酗酒动机的遗传贡献啮齿动物模型。

4区 心理学 Q2 Psychology
John C Crabbe
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引用次数: 0

摘要

总之,关于酒精强化价值的遗传贡献的研究非常少。几乎所有此类研究都对双瓶偏好测试进行了研究。尽管我在解释该测试时提出了一些不足之处,但啮齿类动物基因型在有水可自由饮用的情况下饮用乙醇的意愿提供了酒精相对于其他基因型的强化价值的合理总体估计(Green 和 Grahame,2008 年)。然而,如上所述,偏好饮酒研究可能永远无法避免味觉偏好的干扰作用,而且其摄入量往往不足以产生具有药理学意义的 BAL。因此,改进强化价值测量方法的探索仍在继续。在麦克莱恩(McClearn)在本系列的开创性综述中考虑的潜在动机因素中,我们可以有把握地得出结论:啮齿动物饮酒的主要目的不是获取卡路里。味道(和气味)的作用仍然是一个难题。麦克莱恩的观点似乎是正确的,尤其是那些避免饮酒的基因型,它们很可能是根据胃肠道前的感觉线索来避免饮酒的;然而,胃肠道后遗症也很重要。坎宁安的胃内模型显示,对于最著名的例子,即通常几乎绝对避免饮酒的 DBA/2J 和 HAP-2 小鼠,胃前和胃后调节因素都发挥了作用。随后的大量数据证实了麦克莱恩早先的结论,即至少 C57BL/6J 小鼠不会通过调整摄入量来调节自身摄入的酒精剂量。这就给我们留下了一个难题:为什么几乎所有基因型的小鼠,即使是那些经过多代定向选择培育出的自愿摄入量高的基因型小鼠,也无法自我摄入令人陶醉的酒精量?自麦克莱恩发表评论以来,许多巧妙的酒精动机效应指数测定方法已被广泛使用,新的酒精依赖诱导方法也取代了 1968 年流行的旧方法。我试图找出遗传学在哪些领域大有可为,可以取得丰硕成果,而且总体上认为,我们现在对一些尚待进行的重要实验有了更清晰的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rodent models of genetic contributions to motivation to abuse alcohol.

Rodent models of genetic contributions to motivation to abuse alcohol.

Rodent models of genetic contributions to motivation to abuse alcohol.

Rodent models of genetic contributions to motivation to abuse alcohol.

In summary, there are remarkably few studies focused on the genetic contributions to alcohol's reinforcing values. Almost all such studies examine the two-bottle preference test. Despite the deficiencies I have raised in its interpretation, a rodent genotype's willingness to drink ethanol when water is freely available offers a reasonable aggregate estimate of alcohol's reinforcing value relative to other genotypes (Green and Grahame 2008). As indicated above, however, preference drinking studies will likely never avoid the confounding role of taste preferences and most often yield intake levels not sufficient to yield a pharmacologically significant BAL. Thus, the quest for improved measures of reinforcing value continues. Of the potential motivational factors considered by McClearn in his seminal review in this series, we can safely conclude that rodent alcohol drinking is not primarily directed at obtaining calories. The role of taste (and odor) remains a challenge. McClearn appears to have been correct that especially those genotypes that avoid alcohol are probably doing so based on preingestive sensory cues; however, postingestive consequences are also important. Cunningham's intragastric model shows the role of both preingestional and postingestional modulating factors for the best known examples, the usually nearly absolutely alcohol-avoiding DBA/2J and HAP-2 mice. Much subsequent data reinforce McClearn's earlier conclusion that C57BL/6J mice, at least, do not regulate their intake around a given self-administered dose of alcohol by adjusting their intake. This leaves us with the puzzle of why nearly all genotypes, even those directionally selectively bred for high voluntary intake for many generations, fail to self-administer intoxicating amounts of alcohol. Since McClearn's review, many ingenious assays to index alcohol's motivational effects have been used extensively, and new methods for inducing dependence have supplanted the older ones prevalent in 1968. I have tried to identify promising areas where the power of genetics could be fruitfully harvested and generally feel that we have a much more clear idea now about some important experiments remaining to be performed.

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来源期刊
Nebraska Symposium on Motivation
Nebraska Symposium on Motivation PSYCHOLOGY, SOCIAL-
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