INVOLVEMENT OF LYSOSOMES IN SPONTANEOUS ATHEROGENESIS AND THE EFFECTS OF ESTROGENS
type: CreativeWork
description: Alterations and accumulations of glycosaminoglycans (GAG) and lipids are prominent features in atherosclerotic lesions. Lysosomes are essential for cellular catabolism and are known to be altered in advanced atheroslcerotic lesions; however, their involvement in spontaneous atherogenesis or lesion progression is unclear. Estrogens have been reported to interact with lysosomes and are thought to provide a "protective" effect against development of atherosclerotic lesions. Analysis of lysosomes from sites predisposed to lesions, as well as consideration of the effects of estrogens on lysosomes at different stages of lesion development, may provide insight into biochemical mechanisms of spontaneous atherogenesis and lesion progression. Simultaneous analysis of lesion-resistant aortic segments provides a control for differentiating between aging processes and lesion development. Lysosomal fragility and marker enzyme activities, N-acetyl-B-hexosaminidase (NAHase) and acid phosphatase (APase), were measured in subcellular fractions from upper thoracic aortas (lesion-resistant areas) and celiac bifurcations (site predisposed to lesions) from atherosclerosis-susceptible White Carneau (WC) and atherosclerosis-resistant Show Racer (SR) pigeons at 1 day, 6 weeks, 6 months, and 6 years of age. Isolated arterial segments were also incubated with 17B-estradiol at physiological temperatures to determine the effect on lysosomal fragility and enzyme activities. Lysosomal enzyme activities and protein yields in both aortic sites from 6 week old WC pigeons were higher than in corresponding SR; thus, turnover rates of cellular components would appear higher in the WC than in the SR. However, the lysosomes from 6 week old WC aortas also appeared more fragile than lysosomes from SR aortas. Sine this is prior to appreciable GAG and lipid accumulation in WC celiac sites, excessive release of lysosomal enzymes and/or greater activities of these enzymes may cause alterations in connective ti…
abstract: Alterations and accumulations of glycosaminoglycans (GAG) and lipids are prominent features in atherosclerotic lesions. Lysosomes are essential for cellular catabolism and are known to be altered in advanced atheroslcerotic lesions; however, their involvement in spontaneous atherogenesis or lesion progression is unclear. Estrogens have been reported to interact with lysosomes and are thought to provide a "protective" effect against development of atherosclerotic lesions. Analysis of lysosomes from sites predisposed to lesions, as well as consideration of the effects of estrogens on lysosomes at different stages of lesion development, may provide insight into biochemical mechanisms of spontaneous atherogenesis and lesion progression. Simultaneous analysis of lesion-resistant aortic segments provides a control for differentiating between aging processes and lesion development. Lysosomal fragility and marker enzyme activities, N-acetyl-B-hexosaminidase (NAHase) and acid phosphatase (APase), were measured in subcellular fractions from upper thoracic aortas (lesion-resistant areas) and celiac bifurcations (site predisposed to lesions) from atherosclerosis-susceptible White Carneau (WC) and atherosclerosis-resistant Show Racer (SR) pigeons at 1 day, 6 weeks, 6 months, and 6 years of age. Isolated arterial segments were also incubated with 17B-estradiol at physiological temperatures to determine the effect on lysosomal fragility and enzyme activities. Lysosomal enzyme activities and protein yields in both aortic sites from 6 week old WC pigeons were higher than in corresponding SR; thus, turnover rates of cellular components would appear higher in the WC than in the SR. However, the lysosomes from 6 week old WC aortas also appeared more fragile than lysosomes from SR aortas. Sine this is prior to appreciable GAG and lipid accumulation in WC celiac sites, excessive release of lysosomal enzymes and/or greater activities of these enzymes may cause alterations in connective ti…
author: HOUGH, JANE LINSCOTT
keywords: Chemistry, Biochemistry
date published: 1981-01-01T08:00:00Z
date modified: 2026-07-24T05:23:09Z
provider: University of New Hampshire
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of New Hampshire