Low vasa vasorum densities correlate with inflammation and subintimal thickening: Potential role in location—Determination of atherogenesis
Abstract Objectives To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development. Methods and results Six, 3-month-old, female, crossbred swine were fed 2% high-cholesterol (HC) diet for 3 months prior to euthanasia. Si...
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Published in | Atherosclerosis Vol. 206; no. 2; pp. 362 - 368 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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01.10.2009
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Abstract | Abstract Objectives To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development. Methods and results Six, 3-month-old, female, crossbred swine were fed 2% high-cholesterol (HC) diet for 3 months prior to euthanasia. Six other pigs were fed normal diet (N) for the entire 6 months. Right coronary arteries were harvested and scanned intact with micro-CT (20 μm cubic-voxel-size). After scanning, randomly selected cross-sectional histological sections were stained for nuclear-factor kappaB (NF-κB), hypoxia-inducible factor-1alpha (HIF-1α), macrophages, von-Willebrand-factor, dihydroethidium (DHE), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). The number of positive stained cells, as well as intima-to-media ratio, were compared with VV density (#/mm2 ) obtained from micro-CT images (which closely matched the location of the histological sections) in each of four equal quadrants of the coronary vessel wall. In normal, as well as HC pigs, the number of NF-κB ( r = 0.73 and 0.70), HIF-1α ( r = 0.74 and 0.77), TNF-α ( r = 0.58 and 0.72) and IL-6 ( r = 0.70 and 0.72) positive cells as well as the expression of DHE (Kendall tau coefficient −0.64 and −0.63) inversely correlated with VV density. In HC the VV density also inversely correlated with intima/media ratios ( r = 0.65). Conclusions Our data suggest that low VV density territories within the coronary vessel wall are susceptible to hypoxia, oxidative stress and microinflammation and may therefore be starting points of early atherogenesis. |
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AbstractList | To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development.
Six, 3-month-old, female, crossbred swine were fed 2% high-cholesterol (HC) diet for 3 months prior to euthanasia. Six other pigs were fed normal diet (N) for the entire 6 months. Right coronary arteries were harvested and scanned intact with micro-CT (20mum cubic-voxel-size). After scanning, randomly selected cross-sectional histological sections were stained for nuclear-factor kappaB (NF-kappaB), hypoxia-inducible factor-1alpha (HIF-1alpha), macrophages, von-Willebrand-factor, dihydroethidium (DHE), tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6). The number of positive stained cells, as well as intima-to-media ratio, were compared with VV density (#/mm(2)) obtained from micro-CT images (which closely matched the location of the histological sections) in each of four equal quadrants of the coronary vessel wall. In normal, as well as HC pigs, the number of NF-kappaB (r=0.73 and 0.70), HIF-1alpha (r=0.74 and 0.77), TNF-alpha (r=0.58 and 0.72) and IL-6 (r=0.70 and 0.72) positive cells as well as the expression of DHE (Kendall tau coefficient -0.64 and -0.63) inversely correlated with VV density. In HC the VV density also inversely correlated with intima/media ratios (r=0.65).
