Timberlake William, Leffel Joseph K, Chester Julia A, Froehlich Janice C
Department of Psychological and Brain Sciences, Indiana University, Bloomington, 1101 E. 10th Street, Bloomington, IN 47405, USA.
Alcohol. 2009 Mar;43(2):105-18. doi: 10.1016/j.alcohol.2008.09.007.
Three pairs of Indiana University rat lines (inbred alcohol-preferring and nonpreferring rat lines [P/NPs], high- and low-alcohol-drinking rat lines [HAD/LAD1s and HAD/LAD2s]) were bred in the School of Medicine colony to drink high versus low daily amounts of a 10% vol/vol alcohol test solution (>5.0 g/kg body weight vs. <1.5 g/kg body weight), and a high versus low proportion of alcohol to water (>2:1 vs. <0.5:1) by the end of a 3-week alcohol-water choice condition. This choice phase was always preceded by four days of a forcing procedure with alcohol as the only fluid. The present study examined the contribution of the forcing procedure to the alcohol intake of animals in each pair of lines by comparing daily alcohol intake of rats housed in experimental chambers in a forced group (4 days with only alcohol solution to drink followed by 22 choice days) versus a choice group (both alcohol and water available all 26 days). As expected, under the initial alcohol exposure, high-drinking line rats drank more alcohol than low-drinking line rats, and all forced groups drank more alcohol than choice groups. At the start of the choice phase, all low-drinking line forced groups immediately dropped their alcohol intake to the level of their choice groups. In contrast, all high-drinking line forced groups maintained a high level of alcohol intake under choice, whereas all high-drinking line choice groups slowly increased average alcohol intake across the 22-day choice phase, ending near the average intake of their forced groups. However, a small subset of each high-drinking line choice animals failed to increase alcohol intake until subsequently forced with alcohol for 4 days and tested again in choice. These results indicate that the alcohol-forcing procedure used in deriving these lines resulted in the selection of more than one pathway to a high-drinking phenotype. In addition, high-drinking line animals appeared more sensitive to the differences between laboratory- and colony-testing environments than low-drinking line animals. These data suggest that these high-drinking lines may represent an unexpectedly appropriate complex model of how multiple factors may contribute to the genesis of human alcoholism.
印第安纳大学培育了三对大鼠品系(近交系酒精偏好和非偏好大鼠品系[P/NPs],高酒精饮用量和低酒精饮用量大鼠品系[HAD/LAD1s和HAD/LAD2s]),在医学院的繁殖群体中饲养,使其在为期3周的酒精-水选择条件结束时,每日饮用高剂量与低剂量的10%体积/体积酒精测试溶液(>5.0克/千克体重对<1.5克/千克体重),以及酒精与水的高比例与低比例(>2:1对<0.5:1)。在这个选择阶段之前,总是先进行为期四天的强制程序,只提供酒精作为唯一的液体。本研究通过比较强制组(4天只饮用酒精溶液,随后进行22天的选择期)和选择组(26天内酒精和水都可获取)中饲养在实验室内的大鼠的每日酒精摄入量,来检验强制程序对每对品系动物酒精摄入量的影响。正如预期的那样,在最初接触酒精时,高饮用量品系的大鼠比低饮用量品系的大鼠饮用更多的酒精,并且所有强制组比选择组饮用更多的酒精。在选择阶段开始时,所有低饮用量品系的强制组立即将酒精摄入量降至其选择组的水平。相比之下,所有高饮用量品系的强制组在选择条件下保持高酒精摄入量,而所有高饮用量品系的选择组在22天的选择阶段中平均酒精摄入量缓慢增加,最终接近其强制组的平均摄入量。然而,每个高饮用量品系的选择组中的一小部分动物直到随后再次强制饮用酒精4天并在选择条件下再次测试时才增加酒精摄入量。这些结果表明,用于培育这些品系的酒精强制程序导致选择了不止一条通向高饮用量表型的途径。此外,高饮用量品系的动物似乎比低饮用量品系的动物对实验室测试环境和繁殖群体测试环境之间的差异更敏感。这些数据表明,这些高饮用量品系可能代表了一个意外合适的复杂模型,用于研究多种因素如何可能导致人类酒精中毒的发生。