Hu Wei, Saba Laura, Kechris Katherina, Bhave Sanjiv V, Hoffman Paula L, Tabakoff Boris
Department of Pharmacology, University of Colorado School of Medicine, Mail Stop 8303, P.O. Box 6511, Aurora, CO 80045-0511, USA.
J Pharmacol Exp Ther. 2008 Sep;326(3):792-800. doi: 10.1124/jpet.108.137521. Epub 2008 Jun 11.
Alcohol "sensitivity" has been proposed as a predictive factor for development of alcohol dependence (Schuckit et al., 2005). Most measures of alcohol sensitivity in humans and animals include a component that can be ascribed to acute functional tolerance (AFT). AFT is a form of tolerance that develops within a single period of alcohol exposure and has a genetic component. We used microarray technology as well as quantitative trait locus analysis of phenotypic and gene expression data across 30 BXD recombinant inbred strains of mice, 20 inbred strains of mice, and two replicate lines of mice selectively bred for differences in AFT, to identify differentially expressed candidate genes that contribute to predisposition to AFT. Eight candidate genes were identified by our statistical and filtering methods. The location of brain expression of these genes was mapped using the Allen Brain Atlas (http://www.brain-map.org), and the transcript location and molecular pathway analysis indicated that brain structures and biochemical pathways implicated in long-term potentiation and memory might also participate in the generation of acute functional alcohol tolerance.
酒精“敏感性”已被提出作为酒精依赖发展的一个预测因素(舒基特等人,2005年)。大多数人和动物酒精敏感性的测量方法都包含一个可归因于急性功能性耐受(AFT)的成分。AFT是一种在单次酒精暴露期间产生的耐受形式,具有遗传成分。我们使用微阵列技术以及对30个BXD重组近交系小鼠、20个近交系小鼠和两个因AFT差异而选择性培育的小鼠重复品系的表型和基因表达数据进行数量性状基因座分析,以确定导致AFT易感性的差异表达候选基因。通过我们的统计和筛选方法鉴定出了八个候选基因。利用艾伦脑图谱(http://www.brain-map.org)绘制了这些基因在大脑中的表达位置,转录本位置和分子途径分析表明,与长时程增强和记忆相关的脑结构和生化途径也可能参与急性功能性酒精耐受的产生。