| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Articles |
From the Department of Pathology, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, NC.
Abstract In rabbits, the pulmonary artery and the aorta are susceptible to atherosclerosis. However, susceptibility of the pulmonary artery, compared with the aortic arch, to atherosclerosis and the relationship between the accumulation of cholesterol during the early stages of atherogenesis and the development of atheromatous lesions for these arterial regions remain to be clarified. Cholesterol concentrations for the pulmonary artery and aorta were measured in normal rabbits and in rabbits fed a 0.5% cholesterol diet for 8, 12, and 16 days and 17 weeks. In normal rabbits, the rank order of arterial cholesterol concentrations was pulmonary artery>aortic arch>descending thoracic aorta, with concentrations of total and nonesterified cholesterol 17% and 25% (both P<.05) greater, respectively, for the pulmonary artery than for the descending thoracic aorta. Rank order remained the same during 16 days of cholesterol feeding, but differences between arterial regions were exaggerated. After rabbits were fed cholesterol for 16 days, total and esterified cholesterol concentrations were 57% and 920% (both P<.01) greater, respectively, for the pulmonary artery than for the descending thoracic aorta, with much smaller differences between the aortic regions. In contrast, after rabbits were fed cholesterol for 17 weeks, concentrations of total, esterified, and nonesterified cholesterol were similar for the pulmonary artery and aortic arch, but these forms of cholesterol were increased 100%, 130%, and 53% (all P<.03), respectively, for the aortic arch compared with the descending thoracic aorta. Cholesterol concentrations for the pulmonary artery were positively associated with those for the aortic regions during the first 16 days of cholesterol feeding, but for rabbits fed cholesterol for 17 weeks the associations were either negative or absent. These results indicate that relative rates of cholesterol accumulation in the pulmonary artery and aorta differ at different stages of atherogenesis and suggest that the balance between processes that deliver cholesterol to, and remove cholesterol from, the artery may change in different ways in these arterial regions during atherogenesis.
Key Words: aorta atherosclerosis atherosclerosis susceptibility cholesterol pulmonary artery
This article has been cited by other articles:
![]() |
D. Massaro and G. D. Massaro Apoetm1Unc mice have impaired alveologenesis, low lung function, and rapid loss of lung function Am J Physiol Lung Cell Mol Physiol, May 1, 2008; 294(5): L991 - L997. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. E. Orfanos, J. B. Parkerson, X. Chen, E. L. Fisher, C. Glynos, A. Papapetropoulos, R. G. Gerrity, and J. D. Catravas Reduced lung endothelial angiotensin-converting enzyme activity in Watanabe hyperlipidemic rabbits in vivo Am J Physiol Lung Cell Mol Physiol, June 1, 2000; 278(6): L1280 - L1288. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Grantham, J. A. Schirger, P. W. Wennberg, S. Sandberg, D. M. Heublein, T. Subkowski, and J. C. Burnett Jr Modulation of Functionally Active Endothelin-Converting Enzyme by Chronic Neutral Endopeptidase Inhibition in Experimental Atherosclerosis Circulation, April 25, 2000; 101(16): 1976 - 1981. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. C. Schwenke Gender Differences in Intima-Media Permeability to Low-Density Lipoprotein at Atherosclerosis-Prone Aortic Sites in Rabbits : Lack of Effect of 17ß-Estradiol Arterioscler Thromb Vasc Biol, October 1, 1997; 17(10): 2150 - 2157. [Abstract] [Full Text] |
||||
![]() |
D. C. Schwenke Comparison of Aorta and Pulmonary Artery : II. LDL Transport and Metabolism Correlate With Susceptibility to Atherosclerosis Circ. Res., September 19, 1997; 81(3): 346 - 354. [Abstract] [Full Text] |
||||
|
Circulation Research Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1997 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |