TY - JOUR
T1 - Echocardiographic Characterization of Postnatal Development in Mice with Reduced Arterial Elasticity
AU - Le, Victoria P.
AU - Wagenseil, Jessica E.
N1 - Funding Information:
This work was funded, in part, by National Institutes of Health grants R00 HL087653, R01 HL105314, and R01 HL115560. Dr. Robert Mecham at the Washington University School of Medicine is gratefully acknowledged for providing the Eln mice. The Saint Louis University Center for Cardiovascular Research is gratefully acknowledged for providing the ultrasound equipment. +/−
PY - 2012/12
Y1 - 2012/12
N2 - Decreased expression of elastin results in smaller, less compliant arteries, and high blood pressure. In mice, these differences become more significant with postnatal development. It is known that arterial size and compliance directly affect cardiac function, but the temporal changes in cardiac function have not been investigated in elastin insufficient mice. The aim of this study is to correlate changes in arterial size and compliance with cardiac function in wildtype (WT) and elastin haploinsufficient (Eln+/-) mice from birth to adulthood. Ultrasound scans were performed at the ages of 3, 7, 14, 21, 30, 60, and 90 days on male and female WT and Eln+/- mice. 2-D ultrasound and pulse wave Doppler images were used to measure the dimensions and function of the left ventricle (LV), ascending aorta, and carotid arteries. Eln+/- arteries are smaller and less compliant at most ages, with significant differences from WT as early as 3 days old. Surprisingly, there are no correlations (R2 < 0.2) between arterial size and compliance with measures of LV hypertrophy or systolic function. There are weak correlations (0.2 < R2 < 0.5) between arterial size and compliance with measures of LV diastolic function. Eln+/- mice have similar cardiac function to WT throughout postnatal development, demonstrating the remarkable ability of the developing cardiovascular system to adapt to mechanical and hemodynamic changes. Correlations between arterial size and compliance with diastolic function show that these measures may be useful indicators of early diastolic dysfunction.
AB - Decreased expression of elastin results in smaller, less compliant arteries, and high blood pressure. In mice, these differences become more significant with postnatal development. It is known that arterial size and compliance directly affect cardiac function, but the temporal changes in cardiac function have not been investigated in elastin insufficient mice. The aim of this study is to correlate changes in arterial size and compliance with cardiac function in wildtype (WT) and elastin haploinsufficient (Eln+/-) mice from birth to adulthood. Ultrasound scans were performed at the ages of 3, 7, 14, 21, 30, 60, and 90 days on male and female WT and Eln+/- mice. 2-D ultrasound and pulse wave Doppler images were used to measure the dimensions and function of the left ventricle (LV), ascending aorta, and carotid arteries. Eln+/- arteries are smaller and less compliant at most ages, with significant differences from WT as early as 3 days old. Surprisingly, there are no correlations (R2 < 0.2) between arterial size and compliance with measures of LV hypertrophy or systolic function. There are weak correlations (0.2 < R2 < 0.5) between arterial size and compliance with measures of LV diastolic function. Eln+/- mice have similar cardiac function to WT throughout postnatal development, demonstrating the remarkable ability of the developing cardiovascular system to adapt to mechanical and hemodynamic changes. Correlations between arterial size and compliance with diastolic function show that these measures may be useful indicators of early diastolic dysfunction.
KW - Aorta
KW - Carotid
KW - Compliance
KW - Diastolic dysfunction
KW - Elastin
KW - Stiffness
UR - http://www.scopus.com/inward/record.url?scp=84870462278&partnerID=8YFLogxK
U2 - 10.1007/s13239-012-0108-4
DO - 10.1007/s13239-012-0108-4
M3 - Article
AN - SCOPUS:84870462278
SN - 1869-408X
VL - 3
SP - 424
EP - 438
JO - Cardiovascular Engineering and Technology
JF - Cardiovascular Engineering and Technology
IS - 4
ER -