animals were trained to self administer cocaine (0.75 mg/kg/inj) via an intravenous catheter on a FR5 schedule of reinforcement. Subsequently, subjects were either given bilateral intracerebral injections (0.5 microliter per side) of ibotenic acid (10 micrograms/microliter lesion group) or vehicle (sham group) into the SVP or into the SEA. Four days postlesion, cocaine self-administration on a FR5 schedule was resumed for 3 days. Next, a dose effect function was determined in one 3-h session. Finally, a progressive ratio probe in which the ratio requirement was increased after each reinforcement was tested. Lesions of both the SVP and the SEA produced significant changes in responding for intravenous cocaine on a FR5 schedule of reinforcement as compared to sham lesioned controls, although the effect was found to be greater for the rats bearing lesions of the SEA. While the lesions produced decreases in responding for cocaine at all doses tested in the dose-effect function, the rate of responding was still inversely proportional to the dose in both groups.(ABSTRACT TRUNCATED AT 250 WORDS)
伏隔核区域及其连接与静脉注射自我给药所衡量的可卡因强化作用有关。我们之前的研究表明,伏隔核一个输出区域,即扩展杏仁核的豆状核下区域(SEA)的鹅膏蕈氨酸损伤,导致自我给药可卡因的大鼠获得的最高比率显著下降。在本研究中,探讨了伏隔核的另一个输出区域,即连合部下腹苍白球(SVP)在介导大鼠可卡因自我给药中的重要性。动物通过静脉导管在FR5强化程序上接受训练以自我给药可卡因(0.75mg/kg/注射)。随后,将受试者双侧脑内注射(每侧0.5微升)鹅膏蕈氨酸(10微克/微升损伤组)或赋形剂(假手术组)注入SVP或SEA。损伤后四天,恢复在FR5程序上的可卡因自我给药3天。接下来,在一个3小时的实验中确定剂量效应函数。最后,进行了一个渐进比率探测实验,其中在每次强化后增加比率要求。与假手术损伤对照组相比,SVP和SEA的损伤在FR5强化程序上对静脉注射可卡因的反应产生了显著变化,尽管发现SEA损伤的大鼠效果更大。虽然损伤在剂量效应函数中测试的所有剂量下都导致对可卡因反应的减少,但两组的反应率仍然与剂量成反比。(摘要截断于250字)