Department of Psychiatry, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Mental Health Institute of Central South University, Changsha, Hunan, China.
PLoS One. 2019 Aug 23;14(8):e0221506. doi: 10.1371/journal.pone.0221506. eCollection 2019.
Expression of FosB gene in striatum is essential in addiction establishment. Activated glucocorticoid receptors (GRs) induce FosB gene expression in response to stressor. Therefore, elevation of FosB expression in striatum serves as one mechanism by which stress increases risk for addiction. In this study, adult male Sprague-Dawley rats were used to investigate whether chronic stress result in histone modifications at FosB gene promoter in striatum and how these histone modifications affect FosB expression and the establishment of addiction behavior after administration of drugs of abuse. Animals were randomly assigned to three groups: Electric foot shock (EFS) group received 7-day EFS to induce chronic stress; electric foot shock plus mifepristone (EFS + Mif) group were injected with mifepristone, a nonspecific GRs antagonist, before EFS; control group did not receive any EFS. All groups then received 2-day conditioned place preference (CPP) training with morphine (5 mg/kg body weight) to test vulnerability to drug addiction. Before and after morphine administration, FosB mRNA in striatum was quantified by real-time RT-PCR. Levels of histone H3/H4 acetylation and histone H3K4 dimethylation at FosB promoter in striatum after morphine administration were measured by using chromatin immunoprecipitation (ChIP) plus real-time PCR. EFS group had stronger place preference to morphine and had significantly higher level of FosB mRNA in striatum than the other two groups. H3K4 dimethylation was 2.6-fold higher in EFS group than control group, while no statistical difference in H3/H4 acetylation. Mifepristone administration before EFS decreased histone H3K4 dimethylation and FosB mRNA in striatum, and also diminished morphine-induced conditioned place preference. Altogether, increased level of H3K4 dimethylation at FosB promoter in striatum is partially dependent on the activation of GR and responsible for the elevated level of morphine-induced FosB mRNA in chronic stressed animals.
纹状体中 FosB 基因的表达对于成瘾的建立至关重要。激活的糖皮质激素受体(GRs)在应激反应中诱导 FosB 基因的表达。因此,纹状体中 FosB 表达的升高是应激增加成瘾风险的一种机制。在这项研究中,使用成年雄性 Sprague-Dawley 大鼠来研究慢性应激是否会导致纹状体中 FosB 基因启动子的组蛋白修饰,以及这些组蛋白修饰如何影响 FosB 的表达以及滥用药物后成瘾行为的建立。动物被随机分配到三组:电脚休克(EFS)组接受 7 天的 EFS 以诱导慢性应激;电脚休克加米非司酮(EFS + Mif)组在 EFS 前注射米非司酮,一种非特异性 GRs 拮抗剂;对照组未接受任何 EFS。所有组随后接受 2 天的吗啡(5mg/kg 体重)条件性位置偏好(CPP)训练,以测试对成瘾的易感性。在给予吗啡前后,通过实时 RT-PCR 定量纹状体中的 FosB mRNA。通过染色质免疫沉淀(ChIP)加实时 PCR 测量给予吗啡后纹状体中 FosB 启动子处组蛋白 H3/H4 乙酰化和组蛋白 H3K4 二甲基化的水平。EFS 组对吗啡的位置偏好更强,纹状体中的 FosB mRNA 水平明显高于其他两组。EFS 组的 H3K4 二甲基化水平比对照组高 2.6 倍,而 H3/H4 乙酰化没有统计学差异。EFS 前给予米非司酮可降低纹状体中的组蛋白 H3K4 二甲基化和 FosB mRNA,并且还减弱了吗啡诱导的条件性位置偏好。总之,纹状体中 FosB 启动子处 H3K4 二甲基化水平的升高部分依赖于 GR 的激活,并导致慢性应激动物中吗啡诱导的 FosB mRNA 水平升高。