评估雄性和雌性偏好酒精和非偏好酒精的大鼠的初始/早期厌恶性饮酒。

IF 2.7 Q2 SUBSTANCE ABUSE Alcohol (Hanover, York County, Pa.) Pub Date : 2024-12-26 DOI:10.1111/acer.15518
Kari M. Haines, Nicholle E. Smith, Cristine L. Czachowski
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引用次数: 0

摘要

背景:酒精使用障碍(AUD)的一个特征是不顾负面后果继续饮酒。目前的研究调查了选择性培育的酒精偏好品系的初始/早期厌恶抗性饮酒(ARD),以评估具有最小乙醇史和随后的酒精寻求和饮酒特征的厌恶抗性。此外,使用蔗糖强化剂对嗜酒和非嗜酒大鼠进行ARD评估,以确定ARD是否可能是AUD的遗传风险因素。方法:将四种浓度的奎宁(0.03、0.10、0.30、1.00 g/ l)随机添加到乙醇溶液中,每天30 min,连续12 d。然后在手术室内对寻找和饮酒进行评估。另外一组嗜酒和不嗜酒的大鼠每天使用相同的随机顺序呈现方式,获得相同浓度的奎宁掺杂蔗糖。结果:在乙醇中,所有偏好系表现相似,在最低浓度时表现出对奎宁的抗性。在家中,高酒精饮酒(HAD)1型大鼠与偏好酒精(P)型大鼠喝下高水平的乙醇,而在操作性任务中,高酒精饮酒(HAD)1型大鼠与高酒精饮酒(HAD) 2型大鼠更相似。在蔗糖中,与基线相比,P和HAD2大鼠在低浓度奎宁下表现出厌恶抗性。总体而言,非偏好品系均表现出对奎宁掺杂蔗糖的敏感性。结论:本研究表明,当乙醇为强化剂时,酒精偏好系表现出相似的ARD。在动机反应方面,P大鼠表现出先前观察到的高寻求和饮酒行为。在homecage中,HAD1大鼠的饮水方式与P大鼠相似,这表明不同的条件(即自由获取与操作获取)会影响这些系之间的饮水行为。重要的是,在蔗糖强化剂中,偏爱酒精的老鼠比不喜欢酒精的老鼠更能抵抗厌恶,而不喜欢酒精的老鼠对厌恶表现出更高的敏感性,这表明它们总体上倾向于表现出低水平的强迫行为。
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Assessing initial/early aversion-resistant drinking across male and female alcohol-preferring and non-preferring rats

Background

One trait of alcohol use disorder (AUD) is continuing to drink despite negative consequences. The current study investigated initial/early aversion-resistant drinking (ARD) across selectively bred alcohol-preferring lines to assess aversion resistance with minimal ethanol history and subsequent ethanol-seeking and drinking profiles. Additionally, ARD was assessed in alcohol-preferring and non-preferring rats using a sucrose reinforcer to determine if ARD may be a genetic risk factor for AUD.

Methods

Male and female alcohol-preferring rats were given four concentrations of quinine (0.03, 0.10, 0.30, and 1.00 g/L—in random order) in an ethanol solution in the homecage for 30 min daily across 12 days. Seeking and drinking were then assessed in the operant chambers. Additional groups of alcohol-preferring and non-preferring rats were given access to the same concentrations of quinine-adulterated sucrose using the same daily, random-order presentation.

Results

In ethanol, all preferring lines performed similarly, showing resistance to quinine at the lowest concentration. In the homecage, high-alcohol-drinking (HAD)1 rats drank high levels of ethanol similar to alcohol-preferring (P) rats, whereas in an operant task were more similar to the HAD2 rats. In sucrose, P and HAD2 rats were shown to be aversion resistant at low concentrations of quinine compared to baseline. Overall, the non-preferring lines all demonstrated sensitivity to quinine-adulterated sucrose.

Conclusions

This study demonstrates alcohol-preferring lines show similar ARD when ethanol is the reinforcer. Regarding motivated responding, P rats show high-seeking and drinking behaviors as previously observed. In the homecage, HAD1 rats drink similarly to P rats indicating that different conditions (i.e., free vs. operant access) influence drinking behaviors between these lines. Importantly, in a sucrose reinforcer, alcohol-preferring rats are more aversion-resistant than non-preferring lines, while non-preferring lines show high sensitivity to aversion, suggesting an overall tendency to demonstrate a low level of compulsive behavior.

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The 10-year stability of three subscale scores of the Self-Report of the Effects of Alcohol measure and their relationship to changes in drinking quantities over the same period. Correction to "Effects of prenatal alcohol exposure on cognitive and behavioral development: Findings from a hierarchical meta-analysis of data from six prospective longitudinal U.S. cohorts". Dpp6 knockout mice exhibit increased ethanol conditioned place preference and acute ethanol-induced anxiolytic behavior. Articles of Public Interest Articles of Public Interest
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