Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA 19104, USA.
Psychiatry Res. 2013 Jun 30;208(1):62-6. doi: 10.1016/j.psychres.2013.03.011. Epub 2013 Apr 5.
The opioid receptor family is involved in the development and maintenance of drug addiction. The mu-opioid receptor (MOR) mediates the rewarding effects of multiple drugs, including opiates and cocaine. A number of proteins interact with MOR, potentially modulating MOR function and altering the physiological consequences of drug use. These mu-opioid receptor interacting proteins (MORIPs) are potential therapeutic targets for the treatment of addiction. The Wntless (WLS) protein was recently identified as a MORIP in a yeast two-hybrid screen. In this study, we conducted a case-control association analysis of 16 WLS genetic variants in opioid and cocaine addicted individuals of both African-American (opioid n=336, cocaine n=908) and European-American (opioid n=335, cocaine n=336) ancestry. Of the analyzed SNPs, three were nominally associated with opioid addiction and four were nominally associated with cocaine addiction. None of these associations were significant following multiple testing correction. These data suggest that the common variants of WLS analyzed in this study are not associated with opioid or cocaine addiction. However, this study does not exclude the possibilities that rare variants in WLS may affect susceptibility to drug addiction, or that common variants with small effect size may fall below the detection level of our analysis.
阿片受体家族参与了药物成瘾的发展和维持。μ-阿片受体(MOR)介导多种药物的奖赏效应,包括阿片类药物和可卡因。许多蛋白质与 MOR 相互作用,可能调节 MOR 功能并改变药物使用的生理后果。这些μ-阿片受体相互作用蛋白(MORIPs)是治疗成瘾的潜在治疗靶点。Wntless(WLS)蛋白最近在酵母双杂交筛选中被鉴定为 MORIP。在这项研究中,我们对来自非洲裔美国人(阿片类药物 n=336,可卡因 n=908)和欧洲裔美国人(阿片类药物 n=335,可卡因 n=336)的阿片类药物和可卡因成瘾个体的 16 个 WLS 遗传变异进行了病例对照关联分析。在分析的 SNP 中,有三个与阿片类药物成瘾有显著关联,四个与可卡因成瘾有显著关联。经过多次测试校正后,这些关联都没有统计学意义。这些数据表明,在这项研究中分析的 WLS 常见变体与阿片类或可卡因成瘾无关。然而,本研究不能排除 WLS 中的稀有变体可能影响药物成瘾易感性的可能性,也不能排除常见变体的效应量较小而低于我们分析的检测水平的可能性。