Introduction:
Measurements of cyclic strain give insight into vessel wall properties, offer a better understanding of the pathogenesis of atherosclerosis, and can be used in quantifying loss of vessel compliance. Using dobutamine stimulation to increase heart rate and cardiac output provides a clinically relevant means to begin to understand alterations in cyclic strain during a vascular challenge which mimics some aspects of exercise. Similar work has been completed in murine models, but translating these methods to a species that is an order of magnitude larger allows for a better understanding of how these results could allometrically scale to the human condition. We hypothesize that using a pharmacological cardiovascular stimulant will cause cyclic strain shifts that vary between species.
Materials and Methods:
Cyclic strain was non-invasively quantified using MRI. Young rats and mice were anesthetized using isoflurane and imaged at 7T. 2D and 3D gradient echo data were used to plan ECG-gated acquisitions that included 12 CINE frames across the cardiac cycle, in the infrarenal aorta pre- and post- dobutamine infusion. Vessel strain was quantified in each CINE frame.
Results:
Baseline strain in rats was 17% and 16%, for males and females respectively (A, C). In mice, baseline strain was 22% in males and 18% in females (B, D). After infusion of dobutamine, strain in rats increased to 26% in males and 27% in females, while in mice strain increased to 36% in males and 32% in females.
Conclusions:
In conclusion, there are evident variations in cyclic strain under a cardiovascular challenge between species. With this insight, a clearer understanding of the biomechanical forces experienced by the vasculature in different species may lead to improved extrapolation from mouse to human in understanding the effects of atherosclerosis on vessel compliance and developing therapeutic approaches.