Evidence map›Paper›PMID 26690387›Full record

ArticleScientific reports2015

Disparate metabolic response to fructose feeding between different mouse strains.

M K Montgomery, C E Fiveash, J P Braude, B Osborne, S H J Brown, T W Mitchell, N Turner

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Preclinical models versus clinical renal ischemia reperfusion injury: A systematic review based on metabolic signatures.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Pooled it
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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

7 authors at 2 institutions in 1 country.

M K MontgomeryDepartment of Pharmacology, School of Medical Sciences, UNSW Australia, Sydney, NSW, Australia.
C E FiveashDepartment of Pharmacology, School of Medical Sciences, UNSW Australia, Sydney, NSW, Australia.
J P BraudeDepartment of Pharmacology, School of Medical Sciences, UNSW Australia, Sydney, NSW, Australia.
B OsborneDepartment of Pharmacology, School of Medical Sciences, UNSW Australia, Sydney, NSW, Australia.
S H J BrownSchool of Health Sciences, University of Wollongong, Wollongong, NSW, Australia.
T W MitchellSchool of Health Sciences, University of Wollongong, Wollongong, NSW, Australia.
N TurnerDepartment of Pharmacology, School of Medical Sciences, UNSW Australia, Sydney, NSW, Australia.
UNSW Sydney · AUIllawarra Health and Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diets enriched in fructose (FR) increase lipogenesis in the liver, leading to hepatic lipid accumulation and the development of insulin resistance. Previously, we have shown that in contrast to other mouse strains, BALB/c mice are resistant to high fat diet-induced metabolic deterioration, potentially due to a lack of ectopic lipid accumulation in the liver. In this study we have compared the metabolic response of BALB/c and C57BL/6 (BL6) mice to a fructose-enriched diet. Both strains of mice increased adiposity in response to FR-feeding, while only BL6 mice displayed elevated hepatic triglyceride (TAG) accumulation and glucose intolerance. The lack of hepatic TAG accumulation in BALB/c mice appeared to be linked to an altered balance between lipogenic and lipolytic pathways, while the protection from fructose-induced glucose intolerance in this strain was likely related to low levels of ER stress, a slight elevation in insulin levels and an altered profile of diacylglycerol species in the liver. Collectively these findings highlight the multifactorial nature of metabolic defects that develop in response to changes in the intake of specific nutrients and the divergent response of different mouse strains to dietary challenges.

Indexed as

AdiposityAnimalsBiomarkersBody WeightCells, CulturedEndoplasmic Reticulum StressEnergy MetabolismEnzyme ActivationFatty AcidsFeeding BehaviorFructoseGlucoseHepatocytesInsulinLipid MetabolismLipogenesisBiomarkersFatty AcidsFructoseGlucoseInsulinProtein Kinase C

Identifiers

PMID26690387
PMCPMC4686880
OpenAlexW2418584637

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.