Zaparte Aline, Dore Evan, White Selby, Paliarin Franciely, Gabriel Cameron, Copenhaver Katherine, Basavanhalli Samhita, Garcia Emily, Vaddavalli Rishith, Luo Meng, Taylor Christopher M, Welsh David Allen, Maiya Rajani
Department of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center New Orleans, New Orleans, LA, United States.
Department of Physiology, Louisiana State University Health Sciences Center New Orleans, New Orleans, LA, United States.
Front Neurosci. 2024 May 13;18:1383181. doi: 10.3389/fnins.2024.1383181. eCollection 2024.
Alcohol use disorder (AUD) is a complex and widespread disease with limited pharmacotherapies. Preclinical animal models of AUD use a variety of voluntary alcohol consumption procedures to recapitulate different phases of AUD, including binge alcohol consumption and dependence. However, voluntary alcohol consumption in mice is widely variable, making it difficult to reproduce results across labs. Accumulating evidence indicates that different brands of commercially available rodent chow can profoundly influence alcohol intake. In this study, we investigated the effects of three commercially available and widely used rodent diet formulations on alcohol consumption and preference in C57BL/6 J mice using the 24 h intermittent access procedure. The three brands of chow tested were LabDiet 5,001 (LD5001), LabDiet 5,053 (LD5053), and Teklad 2019S (TL2019S) from two companies (Research Diets and Envigo, respectively). Mice fed LD5001 and LD5053 displayed higher levels of alcohol consumption and preference compared to mice fed TL2019S. We also found that alcohol consumption and preference could be rapidly switched by changing the diet 48 h prior to alcohol administration. Sucrose, saccharin, and quinine preferences were not altered, suggesting that the diets did not alter sweet and bitter taste perception. We also found that mice fed LD5001 displayed increased quinine-resistant alcohol intake compared to mice fed TL2019S, suggesting that diets could influence the development of compulsive behaviors such as alcohol consumption. We profiled the gut microbiome of water- and alcohol-drinking mice that were maintained on different diets and found significant differences in bacterial alpha- and beta-diversities, which could impact the gut-brain axis signaling and alcohol consumption.
酒精使用障碍(AUD)是一种复杂且普遍存在的疾病,可用的药物治疗方法有限。AUD的临床前动物模型采用多种自愿饮酒程序来概括AUD的不同阶段,包括暴饮酒精和依赖。然而,小鼠的自愿饮酒行为差异很大,使得不同实验室难以重复实验结果。越来越多的证据表明,不同品牌的市售啮齿动物饲料会深刻影响酒精摄入量。在本研究中,我们使用24小时间歇性接触程序,研究了三种市售且广泛使用的啮齿动物饮食配方对C57BL/6J小鼠酒精消费和偏好的影响。测试的三种饲料品牌分别是来自两家公司(分别为Research Diets和Envigo)的LabDiet 5001(LD5001)、LabDiet 5053(LD5053)和Teklad 2019S(TL2019S)。与喂食TL2019S的小鼠相比,喂食LD5001和LD5053的小鼠表现出更高的酒精消费量和偏好。我们还发现,在给予酒精前48小时改变饮食,可以迅速改变酒精消费和偏好。蔗糖、糖精和奎宁的偏好没有改变,这表明这些饮食没有改变甜味和苦味的感知。我们还发现,与喂食TL2019S的小鼠相比,喂食LD5001的小鼠对奎宁抗性酒精的摄入量增加,这表明饮食可能会影响强迫行为(如饮酒)的发展。我们对饮用不同饮食的饮水和饮酒小鼠的肠道微生物群进行了分析,发现细菌α-和β-多样性存在显著差异,这可能会影响肠-脑轴信号传导和酒精消费。