Hoffman Paula L, Glanz Jason, Tabakoff Boris
Department of Pharmacology, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
Alcohol Clin Exp Res. 2002 Jul;26(7):1078-87.
There has been considerable interest in identifying biochemical markers indicative of a genetic predisposition to alcohol dependence ("trait markers"), as well as biochemical markers of recent alcohol drinking ("state markers"). Platelet adenylyl cyclase activity has been suggested as a trait and/or as a state marker related to alcohol dependence. We have now measured platelet adenylyl cyclase activity in more than 1400 well-characterized subjects, which allows us to investigate the influence of a broad range of factors on this activity.
Subjects were recruited as part of the WHO/ISBRA Study on State and Trait Markers of Alcohol Use and Dependence and were interviewed by using the WHO/ISBRA Interview Schedule. Adenylyl cyclase activity (basal, cesium fluoride [CsF]-, forskolin- and Gpp(NH)p-stimulated activities) was measured in platelet samples that were obtained at the time of interview. Data were analyzed by multivariate regression analyses.
The multivariate analyses revealed that recent abstinence from alcohol was associated with diminutions in platelet adenylyl cyclase activities. A positive family history of alcohol dependence was associated with higher levels of adenylyl cyclase activities, and there was a significant interaction between the effect of alcohol consumption in the past month and family history of alcohol dependence; that is, the influence of alcohol consumption depended on whether the individual had a positive family history. A history of marijuana abuse also was associated with higher levels of platelet adenylyl cyclase activities, and a history of major depression was associated with lower levels of forskolin- and CsF-stimulated activities. Sex, race, and site of recruitment also affected some adenylyl cyclase activities, but there was no significant association of alcohol dependence or abuse with any of the platelet adenylyl cyclase activities.
The large population and extensive characterization of subjects in this study provided an advantage over previous studies in which only the association of a few individual factors with adenylyl cyclase activity was investigated. The results demonstrate that although platelet adenylyl cyclase activity could be useful as a trait marker of alcohol dependence, its reliability in this regard is diminished by the influence of recent alcohol drinking and other variables. The associations between platelet adenylyl cyclase activities and marijuana abuse, as well as a history of depression, suggest that it may be worthwhile to study the genetic association of adenylyl cyclases (e.g., polymorphisms in the genes that code for particular adenylyl cyclase isoforms) with a predisposition to depression as well as to alcohol or marijuana abuse/dependence.
人们对确定表明酒精依赖遗传易感性的生化标志物(“特质标志物”)以及近期饮酒的生化标志物(“状态标志物”)有着浓厚兴趣。血小板腺苷酸环化酶活性已被认为是与酒精依赖相关的特质和/或状态标志物。我们现已对1400多名特征明确的受试者的血小板腺苷酸环化酶活性进行了测量,这使我们能够研究多种因素对该活性的影响。
受试者作为世界卫生组织/国际生物酒精研究协会酒精使用和依赖的状态与特质标志物研究的一部分被招募,并使用世界卫生组织/国际生物酒精研究协会访谈时间表进行访谈。在访谈时采集的血小板样本中测量腺苷酸环化酶活性(基础活性、氟化铯[CsF]刺激活性、福斯高林刺激活性和鸟苷5'-三磷酸[Gpp(NH)p]刺激活性)。通过多变量回归分析对数据进行分析。
多变量分析显示,近期戒酒与血小板腺苷酸环化酶活性降低有关。酒精依赖的阳性家族史与腺苷酸环化酶活性水平较高有关,且过去一个月饮酒的影响与酒精依赖家族史之间存在显著交互作用;也就是说,饮酒的影响取决于个体是否有阳性家族史。大麻滥用史也与血小板腺苷酸环化酶活性水平较高有关,而重度抑郁史与福斯高林和CsF刺激活性水平较低有关。性别、种族和招募地点也会影响某些腺苷酸环化酶活性,但酒精依赖或滥用与任何血小板腺苷酸环化酶活性均无显著关联。
本研究中大量的人群和受试者的广泛特征为优于以往研究提供了优势,以往研究仅调查了少数个体因素与腺苷酸环化酶活性的关联。结果表明,尽管血小板腺苷酸环化酶活性可能作为酒精依赖的特质标志物有用,但其在这方面的可靠性因近期饮酒和其他变量的影响而降低。血小板腺苷酸环化酶活性与大麻滥用以及抑郁史之间的关联表明,研究腺苷酸环化酶的遗传关联(例如,编码特定腺苷酸环化酶同工型的基因中的多态性)与抑郁易感性以及酒精或大麻滥用/依赖可能是值得的。