Evidence map›Paper›PMID 31188651›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2019

Skeletal muscle energetics are compromised only during high-intensity contractions in the Goto-Kakizaki rat model of type 2 diabetes.

Matthew T Lewis, Jonathan D Kasper, Jason N Bazil, Jefferson C Frisbee, Robert W Wiseman

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. Review
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  5. 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

5 authors at 2 institutions in 2 countries.

Matthew T LewisDepartment of Physiology, Michigan State University, East Lansing, Michigan.
Jonathan D KasperDepartment of Physiology, Michigan State University, East Lansing, Michigan.
Jason N BazilDepartment of Physiology, Michigan State University, East Lansing, Michigan.
Jefferson C FrisbeeDepartment of Medical Biophysics, University of Western Ontario, London, Ontario, Canada.
Robert W WisemanDepartment of Physiology, Michigan State University, East Lansing, Michigan.
Michigan State University · USWestern University · CA

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
Mechanistic Characterization of Calcium and ROS Induced Mitochondrial DysfunctionR00HL121160 · NHLBI · MICHIGAN STATE UNIVERSITY · PI BAZIL, JASON N · 2016 to 2018
$734k
CIHR R5521A02NHLBI NIH HHS R00 HL121160NIDDK NIH HHS R01 DK095210
6 · The paper itself

Abstract

Type 2 diabetes (T2D) presents with hyperglycemia and insulin resistance, affecting over 30 million people in the United States alone. Previous work has hypothesized that mitochondria are dysfunctional in T2D and results in both reduced ATP production and glucose disposal. However, a direct link between mitochondrial function and T2D has not been determined. In the current study, the Goto-Kakizaki (GK) rat model of T2D was used to quantify mitochondrial function in vitro and in vivo over a broad range of contraction-induced metabolic workloads. During high-frequency sciatic nerve stimulation, hindlimb muscle contractions at 2- and 4-Hz intensities, the GK rat failed to maintain similar bioenergetic steady states to Wistar control (WC) rats measured by phosphorus magnetic resonance spectroscopy, despite similar force production. Differences were not due to changes in mitochondrial content in red (RG) or white gastrocnemius (WG) muscles (cytochrome

Indexed as

AnimalsDiabetes Mellitus, Type 2Disease Models, AnimalGlucoseHyperglycemiaInsulin ResistanceMagnetic Resonance SpectroscopyMaleMitochondriaMuscle, SkeletalRatsRats, WistarGlucosehyperglycemiainactivityinsulin resistancemitochondrial oxidative phosphorylationobesity

Identifiers

PMID31188651
PMCPMC6732426
OpenAlexW2950530337

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.