Ikemoto Satoshi
Behavioral Neuroscience Branch, National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services, Baltimore, MD 21224, USA.
Neuropsychopharmacology. 2005 Jun;30(6):1088-95. doi: 10.1038/sj.npp.1300660.
The supramammillary nucleus (SUM), a dorsal layer of the mammillary body, has recently been implicated in positive reinforcement. The present study examined whether GABA(A) receptors in the SUM or adjacent regions are involved in primary reinforcement using intracranial self-administration procedures. Rats learned quickly to lever-press for infusions of the GABA(A) antagonist picrotoxin into the SUM. Although picrotoxin was also self-administered into the posterior hypothalamic nuclei and anterior ventral tegmental area, these regions were less responsive to lower doses of picrotoxin than the SUM. The finding that rats learned to respond selectively on the lever triggering drug infusions is consistent with picrotoxin's reinforcing effect. Coadministration of the GABA(A) agonist muscimol disrupted picrotoxin self-administration, and another GABA(A) antagonist, bicuculline, was also self-administered into the SUM; thus, the reinforcing effect of picrotoxin is mediated by GABA(A) receptors. Since rats did not self-administer the GABA(B) antagonist 2-hydroxysaclofen into the SUM, the role of GABA(B) receptors may be distinct from that of GABA(A) receptors. Pretreatment with the dopamine receptor antagonist SCH 23390 (0.05 mg/kg, i.p.) extinguished picrotoxin self-administration into the SUM, suggesting that the reinforcing effects of GABA(A) receptor blockade depend on normal dopamine transmission. In conclusion, the blockade of GABA(A) receptors in the SUM is reinforcing, and the brain 'reward' circuitry appears to be tonically inhibited via supramammillary GABA(A) receptors and more extensive than the meso-limbic dopamine system.
乳头体上核(SUM)是乳头体的背侧层,最近被认为与正性强化有关。本研究使用颅内自我给药程序,研究了SUM或相邻区域的GABA(A)受体是否参与初级强化。大鼠很快学会按压杠杆,以便将GABA(A)拮抗剂印防己毒素注入SUM。虽然印防己毒素也被自我给药到下丘脑后核和腹侧被盖区前部,但这些区域对较低剂量印防己毒素的反应不如SUM。大鼠学会选择性地对触发药物输注的杠杆做出反应这一发现,与印防己毒素的强化作用一致。同时给予GABA(A)激动剂蝇蕈醇会破坏印防己毒素的自我给药,另一种GABA(A)拮抗剂荷包牡丹碱也被自我给药到SUM;因此,印防己毒素的强化作用是由GABA(A)受体介导的。由于大鼠不会将GABA(B)拮抗剂2-羟基-舒必利自我给药到SUM,GABA(B)受体的作用可能与GABA(A)受体不同。用多巴胺受体拮抗剂SCH 23390(0.05mg/kg,腹腔注射)预处理可消除将印防己毒素自我给药到SUM的行为,这表明GABA(A)受体阻断的强化作用依赖于正常的多巴胺传递。总之,SUM中GABA(A)受体的阻断具有强化作用,大脑“奖赏”回路似乎通过乳头体上GABA(A)受体受到紧张性抑制,且比中脑-边缘多巴胺系统更广泛。