Evidence map›Paper›PMID 40435721›Full record

ArticleEBioMedicine2025

Induction of haemodynamic travelling waves by glial-related vasomotion in a rat model of neuroinflammation: implications for functional neuroimaging.

Mickaël Pereira, Marine Droguerre, Marco Valdebenito, Louis Vidal, Guillaume Marcy, Sarah Benkeder, Paul Marchal, Jean-Christophe Comte, Olivier Pascual, Luc Zimmer and 1 more

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Article in EBioMedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Mickaël PereiraUniversité Claude Bernard Lyon 1, Lyon Neuroscience Research Center, INSERM, CNRS, Lyon, France.
Marine DroguerreTheranexus, Lyon, France.
Marco ValdebenitoCERMEP-Imaging Platform, Lyon, France.
Louis VidalUniversité Claude Bernard Lyon 1, Lyon Neuroscience Research Center, INSERM, CNRS, Lyon, France.
Guillaume MarcyUniversité Claude Bernard Lyon 1, Bioinformatic Platform of the Labex Cortex, Lyon, France.
Sarah BenkederUniversité Claude Bernard Lyon 1, Institut MeLiS, INSERM, CNRS, Lyon, France.
Paul MarchalUniversité Claude Bernard Lyon 1, Institut MeLiS, INSERM, CNRS, Lyon, France.
Jean-Christophe ComteUniversité Claude Bernard Lyon 1, Lyon Neuroscience Research Center, INSERM, CNRS, Lyon, France.
Olivier PascualUniversité Claude Bernard Lyon 1, Institut MeLiS, INSERM, CNRS, Lyon, France.
Luc ZimmerUniversité Claude Bernard Lyon 1, Lyon Neuroscience Research Center, INSERM, CNRS, Lyon, France; CERMEP-Imaging Platform, Lyon, France; Hospices Civils de Lyon, Lyon, France.
Benjamin VidalUniversité Claude Bernard Lyon 1, Lyon Neuroscience Research Center, INSERM, CNRS, Lyon, France; CERMEP-Imaging Platform, Lyon, France. Electronic address: benjamin.vidal@cermep.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCerebral haemodynamics are crucial for brain homoeostasis and serve as a key proxy for brain activity. Although this process involves coordinated interaction between vessels, neurons, and glial cells, its dysregulation in neuroinflammation is not well understood.

methodsWe used in vivo mesoscopic functional ultrasound imaging to monitor cerebral blood volume changes during neuroinflammation in male rats injected with lipopolysaccharide (LPS) in the visual cortex, under resting-state or visual stimulation, combined to advanced ex vivo techniques for glial cell reactivity analysis.

findingsCortical neuroinflammation induced large oscillatory haemodynamic travelling waves in the frequency band of vasomotion (∼0.1 Hz) in both anaesthetized and awake rats. Vasomotor waves travelled through large distances between adjacent penetrating vessels, spanning the entire cortex thickness, and even extending to subcortical areas. Moreover, vasomotion amplitude correlated with microglial morphology changes and was significantly reduced by astrocytic toxins, suggesting that both microglia and astrocytes are involved in the enhancement of vasomotion during neuroinflammation. Notably, functional connectivity was increased under this oscillatory state and functional hyperaemia was exacerbated.

interpretationThese findings further reveal the spatiotemporal properties of cerebral vasomotion and suggest this is a major component of brain haemodynamics in pathological states. Moreover, reactive microglia and astrocytes are participating to increase vasomotion during neuroinflammation. For the field of functional neuroimaging, our results advocate for considering 0.1 Hz haemodynamic oscillations as an important complement to traditional measurements, particularly in neuroinflammatory conditions. Indeed, brain haemodynamics may provide insights not only into neuronal activity but also glial reactivity.

fundingSupported by ANR ("LabCom-NI2D", "Labex Cortex") and Auvergne-Rhône-Alpes Region ("BI2D").

Indexed as

Functional NeuroimagingHemodynamicsNeurogliaNeuroinflammatory DiseasesAnimalsAstrocytesCerebrovascular CirculationDisease Models, AnimalLipopolysaccharidesMaleMicrogliaRatsLipopolysaccharidesFunctional connectivityFunctional ultrasound imagingGliaNeuroinflammationNeurovascular couplingVasomotion

Identifiers

PMID40435721
PMCPMC12159494

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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.