Saunders D E, DiCerbo J A, Williams J R, Hannigan J H
C. S. Mott Center for Human Growth and Development, Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Alcohol. 1997 Sep-Oct;14(5):519-26. doi: 10.1016/s0741-8329(97)00043-8.
High concentrations of alcohol (> or = 1.8%) were shown previously to impair health and viability of cultured hippocampal neurons. Because neurofilament proteins are essential for neuronal process outgrowth and differentiation, the effects of alcohol on these proteins were determined in the neuronal processes of primary cultured gestational day 18 rat hippocampal neurons. At the relatively lower concentrations used in the present study, alcohol caused a concentration-dependent reduction (< or = 47%) in 68 and 200 kDa neurofilament proteins (p < 0.05). Alcohol caused a 32% downward trend in 160 kDa neurofilament protein levels. Alcohol up to 1% (72-h exposure) produced no obvious alterations in neurite extension or explant morphology, and there were no visual signs of cell death. The sensitive MTT dye reduction assay showed no biochemical evidence of decreased cell viability at < or = 0.5% alcohol. The 32-47% reductions in neurofilament protein levels in vitro may hold implications for later hippocampal neuronal differentiation events in animals prenatally exposed to alcohol.
先前的研究表明,高浓度酒精(≥1.8%)会损害培养的海马神经元的健康和活力。由于神经丝蛋白对于神经元突起生长和分化至关重要,因此在原代培养的妊娠第18天大鼠海马神经元的神经突起中,测定了酒精对这些蛋白的影响。在本研究中使用的相对较低浓度下,酒精导致68 kDa和200 kDa神经丝蛋白浓度依赖性降低(≤47%)(p<0.05)。酒精使160 kDa神经丝蛋白水平呈32%的下降趋势。高达1%的酒精(暴露72小时)对神经突延伸或外植体形态没有明显改变,也没有细胞死亡的视觉迹象。灵敏的MTT比色法显示,在≤0.5%酒精浓度下,没有生化证据表明细胞活力下降。体外神经丝蛋白水平降低32%-47%,可能对产前暴露于酒精的动物后期海马神经元分化事件有影响。