Lumeng L, Crabb D W
Indiana University School of Medicine, Indianapolis.
Gastroenterology. 1994 Aug;107(2):572-8. doi: 10.1016/0016-5085(94)90185-6.
There is a great deal of evidence for genetic predisposition to alcoholism; considerably less is known regarding predisposition to alcoholic liver disease. The specific genes involved in either disorder are not well understood, although the enzymes of alcohol metabolism appear to play some role. It will be interesting to determine whether genetic factors that alter the expression of these enzymes, in addition to altering the kinetics of the enzymes, could modify responses to drinking. Work in the next few years will include determination of which responses to alcohol are indeed genetically influenced in twin studies, testing additional candidate genes for alcohol-related traits in populations and families, as well as the application of genomic mapping methodologies to alcoholic pedigrees. The latter strategy will be integrated into the larger number of studies that will grow from the Human Genome Project. Animal studies with selectively bred lines of rodents that differ in voluntary alcohol consumption will lead the way to define the neuronal and behavioral substrates responsible for differences in alcohol-drinking behavior. The use of the quantitative trait locus (QTL) mapping approach in F2 intercross between two inbred strains of rodents with opposite alcohol-response characteristics and in recombinant inbred strains derived from F2 intercross already has and will continue to help identify chromosomal locations of genes relevant to voluntary alcohol consumption. Perhaps in the future selective breeding of rodents and QTL mapping strategies can also be used to determine the biology and genetics of alcohol-induced liver injury.
有大量证据表明酒精成瘾存在遗传易感性;而关于酒精性肝病的易感性,人们了解得则少得多。尽管酒精代谢酶似乎发挥了一定作用,但对于这两种疾病所涉及的具体基因,人们还知之甚少。确定除改变酶的动力学外,那些改变这些酶表达的遗传因素是否会改变对饮酒的反应,将会很有意思。未来几年的工作将包括在双胞胎研究中确定哪些对酒精的反应确实受遗传影响,在人群和家庭中测试与酒精相关性状的其他候选基因,以及将基因组图谱方法应用于酒精成瘾家系。后一种策略将被纳入因人类基因组计划而开展的大量研究中。对自愿饮酒量不同的选择性培育啮齿动物品系进行动物研究,将为确定导致饮酒行为差异的神经元和行为基础指明方向。在具有相反酒精反应特征的两个近交系啮齿动物之间进行F2杂交以及在由F2杂交衍生的重组近交系中使用数量性状基因座(QTL)定位方法,已经并将继续有助于确定与自愿饮酒相关基因的染色体位置。也许未来对啮齿动物的选择性育种和QTL定位策略也可用于确定酒精性肝损伤的生物学和遗传学。