Minneapolis Medical Research Foundation, Minneapolis, MN 55404, United States.
Pharmacol Biochem Behav. 2010 Aug;96(2):217-27. doi: 10.1016/j.pbb.2010.05.008. Epub 2010 May 18.
Animal models of tobacco dependence typically rely on parenteral administration of pure nicotine. Models using cigarette smoke inhalation might more accurately simulate nicotine exposure in smokers. The primary goal of this study was to validate methods for administering cigarette smoke to rats using exposure conditions that were clinically relevant and also produced brain nicotine levels similar to those produced by behaviorally active doses of pure nicotine. A secondary goal was to begin examining the behavioral effects of smoke. Nose-only exposure (NOE) to smoke for 10-45min or whole-body exposure (WBE) to smoke for 1-4h produced serum nicotine concentrations similar to those in smokers (14-55ng/ml), without excessive carbon monoxide exposure. Daily nicotine (0.1mg/kg, s.c.) induced locomotor sensitization whereas 45-min NOE producing brain nicotine levels within the same range did not. Nicotine 0.125mg/kg s.c. reversed withdrawal from a chronic nicotine infusion as measured by elevations in intracranial self-stimulation thresholds whereas 4-h WBE producing similar brain nicotine levels did not. These data demonstrate the feasibility of delivering cigarette smoke to rats at clinically relevant doses, and provide preliminary evidence that the behavioral effects of nicotine delivered in smoke may differ from those of pure nicotine.
动物烟草依赖模型通常依赖于注射纯尼古丁。使用吸烟烟雾吸入的模型可能更准确地模拟吸烟者的尼古丁暴露。本研究的主要目的是验证使用与临床相关的暴露条件向大鼠给予吸烟的方法,并且产生类似于行为活性剂量的纯尼古丁产生的脑内尼古丁水平。次要目标是开始研究烟雾的行为影响。通过鼻内暴露(NOE)吸烟 10-45 分钟或全身暴露(WBE)吸烟 1-4 小时可产生类似于吸烟者的血清尼古丁浓度(14-55ng/ml),而不会暴露于过多的一氧化碳。每天给予尼古丁(0.1mg/kg,皮下注射)可诱导运动敏化,而在相同范围内产生脑内尼古丁水平的 45 分钟 NOE 则不能。尼古丁 0.125mg/kg 皮下注射可逆转慢性尼古丁输注引起的戒断,表现为颅内自我刺激阈值升高,而产生类似脑内尼古丁水平的 4 小时 WBE 则不能。这些数据表明以临床相关剂量向大鼠给予吸烟的可行性,并提供初步证据表明在烟雾中给予尼古丁的行为影响可能与纯尼古丁不同。