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 inAtherosclerosis Vol. 206; no. 2; pp. 362 - 368
Main Authors Gössl, M, Versari, D, Lerman, L.O, Chade, A.R, Beighley, P.E, Erbel, R, Ritman, E.L
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ireland Ltd 01.10.2009
Elsevier
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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.
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
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Issue 2
Keywords Microinflammation
Micro-CT
Vasa vasorum
Atherogenesis
Hypoxia
Vascular disease
Oxygen
Atherosclerosis
Cardiovascular disease
Inflammation
Computerized axial tomography
Thickening
Language English
License CC BY 4.0
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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
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0021915009002068
https://dx.doi.org/10.1016/j.atherosclerosis.2009.03.010
https://www.ncbi.nlm.nih.gov/pubmed/19368925
https://pubmed.ncbi.nlm.nih.gov/PMC4208719
Volume 206
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