Common variants of apolipoprotein A-IV differ in their ability to inhibit low density lipoprotein oxidation
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Wong, Wai-Man R.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Wong, Wai-Man R.
Gerry, Andrew B.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Gerry, Andrew B.
Putt, Wendy
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Putt, Wendy
Roberts, Jane L.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Roberts, Jane L.
Weinberg, Richard B.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Weinberg, Richard B.
Humphries, Steve E.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Humphries, Steve E.
Leake, David S.
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机构:UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Leake, David S.
Talmud, Philippa J.
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UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, EnglandUCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Talmud, Philippa J.
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[1] UCL Royal Free & UCL Med Sch, British Heart Fdn Labs, Ctr Cardiovasc Genet, London WC1E 6JF, England
Apolipoprotein A-IV (apoA-IV) inhibits lipid peroxidation, thus demonstrating potential anti-atherogenic properties. The aim of this study was to investigate how the inhibition of low density lipoprotein (LDL) oxidation was influenced by common apoA-IV isoforms. Recombinant wild type apoA-IV (100 mu g/ml) significantly inhibited the oxidation of LDL (50 mu g protein/ml) by 5 mu M CuSO(4) (P < 0.005), but not by 100 mu M CuSO(4), suggesting that it may act by binding copper ions. ApoA-IV also inhibited the oxidation of LDL by the water-soluble free-radical generator 2,2'-azobis(amidinopropane) dihydrochloride (AAPH; I mM), as shown by the two-fold increase in the time for half maximal conjugated diene formation (T(1/2); P < 0.05) suggesting it can also scavenge free radicals in the aqueous phase. Compared to wild type apoA-IV, apoA-IV-S347 decreased T(1/2) by 15% (P = 0.036) and apoA-IV-H360 increased T(1/2) by 18% (P = 0.046). All apoA-IV isoforms increased the relative electrophoretic mobility of native LDL, suggesting apoA-IV can bind to LDL and acts as a site-specific antioxidant. The reduced inhibition of LDL oxidation by apoA-IV-S347 compared to wild type apoA-IV may account for the previous association of the APOA4 S347 variant with increased CHD risk and oxidative stress. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
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Univ Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
Portella, Rafael de Lima
Barcelos, Romulo Pillon
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Univ Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
Barcelos, Romulo Pillon
de Bem, Andreza Fabro
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Univ Fed Santa Maria, Ctr Ciencias Biol, Dept Bioquim, Florianopolis, SC, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
de Bem, Andreza Fabro
Carratu, Vanessa Santana
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Fundacdo Univ Rio Grande, Dept Quim, Rio Grande, RS, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
Carratu, Vanessa Santana
Bresolin, Leandro
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Univ Fed Acre, Cruzeiro Do Sul, AC, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
Bresolin, Leandro
Teixeira da Rocha, Joao Batista
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Univ Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
Teixeira da Rocha, Joao Batista
Antunes Soares, Felix Alexandre
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Univ Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil