Holmes R S, Meyer J, VandeBerg J L
Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas 78284.
Prog Clin Biol Res. 1990;344:819-41.
The major baboon liver isozyme of alcohol dehydrogenase (ADH-2) has been purified to homogeneity by affinity chromatography, and characterized as a "typical" Class I mammalian ADH isozyme. In contrast to human liver, which possesses three genetic isozymes (alpha 2, beta 2, and gamma 2) and three hybrid isozymes (alpha beta, alpha gamma, and beta gamma) of Class I ADH, baboon liver exhibits activity of a single major Class I isozyme (beta 2). Kinetic analyses, using alcohol substrates of differing chain lengths, and inhibition with pyrazole, support this classification. Agarose-IEF analyses, substrate specificity studies and immunochemical titrations of the major kidney ADH (ADH-1) also support the occurrence of a second Class I isozyme. The baboon was used as a model to study alcohol-induced changes in liver ADH phenotype following moderate and moderately high alcohol consumption. Four male and four female prepubertal baboons were fed nutritionally adequate liquid diets over a 40-week period, including control diets (weeks 1-8, 17-24, 32-40), moderate (12.5 percent of calories) alcohol diet (weeks 9-16), and a moderately high (25 percent of calories) alcohol diet (weeks 25-32). Liver ADH isozyme patterns and Class I ADH activities from biopsy samples, taken every 4 weeks, were monitored during the feeding study. Decreases in both Class I and Class II ADH activities were indicated in most animals, which may reflect adaptive mechanisms in the liver to continuing alcohol metabolism. Moreover, reversible changes were observed, with trends toward a recovery of ADH isozyme activities following return to the control liquid diets. These studies also have particular significance for human biomedical research work on alcohol, since most of the "drinking" population in typical drinking communities are moderate consumers of alcohol. This work, using the baboon as an animal model, has clearly indicated that alcohol consumption at such moderate levels, brings with it adaptations in the level of ADH isozymes in liver, which may play a protective role.
通过亲和层析法已将狒狒肝脏中主要的乙醇脱氢酶同工酶(ADH - 2)纯化至同质,并将其鉴定为“典型的”I类哺乳动物ADH同工酶。与人类肝脏不同,人类肝脏拥有三种I类ADH的基因同工酶(α2、β2和γ2)以及三种杂合同工酶(αβ、αγ和βγ),而狒狒肝脏仅表现出单一主要I类同工酶(β2)的活性。使用不同链长的乙醇底物进行动力学分析以及用吡唑抑制,均支持这一分类。对主要肾脏ADH(ADH - 1)的琼脂糖等电聚焦分析、底物特异性研究和免疫化学滴定也支持第二种I类同工酶的存在。狒狒被用作模型,以研究适度和适度高剂量饮酒后酒精诱导的肝脏ADH表型变化。在40周的时间里,给四只雄性和四只雌性青春期前的狒狒喂食营养充足的流质饮食,包括对照饮食(第1 - 8周、第17 - 24周、第32 - 40周)、适度(热量的12.5%)酒精饮食(第9 - 16周)和适度高(热量的25%)酒精饮食(第25 - 32周)。在喂养研究期间,每4周采集活检样本,监测肝脏ADH同工酶模式和I类ADH活性。大多数动物的I类和II类ADH活性均降低,这可能反映了肝脏对持续酒精代谢的适应性机制。此外,观察到可逆变化,在恢复对照流质饮食后,ADH同工酶活性有恢复的趋势。这些研究对于人类酒精生物医学研究工作也具有特殊意义,因为在典型饮酒社区中,大多数“饮酒”人群是适度饮酒者。这项以狒狒作为动物模型的研究明确表明,适度饮酒会导致肝脏中ADH同工酶水平发生适应性变化,这可能起到保护作用。