Evidence map›Paper›PMID 36730247›Full record

ArticlePloS one2023

High fat diet is protective against kidney injury in hypertensive-diabetic mice, but leads to liver injury.

Véronique Cheff, Mayra Trentin-Sonoda, Amélie Blais, Jean-François Thibodeau, Chet E Holterman, Alex Gutsol, Christopher R J Kennedy, Richard L Hébert

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Current perspective on circadian function of the kidney.American journal of physiology. Renal physiology · 2024
    Review
  3. Article
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 at 2 institutions in 1 country.

Véronique CheffDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Mayra Trentin-SonodaDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.ORCID 0000-0003-2446-7783
Amélie BlaisDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Jean-François ThibodeauDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Chet E HoltermanDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Alex GutsolDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Christopher R J KennedyDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Richard L HébertKidney Research Centre, Division of Nephrology, Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.ORCID 0000-0002-1419-7719
University of Ottawa · CAOttawa Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic kidney disease (CKD) is a worldwide health burden with increases risk of end-stage renal function if left untreated. CKD induced in the context of metabolic syndrome (MS) increases risks of hypertension, hyperglycemia, excess body fat and dyslipidemia. To test if combining a high-fat diet (HFD) regimen onto the hypertensive/ diabetic phenotype would mimic features of MS induced-CKD in mice, hyperglycemia was induced in genetically hypertensive mice (Lin), followed by HFD regimen. For that, 8-week-old male were subjected to streptozotocin (STZ) intraperitoneal (i.p.) injections (50 mg/kg, 5 days consecutive). LinSTZ were fed a 60% kCal HFD for 8 weeks. Lin mice treated with STZ developed polydipsia, became hypertensive and hyperglycemic. HFD induced weight gain, protected against glomerular hypertrophy, scarring, and albuminuria at endpoint compared to regular diet fed LinSTZ. On the other hand, HFD induced steatosis, liver fibrosis, inflammation, and increase in AST/ALT ratio, characteristics of non-alcoholic liver disease. Taken together, our results show that LinSTZ mice fed a HFD did not lead to a more robust model of MS-induced CKD, protected against kidney injury, but inducing liver damage. More studies are necessary to understand the kidney protective mechanisms of HFD when superimposed with hypertension and type 1 diabetes.

Indexed as

Diabetes Mellitus, ExperimentalHyperglycemiaHypertensionRenal Insufficiency, ChronicAnimalsDiet, High-FatKidneyLiverMaleMiceMice, Inbred C57BL

Identifiers

PMID36730247
PMCPMC9894391
OpenAlexW4318930484

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.