Evidence map›Paper›PMID 41760328›Full record

ArticleIn vivo (Athens, Greece)

Protective Effect of Exercise Training Against Age-induced Cerebral Microvascular Rarefaction: VEGF/Flk-1/PI3K/Akt Signaling and GLUT1 Expression.

Sheepsumon Viboolvorakul, Decha Buranajitpirom, Suthiluk Patumraj

Abstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Sheepsumon ViboolvorakulPhysiology Unit, Department of Medical Science, Faculty of Science, Rangsit University, Pathum Thani, Thailand; sheepsumon.v@rsu.ac.th.
Decha BuranajitpiromAnatomy Division, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathum Thani, Thailand.
Suthiluk PatumrajCenter of Excellence for Microcirculation, Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAge-related cerebral microvascular loss is associated with reduced angiogenesis and leads to inadequate tissue perfusion in the brain. Vascular endothelial growth factor (VEGF), crucial for angiogenesis, declines with age. Exercise enhances microvascular density and blood flow, promoting brain health. The specific mechanisms underlying exercise-induced angiogenesis in aging brains remain unclear. This study investigated the impact of exercise on microvessel density, tissue perfusion, and VEGF-angiogenic signaling in aging brains. MATERIALS AND

methodsMale rats were divided into three groups: an age-matched control, a sedentary control, and an exercise-trained group, which underwent swimming exercise. Regional cerebral tissue perfusion (CTP) was assessed in an

resultsMicrovessel density and regional CTP in the sedentary control group were significantly reduced compared to the age-matched control group. The exercise-trained group demonstrated substantial increases in microvessel density and regional CTP compared to the sedentary control group. An increase in GLUT1 in the exercise group indicates microvascular metabolic restoration. VEGF angiogenic protein levels were significantly decreased in the sedentary control group compared to the age-matched control group; however, exercise training significantly increased these protein levels relative to the sedentary control group. Furthermore, we discovered a strong and significant positive correlation among the microvessel density, regional CTP, and VEGF angiogenic proteins across the three groups.

conclusionSwimming exercise training may protect against age-induced cerebral microvascular loss and insufficient brain tissue perfusion through the VEGF-mediated angiogenic signaling cascade. The increase in GLUT1 indicates restored structural and metabolic endothelial function in the aging brain.

Indexed as

AgingGlucose Transporter Type 1Microvascular RarefactionPhysical Conditioning, AnimalSignal TransductionVascular Endothelial Growth Factor AAngiogenesisAnimalsBrainMaleMicrovesselsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRatsVascular Endothelial Growth Factor Receptor-2Glucose Transporter Type 1Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSlc2a1 protein, ratVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2agingangiogenesisbrainExerciseGLUT1VEGF

Identifiers

PMID41760328
PMCPMC12949908

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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.