Herrera Daniel G, Yague Almudena G, Johnsen-Soriano Siv, Bosch-Morell Francisco, Collado-Morente Lucia, Muriach Maria, Romero Francisco J, Garcia-Verdugo J Manuel
Department of Psychiatry, Weill Medical College of Cornell University, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7919-24. doi: 10.1073/pnas.1230907100. Epub 2003 Jun 5.
A major pathogenic mechanism of chronic alcoholism involves oxidative burden to liver and other cell types. We show that adult neurogenesis within the dentate gyrus of the hippocampus is selectively impaired in a rat model of alcoholism, and that it can be completely prevented by the antioxidant ebselen. Rats fed for 6 weeks with a liquid diet containing moderate doses of ethanol had a 66.3% decrease in the number of new neurons and a 227-279% increase in cell death in the dentate gyrus as compared with paired controls. Neurogenesis within the olfactory bulb was not affected by alcohol. Our studies indicate that alcohol abuse, even for a short duration, results in the death of newly formed neurons within the adult brain and that the underlying mechanism is related to oxidative or nitrosative stress. Moreover, these findings suggest that the impaired neurogenesis may be a mechanism mediating cognitive deficits observed in alcoholism.
慢性酒精中毒的一个主要致病机制涉及肝脏和其他细胞类型的氧化负担。我们发现,在酒精中毒大鼠模型中,海马齿状回内的成年神经发生受到选择性损害,而抗氧化剂依布硒仑可以完全预防这种损害。与配对对照组相比,用含中等剂量乙醇的液体饲料喂养6周的大鼠,齿状回中新生神经元数量减少66.3%,细胞死亡增加227 - 279%。嗅球内的神经发生不受酒精影响。我们的研究表明,即使短期酗酒也会导致成人大脑内新形成的神经元死亡,其潜在机制与氧化或亚硝化应激有关。此外,这些发现表明,受损的神经发生可能是介导酒精中毒中观察到的认知缺陷的一种机制。