1994
DOI: 10.1016/0005-2760(94)90050-7
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The effects of free radical scavengers on the oxidation of low-density lipoproteins by macrophages

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Cited by 10 publications
(5 citation statements)
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“…This later effect can result in PON autoinactivation (M. Aviram, unpublished observation). H 2 O 2 is a major ROS produced by arterial wall cells during atherogenesis, and it is converted under oxidative stress into a more potent ROS leading to LDL oxidation (61,62). The ability of HDL-associated PON to hydrolyze H 2 O 2 (in addition to peroxides) may thus play an important role in eliminating potent oxidants that are involved in atherosclerosis.…”
Section: Discussionmentioning
confidence: 99%
“…This later effect can result in PON autoinactivation (M. Aviram, unpublished observation). H 2 O 2 is a major ROS produced by arterial wall cells during atherogenesis, and it is converted under oxidative stress into a more potent ROS leading to LDL oxidation (61,62). The ability of HDL-associated PON to hydrolyze H 2 O 2 (in addition to peroxides) may thus play an important role in eliminating potent oxidants that are involved in atherosclerosis.…”
Section: Discussionmentioning
confidence: 99%
“…Oxidative stress, caused by cells or free radicals, modifies the lipid and protein components of circulating LDL and alters its properties [5][6][7]. The effects exerted by LDL on human endothelial cells were demonstrated to depend qualitatively and quantitatively on the extent of its oxidation [8][9][10][11]. In contrast to native-LDL, oxidised-LDL induces a cytotoxic effect on endothelial cells and a chemotactic stimulation of smooth muscle cells [12,13].…”
Section: Introductionmentioning
confidence: 99%
“…It is also possible that the in vitro oxidation induced by Cu could be particularly drastic and that LDL oxidation induced by other more physiological or mild inducers, such as Table 6. LDL susceptibility to in vitro copper-induced oxidation at the beginning of the study (T0) and after 6-month zinc supplementation (T6)* haem-iron (Grinshtein et al 2003;Klouche et al 2004) or monocytes -macrophages (Wilkins & Leake, 1994;Chisolm et al 1999), may be more appropriate. Consequently, new approaches need to be developed to determine LDL oxidizability with mild inducers, and preferably in their biological medium without isolation and where LDL oxidizability can be measured without elimination of the many protective molecules that LDL may contain when they are in their biological medium.…”
Section: Discussionmentioning
confidence: 99%