Grimm Jeffrey W, Lu Lin, Hayashi Teruo, Hope Bruce T, Su Tsung-Ping, Shaham Yavin
Behavioral Neuroscience Branch, Intramural Research Program/National Institute on Drug Abuse/National Institutes of Health/Department of Health and Human Services, Baltimore, Maryland 21224, USA.
J Neurosci. 2003 Feb 1;23(3):742-7. doi: 10.1523/JNEUROSCI.23-03-00742.2003.
Using a rat model of drug craving, we found that the responsiveness to cocaine cues progressively increases or incubates over the first 60 d of cocaine withdrawal. Here we studied whether alterations in brain-derived neurotrophic factor (BDNF) protein levels within the mesolimbic dopamine system are associated with this incubation phenomenon. BDNF is involved in synaptic plasticity and was found to enhance responding for cues associated with natural rewards. Rats were trained to press a lever to receive intravenous cocaine or oral sucrose for 6 hr/d for 10 d; each earned reward was paired with a tone-light cue. Resumption of lever-pressing behavior was then assessed on days 1, 30, or 90 of reward withdrawal. First, resistance to extinction was assessed during 6 hr in which lever presses were not reinforced and the cue was absent. Second, cue-induced reinstatement was assessed after extinction during 1 hr in which responding led to cue presentations. Other rats were killed without testing on days 1, 30, and 90 of reward withdrawal, and BDNF and nerve growth factor (NGF) protein levels were measured in the ventral tegmental area (VTA), accumbens, and amygdala. Lever pressing during extinction and cue-induced reinstatement tests of cocaine craving progressively increased after cocaine withdrawal. Time-dependent changes also were observed during the tests for sucrose craving, with maximal responding on day 30. BDNF, but not NGF, levels in the VTA, accumbens, and amygdala progressively increased after cocaine, but not sucrose, withdrawal. Time-dependent increases in BDNF levels may lead to synaptic modifications that underlie enhanced responsiveness to cocaine cues after prolonged withdrawal periods.
利用药物渴求的大鼠模型,我们发现,在可卡因戒断的前60天里,对可卡因线索的反应性会逐渐增强或“潜伏期延长”。在此,我们研究了中脑边缘多巴胺系统内脑源性神经营养因子(BDNF)蛋白水平的变化是否与这种潜伏期延长现象相关。BDNF参与突触可塑性,并且已发现其可增强对与自然奖赏相关线索的反应。大鼠接受训练,每天按压杠杆6小时,持续10天,以静脉注射可卡因或口服蔗糖;每次获得的奖赏都与一个声光线索配对。然后在奖赏撤药后的第1天、第30天或第90天评估杠杆按压行为的恢复情况。首先,在6小时内评估消退抵抗,在此期间杠杆按压未得到强化且线索不存在。其次,在消退后的1小时内评估线索诱导的复吸,在此期间反应会导致线索呈现。其他大鼠在奖赏撤药的第1天、第30天和第90天未经测试即被处死,并测量腹侧被盖区(VTA)、伏隔核和杏仁核中的BDNF和神经生长因子(NGF)蛋白水平。可卡因戒断后,在可卡因渴求的消退和线索诱导的复吸测试中,杠杆按压逐渐增加。在蔗糖渴求测试中也观察到了时间依赖性变化,在第30天反应最大。可卡因戒断后,VTA、伏隔核和杏仁核中的BDNF水平逐渐升高,而NGF水平则无变化,但蔗糖戒断后并非如此。BDNF水平的时间依赖性增加可能导致突触修饰,这是长期戒断后对可卡因线索反应增强的基础。