Gorelick David A, Kim Yu Kyeong, Bencherif Badreddine, Boyd Susan J, Nelson Richard, Copersino Marc L, Dannals Robert F, Frost J James
Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD, USA.
Psychopharmacology (Berl). 2008 Nov;200(4):475-86. doi: 10.1007/s00213-008-1225-5. Epub 2008 Sep 2.
Cocaine users have increased regional brain mu-opioid receptor (mOR) binding which correlates with cocaine craving. The relationship of mOR binding to relapse is unknown.
To evaluate regional brain mOR binding as a predictor of relapse to cocaine use is the objective of the study.
Fifteen nontreatment-seeking, adult cocaine users were housed on a closed research ward for 12 weeks of monitored abstinence and then followed for up to 1 year after discharge. Regional brain mOR binding was measured after 1 and 12 weeks using positron emission tomography (PET) with [11C]carfentanil (a selective mOR agonist). Time to first cocaine use (lapse) and to first two consecutive days of cocaine use (relapse) after discharge was based on self-report and urine toxicology.
A shorter interval before relapse was associated with increased mOR binding in frontal and temporal cortical regions at 1 and 12 weeks of abstinence (Ps < 0.001) and with a lesser decrease in binding between 1 and 12 weeks (Ps < 0.0008). There were significant positive correlations between mOR binding at 12 weeks and percent days of cocaine use during first month after relapse (Ps < 0.002). In multiple linear regression analysis, mOR binding contributed significantly to the prediction of time to relapse (R2= 0.79, P < 0.001), even after accounting for clinical variables.
Increased brain mOR binding in frontal and temporal cortical regions is a significant independent predictor of time to relapse to cocaine use, suggesting an important role for the brain endogenous opioid system in cocaine addiction.
可卡因使用者大脑区域的μ-阿片受体(mOR)结合增加,这与对可卡因的渴望相关。mOR结合与复发之间的关系尚不清楚。
本研究的目的是评估大脑区域mOR结合作为可卡因使用复发预测指标的情况。
15名未寻求治疗的成年可卡因使用者被安置在封闭的研究病房中,进行为期12周的监测戒断,出院后随访长达1年。在1周和12周后,使用[11C]卡芬太尼(一种选择性mOR激动剂)的正电子发射断层扫描(PET)测量大脑区域mOR结合。出院后首次使用可卡因(复吸)和连续两天使用可卡因(复发)的时间基于自我报告和尿液毒理学检测。
复发前间隔时间较短与戒断1周和12周时额叶和颞叶皮质区域的mOR结合增加有关(P<0.001),且与1周和12周之间结合减少较少有关(P<0.0008)。12周时的mOR结合与复发后第一个月内使用可卡因的天数百分比之间存在显著正相关(P<0.002)。在多元线性回归分析中,即使考虑了临床变量,mOR结合对复发时间的预测也有显著贡献(R2 = 0.79,P<0.001)。
额叶和颞叶皮质区域大脑mOR结合增加是可卡因使用复发时间的重要独立预测指标,表明大脑内源性阿片系统在可卡因成瘾中起重要作用。