Evidence map›Paper›PMID 38370762›Full record

ArticlebioRxiv : the preprint server for biology2024

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

Aline Zaparte, Evan Dore, Selby White, Franciely Paliarin, Cameron Gabriel, Katherine Copenhaver, Samhita Basavanhalli, Emily Garcia, Rishith Vaddavalli, Meng Luo and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Aline ZaparteDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans.
Evan DoreDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Selby WhiteDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Franciely PaliarinDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Cameron GabrielDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Katherine CopenhaverDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Samhita BasavanhalliDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Emily GarciaDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Rishith VaddavalliDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Meng LuoDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Christopher M TaylorDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
David WelshDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans.
Rajani MaiyaDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans.
Louisiana State University Health Sciences Center New Orleans · US

Funding

Medical Student Alcohol Research Internship (MSARI)T35AA021097 · NIAAA · LSU HEALTH SCIENCES CENTER · PI Scott Edwards, PATRICIA E. MOLINA · 2012 to 2026
$471k
NIAAA NIH HHS T35 AA021097
6 · The paper itself

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 rendering 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/6J mice using the 24h intermittent access procedure. The three brands of chow tested were LabDiet 5001 (LD 5001), LabDiet 5053 (LD 5053), and Teklad 2019S (TL2019S) from two companies (Research Diets and Envigo respectively). Mice fed LD5001 displayed the highest levels of alcohol consumption and preference followed by LD5053 and TL2019S. We also found that alcohol consumption and preference could be rapidly switched by changing the diet 48h prior to alcohol administration. Sucrose, saccharin, and quinine preference were not altered suggesting that the diets did not alter 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" like 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 diversity, which could impact gut-brain axis signaling and alcohol consumption.

Indexed as

AlistipesAnaeroplasmaDubosiellaIntermittent accessLachnospiraceae

Identifiers

PMID38370762
PMCPMC10871281
OpenAlexW4391729414

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.