Evidence map›Paper›PMID 42866253›Full record

ArticleThe journal of nutritional physiology2026

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 read
In one paragraph

Article in The journal of nutritional physiology, 2026. 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

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 Statess.
John C PromDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United Statess.
Pradeep DevkotaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United Statess.
Sireesha YerrathotaDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United Statess.
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 Statess.
Andrew J LutkewitteDepartment of Cell Biology and Physiology, University of Kansas Medical Center, Kansas City, KS, United Statess.

Funding

longitudinal assessment of stress and stress-related concepts across a behavioral weight loss interventionP20GM144269 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Joseph E. Donnelly · 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

The typical Western diet drives obesity and metabolic disease through high intake of saturated fats, sugars, and salt. However, common rodent diet models (High-Fat, High-Sucrose, or HFHS) are often low in salt. We aimed to investigate the chronic metabolic outcomes by feeding C57BL/6J male mice a Low-Fat Diet (LFD), HFHS, or a High-Salt HFHS diet (HFHS + 3% Salt) for 16 weeks, monitoring body composition, glucose tolerance, and tissue function. The HFHS group exhibited the most significant weight gain over 16 weeks. Surprisingly, the addition of salt mitigated hepatic lipid accumulation; the HFHS + Salt group had liver weights and triglyceride levels like the LFD group, while the HFHS group showed elevated levels. However, the high-salt component exacerbated other issues. The HFHS + Salt fed mice displayed the highest degree of glucose intolerance, followed by the HFHS group. Furthermore, gonadal adipose tissue was significantly larger in the HFHS + Salt mice, suggesting the salt component specifically drives expansion in this depot. Paradoxically, salt also appeared to dampen the expression of inflammation-related genes (

Indexed as

adipose tissueinsulin resistancemitochondriasaltWestern diet

Identifiers

PMID42866253
PMCPMC13657138

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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.