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Common variants of apolipoprotein A-IV differ in their ability to inhibit low density lipoprotein oxidation

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Wong, W. M. R., Gerry, A. B., Putt, W., Roberts, J. L., Weinberg, R. B., Humphries, S. E., Leake, D. S. orcid id iconORCID: https://orcid.org/0000-0002-1742-6134 and Talmud, P. J. (2007) Common variants of apolipoprotein A-IV differ in their ability to inhibit low density lipoprotein oxidation. Atherosclerosis, 192 (2). pp. 266-274. ISSN 0021-9150 doi: 10.1016/j.atherosclerosis.2006.07.017

Abstract/Summary

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 CuSO4 (P < 0.005), but not by 100 mu M CuSO4, 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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Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/10119
Item Type Article
Refereed Yes
Divisions Life Sciences > School of Biological Sciences
Interdisciplinary centres and themes > Institute for Cardiovascular and Metabolic Research (ICMR)
Uncontrolled Keywords atherosclerosis, apoA-IV, conjugated dienes, copper, lipid, hydroperoxides, oxidised low density lipoprotein, HUMAN ATHEROSCLEROTIC LESIONS, CORONARY-ARTERY-DISEASE, LIPID-PEROXIDATION, HUMAN-PLASMA, CHOLESTEROL ACYLTRANSFERASE, ENDOTHELIAL-CELLS, COPPER-BINDING, HEART-DISEASE, VITAMIN-C, ACIDIC PH
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