LeSage Mark G, Keyler Daniel E, Hieda Yoko, Collins Greg, Burroughs Danielle, Le Chap, Pentel Paul R
Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.
Psychopharmacology (Berl). 2006 Mar;184(3-4):409-16. doi: 10.1007/s00213-005-0027-2. Epub 2005 Jul 1.
Immunization of rats against nicotine using a nicotine conjugate vaccine reduces the distribution of nicotine to brain in rats and attenuates some of nicotine's physiological and behavioral effects. It is not known whether such a vaccine can attenuate nicotine's reinforcing effects.
The present experiment was conducted to determine whether a nicotine conjugate vaccine could interfere with the acquisition and maintenance of nicotine self-administration (NSA) in rats given 23 h day(-1) access to nicotine.
To examine acquisition of NSA, rats were vaccinated with nicotine or control immunogen prior to being given access to a 0.01 mg kg(-1) infusion(-1) nicotine under a fixed-ratio(FR) 1 schedule for week 1, FR 2 for week 2, and FR 3 for week 3. Acquisition of cocaine self-administration (CSA) was similarly examined to determine the specificity of vaccination effects. To examine maintenance of NSA, rats were initially trained to self-administer nicotine under an FR 3 schedule, and then vaccinated with nicotine or control immunogen while NSA continued to be monitored.
NSA was significantly lower in vaccinated rats compared to controls during the acquisition protocol, with a 38% decrease in the number of infusions during the last week of training. The percentage of rats meeting acquisition criteria in the vaccinated group was lower (36%) than that in the control group (70%), but this difference was not statistically significant. Vaccination did not affect acquisition of CSA, demonstrating its specificity for nicotine. Maintenance of NSA was significantly reduced in vaccinated rats as compared to controls after the final vaccine injection, with a mean reduction of 57%. There was no evidence in either protocol that vaccinated rats attempted to compensate for altered nicotine distribution by increasing nicotine intake.
These data suggest that vaccination against nicotine can reduce the reinforcing effects of nicotine in rats and may have therapeutic potential for the treatment of tobacco dependence.
使用尼古丁结合疫苗对大鼠进行免疫接种可减少尼古丁在大鼠脑中的分布,并减弱尼古丁的一些生理和行为效应。目前尚不清楚这种疫苗是否能减弱尼古丁的强化作用。
进行本实验以确定尼古丁结合疫苗是否会干扰给予23小时/天尼古丁摄入机会的大鼠对尼古丁自我给药(NSA)的获得和维持。
为了检测NSA的获得情况,在给予大鼠按固定比率(FR)1的给药方案,第1周给予0.01mg/kg输注量的尼古丁,第2周给予FR 2,第3周给予FR 3之前,用尼古丁或对照免疫原对大鼠进行疫苗接种。类似地检测可卡因自我给药(CSA)的获得情况以确定疫苗接种效果的特异性。为了检测NSA的维持情况,大鼠最初在FR 3给药方案下训练自我给药尼古丁,然后在继续监测NSA的同时用尼古丁或对照免疫原进行疫苗接种。
在获得性实验方案中,与对照组相比,接种疫苗的大鼠的NSA显著降低,训练最后一周的输注次数减少了38%。接种疫苗组达到获得标准的大鼠百分比(36%)低于对照组(70%),但这种差异无统计学意义。疫苗接种不影响CSA的获得,表明其对尼古丁具有特异性。与对照组相比,最后一次疫苗注射后,接种疫苗的大鼠的NSA维持量显著降低,平均降低了57%。在两个实验方案中均没有证据表明接种疫苗的大鼠试图通过增加尼古丁摄入量来补偿尼古丁分布的改变。
这些数据表明,针对尼古丁的疫苗接种可降低大鼠中尼古丁的强化作用,并且可能对治疗烟草依赖具有治疗潜力。