Liu Xiu, Caggiula Anthony R, Yee Susan K, Nobuta Hiroko, Sved Alan F, Pechnick Robert N, Poland Russell E
Department of Psychology, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Neuropsychopharmacology. 2007 Mar;32(3):710-8. doi: 10.1038/sj.npp.1301129. Epub 2006 Jun 21.
Mecamylamine, a noncompetitive nicotinic cholinergic antagonist, inhibits nicotine self-administration in animals and may attenuate tobacco smoking in humans trying to quit. Our preliminary data suggested that this agent, at a dose of 2 mg/kg (subcutaneous (s.c.)), also attenuates cue-induced relapse to nicotine-seeking behavior in rats. This study determined whether mecamylamine-induced attenuation can be obtained at doses lower than the high 2 mg/kg dose used in the first study, and whether it is specific to nicotine-associated cues. Male Sprague-Dawley rats were trained to intravenously self-administer nicotine (0.03 mg/kg/infusion) on a fixed-ratio 5 schedule. Each infusion was accompanied by a visual cue (1 s onset of a lever light followed by offset of a house light for 20 s during which time no infusions could be obtained). After the nicotine-maintained responding was extinguished by withholding the delivery of nicotine (saline substitution) and its associated cue, reinstatement tests were conducted. Response-contingent re-presentation of the cue without further availability of nicotine significantly reinstated extinguished responding at the previously nicotine-reinforced lever. Pretreatment with mecamylamine (0.5, 1, and 2 mg/kg, s.c.) dose-dependently attenuated the cue-induced reinstatement of lever responding. Mecamylamine did not change food-taking and -seeking responses, whereas the highest dose (2 mg/kg) decreased nicotine self-administration behavior. The results confirm previous findings that stimuli conditioned to nicotine self-administration effectively elicit reinstatement of nicotine-seeking behavior after extinction and demonstrate that mecamylamine, besides suppressing self-administration of nicotine, effectively attenuates cue-induced nicotine-seeking behavior. These findings suggest that the response-reinstatement procedures used in this study may be useful for studying neurobiological mechanisms of nicotine-seeking behavior and that mecamylamine-like drugs may be potential candidates for pharmacological treatment and prevention of relapse to tobacco smoking in abstinent smokers.
美加明是一种非竞争性烟碱型胆碱能拮抗剂,可抑制动物的尼古丁自我给药行为,并可能减少试图戒烟的人的吸烟量。我们的初步数据表明,该药物以2mg/kg(皮下注射)的剂量,也可减少大鼠中线索诱导的尼古丁寻求行为的复发。本研究确定了美加明诱导的减少是否可以在低于第一项研究中使用的2mg/kg高剂量下获得,以及它是否对尼古丁相关线索具有特异性。雄性Sprague-Dawley大鼠被训练在固定比例5的时间表上静脉内自我给药尼古丁(0.03mg/kg/次输注)。每次输注都伴有一个视觉线索(杠杆灯亮起1秒,随后房灯熄灭20秒,在此期间无法获得输注)。在通过停止尼古丁(生理盐水替代)及其相关线索的给药使尼古丁维持的反应消退后,进行恢复测试。在没有进一步提供尼古丁的情况下,线索的反应性重新呈现显著恢复了在先前尼古丁强化杠杆处的消退反应。美加明(0.5、1和2mg/kg,皮下注射)预处理剂量依赖性地减少了线索诱导的杠杆反应恢复。美加明没有改变食物摄取和寻求反应,而最高剂量(2mg/kg)降低了尼古丁自我给药行为。结果证实了先前的发现,即与尼古丁自我给药相关的刺激在消退后有效地引发了尼古丁寻求行为的恢复,并表明美加明除了抑制尼古丁的自我给药外,还有效地减少了线索诱导的尼古丁寻求行为。这些发现表明,本研究中使用的反应恢复程序可能有助于研究尼古丁寻求行为的神经生物学机制,并且美加明样药物可能是戒烟者药物治疗和预防吸烟复发的潜在候选药物。