Our data suggest that low VV density territories within the coronary vessel wall are susceptible to hypoxia, oxidative stress and microinflammation and may therefore be starting points of early atherogenesis. To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development. Six, 3-month-old, female, crossbred swine were fed 2% high-cholesterol (HC) diet for 3 months prior to euthanasia. Six other pigs were fed normal diet (N) for the entire 6 months. Right coronary arteries were harvested and scanned intact with micro-CT (20 μm cubic-voxel-size). After scanning, randomly selected cross-sectional histological sections were stained for nuclear-factor kappaB (NF-κB), hypoxia-inducible factor-1alpha (HIF-1α), macrophages, von-Willebrand-factor, dihydroethidium (DHE), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). The number of positive stained cells, as well as intima-to-media ratio, were compared with VV density (#/mm 2) obtained from micro-CT images (which closely matched the location of the histological sections) in each of four equal quadrants of the coronary vessel wall. In normal, as well as HC pigs, the number of NF-κB ( r = 0.73 and 0.70), HIF-1α ( r = 0.74 and 0.77), TNF-α ( r = 0.58 and 0.72) and IL-6 ( r = 0.70 and 0.72) positive cells as well as the expression of DHE (Kendall tau coefficient −0.64 and −0.63) inversely correlated with VV density. In HC the VV density also inversely correlated with intima/media ratios ( r = 0.65). Our data suggest that low VV density territories within the coronary vessel wall are susceptible to hypoxia, oxidative stress and microinflammation and may therefore be starting points of early atherogenesis. Abstract Objectives To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development. Methods and results Six, 3-month-old, female, crossbred swine were fed 2% high-cholesterol (HC) diet for 3 months prior to euthanasia. Six other pigs were fed normal diet (N) for the entire 6 months. Right coronary arteries were harvested and scanned intact with micro-CT (20 μm cubic-voxel-size). After scanning, randomly selected cross-sectional histological sections were stained for nuclear-factor kappaB (NF-κB), hypoxia-inducible factor-1alpha (HIF-1α), macrophages, von-Willebrand-factor, dihydroethidium (DHE), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). The number of positive stained cells, as well as intima-to-media ratio, were compared with VV density (#/mm2 ) obtained from micro-CT images (which closely matched the location of the histological sections) in each of four equal quadrants of the coronary vessel wall. In normal, as well as HC pigs, the number of NF-κB ( r = 0.73 and 0.70), HIF-1α ( r = 0.74 and 0.77), TNF-α ( r = 0.58 and 0.72) and IL-6 ( r = 0.70 and 0.72) positive cells as well as the expression of DHE (Kendall tau coefficient −0.64 and −0.63) inversely correlated with VV density. In HC the VV density also inversely correlated with intima/media ratios ( r = 0.65). Conclusions Our data suggest that low VV density territories within the coronary vessel wall are susceptible to hypoxia, oxidative stress and microinflammation and may therefore be starting points of early atherogenesis. |
Author | Erbel, R Ritman, E.L Versari, D Beighley, P.E Gössl, M Lerman, L.O Chade, A.R |
AuthorAffiliation | 4 University Duisburg-Essen, West German Heart Center, Hufelandstr. 55, 45122 Essen, Germany 2 Division of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, MN 55905 3 Department of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine, Rochester, MN 55905 1 Department of Internal Medicine, Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, Rochester, MN 55905 |
AuthorAffiliation_xml | – name: 2 Division of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, MN 55905 – name: 4 University Duisburg-Essen, West German Heart Center, Hufelandstr. 55, 45122 Essen, Germany – name: 3 Department of Physiology and Biomedical Engineering, Mayo Clinic College of Medicine, Rochester, MN 55905 – name: 1 Department of Internal Medicine, Division of Cardiovascular Diseases, Mayo Clinic College of Medicine, Rochester, MN 55905 |
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Keywords | Microinflammation Micro-CT Vasa vasorum Atherogenesis Hypoxia Vascular disease Oxygen Atherosclerosis Cardiovascular disease Inflammation Computerized axial tomography Thickening |
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Snippet | Abstract Objectives To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion... To assess the role of coronary vasa vasorum (VV) spatial distribution in determining the location of early atherosclerotic lesion development. Six,... |
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SubjectTerms | Animals Atherogenesis Atherosclerosis (general aspects, experimental research) Atherosclerosis - pathology Biological and medical sciences Blood and lymphatic vessels Blood. Blood coagulation. Reticuloendothelial system Cardiology. Vascular system Cardiovascular Cholesterol, Dietary - pharmacology Coronary Vessels - drug effects Coronary Vessels - pathology Female Hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - metabolism Interleukin-6 - metabolism Medical sciences Micro-CT Microinflammation NF-kappa B - metabolism Pharmacology. Drug treatments Superoxides - metabolism Swine Tumor Necrosis Factor-alpha - metabolism Tunica Intima - metabolism Tunica Intima - pathology Vasa vasorum Vasa Vasorum - pathology |
Title | Low vasa vasorum densities correlate with inflammation and subintimal thickening: Potential role in location—Determination of atherogenesis |
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