June H L, Harvey S C, Foster K L, McKay P F, Cummings R, Garcia M, Mason D, Grey C, McCane S, Williams L S, Johnson T B, He X, Rock S, Cook J M
Psychobiology Program, Department of Psychology, Indiana University-Purdue University, Indianapolis, Indiana 46202, USA.
J Neurosci. 2001 Mar 15;21(6):2166-77. doi: 10.1523/JNEUROSCI.21-06-02166.2001.
GABA receptors within the mesolimbic circuitry have been proposed to play a role in regulating alcohol-seeking behaviors in the alcohol-preferring (P) rat. However, the precise GABA(A) receptor subunit(s) mediating the reinforcing properties of EtOH remains unknown. We examined the capacity of intrahippocampal infusions of an alpha5 subunit-selective ( approximately 75-fold) benzodiazepine (BDZ) inverse agonist [i.e., RY 023 (RY) (tert-butyl 8-(trimethylsilyl) acetylene-5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5a] [1,4] benzodiazepine-3-carboxylate)] to alter lever pressing maintained by concurrent presentation of EtOH (10% v/v) and a saccharin solution (0.05% w/v). Bilateral (1.5-20 microgram) and unilateral (0.01-40 microgram) RY dose-dependently reduced EtOH-maintained responding, with saccharin-maintained responding being reduced only with the highest doses (e.g., 20 and 40 microgram). The competitive BDZ antagonist ZK 93426 (ZK) (7 microgram) reversed the RY-induced suppression on EtOH-maintained responding, confirming that the effect was mediated via the BDZ site on the GABA(A) receptor complex. Intrahippocampal modulation of the EtOH-maintained responding was site-specific; no antagonism by RY after intra-accumbens [nucleus accumbens (NACC)] and intraventral tegmental [ventral tegmental area (VTA)] infusions was observed. Because the VTA and NACC contain very high densities of alpha1 and alpha2 subunits, respectively, we determined whether RY exhibited a "negative" or "neutral" pharmacological profile at recombinant alpha1beta3gamma2, alpha2beta3gamma2, and alpha5beta3gamma2 receptors expressed in Xenopus oocytes. RY produced "classic" inverse agonism at all alpha receptor subtypes; thus, a neutral efficacy was not sufficient to explain the failure of RY to alter EtOH responding in the NACC or VTA. The results provide the first demonstration that the alpha5-containing GABA(A) receptors in the hippocampus play an important role in regulating EtOH-seeking behaviors.
中脑边缘回路中的γ-氨基丁酸(GABA)受体被认为在调节嗜酒(P)大鼠的觅酒行为中发挥作用。然而,介导乙醇强化特性的确切GABA A受体亚基仍不清楚。我们研究了海马内注射α5亚基选择性(约75倍)苯二氮䓬(BDZ)反向激动剂[即RY 023(RY)(叔丁基8-(三甲基甲硅烷基)乙炔-5,6-二氢-5-甲基-6-氧代-4H-咪唑并[1,5a][1,4]苯二氮䓬-3-羧酸盐)]改变由同时呈现乙醇(10% v/v)和糖精溶液(0.05% w/v)维持的杠杆按压行为的能力。双侧(1.5 - 20微克)和单侧(0.01 - 40微克)的RY剂量依赖性地减少了由乙醇维持的反应,而只有最高剂量(如20和40微克)才会减少由糖精维持的反应。竞争性BDZ拮抗剂ZK 93426(ZK)(7微克)逆转了RY对乙醇维持反应的抑制作用,证实该效应是通过GABA A受体复合物上的BDZ位点介导的。海马内对乙醇维持反应的调节具有位点特异性;在伏隔核[伏隔核(NACC)]和腹侧被盖区[腹侧被盖区(VTA)]内注射后未观察到RY的拮抗作用。由于VTA和NACC分别含有非常高密度的α1和α2亚基,我们确定RY在非洲爪蟾卵母细胞中表达的重组α1β3γ2、α2β3γ2和α5β3γ2受体上是否表现出“负性”或“中性”药理学特征。RY在所有α受体亚型上均产生“经典”反向激动作用;因此,中性效能不足以解释RY未能改变NACC或VTA中乙醇反应的原因。结果首次证明海马中含α5的GABA A受体在调节觅酒行为中起重要作用。