Evidence map›Paper›PMID 38853960›Full record

ArticleResearch square2024

Transfer with microbiota from lean donors prevents excessive weight gain and restores gut-brain vagal signaling in obese rats maintained on a high fat diet.

Dulce M Minaya, Jiyoung S Kim, Rebecca Kirkland, Jillian Allen, Sitara Cullinan, Neil Maclang, Guillaume de Lartigue, Claire B de La Serre

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In one paragraph

Article in Research square, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Dulce M MinayaDepartment of Nutritional Science, University of Georgia, Athens, GA.
Jiyoung S KimEmory University School of Medicine, Atlanta, GA.
Rebecca KirklandDepartment of Nutritional Science, University of Georgia, Athens, GA.
Jillian AllenDepartment of Nutritional Science, University of Georgia, Athens, GA.
Sitara CullinanDepartment of Nutritional Science, University of Georgia, Athens, GA.
Neil MaclangDepartment of Nutritional Science, University of Georgia, Athens, GA.
Guillaume de LartigueMonell Chemical Senses Center, Philadelphia, PA.
Claire B de La SerreDepartment of Biomedical Sciences, Colorado State University, Fort Collins, CO.

Funding

Consequence and mechanism of diet-driven vagal remodeling on gut-brain feedingbehaviorR01DK125890 · NIDDK · UNIVERSITY OF GEORGIA · PI DE LA SERRE, CLAIRE, DE LARTIGUE, GUILLAUME FH · 2020 to 2023
$1.8M
NIDDK NIH HHS R01 DK125890
6 · The paper itself

Abstract

Background: The collection of microorganisms, mainly bacteria, which live in the gastrointestinal (GI) tract are collectible known as the gut microbiota. GI bacteria play an active role in regulation of the host's immune system and metabolism, as well as certain pathophysiological processes. Diet is the main factor modulating GI microbiota composition and recent studies have shown that high fat (HF) diets induce detrimental changes, known as dysbiosis, in the GI bacterial makeup. HF diet induced microbiota dysbiosis has been associated with structural and functional changes in gut-brain vagally mediated signaling system, associated with overeating and obesity. Although HF-driven changes in microbiota composition are sufficient to alter vagal signaling, it is unknown if restoring normal microbiota in obesity can improve gut-brain signaling and metabolic outcomes. In this study, we evaluated the effect of lean gut microbiota transfer in obese, vagally compromised, rats on gut-brain communication, food intake, and body weight. Male Sprague-Dawley rats were maintained on regular chow, or 45% HF diet for nine weeks followed by three weeks of microbiota depletion using an antibiotic cocktail. The animals were then divided into four groups (n=10 each): Results: We found that transferring a LF microbiota to HF fed animals (HF-LF) reduced caloric intake during the light phase when compared with HF-HF rats and prevented additional excessive weight gain. We did not observe significant changes in the density of vagal afferents terminating in the brainstem among the groups, however, HF-LF animals displayed an increase in postprandial activation of both primary sensory neurons innervating the GI tract and brainstem secondary neurons. Conclusions: We concluded from these data that normalizing microbiota composition in obese rats improves gut-brain communication and restores normal feeding patterns which was associated with a reduction in weight gain.

Indexed as

DysbiosisGut-brain axisGut microbiotaMicrobiota TransferObesity

Identifiers

PMID38853960
PMCPMC11160927

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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.