Peroxynitrite, the oxidant formed from the diffusion-limited reaction between nitric oxide and superoxide, has been shown to modify low-density lipoprotein (LDL) into a pro-atherogenic form. LDL contains both alpha-tocopherol and gamma-tocopherol. We have shown that peroxynitrite oxidizes alpha-tocopherol to alpha-tocopherol quinone. It has recently been reported by Christian et al. (Proc. Natl. Acad. Sci. USA 94:3217-3222) that gamma-tocopherol is oxidized to 5-NO2-gamma-tocopherol by peroxynitrite and the gamma-tocopherol may be a more specific scavenger of peroxynitrite than alpha-tocopherol. As both alpha-tocopherol and gamma-tocopherol are present in LDL, it is important to determine which of these reactions is favored. Endogenous levels of both alpha-tocopherol and gamma-tocopherol were monitored when LDL was oxidized in the presence of the peroxynitrite generator, SIN-1. Peroxynitrite generated from SIN-1 reacted preferentially with alpha-tocopherol, sparing gamma-tocopherol levels until alpha-tocopherol was depleted. This same sparing effect was demonstrated when dilauryl phosphatidylcholine liposomes containing alpha-tocopherol and gamma-tocopherol were incubated with SIN-1. These data suggest that peroxynitrite reacts preferentially with alpha-tocopherol. We conclude that the reaction between peroxynitrite and gamma-tocopherol is not siginficant until alpha-tocopherol levels have been depleted. ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001008-26
Application #
6448017
Study Section
Project Start
2001-03-01
Project End
2002-02-28
Budget Start
Budget End
Support Year
26
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Type
DUNS #
073134603
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Mao, Li; Liu, Yu-Xiang; Huang, Chun-Hua et al. (2015) Intrinsic Chemiluminescence Generation during Advanced Oxidation of Persistent Halogenated Aromatic Carcinogens. Environ Sci Technol 49:7940-7
Shan, Guo-Qiang; Yu, Ao; Zhao, Chuan-Fang et al. (2015) A combined experimental and computational investigation on the unusual molecular mechanism of the Lossen rearrangement reaction activated by carcinogenic halogenated quinones. J Org Chem 80:180-9
Li, Yan; Huang, Chun-Hua; Liu, Yu-Xiang et al. (2014) Detoxifying polyhalogenated catechols through a copper-chelating agent by forming stable and redox-inactive hydrogen-bonded complexes with an unusual perpendicular structure. Chemistry 20:13028-33
Sheng, Zhi-Guo; Huang, Wei; Liu, Yu-Xiang et al. (2013) Ofloxacin induces apoptosis via ?1 integrin-EGFR-Rac1-Nox2 pathway in microencapsulated chondrocytes. Toxicol Appl Pharmacol 267:74-87
Sheng, Zhi-Guo; Huang, Wei; Liu, Yu-Xiang et al. (2013) Bisphenol A at a low concentration boosts mouse spermatogonial cell proliferation by inducing the G protein-coupled receptor 30 expression. Toxicol Appl Pharmacol 267:88-94
Shao, Jie; Huang, Chun-Hua; Kalyanaraman, Balaraman et al. (2013) Potent methyl oxidation of 5-methyl-2'-deoxycytidine by halogenated quinoid carcinogens and hydrogen peroxide via a metal-independent mechanism. Free Radic Biol Med 60:177-82
Sheng, Zhi-Guo; Li, Yan; Fan, Rui-Mei et al. (2013) Lethal synergism between organic and inorganic wood preservatives via formation of an unusual lipophilic ternary complex. Toxicol Appl Pharmacol 266:335-44
Qin, Hao; Huang, Chun-Hua; Mao, Li et al. (2013) Molecular mechanism of metal-independent decomposition of lipid hydroperoxide 13-HPODE by halogenated quinoid carcinogens. Free Radic Biol Med 63:459-66
Huang, Chun-Hua; Shan, Guo-Qiang; Mao, Li et al. (2013) The first purification and unequivocal characterization of the radical form of the carbon-centered quinone ketoxy radical adduct. Chem Commun (Camb) 49:6436-8
Liddle, Brendan J; Wanniarachchi, Sarath; Hewage, Jeewantha S et al. (2012) Electronic communication across diamagnetic metal bridges: a homoleptic gallium(III) complex of a redox-active diarylamido-based ligand and its oxidized derivatives. Inorg Chem 51:12720-8

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