Evidence map›Paper›PMID 30571284›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2019

Type 2 diabetes mellitus in the Goto-Kakizaki rat impairs microvascular function and contributes to premature skeletal muscle fatigue.

Jefferson C Frisbee, Matthew T Lewis, Jonathan D Kasper, Paul D Chantler, Robert W Wiseman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  12. Skeletal muscle energetics are compromised only during high-intensity contractions in the Goto-Kakizaki rat model of type 2 diabetes.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  13. Endothelium-dependent impairments to cerebral vascular reactivity with type 2 diabetes mellitus in the Goto-Kakizaki rat.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    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

5 authors at 3 institutions in 2 countries.

Jefferson C FrisbeeDepartment of Medical Biophysics, Western University , London, Ontario , Canada.
Matthew T LewisDepartment of Physiology, Michigan State University , East Lansing, Michigan.
Jonathan D KasperDepartment of Physiology, Michigan State University , East Lansing, Michigan.
Paul D ChantlerDivision of Exercise Physiology, West Virginia University , Morgantown, West Virginia.
Robert W WisemanDepartment of Physiology, Michigan State University , East Lansing, Michigan.
Michigan State University · USWestern University · CAWest Virginia University · US

Funding

Mechanisms of Metabolic Dysfunction in Type 2 DiabetesR01DK095210 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BEARD, DANIEL A, WISEMAN, ROBERT W · 2012 to 2016
$2.7M
Skeletal Muscle Microcirculation in Obese Zucker RatsR01DK064668 · NIDDK · WEST VIRGINIA UNIVERSITY · PI FRISBEE, JEFFERSON C · 2004 to 2009
$1.1M
NIDDK NIH HHS R01 DK064668NIDDK NIH HHS R01 DK095210
6 · The paper itself

Abstract

Despite extensive investigation into the impact of metabolic disease on vascular function and, by extension, tissue perfusion and organ function, interpreting results for specific risk factors can be complicated by the additional risks present in most models. To specifically determine the impact of type 2 diabetes without obesity on skeletal muscle microvascular structure/function and on active hyperemia with elevated metabolic demand, we used 17-wk-old Goto-Kakizaki (GK) rats to study microvascular function at multiple levels of resolution. Gracilis muscle arterioles demonstrated blunted dilation to acetylcholine (both ex vivo proximal and in situ distal arterioles) and elevated shear (distal arterioles only). All other alterations to reactivity appeared to reflect compromised endothelial function associated with increased thromboxane (Tx)A

Indexed as

AnimalsBridged Bicyclo Compounds, HeterocyclicCyclic N-OxidesDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Endothelium, VascularFatty Acids, UnsaturatedHydrazinesHyperemiaImidazolesMetabolic SyndromeMicrocirculationMuscle FatigueMuscle, SkeletalMuscle, Smooth, VascularObesityBridged Bicyclo Compounds, HeterocyclicCyclic N-OxidesdazmegrelFatty Acids, UnsaturatedHydrazinesImidazolesSpin LabelsSQ 29548tempolanimal models of diabetesendothelial dysfunctionmetabolic diseaseregulation of blood flowvascular dysfunction

Identifiers

PMID30571284
PMCPMC6459383
OpenAlexW2906369865

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.