Evidence map›Paper›PMID 35095472›Full record

ArticleFrontiers in aging neuroscience2021

Impaired Glymphatic Function and Pulsation Alterations in a Mouse Model of Vascular Cognitive Impairment.

Mosi Li, Akihiro Kitamura, Joshua Beverley, Juraj Koudelka, Jessica Duncombe, Ross Lennen, Maurits A Jansen, Ian Marshall, Bettina Platt, Ulrich K Wiegand and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
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

39 citing papers in PubMed, 50 citations in OpenAlex.

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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

14 authors at 5 institutions in 3 countries.

Mosi LiCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Akihiro KitamuraCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Joshua BeverleyCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Juraj KoudelkaCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Jessica DuncombeCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Ross LennenCentre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Maurits A JansenCentre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Ian MarshallCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Bettina PlattSchool of Medicine, Medical Sciences and Nutrition, College of Life Sciences and Medicine, University of Aberdeen, Aberdeen, United Kingdom.
Ulrich K WiegandCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Roxana O CarareFaculty of Medicine, University of Southampton, Southampton, United Kingdom.
Rajesh N KalariaTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Jeffrey J IliffVISN 20 Mental Illness Research, Education and Clinical Center, VA Puget Sound Health Care System, Seattle, WA, United States.
Karen HorsburghCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
University of Edinburgh · GBNewcastle University · GBUniversity of Aberdeen · GBUniversity of Southampton · GBVA Portland Health Care System · US

Funding

Defining the role of age-related glymphatic pathway impairment in amyloid beta plaque depositionR01AG054456 · NIA · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI ILIFF, JEFFREY J · 2017 to 2021
$1.8M
Medical Research Council MR/K015710/1NIA NIH HHS R01 AG054456
6 · The paper itself

Abstract

Large vessel disease and carotid stenosis are key mechanisms contributing to vascular cognitive impairment (VCI) and dementia. Our previous work, and that of others, using rodent models, demonstrated that bilateral common carotid stenosis (BCAS) leads to cognitive impairment via gradual deterioration of the neuro-glial-vascular unit and accumulation of amyloid-β (Aβ) protein. Since brain-wide drainage pathways (glymphatic) for waste clearance, including Aβ removal, have been implicated in the pathophysiology of VCI via glial mechanisms, we hypothesized that glymphatic function would be impaired in a BCAS model and exacerbated in the presence of Aβ. Male wild-type and Tg-SwDI (model of microvascular amyloid) mice were subjected to BCAS or sham surgery which led to a reduction in cerebral perfusion and impaired spatial learning acquisition and cognitive flexibility. After 3 months survival, glymphatic function was evaluated by cerebrospinal fluid (CSF) fluorescent tracer influx. We demonstrated that BCAS caused a marked regional reduction of CSF tracer influx in the dorsolateral cortex and CA1-DG molecular layer. In parallel to these changes increased reactive astrogliosis was observed post-BCAS. To further investigate the mechanisms that may lead to these changes, we measured the pulsation of cortical vessels. BCAS impaired vascular pulsation in pial arteries in WT and Tg-SwDI mice. Our findings show that BCAS influences VCI and that this is paralleled by impaired glymphatic drainage and reduced vascular pulsation. We propose that these additional targets need to be considered when treating VCI.

Indexed as

amyloid-β (Aβ)carotid stenosiscerebral amyloid angiopathy (CAA)glymphatic functionvascular cognitive impairmentvascular pulsation

Identifiers

PMID35095472
PMCPMC8793139
OpenAlexW4206333356

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.