Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR, USA.
Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, 505 NW 185th Ave, Beaverton, OR, USA.
Psychopharmacology (Berl). 2018 Jan;235(1):109-120. doi: 10.1007/s00213-017-4748-9. Epub 2017 Oct 19.
Abstinence-based approaches to treating alcohol use disorder (AUD) are highly prevalent, but abstinence from chronic drinking may exacerbate subsequent levels of alcohol intake in relapse.
Use a non-human primate model that encompasses a range of chronic voluntary ethanol drinking to isolate biological responses to repeated cycles of imposed abstinence as a function of baseline voluntary alcohol drinking levels.
Over a 26-month protocol, young adult male rhesus macaques were first induced to drink alcohol and then given continuous access to 4% (w/v) ethanol (n = 8) or water (n = 4) for approximately 14 months, followed by three 28- to 35-day abstinence phases, with 3 months of ethanol access in between. Ethanol intake and blood ethanol concentration (BEC) were the primary dependent variables. Observational signs of physical dependence and circulating ACTH and cortisol were monitored.
Prior to abstinence, stable, categorical, individual differences in voluntary ethanol intake under chronic access conditions were found. Following abstinence, categorical "non-heavy" drinking subjects increased drinking transiently (increased between 0.7 and 1.4 g/kg/day in first month after abstinence) but returned to baseline after 3 months. Categorical "heavy" drinkers, however, maintained drinking 1.0-2.6 g/kg above baseline for over 3 months following abstinence. Signs of physical dependence were rare, although huddling and social withdrawal increased in ethanol and control subjects. The most prominent effect on hormonal measures was heightened cortisol during abstinence that increased to a greater extent in ethanol subjects.
Involuntary abstinence increases drinking in the absence of overt physical withdrawal symptoms, and heavy drinkers are more robustly affected compared to non-heavy drinkers.
基于戒除的方法治疗酒精使用障碍(AUD)非常普遍,但戒除慢性饮酒可能会加剧随后的复饮期间的酒精摄入量。
使用涵盖一系列慢性自愿饮酒的非人类灵长类动物模型,来分离反复强制戒断作为基线自愿饮酒水平的函数的生物学反应。
在 26 个月的方案中,年轻成年雄性恒河猴首先被诱导饮酒,然后连续接触 4%(w/v)乙醇(n=8)或水(n=4)约 14 个月,随后进行三个 28-35 天的戒断阶段,中间有 3 个月的乙醇摄入。乙醇摄入量和血液乙醇浓度(BEC)是主要的依赖变量。监测身体依赖的观察迹象和循环促肾上腺皮质激素(ACTH)和皮质醇。
在戒断之前,在慢性接触条件下发现了自愿乙醇摄入量的稳定、分类和个体差异。戒断后,分类为“非重度”饮酒者的饮酒量短暂增加(在戒断后的第一个月增加了 0.7 至 1.4 g/kg/天),但在 3 个月后恢复到基线。然而,分类为“重度”饮酒者在戒断后 3 个月以上仍保持 1.0-2.6 g/kg/天以上的饮酒量。身体依赖的迹象很少见,尽管乙醇和对照组的抱成团和社交回避增加。对激素测量最显著的影响是戒断期间皮质醇升高,在乙醇组中升高更为明显。
非自愿戒断会增加饮酒量,而没有明显的身体戒断症状,与非重度饮酒者相比,重度饮酒者受影响更为严重。