Department of Psychiatry, Center for Addiction Research, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
J Neural Transm (Vienna). 2010 Apr;117(4):513-9. doi: 10.1007/s00702-010-0378-7. Epub 2010 Feb 27.
Hypothalamic-pituitary-adrenal (HPA) axis dysfunction has been implicated in the pathogenesis of addictive behaviour and especially in alcohol craving. The pro-opiomelanocortin gene (POMC), encoding a 241 amino acids stretching polypeptide hormone precursor, plays an important role in the regulation of the HPA, and is prone to epigenetic regulation due to promoter-related DNA methylation. Aim of the present study therefore was to investigate possible differences in promoter-related DNA methylation in patients suffering from alcohol dependence compared to healthy controls. We analysed the DNA methylation of the 5' promoter of the POMC gene that is embedded in a CpG island using bisulfite sequencing in 145 alcohol-dependent patients and 37 healthy controls taken from the Franconian Alcoholism Research Studies. We found only marginal, hence significant differences at single CpG sites between patients and controls. We identified a cluster of CpGs showing a significant association with alcohol craving in the patients group. These results implicate that epigenetic changes possibly due to alcohol intake may contribute to craving via promoting HPA-axis dysfunction. Further studies should more closely investigate the impact of these changes on the several derivatives of the POMC gene.
下丘脑-垂体-肾上腺(HPA)轴功能障碍与成瘾行为的发病机制有关,尤其是与酒精渴求有关。编码 241 个氨基酸延伸多肽激素前体的前阿黑皮素原基因(POMC)在 HPA 的调节中起着重要作用,由于启动子相关的 DNA 甲基化,它容易受到表观遗传调节。因此,本研究的目的是调查与健康对照组相比,酒精依赖患者中与启动子相关的 DNA 甲基化是否存在差异。我们使用 bisulfite 测序分析了来自弗兰肯酗酒研究的 145 名酒精依赖患者和 37 名健康对照者的 POMC 基因 5'启动子的 DNA 甲基化情况,该启动子嵌入一个 CpG 岛。我们只在患者和对照组之间的单个 CpG 位点发现了边缘性但有统计学意义的差异。我们确定了一组与患者组中酒精渴求显著相关的 CpG 位点。这些结果表明,由于饮酒引起的表观遗传变化可能通过促进 HPA 轴功能障碍导致渴求。进一步的研究应更密切地调查这些变化对 POMC 基因的几个衍生物的影响。