Evidence map›Paper›PMID 41226315›Full record

ArticleInternational journal of molecular sciences2025

Augmented Flow-Induced Outward Remodelling Occurs with Ageing in Mice.

Bethan Brown, Helen Williams, Samson Egbulonu, Andrew Bond, Jason Johnson, Sarah George

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Bethan BrownTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.
Helen WilliamsTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.ORCID 0000-0003-3467-3054
Samson EgbulonuTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.
Andrew BondTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.ORCID 0000-0002-4255-4488
Jason JohnsonTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.ORCID 0000-0003-0630-9183
Sarah GeorgeTranslational Health Sciences, Bristol Medical School, University of Bristol, Level 7 Bristol Royal Infirmary, Bristol BS2 8HW, UK.ORCID 0000-0002-1426-8257

Funding

British Heart Foundation FS/13/68/30489British Heart Foundation SS/CH/92027/7163
6 · The paper itself

Abstract

Outward remodelling of arteries is a feature of cardiovascular pathologies such as atherosclerosis and aneurysm, so a greater understanding of the processes involved in remodelling may aid the development of improved therapies for patients. As ageing increases the risk of atherosclerosis and aneurysmal disease, it was therefore hypothesised that ageing affects arterial remodelling and thereby contributes to these diseases. To test this hypothesis, we compared right carotid artery remodelling in young (2 months, n = 13) and old (18-20 months, n = 13) mice resulting from increased blood flow after ligation of the left carotid artery. The media area, thickness, collagen content and α-SM-actin content per cell of control right carotid arteries from old mice were significantly greater than observed in young mice. Positive remodelling was observed in the carotid arteries of both old and young mice 21 days after ligation of the left carotid artery. However, arteries from old mice had a significantly larger increase in lumen size and reduction in media area, thickness and α-SM-actin content per cell compared to young arteries, indicative of augmented positive remodelling in arteries from old mice. Remodelling was associated with significantly increased MMP-2 protein in arteries from young mice, but this was not observed in arteries from old mice. This study demonstrates that the extent of positive remodelling of carotid arteries is greater in old mice than in young mice and results in a potentially less resilient medial layer with decreased α-SM-actin content per cell, elastin and collagen that may promote atherosclerosis and aneurysm formation.

Indexed as

AgingCarotid ArteriesVascular RemodelingActinsAnimalsCollagenMaleMatrix Metalloproteinase 2MiceMice, Inbred C57BLActinsCollagenMatrix Metalloproteinase 2ageingarterycardiovascular diseaseflow remodelling

Identifiers

PMID41226315
PMCPMC12610229

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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.