Evidence map›Paper›PMID 39596183›Full record

ArticleInternational journal of molecular sciences2024

Oxidative Stress and Histomorphometric Remodeling: Two Key Intestinal Features of Type 2 Diabetes in Goto-Kakizaki Rats.

Marisa Esteves-Monteiro, Mariana Ferreira-Duarte, Cláudia Vitorino-Oliveira, José Costa-Pires, Sara Oliveira, Paulo Matafome, Manuela Morato, Patrícia Dias-Pereira, Vera Marisa Costa, Margarida Duarte-Araújo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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
–field-weighted citation impact
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

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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.

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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

10 authors.

Marisa Esteves-MonteiroAssociated Laboratory for Green Chemistry (LAQV) Network of Chemistry and Technology (REQUIMTE), University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-0585-3905
Mariana Ferreira-DuarteAssociated Laboratory for Green Chemistry (LAQV) Network of Chemistry and Technology (REQUIMTE), University of Porto, 4050-313 Porto, Portugal.
Cláudia Vitorino-OliveiraInstitute for Health and Bioeconomy (i4HB), Laboratory of Toxicology, Department of Biological Sciences, FFUP, 4050-313 Porto, Portugal.
José Costa-PiresDepartment of Immuno-Physiology and Pharmacology, Institute of Biomedical Sciences Abel Salazar, University of Porto (ICBAS-UP), 4050-313 Porto, Portugal.
Sara OliveiraCoimbra Institute for Clinical and Biomedical Research (iCBR) and Institute of Physiology, Faculty of Medicine, University of Coimbra (UC), 3000-548 Coimbra, Portugal.ORCID 0000-0002-0423-7959
Paulo MatafomeCoimbra Institute for Clinical and Biomedical Research (iCBR) and Institute of Physiology, Faculty of Medicine, University of Coimbra (UC), 3000-548 Coimbra, Portugal.ORCID 0000-0002-3422-290X
Manuela MoratoAssociated Laboratory for Green Chemistry (LAQV) Network of Chemistry and Technology (REQUIMTE), University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-9509-0613
Patrícia Dias-PereiraDepartment of Pathology and Molecular Immunology, ICBAS-UP, 4050-313 Porto, Portugal.ORCID 0000-0002-8845-794X
Vera Marisa CostaInstitute for Health and Bioeconomy (i4HB), Laboratory of Toxicology, Department of Biological Sciences, FFUP, 4050-313 Porto, Portugal.ORCID 0000-0002-0471-2756
Margarida Duarte-AraújoAssociated Laboratory for Green Chemistry (LAQV) Network of Chemistry and Technology (REQUIMTE), University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0003-4727-727X

Funding

Fundação para a Ciência e Tecnologia UIDP/50006/2020 DOI 10.54499/UIDP/50006/2020; 2020.06502.BDUniversidade de Coimbra UIDB//04539/2020, UIDP//04539/2020, and LA/P/0058/2020, CIBB
6 · The paper itself

Abstract

Gastrointestinal complications of diabetes are often overlooked, despite affecting up to 75% of patients. This study innovatively explores local glutathione levels and morphometric changes in the gut of Goto-Kakizaki (GK) rats, a type 2 diabetes animal model. Segments of the intestine, cecum, and colon were collected for histopathological analysis and glutathione quantification. A significant increase in the total thickness of the intestinal wall of GK rats was observed, particularly in the duodenum (1089.02 ± 39.19 vs. 864.19 ± 37.17 µm), ileum (726.29 ± 24.75 vs. 498.76 ± 16.86 µm), cecum (642.24 ± 34.15 vs. 500.97 ± 28.81 µm), and distal colon (1211.81 ± 51.32 vs. 831.71 ± 53.2 µm). Additionally, diabetic rats exhibited thickening of the muscular layers in all segments, except for the duodenum, which was also the only portion where the number of smooth muscle cells did not decrease. Moreover, myenteric neuronal density was lower in GK rats, suggesting neurological loss. Total glutathione levels were lower in all intestinal segments of diabetic rats (except duodenum), and the reduced/oxidized glutathione ratio (GSH/GSSG) was significantly decreased in GK rats, indicating increased oxidative stress. These findings strongly indicate that GK rats undergo significant intestinal remodeling, notable shifts in neuronal populations, and heightened oxidative stress-factors that likely contribute to the functional gastrointestinal alterations seen in diabetic patients.

Indexed as

Diabetes Mellitus, Type 2GlutathioneOxidative StressAnimalsDiabetes Mellitus, ExperimentalDisease Models, AnimalDuodenumIntestinal MucosaIntestinesMaleRatsGlutathionediabetesGK ratsgut remodelingoxidative stress

Identifiers

PMID39596183
PMCPMC11594829

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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.