London E D, Fanelli R J, Kimes A S, Moses R L
Addiction Research Center, National Institute on Drug Abuse, Baltimore, MD 21224.
Brain Res. 1990 Jun 18;520(1-2):208-14. doi: 10.1016/0006-8993(90)91707-n.
Effects of chronic nicotine on glucose utilization in 45 CNS regions were examined using the 2-deoxy-D-[1-14C]glucose technique in rats. Either L-nicotine (1.0 mg/kg) or saline was injected subcutaneously twice daily for 10 days and once the morning of day 11. On the following afternoon, rats received either nicotine challenge (0.3 mg/kg) or saline subcutaneously 2 min before an intravenous pulse of 2-deoxy-D-[1-14C]glucose. Drug-naive rats given nicotine challenge showed increases of glucose utilization in thalamic nuclei and components of the visual system. Tolerance to nicotine challenge in rats given nicotine chronically was seen in the ventral tegmental area, some components of visual pathways, the cerebellum, and vestibular nuclei; no regions showed sensitization. The percent of rats manifesting most nicotine-induced behaviors either increased (Straub tail, locomotor stimulation, tremors) or did not change (ataxia) over the 10 days of chronic treatment. Plasma from rats given nicotine chronically showed low concentrations of nicotine (12 +/- 1 ng/ml) and higher concentrations of cotinine (124 +/- 6 ng/ml) at the time of assay, with no apparent effect of chronic treatment on nicotine levels after the challenge dose. Changes in regional brain activity, as measured by the 2-deoxy-D-[1-14C]glucose technique, generally do not explain the observed sensitization to nicotine in behavioral assays.
利用2-脱氧-D-[1-¹⁴C]葡萄糖技术检测了慢性尼古丁对大鼠45个中枢神经系统区域葡萄糖利用的影响。每天皮下注射L-尼古丁(1.0毫克/千克)或生理盐水两次,共10天,并在第11天上午注射一次。在接下来的下午,大鼠在静脉注射2-脱氧-D-[1-¹⁴C]葡萄糖脉冲前2分钟皮下注射尼古丁激发剂(0.3毫克/千克)或生理盐水。给予尼古丁激发的未接触过药物的大鼠丘脑核和视觉系统各部分的葡萄糖利用增加。长期给予尼古丁的大鼠对尼古丁激发的耐受性出现在腹侧被盖区、视觉通路的一些部分、小脑和前庭核;没有区域出现敏化现象。在慢性治疗的10天里,表现出大多数尼古丁诱导行为的大鼠百分比要么增加(Straub尾、运动兴奋、震颤),要么没有变化(共济失调)。长期给予尼古丁的大鼠血浆在检测时显示尼古丁浓度较低(12±1纳克/毫升),可替宁浓度较高(124±6纳克/毫升),给予激发剂量后,慢性治疗对尼古丁水平没有明显影响。用2-脱氧-D-[1-¹⁴C]葡萄糖技术测量的区域脑活动变化通常无法解释行为试验中观察到的对尼古丁的敏化现象。