Evidence map›Paper›PMID 40209503›Full record

ArticleBiochemical and biophysical research communications2025

Quantifying renal lipid accumulation in obese murine models using Magnetic Resonance Imaging (MRI).

Jamie Lynne Lois Q Balugo, Joshua D Samuels, Joshua L Milstein, Maurits A Jansen, Thurl E Harris, Silas A Culver

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2025. 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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0citing papers in PubMed
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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

6 authors.

Jamie Lynne Lois Q BalugoDivision of Endocrinology, Department of Medicine, University of Virginia Health System, 450 Ray C. Hunt Dr, Charlottesville, VA, 22903, USA. Electronic address: JB7WR@uvahealth.org.
Joshua D SamuelsDepartment of Neuroscience, University of Virginia Health System, 409 Lane Rd, Charlottesville, VA, 22908, USA. Electronic address: rhk9gh@virginia.edu.
Joshua L MilsteinDepartment of Neuroscience, University of Virginia Health System, 409 Lane Rd, Charlottesville, VA, 22908, USA. Electronic address: jm7kf@virginia.edu.
Maurits A JansenMolecular Imaging Core and Department of Radiology and Medical Imaging, University of Virginia, 480 Ray C. Hunt Dr, Charlottesville, VA, 22903, USA. Electronic address: vtf5vq@virginia.edu.
Thurl E HarrisDepartment of Pharmacology, University of Virginia Health System, 1340 Jefferson Park Ave, Charlottesville, VA, 22903, USA. Electronic address: teh3c@virginia.edu.
Silas A CulverDivision of Endocrinology, Department of Medicine, University of Virginia Health System, 450 Ray C. Hunt Dr, Charlottesville, VA, 22903, USA. Electronic address: SAC7ZU@uvahealth.org.

Funding

Small-Animal 9.4T MRI for Biomedical ResearchS10OD025024 · OD · UNIVERSITY OF VIRGINIA · PI BERR, STUART S. · 2019 to 2019
$2.0M
Role of Atp6ap2 in renal proximal tubule lipotoxicityK08DK132463 · NIDDK · UNIVERSITY OF VIRGINIA · PI Silas A Culver · 2023 to 2026
$662k
NIDDK NIH HHS K08 DK132463NIH HHS S10 OD025024
6 · The paper itself

Abstract

Renal cortical lipid content is increased in obesity and contributes to obesity-related kidney dysfunction. Studying this phenomenon requires reliable tools to quantitate renal cortical lipid in preclinical models. However, most current preclinical methods require euthanizing the model. MRI has been used to measure lipid content in other organ systems but, to our knowledge, has not been employed in quantifying kidney lipid in mice. Eleven-week old male C57BL/6 mice were fed either standard chow (ND) (12 % fat) or high fat diet (HFD) (45 % fat) for 12 weeks. At the end of this period, a 9.4 T Bruker MRI was utilized to perform fat-water separation imaging based on the Dixon method. These images were utilized to calculate a proton-density fat fraction for regions of interest within the renal cortex. For validation, frozen kidney sections underwent immunofluorescent LipidSpot™ staining for quantitation of lipid droplet area. After 12 weeks on diet, the average body weight of HFD fed mice was 34.63g compared to 27.84g in ND controls (p < 0.001). Consistent with prior studies, MRI demonstrated increased hepatic fat content of 13.34 % in HFD fed mice compared to 8.3 % in ND controls (p < 0.05). Renal cortical lipid measured by MRI averaged 7.35 % in HFD fed mice compared to 4.75 % in ND controls (p < 0.05). On histologic analysis, HFD fed mice had a ratio of lipid droplet area to DAPI of 0.866 compared to 0.221 in ND fed mice (p < 0.05). These results demonstrate that MRI can be used effectively to measure changes in renal cortical lipid content in mice.

Indexed as

KidneyKidney CortexLipid MetabolismMagnetic Resonance ImagingObesityAnimalsDiet, High-FatDisease Models, AnimalMaleMiceMice, Inbred C57BLKidneyLipidMRIObesity

Identifiers

PMID40209503
PMCPMC12094437

What Socratic holds

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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 Socratic graph.