Department of Clinical Neuroscience, Division of Psychiatry, Karolinska Institutet, Sweden.
Brain Res. 2009 Dec 11;1305 Suppl:S2-6. doi: 10.1016/j.brainres.2009.09.093. Epub 2009 Sep 30.
Acamprosate is a widely utilized, efficacious treatment for relapse prevention in alcohol dependent patients. The mechanism of acamprosate action is hypothesized to be by modulation of craving responses. Previous research has suggested that acamprosate may affect the hypothalamic pituitary adrenal (HPA) axis as well as beta-endorphin. The aim of the present study was to investigate if acamprosate attenuates alcohol craving following a short-term treatment, and if craving and drinking measures are correlated to changes in HPA-axis hormones and beta-endorphin. In a double-blind design, 56 alcohol dependent treatment seeking patients were randomized to 21 days of either acamprosate (1998 mg/day) or placebo treatment. Subjective, physiological and biological measurements were recorded at inclusion and on day 21. The results showed that acamprosate treated patients showed significantly reduced craving compared to placebo. Further, a significant correlation was shown between craving and alcohol consumption during study. No changes in hormonal levels were found in acamprosate treated patients compared to placebo.
钙通道调节剂乙酰谷酰胺是一种广泛应用于临床的抗酒渴求药物,其作用机制可能是通过调节酒渴求反应。已有研究提示钙通道调节剂可能影响下丘脑-垂体-肾上腺(HPA)轴及β-内啡肽。本研究旨在观察钙通道调节剂短期治疗能否减轻酒渴求,并探讨 HPA 轴激素和β-内啡肽的变化与酒渴求及饮酒的关系。采用随机、双盲、安慰剂对照的方法,将 56 例酒精依赖患者分为钙通道调节剂(1998mg/d)组和安慰剂组,进行为期 21 天的治疗。分别于入组时和治疗第 21 天记录患者的主观、生理和生物学指标。结果显示,钙通道调节剂组患者的酒渴求明显低于安慰剂组,而且治疗期间患者的酒渴求与饮酒量呈显著正相关。与安慰剂组相比,钙通道调节剂组患者的激素水平无明显变化。