Evidence map›Paper›PMID 28232454›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2017

A longitudinal study of whole body, tissue, and cellular physiology in a mouse model of fibrosing NASH with high fidelity to the human condition.

Anuradha Krishnan, Tasduq Sheikh Abdullah, Taofic Mounajjed, Stella Hartono, Andrea McConico, Thomas White, Nathan LeBrasseur, Ian Lanza, Sreekumaran Nair, Gregory Gores and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Ethanol reshapes FFC-driven steatohepatitis through time-dependent fibrosis and lipid-droplet remodeling.American journal of physiology. Gastrointestinal and liver physiology · 2026
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  18. Heat-InactivatedInternational journal of molecular sciences · 2022
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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

11 authors at 4 institutions in 2 countries.

Anuradha KrishnanDivision of Gastroenterology, Mayo Clinic, Rochester, Minnesota.
Tasduq Sheikh AbdullahIndian Institute of Integrative Medicine, Council of Scientific and Industrial Research, Jammu and Kashmir, India.
Taofic MounajjedDivision of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota.
Stella HartonoDivision of Immunology, Mayo Clinic, Rochester, Minnesota.
Andrea McConicoDivision of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota.
Thomas WhiteRobert and Arlene Kogod Centre for Aging, Mayo Clinic, Rochester, Minnesota.
Nathan LeBrasseurRobert and Arlene Kogod Centre for Aging, Mayo Clinic, Rochester, Minnesota.
Ian LanzaDivision of Endocrinology, Mayo Clinic, Rochester, Minnesota; and.
Sreekumaran NairDivision of Endocrinology, Mayo Clinic, Rochester, Minnesota; and.
Gregory GoresDivision of Gastroenterology, Mayo Clinic, Rochester, Minnesota.
Michael CharltonDivision of Gastroenterology, Mayo Clinic, Rochester, Minnesota; mcharlton@medicine.bsd.uchicago.edu michael.charlton@imail.org.
Mayo Clinic · USMayo Clinic in Florida · USIndian Institute of Integrative Medicine · INIntermountain Healthcare · US

Funding

MECHANISMS OF LIVER CELL INJURYR01DK041876 · NIDDK · MAYO CLINIC ROCHESTER · PI GORES, GREGORY J. · 1992 to 2019
$3.6M
Mechanistic Role of CD4+ T-Cells in Atherosclerotic Renal Artery StenosisF30DK102232 · NIDDK · MAYO CLINIC ROCHESTER · PI HARTONO, STELLA P · 2014 to 2016
$133k
NIDDK NIH HHS F30 DK102232NIDDK NIH HHS R01 DK041876
6 · The paper itself

Abstract

The sequence of events that lead to inflammation and fibrosing nonalcoholic steatohepatitis (NASH) is incompletely understood. Hence, we investigated the chronology of whole body, tissue, and cellular events that occur during the evolution of diet-induced NASH. Male C57Bl/6 mice were assigned to a fast-food (FF; high calorie, high cholesterol, high fructose) or standard-chow (SC) diet over a period of 36 wk. Liver histology, body composition, mitochondrial respiration, metabolic rate, gene expression, and hepatic lipid content were analyzed. Insulin resistance [homeostasis model assessment-insulin resistance (HOMA-IR)] increased 10-fold after 4 wk. Fibrosing NASH was fully established by 16 wk. Total hepatic lipids increased by 4 wk and remained two- to threefold increased throughout. Hepatic triglycerides declined from sixfold increase at 8 wk to threefold increase by 36 wk. In contrast, hepatic cholesterol levels steadily increased from baseline at 8 wk to twofold by 36 wk. The hepatic immune cell population altered over time with macrophages persisting beyond 16 wk. Mitochondrial oxygen flux rates of FF mice diet were uniformly lower with all the tested substrates (13-276 pmol·s

Indexed as

AdiposityAnimalsBiomarkersBlood GlucoseDiet, High-FatDisease Models, AnimalDisease ProgressionEnergy MetabolismHumansInflammation MediatorsInsulinInsulin ResistanceLipidsLiverLiver CirrhosisMaleBiomarkersBlood GlucoseInflammation MediatorsInsulinLipidsfatty liverhepatic fibrosisinflammation metabolic functioninsulin resistancemitochondrial respiration

Identifiers

PMID28232454
PMCPMC6146305
OpenAlexW2590703216

What OpenQuestion holds

Textmetadata
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.