Worrall S, de Jersey J, Shanley B C, Wilce P A
Department of Biochemistry, University of Queensland, Australia.
Alcohol Alcohol. 1991;26(4):437-44. doi: 10.1093/oxfordjournals.alcalc.a045136.
Liver cytosolic fractions, obtained from rats pair-fed diets supplemented with either ethanol or an isocaloric amount of sucrose for periods from 3 weeks to 27 months, were tested for the presence of acetaldehyde-modified proteins by immunoblotting, using a partially purified antiserum raised in rabbits against proteins modified by acetaldehyde in vitro. The antiserum reacted with a large number of proteins in cytosolic fractions from ethanol-fed rats but did not react with any proteins in the same fraction from control animals. The duration of the ethanol-containing diet did not appear to influence the number of proteins modified or the total amount of modification within the time range tested. These results indicate that many proteins in rat liver cytosol are targets for modification by acetaldehyde in vivo.
从对喂的大鼠中获得肝脏胞质部分,这些大鼠的饮食分别补充了乙醇或等热量的蔗糖,持续时间从3周至27个月,通过免疫印迹法检测乙醛修饰蛋白的存在,使用在兔子体内针对体外被乙醛修饰的蛋白产生的部分纯化抗血清。该抗血清与来自喂食乙醇大鼠的胞质部分中的大量蛋白发生反应,但与来自对照动物相同部分中的任何蛋白均无反应。在所测试的时间范围内,含乙醇饮食的持续时间似乎不影响被修饰蛋白的数量或修饰总量。这些结果表明,大鼠肝脏胞质溶胶中的许多蛋白是体内乙醛修饰的靶点。