Shi Jie, Zhao Li-Yan, Copersino Marc L, Fang Yu-Xia, Chen Yingmao, Tian Jiahe, Deng Yanping, Shuai Yinliang, Jin Jun, Lu Lin
National Institute on Drug Dependence, Peking University, Beijing 100083, China.
Eur J Pharmacol. 2008 Jan 28;579(1-3):160-6. doi: 10.1016/j.ejphar.2007.09.042. Epub 2007 Oct 10.
It has been documented that methadone maintenance treatment is effective in reducing drug craving and relevant risk behaviors in heroin users. However, it is not understood whether methadone maintenance treatment impairs the dopamine transporter in the striatum. To establish whether chronic opiate use might impair brain dopamine neurons in humans, we assessed dopamine transporter (DAT) uptake function in the striatum (caudate and putamen), and analyzed the correlation between DAT in the striatum and heroin craving and subjective anxiety in former heroin users with prolonged abstinence and in patients receiving methadone maintenance treatment. Binding of [(11)C]-2beta-carbomethoxy-3beta-aryltropane ([(11)C] CFT) as a brain dopamine transporter ligand was measured with positron emission tomography (PET) in eleven former heroin users with prolonged abstinence, ten patients receiving methadone maintenance treatment and ten healthy control subjects. Heroin craving and subjective anxiety in prolonged abstinence and methadone maintenance treatment groups were assessed and the correlations between DAT of striatum and heroin craving or subjective anxiety were determined. In comparison with healthy control subjects, methadone maintenance treatment subjects had lower DAT uptake function in the bilateral caudate and putamen and prolonged abstinence subjects showed significantly lower DAT uptake function in the bilateral caudate. Moreover, in comparison to the prolonged abstinence subjects, the methadone maintenance treatment subjects showed significant decreases of DAT uptake in the bilateral putamen. DAT uptake function in bilateral striatum was not associated with heroin craving in prolonged abstinence or in methadone maintenance treatment subjects; however, DAT uptake function in the bilateral caudate was significantly correlated with subjective anxiety in methadone maintenance treatment subjects. Our findings suggest that chronic opioid use induces long-lasting striatum dopamine neuron impairment, and prolonged withdrawal from opioids can benefit the recovery of impaired dopamine neurons in the brain.
有文献记载,美沙酮维持治疗在减少海洛因使用者的药物渴望及相关危险行为方面是有效的。然而,尚不清楚美沙酮维持治疗是否会损害纹状体中的多巴胺转运体。为了确定长期使用阿片类药物是否可能损害人类大脑中的多巴胺神经元,我们评估了纹状体(尾状核和壳核)中的多巴胺转运体(DAT)摄取功能,并分析了长期戒断的前海洛因使用者和接受美沙酮维持治疗的患者纹状体中DAT与海洛因渴望及主观焦虑之间的相关性。使用正电子发射断层扫描(PET)测量了11名长期戒断的前海洛因使用者、10名接受美沙酮维持治疗的患者和10名健康对照者作为脑多巴胺转运体配体的[(11)C]-2β-甲氧基羰基-3β-芳基托烷([(11)C]CFT)的结合情况。评估了长期戒断组和美沙酮维持治疗组的海洛因渴望及主观焦虑情况,并确定了纹状体DAT与海洛因渴望或主观焦虑之间的相关性。与健康对照者相比,美沙酮维持治疗组受试者双侧尾状核和壳核的DAT摄取功能较低,长期戒断者双侧尾状核的DAT摄取功能显著较低。此外,与长期戒断者相比,美沙酮维持治疗组受试者双侧壳核的DAT摄取显著降低。长期戒断者或美沙酮维持治疗组受试者双侧纹状体的DAT摄取功能与海洛因渴望无关;然而,美沙酮维持治疗组受试者双侧尾状核的DAT摄取功能与主观焦虑显著相关。我们的研究结果表明,长期使用阿片类药物会导致纹状体多巴胺神经元长期受损,而长期停用阿片类药物有助于受损的脑多巴胺神经元恢复。