2024-03-28T09:56:25Z
https://nagoya.repo.nii.ac.jp/oai
oai:nagoya.repo.nii.ac.jp:00014770
2023-01-16T04:02:12Z
499:960:1165
Lipid peroxide and transition metals are required for the toxicity of oxidized low density lipoprotein to cultured endothelial cells
Kuzuya, Masafumi
Naito, Michitaka
Funaki, Chiaki
Hayashi, Toshio
Asai, Kanichi
Kuzuya, Fumio
open access
This is the author's version of a work that was accepted for publication in Biochimica et Biophysica Acta (BBA) : Molecular Basis of Disease. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms, may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Biochimica et Biophysica Acta (BBA) : Molecular Basis of Disease. v.1096, n.2, 1991, p.155–161 http://dx.doi.org/10.1016/0925-4439(91)90054-D
Oxidized los density lipoprotein
Altherosclerosis
Lipid peroxidation
Cytotoxicity
Transition metal
(Bovine aortic endothelial cell)
The toxicity of oxidized low density lipoprotein (Ox-LDL) to cultured vascular endothelial cells was investigated. The modification of low density lipoprotein (LDL) by copper led to the production of thiobarbituric acid-reacting substance (TBARS) and lipid hydroperoxide (LPO). TBARS was distributed not only in lipoprotein, but also in the aqueous phase, whereas LPO was observed only in the lipoprotein particle. During the incubation of LDL with copper, the copper bound to lipoprotein and formed a complex. The toxicity of products resulting from the oxidation of LDL to endothelial cells was recognized in Ox-LDL particles, not in the aqueous phase. Following dialysis of Ox-LDL against EDTA, copper which had bound to the OX-LDL particle was released and the toxicity of Ox-LDL disappeared. The addition of copper to the dialyzed Ox-LDL restored the cytotoxicity. To a lesser extent this effect was also observed with the addition of iron. A study of the time-course of LDL oxidation showed that the toxicity of Ox-LDL depends upon the level of LPO, not upon the content of TBARS, the extent of negative charge or the protein adduct of aldehydes. These results demonstrate that transition metal is required for Ox-LDL toxicity and the toxic moiety of the products resulting from LDL oxidation is LPO associated with the Ox-LDL particle.
名古屋大学博士学位論文 学位の種類 : 博士(医学)(課程) 学位授与年月日:平成3年3月8日 葛谷雅文氏の博士論文として提出された
Elsevier
1991-02
eng
doctoral thesis
http://hdl.handle.net/2237/16697
https://nagoya.repo.nii.ac.jp/records/14770
https://doi.org/10.1016/0925-4439(91)90054-D
0925-4439
Biochimica et Biophysica Acta (BBA) : Molecular Basis of Disease
1096
2
155
161
甲第2403号
博士(医学)
1991-02-01
13901
名古屋大学
NAGOYA University
https://nagoya.repo.nii.ac.jp/record/14770/files/k2403.pdf
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2018-02-20