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Standard rodent diets differentially impact alcohol consumption, preference, and gut microbiome diversity.

作者信息

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

机构信息

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.

出版信息

Front Neurosci. 2024 May 13;18:1383181. doi: 10.3389/fnins.2024.1383181. eCollection 2024.


DOI:10.3389/fnins.2024.1383181
PMID:38803684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11129685/
Abstract

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/0080c96aa0ba/fnins-18-1383181-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/aaba7f1b37ae/fnins-18-1383181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/007caacea8a1/fnins-18-1383181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/2929258eaebd/fnins-18-1383181-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/02ed81d43896/fnins-18-1383181-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/9284d3ec146a/fnins-18-1383181-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/2551186cc6a5/fnins-18-1383181-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/599af42a24ff/fnins-18-1383181-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/0080c96aa0ba/fnins-18-1383181-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/aaba7f1b37ae/fnins-18-1383181-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/007caacea8a1/fnins-18-1383181-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/2929258eaebd/fnins-18-1383181-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/02ed81d43896/fnins-18-1383181-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/9284d3ec146a/fnins-18-1383181-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/2551186cc6a5/fnins-18-1383181-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/599af42a24ff/fnins-18-1383181-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cba5/11129685/0080c96aa0ba/fnins-18-1383181-g008.jpg

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引用本文的文献

[1]
Role of Lactobacillus plantarum-Derived Extracellular Vesicles in Regulating Alcohol Consumption.

Mol Neurobiol. 2025-3

本文引用的文献

[1]
Gut-Liver-Brain Axis and Alcohol Use Disorder: Treatment Potential of Fecal Microbiota Transplantation.

Alcohol Res. 2024

[2]
Bitter taste function-related genes are implicated in the behavioral association between taste preference and ethanol preference in male mice.

Physiol Behav. 2024-3-15

[3]
Resistant starches from dietary pulses modulate the gut metabolome in association with microbiome in a humanized murine model of ageing.

Sci Rep. 2023-6-29

[4]
The best practice for microbiome analysis using R.

Protein Cell. 2023-10-25

[5]
Animal models of compulsion alcohol drinking: Why we love quinine-resistant intake and what we learned from it.

Front Psychiatry. 2023-3-24

[6]
Exploring the links between gut microbiota and excitatory and inhibitory brain processes in alcohol use disorder: A TMS study.

Neuropharmacology. 2023-3-1

[7]
The Impact of Taste Preference-Related Gene Polymorphisms on Alcohol Consumption Behavior: A Systematic Review.

Int J Mol Sci. 2022-12-15

[8]
Reduced alcohol preference and intake after fecal transplant in patients with alcohol use disorder is transmissible to germ-free mice.

Nat Commun. 2022-10-19

[9]
Targeting Unmet Clinical Needs in the Treatment of Alcohol Use Disorder.

Front Psychiatry. 2022-6-9

[10]
Beta-diversity distance matrices for microbiome sample size and power calculations - How to obtain good estimates.

Comput Struct Biotechnol J. 2022-4-27

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