ArticleNeurophotonics2025
Semi-automated analysis of cerebral capillary red blood cell velocities allows modeling of transit time distribution after experimental subarachnoid hemorrhage in mice.
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.
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Who cites it
3 citing papers in PubMed.
- The Effects of Milrinone Systemic Administration on Cerebral Perfusion as Measured with Computed Tomography in Aneurysmal Subarachnoid Hemorrhage Patients.Neurocritical care · 2026Observational
- 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 · 2026Article
- Introduction to the Special Issue "Understanding Brain Disease with Live Imaging".Neurophotonics · 2025Article
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4 authors.
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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.
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