Nickell Chelsea R Geil, Peng Hui, Hayes Dayna M, Chen Kevin Y, McClain Justin A, Nixon Kimberly
Department of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, United States.
Front Psychiatry. 2017 Dec 15;8:283. doi: 10.3389/fpsyt.2017.00283. eCollection 2017.
Excessive alcohol consumption during adolescence remains a significant health concern as alcohol drinking during adolescence increases the likelihood of an alcohol use disorder in adulthood by fourfold. Binge drinking in adolescence is a particular problem as binge-pattern consumption is the biggest predictor of neurodegeneration from alcohol and adolescents are particularly susceptible to the damaging effects of alcohol. The adolescent hippocampus, in particular, is highly susceptible to alcohol-induced structural and functional effects, including volume and neuron loss. However, hippocampal structure and function may recover with abstinence and, like in adults, a reactive burst in hippocampal neurogenesis in abstinence may contribute to that recovery. As the mechanism of this reactive neurogenesis is not known, the current study investigated potential mechanisms of reactive neurogenesis in binge alcohol exposure in adolescent, male rats. In a screen for cell cycle perturbation, a dramatic increase in the number of cells in all phases of the cycle was observed at 7 days following binge ethanol exposure as compared to controls. However, the proportion of cells in each phase was not different between ethanol-exposed rats and controls, indicating that cell cycle dynamics are not responsible for the reactive burst in neurogenesis. Instead, the marked increase in hippocampal proliferation was shown to be due to a twofold increase in proliferating progenitor cells, specifically an increase in cells colabeled with the progenitor cell marker Sox2 and S-phase (proliferation) marker, BrdU, in ethanol-exposed rats. To further characterize the individual subtypes of neural progenitor cells (NPCs) affected by adolescent binge ethanol exposure, a fluorescent quadruple labeling technique was utilized to differentiate type 1, 2a, 2b, and 3 progenitor cells simultaneously. At one week into abstinence, animals in the ethanol exposure groups had an increase in proliferating type 2 (intermediate progenitors) and type 3 (neuroblast) progenitors but not type 1 neural stem cells. These results together suggest that activation of type 2 NPCs out of quiescence is likely the primary mechanism for reactive hippocampal neurogenesis following adolescent alcohol exposure.
青少年时期过度饮酒仍然是一个重大的健康问题,因为青少年饮酒会使成年后患酒精使用障碍的可能性增加四倍。青少年时期的暴饮是一个特别的问题,因为暴饮模式的饮酒是酒精导致神经退行性变的最大预测因素,而且青少年特别容易受到酒精的损害作用影响。尤其是青少年的海马体,对酒精引起的结构和功能影响高度敏感,包括体积减小和神经元丢失。然而,海马体的结构和功能可能会随着戒酒而恢复,并且与成年人一样,戒酒时海马体神经发生的反应性激增可能有助于这种恢复。由于这种反应性神经发生的机制尚不清楚,本研究调查了青春期雄性大鼠暴饮酒精后反应性神经发生的潜在机制。在一项细胞周期扰动筛查中,与对照组相比,暴饮乙醇暴露7天后,观察到细胞周期各阶段的细胞数量显著增加。然而,乙醇暴露组大鼠和对照组之间各阶段细胞的比例没有差异,这表明细胞周期动力学不是神经发生反应性激增的原因。相反,海马体增殖的显著增加被证明是由于增殖祖细胞增加了两倍,具体而言,在乙醇暴露的大鼠中,与祖细胞标记物Sox2和S期(增殖)标记物BrdU共标记的细胞增加。为了进一步表征受青少年暴饮乙醇暴露影响的神经祖细胞(NPC)的个体亚型,采用荧光四重标记技术同时区分1型、2a型、2b型和3型祖细胞。在戒酒一周时,乙醇暴露组的动物中增殖的2型(中间祖细胞)和3型(神经母细胞)祖细胞增加,但1型神经干细胞没有增加。这些结果共同表明,2型NPC从静止状态的激活可能是青少年酒精暴露后海马体反应性神经发生的主要机制。