Rabbits were induced to form atheromatous cardiovascular lesions by subjecting them to treatments of a single BSA injection plus a 2-wk period of cholesterol diet, or to the diet alone. Microscopic examination of the hearts at the end of the 2-wk induction period, or after having been returned to regular diet for 5 or 8 wk, showed that lesion incidence in the cholesterol-only animall decreased markedly during the 8-wk rest period, while little change in incidence occurred in animals with lesions from the combined treatment. This finding was taken to mean that the latter type of lesion was less reversible, and therefore perhaps more pathologically significant, than the former type. It was felt that lipid deposition was not solely responsible for this prolongation, since it was present in diet-only lesions which disappeared with time, and also seemed to be disappearing from the prolonged lesions in all treatment groups. On the other hand, elastic tissue was demonstrated only in lesions arising from the combined treatment, and it is hypothesized that this feature is implicated in the prolongation of these lesions.
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1 November 1970
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November 01 1970
FURTHER STUDIES ON THE REVERSIBILITY OF SERUM SICKNESS CHOLESTEROL-INDUCED ATHEROSCLEROSIS
M. Van Winkle,
M. Van Winkle
From the Biological Sciences Department, Riker Laboratories, Northridge, California 91324
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L. Levy
L. Levy
From the Biological Sciences Department, Riker Laboratories, Northridge, California 91324
Search for other works by this author on:
M. Van Winkle
From the Biological Sciences Department, Riker Laboratories, Northridge, California 91324
L. Levy
From the Biological Sciences Department, Riker Laboratories, Northridge, California 91324
Received:
May 22 1970
Online ISSN: 1540-9538
Print ISSN: 0022-1007
Copyright © 1970 by The Rockefeller University Press
1970
J Exp Med (1970) 132 (5): 858–867.
Article history
Received:
May 22 1970
Citation
M. Van Winkle, L. Levy; FURTHER STUDIES ON THE REVERSIBILITY OF SERUM SICKNESS CHOLESTEROL-INDUCED ATHEROSCLEROSIS . J Exp Med 1 November 1970; 132 (5): 858–867. doi: https://doi.org/10.1084/jem.132.5.858
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