Department of Psychology, Texas A&M University, 425 Ross Street, College Station, TX 77843-4235, USA.
Departments of Animal Science and Veterinary Integrative Biosciences, Texas A&M University, 474 Olsen Blvd, College Station, TX 77843-2471, USA.
Alcohol Alcohol. 2020 Oct 20;55(6):608-615. doi: 10.1093/alcalc/agaa035.
Rodent studies propose potential mechanisms linking excessive drinking and pain hypersensitivity (hyperalgesia), such that stress hormones (i.e. epinephrine and cortisol) mediate induction and maintenance of alcohol withdrawal-induced hyperalgesia. The first aim of this study was to examine whether hyperalgesia would occur within 48 h after a drinking episode in healthy young adult binge drinkers. The second was to examine whether stress hormones and negative effect would be associated with binge drinking or alcohol withdrawal-associated hyperalgesia.
A cross-sectional experiment was conducted in five groups with naturally occurring drinking (mean age = 19.6, range 18-29 years): abstainers (n = 43, 54% female), moderate drinkers with (n = 50, 50% female) or without recent drinking (i.e. within 48 h, n = 23, 26% female) and binge drinkers with (n = 36, 58% female) or without recent drinking (n = 25, 44% female). All types of drinkers endorsed drinking about 2-3 times a month and 2-3 years of drinking history.
Muscle pressure pain thresholds were significantly lower in the binge group with recent drinking compared to other groups, but cutaneous mechanical and heat pain thresholds were not significantly different across the five groups. Basal epinephrine levels were significantly higher in binge groups regardless of recent drinking, but cortisol and negative effect were not significantly different across the five groups.
This is the first study to show that alcohol withdrawal-associated muscle hyperalgesia may occur in healthy episodic binge drinkers with only 2-3 years of drinking history, and epinephrine may play a role in binge drinking-associated hyperalgesia.
啮齿动物研究提出了将过度饮酒与疼痛敏感性(痛觉过敏)联系起来的潜在机制,例如应激激素(即肾上腺素和皮质醇)介导酒精戒断引起的痛觉过敏的诱导和维持。本研究的第一个目的是检验健康年轻的习惯性暴饮者在饮酒后 48 小时内是否会发生痛觉过敏。第二个目的是检验应激激素和负性效价是否与暴饮或与酒精戒断相关的痛觉过敏有关。
在五个自然饮酒的组别中进行了一项横断面实验(平均年龄 19.6 岁,范围 18-29 岁):不饮酒者(n=43,54%女性)、有或无近期饮酒(即在 48 小时内,n=23,26%女性)的中度饮酒者和有或无近期饮酒(n=25,44%女性)的暴饮者(n=36,58%女性)。所有类型的饮酒者均报告每月饮酒 2-3 次,饮酒史 2-3 年。
与其他组相比,近期有暴饮的暴饮组的肌肉压力痛觉阈值显著降低,但五组间的皮肤机械痛觉和热痛觉阈值无显著差异。无论是否有近期饮酒,暴饮组的基础肾上腺素水平均显著升高,但皮质醇和负性效价在五组间无显著差异。
这是第一项表明,与酒精戒断相关的肌肉痛觉过敏可能发生在仅有 2-3 年饮酒史的健康偶发性暴饮者中,并且肾上腺素可能在暴饮相关的痛觉过敏中起作用的研究。