Evidence map›Paper›PMID 40599192›Full record

ArticleWorld journal of gastroenterology2025

miR-10a-5p and miR-10b-5p restore colonic motility in aged mice.

Gain Baek, Rajan Singh, Se Eun Ha, Hayeong Cho, Sesh Padmanabhan, Vachan Vishwanath, Min Seob Kim, Dahyun Seon, Jisong You, Moon Young Lee and 1 more

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2025. 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
–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

3 citing papers in PubMed.

  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

11 authors.

Gain BaekDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Rajan SinghDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Se Eun HaDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Hayeong ChoDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Sesh PadmanabhanDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Vachan VishwanathDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States.
Min Seob KimDepartment of Physiology, Wonkwang University, Iksan 54538, South Korea.
Dahyun SeonDepartment of Physiology, Wonkwang University, Iksan 54538, South Korea.
Jisong YouDepartment of Physiology, Wonkwang University, Iksan 54538, South Korea.
Moon Young LeeDepartment of Physiology, Wonkwang University, Iksan 54538, South Korea.
Seungil RoDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, United States. sro@med.unr.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe previously identified miR-10b-5p as a key regulator of gastrointestinal (GI) motility through its essential role in the development and function of interstitial cells of Cajal (ICC), the pacemaker cells of the gut. Loss of miR-10b-5p in ICC impairs intestinal motility and contributes to constipation, a common condition in the elderly. Notably, miR-10b-5p is co-expressed with its paralog, miR-10a-5p, in ICC.

aimTo investigate the roles of miR-10a-5p and miR-10b-5p in age-associated intestinal dysmotility and assess the therapeutic potential of restoring their expression.

methodsWe employed aged mice,

resultsAged mice exhibited delayed GI and colonic transit, reduced fecal output, and diminished expression of miR-10a-5p and miR-10b-5p, which peaked during late embryonic and early postnatal stages and declined with age. This decline paralleled ICC network deterioration in the colon. All KO models exhibited impaired motility and ICC loss, with

conclusionmiR-10a-5p and miR-10b-5p are essential for ICC maintenance and colonic motility, and their age-related decline contributes to GI dysmotility in both mice and humans. Restoring their levels offers a promising therapeutic strategy for treating age-related constipation and other motility disorders.

Indexed as

AgingColonConstipationGastrointestinal MotilityInterstitial Cells of CajalMicroRNAsAnimalsDisease Models, AnimalFemaleGastrointestinal TransitHumansMaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMIRN10 microRNA, humanMIRN10 microRNA, mouseAged miceConstipationGastrointestinal dysmotilityInterstitial cells of CajalMicroRNAs

Identifiers

PMID40599192
PMCPMC12207554

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.