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A novel MRI analysis for assessment of microvascular vasomodulation in low-perfusion skeletal muscle

Compromised microvascular reactivity underlies many conditions and injuries, but its assessment remains difficult, particularly in low perfusion tissues. In this paper, we develop a new mathematical model for the assessment of vasomodulation in low perfusion settings. A first-order model was develop...

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Detalles Bibliográficos
Autores principales: Zakher, Eric, Ganesh, Tameshwar, Cheng, Hai-Ling Margaret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070083/
https://www.ncbi.nlm.nih.gov/pubmed/32170106
http://dx.doi.org/10.1038/s41598-020-61682-z
Descripción
Sumario:Compromised microvascular reactivity underlies many conditions and injuries, but its assessment remains difficult, particularly in low perfusion tissues. In this paper, we develop a new mathematical model for the assessment of vasomodulation in low perfusion settings. A first-order model was developed to approximate changes in T(1) relaxation times as a result of vasomodulation. Healthy adult rats (N = 6) were imaged on a 3-Tesla clinical MRI scanner, and vasoactive response was probed on gadofosveset using hypercapnic gases at 20% and 5% CO(2) to induce vasoconstriction and vasodilation, respectively. MRI included dynamic 3D T(1) mapping and T(1)-weighted images during gas challenge; heart rate was continuously monitored. Laser Doppler perfusion measurements were performed to corroborate MRI findings. The model was able to identify hypercapnia-mediated vasoconstriction and vasodilation through the partial derivative [Formula: see text] . MRI on animals revealed gradual vasoconstriction in the skeletal muscle bed in response to 20% CO(2) followed by gradual vasodilation on transitioning to 5% CO(2). These trends were confirmed on laser Doppler perfusion measurements. Our new mathematical model has the potential for detecting microvascular dysfunction that manifests in the early stages across multiple metabolic and ischemic pathologies.