Evidence map›Paper›PMID 41279327›Full record

ArticlebioRxiv : the preprint server for biology2025

The Impact of a Western Diet with High Salt on Metabolic Outcomes in Male C57bl/6J Mice.

Michael E Ponte, John C Prom, Pradeep Devkota, Sireesha Yerrathota, Mea Carradine, Larry Ha, E Matthew Morris, Andrew J Lutkewitte

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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.

No citing paper in PubMed yet.

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

8 authors.

Michael E PonteDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.ORCID 0009-0004-7490-2573
John C PromDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.
Pradeep DevkotaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.
Sireesha YerrathotaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.
Mea CarradineKansas University Cancer Center, University of Kansas Medical Center, Kansas City, KS, United States.
Larry HaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
E Matthew MorrisDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.ORCID 0000-0001-7046-3623
Andrew J LutkewitteDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United States.

Funding

longitudinal assessment of stress and stress-related concepts across a behavioral weight loss interventionP20GM144269 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Chelsea L Kracht, John P Thyfault · 2022 to 2026
$14.9M
Translating Obesity, Metabolic Dysfunction and Comorbid Disease StatesT32DK128770 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI John P Thyfault, Douglas E Wright · 2022 to 2026
$806k
Adipose-Specific Phosphatidic Acid Phosphatase Activity of Lipin 1 Regulates Systemic Insulin SensitivityK01DK126990 · NIDDK · WASHINGTON UNIVERSITY · PI LUTKEWITTE, ANDREW · 2021 to 2024
$466k
NIDDK NIH HHS K01 DK126990NIDDK NIH HHS T32 DK128770NIGMS NIH HHS P20 GM144269
6 · The paper itself

Abstract

Objective: The Western diet promotes obesity and metabolic disease by increasing caloric intake and systemic inflammation. The typical Western diet is high in saturated fats, sugars, and salt. In pre-clinical rodent studies, the "Western" diet (also called the high-fat high-sucrose diet (HFHS)) is high in saturated fats and sugars (typically sucrose) but low in salt (<1% salt). As such, we sought investigate the impact of a chronic 3% NaCl Western diet (high-fat, high-sucrose + high salt (HFHS + Salt)) diet on systemic organ metabolism, liver mitochondrial function, and adipose tissue. Methods: Thirty-six 8 week-old C57Bl/6J male mice were fed either a low-fat diet (LFD), a HFHS, or a HFHS + Salt diet for 16 weeks. Body weight, body composition, and food intake were monitored weekly. Glucose tolerance tests (GTT) and insulin concentrations were measured after 8 weeks of diet intervention to assess glucose and insulin homeostasis. Mice were euthanized at 16 weeks for liver mitochondrial respiration and tissue analysis. Results: Over 16 weeks, the HFHS fed group gained significantly more weight than the other diet groups. Liver weights were similar in LFD and HFHS + Salt groups but higher in the HFHS group. Liver triglycerides (TAGs) were also similar between LFD and HFHS + Salt groups, while HFHS had elevated liver TAGs. Inguinal and brown adipose tissue depots were larger in both HFHS and HFHS + Salt vs. LFD. Surprisingly, the gonadal adipose tissue was significantly larger in the HFHS + Salt compared to HFHS and LFD groups - suggesting that a HFHS + Salt exacerbates gonadal adipose expansion more than typical rodent HFHS. Paradoxically, the addition of salt appears to have dampened expression of inflammation related genes ( Conclusion: While the excess salt mitigated some HFHS effects on weight gain and hepatic lipid accumulation, it exacerbated gonadal adipose expansion and impaired glucose tolerance. HFHS increased mitochondrial respiration, but salt addition appeared to dampen this effect. Dietary salt, within a high-fat/high-sucrose context, has differential impacts on metabolic outcomes compared to HFHS alone, underscoring the need for further research to fully understand how Western diets (high-fat, high-sucrose,

Indexed as

adipose tissueinsulin resistancemitochondriasaltWestern diet

Identifiers

PMID41279327
PMCPMC12632855

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.