Evidence map›Paper›PMID 28655717›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2017

Deletion of UCP1 enhances ex vivo aortic vasomotor function in female but not male mice despite similar susceptibility to metabolic dysfunction.

Nathan C Winn, Zachary I Grunewald, Michelle L Gastecki, Makenzie L Woodford, Rebecca J Welly, Stephanie L Clookey, James R Ball, T'Keaya L Gaines, Natalia G Karasseva, Jill A Kanaley and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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
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  7. Hyperinsulinemia blunts sympathetic vasoconstriction: a possible role of β-adrenergic activation.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
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  15. Removal of interscapular brown adipose tissue increases aortic stiffness despite normal systemic glucose metabolism in mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    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

13 authors at 3 institutions in 1 country.

Nathan C WinnNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Zachary I GrunewaldNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Michelle L GasteckiNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Makenzie L WoodfordNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Rebecca J WellyNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Stephanie L ClookeyNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
James R BallNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
T'Keaya L GainesNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Natalia G KarassevaTransgenic Animal Core, University of Missouri, Columbia, Missouri.
Jill A KanaleyNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.
Harold S SacksEndocrine and Diabetes Division, Veterans Affairs Greater Los Angeles Healthcare System and Department of Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California.
Victoria J Vieira-PotterNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri.ORCID 0000-0001-7563-0806
Jaume PadillaNutrition and Exercise Physiology, University of Missouri, Columbia, Missouri; padillaja@missouri.edu.
University of Missouri · USUniversity of Missouri Health System · USVA Greater Los Angeles Healthcare System · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
MINORITY BIOMEDICAL RESEARCHERS TRAINING INITIATIVER25GM056901 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI HANNINK, MARK · 1999 to 2019
$8.4M
Vascular Insulin Resistance in Obesity: Role of Endoplasmic Reticulum StressK01HL125503 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI PADILLA, JAUME · 2015 to 2018
$564k
Targeting endoplasmic reticulum stress to correct vascular insulin resistance and glycemic dysregulation in diabetesR21DK105368 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI PADILLA, JAUME · 2015 to 2016
$422k
NCI NIH HHS P30 CA086862NHLBI NIH HHS K01 HL125503NIDDK NIH HHS R21 DK105368NIGMS NIH HHS R25 GM056901
6 · The paper itself

Abstract

Females are typically more insulin sensitive than males, which may be partly attributed to greater brown adipose tissue (BAT) activity and uncoupling protein 1 (UCP1) content. Accordingly, we tested the hypothesis that UCP1 deletion would abolish sex differences in insulin sensitivity and that whitening of thoracic periaortic BAT caused by UCP1 loss would be accompanied with impaired thoracic aortic function. Furthermore, because UCP1 exerts antioxidant effects, we examined whether UCP1 deficiency-induced metabolic dysfunction was mediated by oxidative stress. Compared with males, female mice had lower HOMA- and AT-insulin resistance (IR) despite no significant differences in BAT UCP1 content. UCP1 ablation increased HOMA-IR, AT-IR, and whitening of BAT in both sexes. Expression of UCP1 in thoracic aorta was greater in wild-type females compared with males. Importantly, deletion of UCP1 enhanced aortic vasomotor function in females only. UCP1 ablation did not promote oxidative stress in interscapular BAT. Furthermore, daily administration of the free radical scavenger tempol for 8 wk did not abrogate UCP1 deficiency-induced increases in adiposity, hyperinsulinemia, or liver steatosis. Collectively, we report that

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAdiposityAnimalsAortaFatty LiverFemaleHyperinsulinismInsulin ResistanceIn Vitro TechniquesMaleMiceMice, KnockoutOxidative StressSex FactorsUncoupling Protein 1Ucp1 protein, mouseUncoupling Protein 1brown adipose tissueinsulin resistanceoxidative stressvascular function

Identifiers

PMID28655717
PMCPMC5668596
OpenAlexW2727628885

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.