Evidence map›Paper›PMID 27554472›Full record

ArticleDiabetes2016

Deficiency in the Heat Stress Response Could Underlie Susceptibility to Metabolic Disease.

Robert S Rogers, E Matthew Morris, Joshua L Wheatley, Ashley E Archer, Colin S McCoin, Kathleen S White, David R Wilson, Grace M E Meers, Lauren G Koch, Steven L Britton and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
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  8. Article
  9. Endothelial HSP72 is not reduced in type 2 diabetes nor is it a key determinant of endothelial insulin sensitivity.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  10. Review
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  16. Article
  17. Heat therapy: possible benefits for cognitive function and the aging brain.Journal of applied physiology (Bethesda, Md. : 1985) · 2020
    Review
  18. Article
  19. Article
  20. Review
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

12 authors at 3 institutions in 1 country.

Robert S RogersDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
E Matthew MorrisDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
Joshua L WheatleyDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
Ashley E ArcherDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
Colin S McCoinDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
Kathleen S WhiteDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
David R WilsonDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.
Grace M E MeersDepartment of Medicine-Gastroenterology and Hepatology, University of Missouri, Columbia, MO.
Lauren G KochDepartment of Anesthesiology, University of Michigan, Ann Arbor, MI.
Steven L BrittonDepartment of Anesthesiology, University of Michigan, Ann Arbor, MI.
John P ThyfaultDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS.ORCID http://orcid.org/0000-0001-7920-7466
Paige C GeigerDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS pgeiger@kumc.edu.
University of Kansas Medical Center · USUniversity of Michigan · USUniversity of Missouri · US

Funding

Research Design and Analysis Core (RDAC)P30HD002528 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI FOWLER, STEPHEN CLETIUS · 1985 to 2015
$22.1M
Exercise &Health: Integration from Molecule to PatientT32AR048523 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI TERJUNG, RONALD L · 2003 to 2013
$2.5M
Resource for Rat Genetic Models of Aerobic CapacityP40OD021331 · OD · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI KOCH, LAUREN GERARD · 2015 to 2019
$1.9M
Biology of Aerobic Capacity and Insulin ResistanceR01DK077200 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2008 to 2012
$1.5M
Aerobic fitness, mitochondrial dysfunction, and fatty liver diseaseR01DK088940 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI THYFAULT, JOHN P · 2011 to 2015
$1.5M
Inflammation resolving mechanism dysregulation in postoperative cognitive declineR01GM104194 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MAZE, MERVYN · 2013 to 2016
$1.2M
Targeting stress-mediated pathways in the treatment of muscle insulin resistanceR01AG031575 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI GEIGER, PAIGE C · 2010 to 2014
$1.2M
NIAMS NIH HHS T32 AR048523NIA NIH HHS R01 AG031575NICHD NIH HHS P30 HD002528NIDDK NIH HHS R01 DK077200NIDDK NIH HHS R01 DK088940NIGMS NIH HHS R01 GM104194NIH HHS P40 OD021331
6 · The paper itself

Abstract

Heat treatment (HT) effectively prevents insulin resistance and glucose intolerance in rats fed a high-fat diet (HFD). The positive metabolic actions of heat shock protein 72 (HSP72), which include increased oxidative capacity and enhanced mitochondrial function, underlie the protective effects of HT. The purpose of this study was to test the ability of HSP72 induction to mitigate the effects of consumption of a short-term 3-day HFD in rats selectively bred to be low-capacity runners (LCRs) and high-capacity runners (HCRs)-selective breeding that results in disparate differences in intrinsic aerobic capacity. HCR and LCR rats were fed a chow or HFD for 3 days and received a single in vivo HT (41°C, for 20 min) or sham treatment (ST). Blood, skeletal muscles, liver, and adipose tissues were harvested 24 h after HT/ST. HT decreased blood glucose levels, adipocyte size, and triglyceride accumulation in liver and muscle and restored insulin sensitivity in glycolytic muscles from LCR rats. As expected, HCR rats were protected from the HFD. Importantly, HSP72 induction was decreased in LCR rats after only 3 days of eating the HFD. Deficiency in the highly conserved stress response mediated by HSPs could underlie susceptibility to metabolic disease with low aerobic capacity.

Indexed as

Adipose Tissue, WhiteAnimalsBlood GlucoseBlotting, WesternBody CompositionDiet, High-FatEnergy IntakeHeat-Shock ResponseInsulin ResistanceMaleMetabolic DiseasesMuscle, SkeletalRatsTriglyceridesBlood GlucoseTriglycerides

Identifiers

PMID27554472
PMCPMC5079638
OpenAlexW2517182034

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.