Evidence map›Paper›PMID 23321322›Full record

ArticleThe American journal of pathology2013

Alterations in glucose homeostasis in a murine model of Chagas disease.

Fnu Nagajyothi, Regina Kuliawat, Christine M Kusminski, Fabiana S Machado, Mahalia S Desruisseaux, Dazhi Zhao, Gary J Schwartz, Huan Huang, Chris Albanese, Michael P Lisanti and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. DIAGNOSIS AND TREATMENT OF A NATURAL INFECTION WITHJournal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Limited Foxp3Frontiers in immunology · 2018
    Article
  11. Review
  12. Article
  13. Adipose Tissue: A Safe Haven for Parasites?Trends in parasitology · 2017
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. The cell biology of fat expansion.The Journal of cell biology · 2015
    Review
  19. Article
  20. 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

17 authors at 6 institutions in 5 countries.

Fnu NagajyothiDivision of Parasitology and Tropical Medicine, Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Regina Kuliawat
Christine M Kusminski
Fabiana S Machado
Mahalia S Desruisseaux
Dazhi Zhao
Gary J Schwartz
Huan Huang
Chris Albanese
Michael P Lisanti
Rajat Singh
Feng Li
Louis M Weiss
Stephen M Factor
Jeffrey E Pessin
Philipp E Scherer
Herbert B Tanowitz
Albert Einstein College of Medicine · USThe University of Texas Southwestern Medical Center · USGeorgetown University · USHunan University of Traditional Chinese Medicine · CNManchester Academic Health Science Centre · GBUniversidade Federal de Minas Gerais · BR

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI FLEISCHER, NORMAN S. · 1986 to 2014
$29.8M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Novel Mechanisms Regulating the Adipocyte-Brain-Hepatocyte AxisP01DK088761 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GORDILLO, RUTH · 2010 to 2019
$17.4M
Adiponectin, A Protein Secreted From Adipose TissueR01DK055758 · NIDDK · YESHIVA UNIVERSITY · PI SCHERER, PHILIPP E · 2000 to 2024
$10.9M
Einstein's Nathan Shock Center of Excellence in Basic Biology of AgingP30AG038072 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VIJG, JAN · 2010 to 2024
$10.8M
REGULATION OF THE INSULIN RECEPTOR KINASER01DK033823 · NIDDK · UNIVERSITY OF IOWA · PI KURLAND, IRWIN JACK, PESSIN, JEFFREY E. · 1986 to 2022
$6.7M
Intracellular signaling by the insulin receptor kinaseR37DK033823 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI PESSIN, JEFFREY E. · 2005 to 2014
$4.2M
T. cruzi: pathogenesis modulation by eicosanoidsR01AI076248 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI TANOWITZ, HERBERT BERNARD · 2008 to 2012
$2.3M
Cerebral Malaria: Mechanisms of disease and neurological salvageR01NS069577 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DESRUISSEAUX, MAHALIA S · 2011 to 2015
$1.8M
Comprehensive MRI, MRS and Molecular Analyses: Pten-based Prostate Cancer ModelsR01CA129003 · NCI · GEORGETOWN UNIVERSITY · PI ALBANESE, CHRISTOPHER · 2007 to 2012
$1.4M
NCI NIH HHS CA-129003NCI NIH HHS P30 CA013330NCI NIH HHS P30CA013330NCI NIH HHS R01 CA129003NHLBI NIH HHS HL-112099NHLBI NIH HHS R21 HL112099NIAID NIH HHS AI-76248NIAID NIH HHS R01 AI076248NIA NIH HHS P30 AG038072NIA NIH HHS P30AG038072NIDDK NIH HHS DK020541NIDDK NIH HHS DK-033823NIDDK NIH HHS DK087776NIDDK NIH HHS K01 DK087776NIDDK NIH HHS P01 DK088761NIDDK NIH HHS P01-DK088761NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK026687NIDDK NIH HHS P60 DK020541NIDDK NIH HHS R01 DK033823NIDDK NIH HHS R01 DK055758NIDDK NIH HHS R01-DK55758NIDDK NIH HHS R37 DK033823NINDS NIH HHS NS069577NINDS NIH HHS R01 NS069577
6 · The paper itself

Abstract

Chagas disease, caused by Trypanosoma cruzi, is an important cause of morbidity and mortality primarily resulting from cardiac dysfunction, although T. cruzi infection results in inflammation and cell destruction in many organs. We found that T. cruzi (Brazil strain) infection of mice results in pancreatic inflammation and parasitism within pancreatic β-cells with apparent sparing of α cells and leads to the disruption of pancreatic islet architecture, β-cell dysfunction, and surprisingly, hypoglycemia. Blood glucose and insulin levels were reduced in infected mice during acute infection and insulin levels remained low into the chronic phase. In response to the hypoglycemia, glucagon levels 30 days postinfection were elevated, indicating normal α-cell function. Administration of L-arginine and a β-adrenergic receptor agonist (CL316, 243, respectively) resulted in a diminished insulin response during the acute and chronic phases. Insulin granules were docked, but the lack of insulin secretion suggested an inability of granules to fuse at the plasma membrane of pancreatic β-cells. In the liver, there was a concomitant reduced expression of glucose-6-phosphatase mRNA and glucose production from pyruvate (pyruvate tolerance test), demonstrating defective hepatic gluconeogenesis as a cause for the T. cruzi-induced hypoglycemia, despite reduced insulin, but elevated glucagon levels. The data establishes a complex, multi-tissue relationship between T. cruzi infection, Chagas disease, and host glucose homeostasis.

Indexed as

HomeostasisAdipose Tissue, WhiteAnimalsBlood GlucoseChagas DiseaseDisease Models, AnimalFluorescent Antibody TechniqueGlucagonGluconeogenesisGlucoseInsulinLiverMaleMicePancreasTrypanosoma cruziBlood GlucoseGlucagonGlucoseInsulin

Identifiers

PMID23321322
PMCPMC3586686
OpenAlexW2039021392

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.