Evidence map›Paper›PMID 40386649›Full record

ArticleNeurophotonics2025

Semi-automated analysis of cerebral capillary red blood cell velocities allows modeling of transit time distribution after experimental subarachnoid hemorrhage in mice.

Kévin Chalard, Yan Chastagnier, Julie Perroy, Vivien Szabo

Abstract read
In one paragraph

Article in Neurophotonics, 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. Observational
  2. Assessing cerebral capillary function and stalling using single capillary reporters in ultrasound localization microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
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

4 authors.

Kévin ChalardUniversity of Montpellier, IGF, CNRS, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0002-0727-064X
Yan ChastagnierUniversity of Montpellier, IGF, CNRS, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0002-1239-0048
Julie PerroyUniversity of Montpellier, IGF, CNRS, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0001-6199-0448
Vivien SzaboUniversity of Montpellier, IGF, CNRS, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0002-0079-7596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Microvascular dysfunction stems from the origin of various neurological diseases. Among these, delayed cerebral ischemia following subarachnoid hemorrhage (SAH) is a major complication. Even though pathogenesis remains poorly understood, hypotheses converge toward early and persistent microvascular dysfunction. In this context, mathematical models have been developed to study oxygen delivery using theoretical distributions of capillary flux. However, these distributions lack experimental validation. Aim: We propose experimental recording of capillary red blood cell (RBC) velocities in a superficial cortical microvascular network in a mouse model of SAH, testing theoretical transit time distributions and their implications on tissue oxygenation. Approach: We performed optical recording of RBC velocities. We propose a complete software, available on GitHub, for velocity semi-automated measurement. Experimental data were fitted with Gamma and Cauchy probability distribution functions (PDFs). Corresponding maximal oxygen metabolic rates ( Results: Data showed that transit time distributions changed after SAH, such that they followed a Cauchy distribution. Corresponding Conclusions: We provide distributions of transit times in an SAH mouse model, allowing us to discuss PDF implications for maximal oxygen consumption.

Indexed as

cerebral blood flowopticssubarachnoid hemorrhage

Identifiers

PMID40386649
PMCPMC12081204

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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.