Evidence map›Paper›PMID 41083686›Full record

ArticleScientific reports2025

Inflammatory and morphological changes in the colon reflect early aging induced by D-galactose in rats.

Cherry Azaria, Bilqis Zahra Nabila, Yustina Andwi Ari Sumiwi, Rina Susilowati, Dewajani Purnomosari

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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
–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

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.

  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

5 authors.

Cherry AzariaDoctoral Program Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Jalan Farmako, Sekip Utara, Yogyakarta, 55281, Indonesia.ORCID http://orcid.org/0009-0007-3563-6569
Bilqis Zahra NabilaDepartment Histology and Cell Biology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Jalan Farmako, Sekip Utara, Yogyakarta, 55281, Indonesia.ORCID http://orcid.org/0009-0009-2167-7057
Yustina Andwi Ari SumiwiDepartment Histology and Cell Biology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Jalan Farmako, Sekip Utara, Yogyakarta, 55281, Indonesia.ORCID http://orcid.org/0000-0001-5576-4081
Rina SusilowatiDepartment Histology and Cell Biology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Jalan Farmako, Sekip Utara, Yogyakarta, 55281, Indonesia.ORCID http://orcid.org/0000-0001-8248-5803
Dewajani PurnomosariDepartment Histology and Cell Biology, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Jalan Farmako, Sekip Utara, Yogyakarta, 55281, Indonesia. d.purnomosari@ugm.ac.id.ORCID http://orcid.org/0000-0002-3972-8387

Funding

Ministry of Education, Culture, Research and Technology Republic of Indonesia 3099/UNI1/DITLIT/Dit-Lit/PT.01.03/2023
6 · The paper itself

Abstract

Aging leads to a decline in function and structural changes. To mimic these processes, D-galactose (D-Gal) administration is widely used as a pro-aging model in animal studies due to its reproducibility and practicality. In this study, D-Gal was administered via intraperitoneal injection to induce aging in rats. This study aimed to investigate age-related changes in colon function and structure in an animal model through histological analysis and immunohistochemical assessment of aging biomarkers. Twelve-week-old male Sprague Dawley rats were divided into control and GAL groups. The functional test was performed by measuring the colon transit time duration and faecal output amount. Structural analysis was performed by histological examination using hematoxyllin-eosin staining and immunohistochemistry against p16Ink4A and lamin B1 antibodies. Colon transit time in the GAL group was significantly faster, but fecal pellet output and body weight in the GAL group had lower values. Microscopic examination revealed significant differences (p = 0.00) between the GAL and control groups. The GAL group exhibited mild epithelial (score 1) and muscle tissue damage (score 2), along with leukocyte infiltration (score 3). The immunohistochemistry results showed a significant difference in the GAL group (p < 0.05) for p16Ink4A and lamin B1 antibodies, which confirmed the ongoing aging process. Mild structural and functional changes, accompanied by significant inflammation, suggest that the D-Gal-induced aging model accelerates colon aging.

Indexed as

AgingColonGalactoseInflammationAnimalsCyclin-Dependent Kinase Inhibitor p16MaleRatsRats, Sprague-DawleyCyclin-Dependent Kinase Inhibitor p16GalactoseAge-inducedColon inflammationd-GalactoseEarly aging

Identifiers

PMID41083686
PMCPMC12518535

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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.