Myrick Hugh, Anton Raymond F, Li Xingbao, Henderson Scott, Randall Patrick K, Voronin Konstantin
Research and Development Service, Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, SC, USA.
Arch Gen Psychiatry. 2008 Apr;65(4):466-75. doi: 10.1001/archpsyc.65.4.466.
Medication for the treatment of alcoholism is currently not particularly robust. Neuroimaging techniques might predict which medications could be useful in the treatment of alcohol dependence.
To explore the effect of naltrexone, ondansetron hydrochloride, or the combination of these medications on cue-induced craving and ventral striatum activation.
Functional brain imaging was conducted during alcohol cue presentation.
Participants were recruited from the general community following media advertisement. Experimental procedures were performed in the magnetic resonance imaging suite of a major training hospital and medical research institute.
Ninety non-treatment-seeking alcohol-dependent (by DSM-IV criteria) and 17 social drinking (< 14 drinks per week) paid volunteers recruited through advertisements at an academic center.
A taste of alcohol and a series of alcohol-related pictures, neutral beverage pictures, and visual control images were provided to volunteers after 7 days of double-blind randomly assigned daily dosing with 50 mg of naltrexone (n = 23), 0.50 mg of ondansetron hydrochloride (n = 23), the combination of the 2 medications (n = 20), or matching placebos (n = 24).
Difference in brain blood oxygen level-dependent magnetic resonance when viewing alcohol pictures vs neutral beverage pictures with a particular focus on ventral striatum activity comparison across medication groups. Self-ratings of alcohol craving.
The combination treatment decreased craving for alcohol. Naltrexone with (P = .02) or without (P = .049) ondansetron decreased alcohol cue-induced activation of the ventral striatum. Ondansetron by itself was similar to naltrexone and the combination in the overall analysis but intermediate in a region-specific analysis.
Consistent with animal data that suggest that both naltrexone and ondansetron reduce alcohol-stimulated dopamine output in the ventral striatum, the current study found evidence that these medications, alone or in combination, could decrease alcohol cue-induced activation of the ventral striatum, consistent with their putative treatment efficacy.
目前用于治疗酒精成瘾的药物效果并不特别显著。神经影像学技术或许能够预测哪些药物对治疗酒精依赖有效。
探究纳曲酮、盐酸昂丹司琼或这两种药物联合使用对线索诱发的渴望及腹侧纹状体激活的影响。
在呈现酒精线索期间进行功能性脑成像。
通过媒体广告从普通社区招募参与者。实验程序在一家大型教学医院和医学研究所的磁共振成像室进行。
通过在学术中心发布广告招募的90名未寻求治疗的酒精依赖者(符合《精神疾病诊断与统计手册》第四版标准)和17名社交饮酒者(每周饮酒少于14杯)付费志愿者。
在对志愿者进行为期7天的双盲随机每日给药后,提供一次酒精品尝以及一系列与酒精相关的图片、中性饮料图片和视觉对照图像,给药方案为50毫克纳曲酮(n = 23)、0.50毫克盐酸昂丹司琼(n = 23)、两种药物联合使用(n = 20)或匹配的安慰剂(n = 24)。
观看酒精图片与中性饮料图片时脑血氧水平依赖磁共振的差异,特别关注各药物组腹侧纹状体活动的比较。对酒精渴望的自我评分。
联合治疗降低了对酒精的渴望。纳曲酮单独使用(P = 0.02)或与昂丹司琼联合使用(P = 0.049)均降低了酒精线索诱发的腹侧纹状体激活。在总体分析中,昂丹司琼本身与纳曲酮及联合用药相似,但在区域特异性分析中处于中间水平。
与动物数据一致,即纳曲酮和昂丹司琼均可降低腹侧纹状体中酒精刺激的多巴胺输出,本研究发现证据表明这些药物单独或联合使用均可降低酒精线索诱发的腹侧纹状体激活,这与其假定的治疗效果相符。