间歇性接触酒精后,5 项选择连续反应时间任务中对酒精的参与度会上升。

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Alcohol Pub Date : 2024-01-28 DOI:10.1016/j.alcohol.2024.01.004
Phillip Starski , Addyson Siegle , F. Woodward Hopf
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引用次数: 0

摘要

过量摄入酒精在酒精使用障碍的发展中起着重要作用,每年影响 1,500 万美国人,其中约 88,000 人死于与酒精相关的死亡。导致酒精使用障碍的几个因素包括冲动、动机和注意力。以前的研究曾使用 "5-选择连续反应时间任务"(5-Choice)来分析使用糖的这些行为类型,但最近我们公布了使用 10%酒精作为奖励的研究结果。本研究分析了 48 只小鼠,这些小鼠在 "5-选择 "中接受了对酒精做出反应的训练。所有小鼠首先按酒精偏好进行分配和分析,然后再按消耗量进行分析。在这里,我们对一种名为 "参与度 "的新分类产生了兴趣。高参与度小鼠和低参与度小鼠是根据最后的后期训练中正确反应的数量来确定的。有趣的是,在早期训练阶段,小鼠开始根据它们与任务的互动情况将自己分成两组。在这两个训练阶段中,与低参与度小鼠相比,高参与度小鼠的试验次数和正确反应次数更多,遗漏比例更低。经过三周的间歇性同笼饮水训练后,低参与度小鼠与高参与度小鼠相比,表现出更多的坚持性反应。此外,与高参与度小鼠相比,低参与度小鼠的奖赏和正确潜伏期都有所缩短,这表明小鼠的饮酒动机有所增加。总体而言,参与度分析显示出两个明显不同的群体,其中只有一个群体的工作动机是酒精。5-选择中这两种不同的表型可用于模拟酒精动机行为,这有助于我们进一步了解酒精使用障碍。
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Engagement for alcohol escalates in the 5-choice serial reaction time task after intermittent access

Excessive intake plays a significant role in the development of alcohol use disorder and impacts 15 million Americans annually, with approximately 88 000 dying from alcohol related deaths. Several facets we contribute to alcohol use disorder include impulsivity, motivation, and attention. Previous studies have used the 5-Choice Serial Reaction Time Task (5-Choice) to analyze these types of behaviors using sugar, but recently we have published using 10% alcohol as the reward. This study analyzed 48 mice that were trained to respond for alcohol in the 5-Choice. All mice distributed and analyzed first by alcohol preference and then by consumption. Here, we became interested in a new classification called “engagement”. High-engaged and low-engaged mice were determined by the number of correct responses during final Late-Stage training sessions. Interestingly, during Early-Stage training, the mice began to separate themselves into two groups based on their interaction with the task. Throughout both training stages, high-engaged mice displayed a greater number of trials and correct responses, as well as a lower percentage of omissions compared to low-engaged mice. Following three weeks of intermittent access homecage drinking, low-engaged mice showed greater increase in perseverative responding relative to high-engaged. Additionally, low-engaged mice decreased their reward and correct latencies compared to high-engaged mice suggesting an increase in motivation for alcohol. Overall, engagement analysis presents two clearly different groups, with only one being motivated to work for alcohol. These two distinct phenotypes in the 5-Choice could be used to model alcohol motivated behavior, which could help us further understand alcohol use disorder.

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来源期刊
Alcohol
Alcohol 医学-毒理学
CiteScore
4.60
自引率
4.30%
发文量
74
审稿时长
15.6 weeks
期刊介绍: Alcohol is an international, peer-reviewed journal that is devoted to publishing multi-disciplinary biomedical research on all aspects of the actions or effects of alcohol on the nervous system or on other organ systems. Emphasis is given to studies into the causes and consequences of alcohol abuse and alcoholism, and biomedical aspects of diagnosis, etiology, treatment or prevention of alcohol-related health effects. Intended for both research scientists and practicing clinicians, the journal publishes original research on the neurobiological, neurobehavioral, and pathophysiological processes associated with alcohol drinking, alcohol abuse, alcohol-seeking behavior, tolerance, dependence, withdrawal, protracted abstinence, and relapse. In addition, the journal reports studies on the effects alcohol on brain mechanisms of neuroplasticity over the life span, biological factors associated with adolescent alcohol abuse, pharmacotherapeutic strategies in the treatment of alcoholism, biological and biochemical markers of alcohol abuse and alcoholism, pathological effects of uncontrolled drinking, biomedical and molecular factors in the effects on liver, immune system, and other organ systems, and biomedical aspects of fetal alcohol spectrum disorder including mechanisms of damage, diagnosis and early detection, treatment, and prevention. Articles are published from all levels of biomedical inquiry, including the following: molecular and cellular studies of alcohol''s actions in vitro and in vivo; animal model studies of genetic, pharmacological, behavioral, developmental or pathophysiological aspects of alcohol; human studies of genetic, behavioral, cognitive, neuroimaging, or pathological aspects of alcohol drinking; clinical studies of diagnosis (including dual diagnosis), treatment, prevention, and epidemiology. The journal will publish 9 issues per year; the accepted abbreviation for Alcohol for bibliographic citation is Alcohol.
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