Why the study?
The capacity of small cerebral arteries to adapt to pressure fluctuations plays a fundamental physiological role and is relevant across different pathological conditions, requiring quantitative evaluation.
A novel multiscale computational model successfully links pressure-induced smooth muscle cell signaling to tissue-level vascular tone generation in small cerebral arteries.
New SCA pressure-tone model may guide mechanistic research; leaves open clinical translation pending experimental validation.
The capacity of small cerebral arteries (SCAs) to adapt to pressure fluctuations has a fundamental physiological role and appears to be relevant in different pathological conditions. Here, we present a new computational model for quantifying the link, and its contributors, between luminal pressure and vascular tone generation in SCAs. This is assembled by combining a chemical sub-model, representing pressure-induced smooth muscle cell (SMC) signalling, with a mechanical sub-model for the tone generation and its transduction at tissue level. The devised model can accurately reproduce the impact of luminal pressure on different cytoplasmic components involved in myogenic signalling, both in the control case and when combined with some specific pharmacological interventions. Furthermore, the model is also able to capture and predict experimentally recorded pressure-outer diameter relationships obtained for vessels under control conditions, both in a Ca ²⁺ 2 + -free bath and under drug inhibition. The modularity of the proposed framework allows the integration of new components for the study of a broad range of processes involved in the vascular function.
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Coccarelli et al. (2023) studied this question.
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