Evidence map›Paper›PMID 38453236›Full record

ArticleBMJ open diabetes research & care2024

Colonic epithelial hypoxia remains constant during the progression of diabetes in male UC Davis type 2 diabetes mellitus rats.

Brian D Piccolo, James L Graham, Leslie Tabor-Simecka, Christopher E Randolph, Becky Moody, Michael S Robeson, Ping Kang, Renee Fox, Renny Lan, Lindsay Pack and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

15 authors at 6 institutions in 1 country.

Brian D PiccoloUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA bdpiccolo@uams.edu.ORCID 0000-0002-1789-4587
James L GrahamDepartment of Nutrition, University of California Davis, Davis, California, USA.
Leslie Tabor-SimeckaUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Christopher E RandolphCenter for Translational Pediatric Research, Arkansas Children's Research Institute, Little Rock, Arkansas, USA.
Becky MoodyUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Michael S RobesonDepartment of Biomedical Informatics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Ping KangUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Renee FoxUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Renny LanUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Lindsay PackUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Noah WofordCollege of Osteopathic Medicine, Lincoln Memorial University, Harrogate, Tennessee, USA.
Laxmi YeruvaUSDA-ARS Arkansas Children's Nutrition Center, Little Rock, Arkansas, USA.
Tanya LeRoithDepartment of Biomedical Science and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, USA.
Kimber L StanhopeDepartment of Nutrition, University of California Davis, Davis, California, USA.
Peter J HavelDepartment of Nutrition, University of California Davis, Davis, California, USA.
Arkansas Children's Nutrition Center · USUniversity of California, Davis · USArkansas Children's Hospital · USLincoln Memorial University · USUniversity of Arkansas for Medical Sciences · USVirginia Tech · US

Funding

Expanding Translational Research in ArkansasUL1TR003107 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI JAMES, LAURA P · 2019 to 2023
$21.6M
Adverse Metabolic Effects of Dietary Sugar _ Ad Libitum vs Energy-Balanced DietsR01HL121324 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAVEL, PETER J, SCHWARZ, JEAN-MARC · 2014 to 2019
$4.2M
Mouse Metabolic Phenotyping Center (MMPC) at UC DavisU24DK092993 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2011 to 2015
$4.1M
Institutional Career DevelopmentKL2TR003108 · NCATS · UNIV OF ARKANSAS FOR MED SCIS · PI ARTHUR, JOHN M., BORSHEIM, ELISABET · 2019 to 2023
$2.3M
Effects of 2wk fructose & HFCS consumption on lipid dysregulation & insulin resisR01HL091333 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAVEL, PETER J · 2008 to 2012
$2.0M
Fatty acid sources of fructose and HFCS-induced postprandial hypertriglyceridemiaR01HL107256 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HAVEL, PETER J, SCHWARZ, JEAN-MARC · 2011 to 2014
$1.5M
Surgical amelioration of type 2 diabetes: Hormones, microbiota and mitochondriaRC1DK087307 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GIULIVI, CECILIA, HAVEL, PETER J · 2009 to 2010
$985k
Extracellular vesicles miRNA cargo induces inflammation during chlamydial infectionR21AI146521 · NIAID · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI FERRUZZI, MARIO G · 2019 to 2020
$422k
NCATS NIH HHS KL2 TR003108NCATS NIH HHS UL1 TR003107NHLBI NIH HHS R01 HL091333NHLBI NIH HHS R01 HL107256NHLBI NIH HHS R01 HL121324NIAID NIH HHS R21 AI146521NIDDK NIH HHS RC1 DK087307NIDDK NIH HHS U24 DK092993
6 · The paper itself

Abstract

introductionColonocyte oxidation of bacterial-derived butyrate has been reported to maintain synergistic obligate anaerobe populations by reducing colonocyte oxygen levels; however, it is not known whether this process is disrupted during the progression of type 2 diabetes. Our aim was to determine whether diabetes influences colonocyte oxygen levels in the University of California Davis type 2 diabetes mellitus (UCD-T2DM) rat model. RESEARCH DESIGN AND

methodsAge-matched male UCD-T2DM rats (174±4 days) prior to the onset of diabetes (PD, n=15), within 1 month post-onset (RD, n=12), and 3 months post-onset (D3M, n=12) were included in this study. Rats were administered an intraperitoneal injection of pimonidazole (60 mg/kg body weight) 1 hour prior to euthanasia and tissue collection to estimate colonic oxygen levels. Colon tissue was fixed in 10% formalin, embedded in paraffin, and processed for immunohistochemical detection of pimonidazole. The colonic microbiome was assessed by 16S gene rRNA amplicon sequencing and content of short-chain fatty acids was measured by liquid chromatography-mass spectrometry.

resultsHbA1c % increased linearly across the PD (5.9±0.1), RD (7.6±0.4), and D3M (11.5±0.6) groups, confirming the progression of diabetes in this cohort. D3M rats had a 2.5% increase in known facultative anaerobes,

conclusionsThe advancement of diabetes in UCD-T2DM rats was associated with an increase in facultative anaerobes; however, this was not explained by changes in colonocyte oxygen levels. The mechanisms underlying shifts in gut microbe populations associated with the progression of diabetes in the UCD-T2DM rat model remain to be identified.

Indexed as

Diabetes Mellitus, Type 2NitroimidazolesAnimalsHumansHypoxiaInfant, NewbornMaleOxygenRatsNitroimidazolesOxygenpimonidazoleDiabetes Mellitus, ExperimentalGastrointestinal TractHypoxiaMicrobiology

Identifiers

PMID38453236
PMCPMC10921531
OpenAlexW4392561047

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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.