Central Artery Hemodynamics in Angiotensin II-Induced Hypertension and Effects of Anesthesia

• Published in: Annals of biomedical engineering Vol. 52; no. 4; pp. 1051 - 1066
• Main Authors: Hopper, S. E., Weiss, D., Mikush, N., Jiang, B., Spronck, B., Cavinato, C., Humphrey, J. D., Figueroa, C. A.
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01-04-2024; Springer Nature B.V
• Subjects: Anesthesia; Angiotensin; Angiotensin II; Animal models; Aorta; Biochemistry; Biological and Medical Physics; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Biophysics; Cardiovascular diseases; Classical Mechanics; Coronary vessels; Hemodynamics; Hypertension; Isoflurane; Original Article; Risk factors; Stiffness; Thorax; Workflow; Hypertension; Pulse pressure; Aorta; Stiffness; Mouse; Isoflurane
• ISSN: 0090-6964; 1573-9686; 1573-9686
• DOI: 10.1007/s10439-024-03440-0

Systemic hypertension is a strong risk factor for cardiovascular, neurovascular, and renovascular diseases. Central artery stiffness is both an initiator and indicator of hypertension, thus revealing a critical relationship between the wall mechanics and hemodynamics. Mice have emerged as a critical animal model for studying effects of hypertension and much has been learned. Regardless of the specific mouse model, data on changes in cardiac function and hemodynamics are necessarily measured under anesthesia. Here, we present a new experimental-computational workflow to estimate awake cardiovascular conditions from anesthetized data, which was then used to quantify effects of chronic angiotensin II-induced hypertension relative to normotension in wild-type mice. We found that isoflurane anesthesia had a greater impact on depressing hemodynamics in angiotensin II-infused mice than in controls, which led to unexpected results when comparing anesthetized results between the two groups of mice. Through comparison of the awake simulations, however, in vivo relevant effects of angiotensin II-infusion on global and regional vascular structure, properties, and hemodynamics were found to be qualitatively consistent with expectations. Specifically, we found an increased in vivo vascular stiffness in the descending thoracic aorta and suprarenal abdominal aorta, leading to increases in pulse pressure in the distal aorta. These insights allow characterization of the impact of regionally varying vascular remodeling on hemodynamics and mouse-to-mouse variations due to induced hypertension.