TY - JOUR
T1 - Adventitial vasa vasorum heterogeneity among different vascular beds
AU - Galili, Offer
AU - Herrmann, Joerg
AU - Woodrum, Julie
AU - Sattler, Katherine J.
AU - Lerman, Lilach O.
AU - Lerman, Amir
PY - 2004/9
Y1 - 2004/9
N2 - Different vascular beds show substantial variation in their susceptibilities for development of vascular disease like atherosclerosis, and thereby exhibit a variety of different clinical presentations. Yet, the underlying mechanism of this heterogeneity is not well defined. Recent evidence suggests a role for the vasa vasorum (VV) in vascular disease. We hypothesized that there is a differential distribution structure of adventitial VV in different vascular beds. Hence, the current study was designed to characterize and compare the structure of the adventitial VV in the coronary and the peripheral circulation. Samples of vessels from different vascular beds were obtained from 6 female crossbred domestic pigs. The samples were scanned using micro-computed tomography, and the images reconstructed and analyzed to characterize VV architecture, including vessel wall area, VV count, VV density, intravessel spatial distribution, mean diameter of first- and second-order VVs and the ratio of second- to first-order VVs. There were significant differences in VV density among different vascular beds. Density was highest in coronary arteries (2.91 ± 0.26 vessels/mm 2, P < .05, vs renal, carotid, and femoral arteries), intermediate in renal arteries (1.45 ± 0.22 vessels/mm 2, P < .05, vs femoral artery) and carotid arteries (0.64 ± 0.08 vessels/mm 2, P < .05, vs femoral artery), and lowest in femoral arteries (0.23 ± 0.05 vessels/mm 2). A similar pattern for the ratio of second- to first-order VV was also observed. Random intravessel spatial distribution of VVs was seen in all vascular beds. The current study demonstrates a differential structure of the adventitial VV in different vascular beds. This intra- and intervessel heterogeneity in VV anatomy is a phenotypic variability that might determine a differential local response to systemic risk factors and, thereby, variable propensity for vascular disease among different vascular beds. Atherosclerosis is a diffuse disease with differential expression among different vascular beds, inflicting a spectrum of vascular diseases. The majority of research efforts focus on the inner and medial vascular layers, which are in fact affected at the late stage of atherosclerosis. However, recent evidence suggests that the outer wall, including the adventitial layer and the vasa vasorum, plays a significant role in maintaining vessel integrity, contributing to the initiation and progression of atherosclerosis. The current article extends these previous observations. Using a novel imaging technology, micro-computed tomography, we demonstrate structural heterogeneity of the adventitial vasa vasorum among different vascular beds. This heterogeneity in VV anatomy is a phenotypic variability that might determine a differential local response to systematic risk factors and a concomitant variable propensity for vascular disease among different vascular beds.Furthermore, it suggests that anti-angiogenic treatment aimed at attenuating the VV neovascularization may have a potential preventive or reversal measure against the progression of atherosclerosis.
AB - Different vascular beds show substantial variation in their susceptibilities for development of vascular disease like atherosclerosis, and thereby exhibit a variety of different clinical presentations. Yet, the underlying mechanism of this heterogeneity is not well defined. Recent evidence suggests a role for the vasa vasorum (VV) in vascular disease. We hypothesized that there is a differential distribution structure of adventitial VV in different vascular beds. Hence, the current study was designed to characterize and compare the structure of the adventitial VV in the coronary and the peripheral circulation. Samples of vessels from different vascular beds were obtained from 6 female crossbred domestic pigs. The samples were scanned using micro-computed tomography, and the images reconstructed and analyzed to characterize VV architecture, including vessel wall area, VV count, VV density, intravessel spatial distribution, mean diameter of first- and second-order VVs and the ratio of second- to first-order VVs. There were significant differences in VV density among different vascular beds. Density was highest in coronary arteries (2.91 ± 0.26 vessels/mm 2, P < .05, vs renal, carotid, and femoral arteries), intermediate in renal arteries (1.45 ± 0.22 vessels/mm 2, P < .05, vs femoral artery) and carotid arteries (0.64 ± 0.08 vessels/mm 2, P < .05, vs femoral artery), and lowest in femoral arteries (0.23 ± 0.05 vessels/mm 2). A similar pattern for the ratio of second- to first-order VV was also observed. Random intravessel spatial distribution of VVs was seen in all vascular beds. The current study demonstrates a differential structure of the adventitial VV in different vascular beds. This intra- and intervessel heterogeneity in VV anatomy is a phenotypic variability that might determine a differential local response to systemic risk factors and, thereby, variable propensity for vascular disease among different vascular beds. Atherosclerosis is a diffuse disease with differential expression among different vascular beds, inflicting a spectrum of vascular diseases. The majority of research efforts focus on the inner and medial vascular layers, which are in fact affected at the late stage of atherosclerosis. However, recent evidence suggests that the outer wall, including the adventitial layer and the vasa vasorum, plays a significant role in maintaining vessel integrity, contributing to the initiation and progression of atherosclerosis. The current article extends these previous observations. Using a novel imaging technology, micro-computed tomography, we demonstrate structural heterogeneity of the adventitial vasa vasorum among different vascular beds. This heterogeneity in VV anatomy is a phenotypic variability that might determine a differential local response to systematic risk factors and a concomitant variable propensity for vascular disease among different vascular beds.Furthermore, it suggests that anti-angiogenic treatment aimed at attenuating the VV neovascularization may have a potential preventive or reversal measure against the progression of atherosclerosis.
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U2 - 10.1016/j.jvs.2004.06.032
DO - 10.1016/j.jvs.2004.06.032
M3 - Article
C2 - 15337884
AN - SCOPUS:4444246945
SN - 0741-5214
VL - 40
SP - 529
EP - 535
JO - Journal of vascular surgery
JF - Journal of vascular surgery
IS - 3
ER -