Evidence map›Paper›PMID 35385494›Full record

ArticlePloS one2022

Sex differences in the fecal microbiome and hippocampal glial morphology following diet and antibiotic treatment.

Anju Saxena, Roberta R M Moran, Meghan R Bullard, Emma O Bondy, Matthew Foster Smith, Lainie Morris, Nicaella Fogle, Jagroop Singh, Brendan Jarvis, Tammy Ray and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

7 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Anju SaxenaNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Roberta R M MoranNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Meghan R BullardDepartment of Biology, Furman University, Greenville, South Carolina, United States of America.
Emma O BondyNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Matthew Foster SmithNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Lainie MorrisDepartment of Biology, Furman University, Greenville, South Carolina, United States of America.
Nicaella FogleNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Jagroop SinghDepartment of Biology, Furman University, Greenville, South Carolina, United States of America.
Brendan JarvisNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Tammy RayNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Juhi SaxenaNeurosciences, Furman University, Greenville, South Carolina, United States of America.
Linnea Ruth FreemanNeurosciences, Furman University, Greenville, South Carolina, United States of America.ORCID 0000-0001-5507-8903
Furman University · US

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
NIGMS NIH HHS P20 GM103499
6 · The paper itself

Abstract

Rising obesity rates have become a major public health concern within the United States. Understanding the systemic and neural effects of obesity is crucial in designing preventive and therapeutic measures. In previous studies, administration of a high fat diet has induced significant weight gain for mouse models of obesity. Interestingly, sex differences in high-fat diet-induced weight gain have been observed, with female mice gaining significantly less weight compared to male mice on the same high-fat diet. It has also been observed that consumption of a high-fat diet can increase neurogliosis, but the mechanism by which this occurs is still not fully understood. Recent research has suggested that the gut microbiome may mediate diet-induced glial activation. The current study aimed to (1) analyze changes to the gut microbiome following consumption of a high fat (HF) diet as well as antibiotic treatment, (2) evaluate hippocampal microgliosis and astrogliosis, and (3) identify sex differences within these responses. We administered a low fat (Research Diets D12450 K) or high fat diet (Research Diets D12451) to male and female C57Bl/6 mice for sixteen weeks. Mice received an antibiotic cocktail containing 0.5g/L of vancomycin, 1.0 g/L ampicillin, 1.0 g/L neomycin, and 1.0 g/L metronidazole in their drinking water during the last six weeks of the study and were compared to control mice receiving normal drinking water throughout the study. We observed a significant reduction in gut microbiome diversity for groups that received the antibiotic cocktail, as determined by Illumina next-generation sequencing. Male mice fed the HF diet (± antibiotics) had significantly greater body weights compared to all other groups. And, female mice fed the low fat (LF) diet and administered antibiotics revealed significantly decreased microgliosis and astrogliosis in the hippocampus compared to LF-fed females without antibiotics. Interestingly, male mice fed the LF diet and administered antibiotics revealed significantly increased microgliosis, but decreased astrogliosis, compared to LF-fed males without antibiotics. The observed sex differences in LF-fed mice given antibiotics brings forward questions about sex differences in nutrient metabolism, gut microbiome composition, and response to antibiotics.

Indexed as

Drinking WaterMicrobiotaAnimalsAnti-Bacterial AgentsDiet, High-FatFemaleGliosisHippocampusMaleMiceMice, Inbred C57BLObesitySex CharacteristicsWeight GainAnti-Bacterial AgentsDrinking Water

Identifiers

PMID35385494
PMCPMC8985946
OpenAlexW4226495128

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.