Evidence map›Paper›PMID 28713178›Full record

ArticleThe Polar record2015

Glucose transporter-4 in white blood cells of young and old sled dogs: a model for human biomarker development.

Theresia M Schnurr, Arleigh J Reynolds, Lawrence K Duffy, Kriya L Dunlap

Open access · bronzeAbstract read
In one paragraph

Article in The Polar record, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

4 authors at 1 institution in 1 country.

Theresia M SchnurrDepartment of Chemistry and Biochemistry and Institute of Arctic Biology, University of Alaska Fairbanks, PO BOX 756160, Fairbanks, AK 99775, USA.
Arleigh J ReynoldsDepartment of Chemistry and Biochemistry and Institute of Arctic Biology, University of Alaska Fairbanks, PO BOX 756160, Fairbanks, AK 99775, USA.
Lawrence K DuffyDepartment of Chemistry and Biochemistry and Institute of Arctic Biology, University of Alaska Fairbanks, PO BOX 756160, Fairbanks, AK 99775, USA.
Kriya L DunlapDepartment of Chemistry and Biochemistry and Institute of Arctic Biology, University of Alaska Fairbanks, PO BOX 756160, Fairbanks, AK 99775, USA.
University of Alaska Fairbanks · US

Funding

The Administrative CoreP20GM103395 · NIGMS · UNIVERSITY OF ALASKA FAIRBANKS · PI BRIAN M BARNES · 2012 to 2026
$66.1M
VIROLOGISTP20RR016466 · NCRR · UNIVERSITY OF ALASKA FAIRBANKS · PI LEIGH, MARY BETH · 2001 to 2011
$37.0M
Rac-1 mediated superoxide signaling in neuronsU54NS041069 · NINDS · UNIVERSITY OF ALASKA FAIRBANKS · PI DUFFY, LAWRENCE K · 2000 to 2011
$14.1M
NCRR NIH HHS P20 RR016466NIGMS NIH HHS P20 GM103395NINDS NIH HHS U54 NS041069
6 · The paper itself

Abstract

The insulin responsive glucose transporter, GLUT4 is found predominantly in muscle and adipose cells. Maratou and others (2007) reported that there is GLUT4 in white blood cells (WBC) collected from human subjects in response to insulin activation. This study was designed to validate the presence of GLUT4 in white blood cells of sled dogs and furthermore to investigate whether changes in levels of the GLUT4 protein might be associated with aging. Additionally, we examined the blood insulin concentration of two populations of dogs, young and old, before and after a meal to observe their insulin response. It is documented in skeletal muscle that GLUT4 expression is increased as a result of conditioning, making sled dogs an excellent model in the circumpolar north for studying the effects of exercise, nutrition and diabetes (Felsburg 2002; Kararli 2006). Blood was withdrawn from 11 healthy sled dogs: 6 young (1-5 years) and physically fit, conditioned for racing and 5 old (7-13 years), retired from racing. The insulin response was determined using blood plasma and ELISA. The buffy coat (containing WBC) was collected with a glass pipette after centrifugation and washed and suspended in 1x phosphate buffer. GLUT4 was measured using ELISA kits (USCN Life Sciences). The results validate that GLUT4 is present in white blood cells in sled dogs. Age had no significant effect in the concentration of GLUT4 between the populations of old and young dogs. A significant difference in insulin levels pre and post meal in young (0.13 ± 0.03 ng/mL (pre), 0.22 ± 0.04 ng/mL (post), p < 0.05) and old (0.13 ± 0.02 ng/mL (pre), 0.22 ± 0.03 ng/mL (post), p < 0.05) dogs was observed, displaying the typical postprandial insulin spike. No significant difference was found in insulin concentration comparing old versus young dogs. Our data shows that white blood cells in young (40.4 ± 2.4 ng/mL) and old (35.3 ± 8.8 ng/mL) sled dogs have quantifiable but non-significant different GLUT4 levels (p > 0.05). Detecting GLUT4 via an ELISA in white blood cells, opens up minimally invasive avenues for studying the underlying molecular mechanisms associated with insulin resistance in more complex, dynamic and physiological systems. This project was the first step in developing a protocol for this simple, technique with a potential clinical application for diagnosing insulin resistance.

Identifiers

PMID28713178
PMCPMC5507629
OpenAlexW2045461010

What OpenQuestion holds

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Registered trials

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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.