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长期酒精依赖后大鼠前脑神经发生的长期抑制和神经元祖细胞的丧失。

Long-term suppression of forebrain neurogenesis and loss of neuronal progenitor cells following prolonged alcohol dependence in rats.

机构信息

Laboratory of Clinical and Translational Studies, NIH/NIAAA, Bethesda, MD, USA.

出版信息

Int J Neuropsychopharmacol. 2010 Jun;13(5):583-93. doi: 10.1017/S1461145710000246. Epub 2010 Mar 25.

Abstract

Alcohol dependence leads to persistent neuroadaptations, potentially related to structural plasticity. Previous work has shown that hippocampal neurogenesis is modulated by alcohol, but effects of chronic alcohol on neurogenesis in the forebrain subventricular zone (SVZ) have not been reported. Effects in this region may be relevant for the impairments in olfactory discrimination present in alcoholism. Here, we examined the effects of prolonged alcohol dependence on neurogenesis. Rats were sacrificed directly after 7 wk of intermittent alcohol vapour exposure, or 3, 7 or 21 d into abstinence. Proliferation was assessed using BrdU and Ki67 immunoreactivity, newly differentiated neurons (neurogenesis) as doublecortin-immunoreactivity (DCX-IR), and neural stem cells using the SOX2 marker. In the dentate gyrus, chronic dependence resulted in a pattern similar to that previously reported for acute alcohol exposure: proliferation and neurogenesis were suppressed by the end of exposure, rebounded on day 3 of abstinence, and returned to control levels by days 7 and 21. In the SVZ, proliferation was also suppressed at the end of alcohol exposure, followed by a proliferation burst 3 d into abstinence. However, in this area, there was a trend for reduced proliferation on days 7 and 21 of abstinence, and this was accompanied by significant suppression of DCX-IR, indicating a long-term suppression of forebrain neurogenesis. Finally, a decrease in the SOX2 stem cell marker was detected at days 7 and 21, suggesting long-term reduction of the SVZ stem cell pool. While suppression of hippocampal neurogenesis by alcohol dependence is transient, the suppression in the forebrain SVZ appears long-lasting.

摘要

酒精依赖导致持续的神经适应性改变,可能与结构可塑性有关。以前的工作表明,海马神经发生受酒精调节,但慢性酒精对前脑室下区(SVZ)神经发生的影响尚未报道。该区域的影响可能与酒精中毒中存在的嗅觉辨别障碍有关。在这里,我们研究了长期酒精依赖对神经发生的影响。在间歇性酒精蒸气暴露 7 周后,或在戒断 3、7 或 21 天时,大鼠被处死。使用 BrdU 和 Ki67 免疫反应性、双皮质素免疫反应性(DCX-IR)评估增殖,使用 SOX2 标志物评估新分化神经元(神经发生)和神经干细胞。在齿状回,慢性依赖导致的模式类似于先前报道的急性酒精暴露:暴露结束时增殖和神经发生受到抑制,戒断第 3 天反弹,戒断第 7 天和第 21 天恢复到对照水平。在 SVZ 中,增殖在酒精暴露结束时也受到抑制,随后在戒断第 3 天出现增殖爆发。然而,在该区域,戒断第 7 天和第 21 天的增殖有减少的趋势,这伴随着 DCX-IR 的显著抑制,表明前脑神经发生的长期抑制。最后,在戒断第 7 天和第 21 天检测到 SOX2 干细胞标志物减少,表明 SVZ 干细胞池长期减少。虽然酒精依赖对海马神经发生的抑制是短暂的,但对前脑 SVZ 的抑制似乎是持久的。

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