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Atherosclerosis and Lipoproteins |
From the Department of Physiology (J.G., J.W., U.H., L.-m.G.), Institute of Neuroscience and Physiology, and the Department of Clinical Physiology (B.W., L.-m.G.), Cardiovascular Institute, The Sahlgrenska Academy, Göteborg University, Sweden.
Correspondence to Li-ming Gan, MD, PhD, Department of Clinical Physiology, Cardiovascular Institute, Sahlgrenska University Hospital, SE 413 45 Göteborg, Sweden. E-mail li-ming.gan{at}hjl.gu.se
Background We aimed to establish a completely noninvasive technique to assess coronary artery atherosclerosis in living mice using proximal to middle left coronary artery (LCA) velocity ratio as assessed with color Doppler echocardiography (CDE).
Methods and Results Three groups of apolipoprotein E/low-density lipoprotein receptor double-knockout (apoE/LDLr dko) mice 10, 40, and 80 weeks of age and 3 additional age-matched groups of C57BL/6 mice were examined under anesthesia. Coronary flow velocity in proximal (Vprox) and middle part (Vmid) of LCA was measured using CDE. A 40-MHz ultrasound biomicroscope (UBM) was used to visualize lumen and outer vessel diameter in the proximal LCA. Flow velocity in the proximal LCA increased significantly with age and remained constant in the middle part in the apoE/LDLr dko mice, whereas velocities at both the sites remained unchanged in C57 mice. CDE-assessed flow velocity ratio (Vprox/Vmid) increased significantly with age in apoE/LDLr dko mice (P=0.0055) and correlated significantly to percentage wall thickness, as assessed by UBM (P=0.0044; r=0.65) and histology (P=0.0002; r=0.78). Wall thickness increased with age in the apoE/LDLr dko mice as measured with UBM (P=0.0093; r=0.49), which was also confirmed with histology (P<0.0001; r=0.73).
Conclusions CDE and UBM are useful noninvasive tools to quantify mouse coronary artery atherosclerosis in vivo.
We demonstrated that mouse proximal left coronary artery (LCA) atherosclerosis could be quantified noninvasively in vivo using the proximal to the middle LCA flow velocity ratio, as measured by color Doppler echocardiography. The findings were further validated in vivo by ultrasound biomicroscopy and ex vivo by histology.
Key Words: coronary artery velocity ratio atherosclerosis mouse color Doppler echocardiography ultrasound biomicroscopy
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