Xu Xuting, Ji Huihui, Liu Guili, Wang Qinwen, Liu Huifen, Shen Wenwen, Li Longhui, Xie Xiaohu, Zhou Wenhua, Duan Shiwei
Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China.
Laboratory of Behavioral Neuroscience, Ningbo Addiction Research and Treatment Center, Ningbo, Zhejiang 315010, China.
Gene. 2016 Jun 10;584(1):54-59. doi: 10.1016/j.gene.2016.03.010. Epub 2016 Mar 11.
As a member of the neurotrophic factor family, brain derived neurotrophic factor (BDNF) plays an important role in the survival and differentiation of neurons. The aim of our work was to evaluate the role of BDNF promoter methylation in drug addiction. A total of 60 drug abusers (30 heroin and 30 methylamphetamine addicts) and 52 healthy age- and gender-matched controls were recruited for the current case control study. Bisulfite pyrosequencing technology was used to determine the methylation levels of five CpGs (CpG1-5) on the BDNF promoter. Among the five CpGs, CpG5 methylation was significantly lower in drug abusers than controls. Moreover, significant associations were found between CpG5 methylation and addictive phenotypes including tension-anxiety, anger-hostility, fatigue-inertia, and depression-dejection. In addition, luciferase assay showed that the DNA fragment of BDNF promoter played a key role in the regulation of gene expression. Our results suggest that BDNF promoter methylation is associated with drug addiction, although further studies are needed to understand the mechanisms by which BDNF promoter methylation contributes to the pathophysiology of drug addiction.
作为神经营养因子家族的一员,脑源性神经营养因子(BDNF)在神经元的存活和分化中发挥着重要作用。我们研究的目的是评估BDNF启动子甲基化在药物成瘾中的作用。本病例对照研究共招募了60名药物滥用者(30名海洛因成瘾者和30名甲基苯丙胺成瘾者)以及52名年龄和性别匹配的健康对照者。采用亚硫酸氢盐焦磷酸测序技术测定BDNF启动子上五个CpG位点(CpG1 - 5)的甲基化水平。在这五个CpG位点中,药物滥用者的CpG5甲基化水平显著低于对照组。此外,还发现CpG5甲基化与成瘾表型(包括紧张 - 焦虑、愤怒 - 敌意、疲劳 - 惰性和抑郁 - 沮丧)之间存在显著关联。另外,荧光素酶报告基因检测表明,BDNF启动子的DNA片段在基因表达调控中起关键作用。我们的结果表明,BDNF启动子甲基化与药物成瘾有关,尽管需要进一步研究来了解BDNF启动子甲基化导致药物成瘾病理生理过程的机制。