Department of Psychology and Neuroscience, University of Colorado, UCB 345, Boulder, CO 80309-0345, USA.
Psychopharmacology (Berl). 2009 Oct;206(3):469-78. doi: 10.1007/s00213-009-1624-2. Epub 2009 Jul 30.
Dopamine (DA) receptor stimulation in the nucleus accumbens (NAc) plays an important role in regulating cocaine-seeking behavior. Adenosine receptors antagonize the effects of DA receptor stimulation on intracellular signaling, neuronal output, and behavior.
The goal of the present study is to determine the effects of adenosine A(2A) receptor stimulation on reinstatement of cocaine-seeking behavior in rats.
Rats were trained to lever press for cocaine in daily self-administration sessions on a fixed-ratio 1 schedule for 3 weeks. After 1 week of abstinence, lever pressing was extinguished in six daily extinction sessions. We subsequently assessed the effects of the adenosine A(2A) receptor agonist, CGS 21680, on cocaine-, quinpirole (D(2) agonist)-, and cue-induced reinstatement to cocaine seeking. We also assessed the effects of CGS 21680 on sucrose seeking in rats extinguished from sucrose self-administration.
Pretreatment of CGS 21680 dose-dependently blunted cocaine-induced reinstatement (15 mg/kg, i.p.). Pretreatment with CGS 21680 (0.03 mg/kg, i.p.) also attenuated quinpirole- and cue-induced reinstatement. A minimally effective dose of CGS 21680 failed to alter cocaine-induced locomotor activity or sucrose seeking.
Stimulation of adenosine A(2A) receptors antagonizes reinstatement of cocaine seeking elicited by cocaine, DA D(2)-receptor stimulation, and cocaine-conditioned cues. These findings suggest that adenosine A(2A) receptor stimulation may oppose DA D(2) receptor signaling in the NAc that mediates cocaine relapse.
伏隔核(NAc)中的多巴胺(DA)受体刺激在调节可卡因寻求行为中起着重要作用。腺苷受体拮抗 DA 受体刺激对细胞内信号转导、神经元输出和行为的影响。
本研究的目的是确定腺苷 A(2A)受体刺激对可卡因寻求行为复燃的影响。
大鼠经过 3 周的每日可卡因自我给药训练,以固定比例 1 进行按压杠杆。在 1 周的禁欲后,在 6 次每日消退中进行按压杠杆的消退。随后,我们评估了腺苷 A(2A)受体激动剂 CGS 21680 对可卡因、喹吡罗(D2 激动剂)和线索诱导的可卡因寻求复燃的影响。我们还评估了 CGS 21680 在蔗糖自我给药消退的大鼠中对蔗糖寻求的影响。
CGS 21680 的预处理剂量依赖性地削弱了可卡因诱导的复燃(15mg/kg,ip)。CGS 21680(0.03mg/kg,ip)的预处理也减弱了喹吡罗和线索诱导的复燃。CGS 21680 的最小有效剂量未能改变可卡因诱导的运动活动或蔗糖寻求。
腺苷 A(2A)受体的刺激拮抗可卡因、DA D2 受体刺激和可卡因条件线索引起的可卡因寻求复燃。这些发现表明,腺苷 A(2A)受体刺激可能在伏隔核中拮抗介导可卡因复发的 DA D2 受体信号。