Di Ciano Patricia, Guranda Mihail, Lagzdins Dina, Tyndale Rachel F, Gamaleddin Islam, Selby Peter, Boileau Isabelle, Le Foll Bernard
Translational Addiction Research Laboratory, CAMH, Toronto, ON, Canada.
Pharmacogenetics Laboratory, CAMH, Toronto, ON, Canada.
Neuropsychopharmacology. 2016 May;41(6):1513-20. doi: 10.1038/npp.2015.305. Epub 2015 Oct 7.
Varenicline, a nicotinic partial agonist, is the most effective treatment for tobacco use disorder. However, its mechanism of action is still unclear and may involve stimulating dopaminergic transmission. Here we used PET imaging with [(11)C]-(+)-PHNO to explore for the first time the impact of varenicline on dopamine transmission in the D2-rich striatum and D3-rich extra-striatal regions and its relationship with craving, withdrawal and smoking. Eleven treatment-seeking smokers underwent two PET scans with [(11)C]-(+)-PHNO, each following 12-h overnight smoking abstinence both prior to receiving varenicline and following 10-11 days of varenicline treatment (ie, at steady-state drug levels). Subjective measures of craving and urges to smoke were also assessed on the days of the PET scans. Varenicline treatment significantly reduced [(11)C]-(+)-PHNO binding in the dorsal caudate (p=0.008) and reduced some craving measures. These findings provide the first evidence that varenicline is able to increase DA levels in the human brain, a factor that may contribute to its therapeutic efficacy.
伐尼克兰是一种烟碱类部分激动剂,是治疗烟草使用障碍最有效的药物。然而,其作用机制仍不清楚,可能涉及刺激多巴胺能传递。在此,我们首次使用[(11)C]-(+)-PHNO进行PET成像,以探究伐尼克兰对富含D2的纹状体和富含D3的纹状体以外区域多巴胺传递的影响,以及它与渴望、戒断和吸烟的关系。11名寻求治疗的吸烟者接受了两次[(11)C]-(+)-PHNO PET扫描,一次是在服用伐尼克兰之前,另一次是在服用伐尼克兰10 - 11天之后(即处于稳态药物水平),每次扫描前均需过夜戒烟12小时。在PET扫描当天还评估了对吸烟的渴望和冲动的主观测量指标。伐尼克兰治疗显著降低了背侧尾状核中[(11)C]-(+)-PHNO的结合(p = 0.008),并减少了一些对吸烟渴望的测量指标。这些发现首次证明伐尼克兰能够提高人脑中的多巴胺水平,这一因素可能有助于其治疗效果。