Human serum paraoxonase (PON 1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants.
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B. La Du | S Billecke | M Aviram | C L Bisgaier | R S Newton | C. Bisgaier | M. Aviram | M Rosenblat | J Erogul | R Sorenson | B La Du | R. Newton | M. Rosenblat | S. Billecke | R. Sorenson | J. Erogul | B. Du
[1] B. La Du,et al. Paraoxonase active site required for protection against LDL oxidation involves its free sulfhydryl group and is different from that required for its arylesterase/paraoxonase activities: selective action of human paraoxonase allozymes Q and R. , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[2] C. Bisgaier,et al. Atorvastatin and gemfibrozil metabolites, but not the parent drugs, are potent antioxidants against lipoprotein oxidation. , 1998, Atherosclerosis.
[3] P. Belinky,et al. Structural aspects of the inhibitory effect of glabridin on LDL oxidation. , 1998, Free radical biology & medicine.
[4] B. La Du,et al. Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions. A possible peroxidative role for paraoxonase. , 1998, The Journal of clinical investigation.
[5] R. Coleman,et al. Reduced progression of atherosclerosis in apolipoprotein E-deficient mice following consumption of red wine, or its polyphenols quercetin or catechin, is associated with reduced susceptibility of LDL to oxidation and aggregation. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[6] S. Buch,et al. Licorice extract and its major polyphenol glabridin protect low-density lipoprotein against lipid peroxidation: in vitro and ex vivo studies in humans and in atherosclerotic apolipoprotein E-deficient mice. , 1997, The American journal of clinical nutrition.
[7] Yasuhiro Watanabe,et al. Cigarette smoke extract inhibits plasma paraoxonase activity by modification of the enzyme's free thiols. , 1997, Biochemical and biophysical research communications.
[8] M. Odawara,et al. Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus. , 1997, The Journal of clinical endocrinology and metabolism.
[9] G. Fonarow,et al. Mildly oxidized LDL induces an increased apolipoprotein J/paraoxonase ratio. , 1997, The Journal of clinical investigation.
[10] E. Topol,et al. Current Review of Interventional Cardiology , 1997 .
[11] T. Suehiro,et al. Paraoxonase gene polymorphism in Japanese subjects with coronary heart disease. , 1996, International journal of cardiology.
[12] B. L. Du,et al. Structural and functional diversity of paraoxonases , 1996, Nature Medicine.
[13] P. Edwards,et al. The Yin and Yang of oxidation in the development of the fatty streak. A review based on the 1994 George Lyman Duff Memorial Lecture. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[14] T. Forte,et al. Minimally oxidized LDL is a potent inhibitor of lecithin:cholesterol acyltransferase activity. , 1996, Journal of lipid research.
[15] R. Hegele,et al. Paraoxonase: biochemistry, genetics and relationship to plasma lipoproteins , 1996, Current opinion in lipidology.
[16] D. Shih,et al. Genetic-dietary regulation of serum paraoxonase expression and its role in atherogenesis in a mouse model. , 1996, The Journal of clinical investigation.
[17] P. Shah,et al. Active oxygen species and lysophosphatidylcholine are involved in oxidized low density lipoprotein activation of smooth muscle cell DNA synthesis. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[18] A. Marian,et al. A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease. , 1995, The Journal of clinical investigation.
[19] J. Berliner,et al. Protective effect of high density lipoprotein associated paraoxonase. Inhibition of the biological activity of minimally oxidized low density lipoprotein. , 1995, The Journal of clinical investigation.
[20] A. Boulton,et al. Serum paraoxonase activity, concentration, and phenotype distribution in diabetes mellitus and its relationship to serum lipids and lipoproteins. , 1995, Arteriosclerosis, thrombosis, and vascular biology.
[21] G. Charpentier,et al. Gln-Arg192 polymorphism of paraoxonase and coronary heart disease in type 2 diabetes , 1995, The Lancet.
[22] C. Kuo,et al. Comparison of purified human and rabbit serum paraoxonases. , 1995, Drug metabolism and disposition: the biological fate of chemicals.
[23] O. Lockridge,et al. Reconsideration of the catalytic center and mechanism of mammalian paraoxonase/arylesterase. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[24] P. Durrington,et al. HDL, its enzymes and its potential to influence lipid peroxidation , 1995 .
[25] L. Sultatos,et al. Kinetic mechanism of the detoxification of the organophosphate paraoxon by human serum A-esterase. , 1994, Drug metabolism and disposition: the biological fate of chemicals.
[26] J. Gaziano,et al. Content of antioxidants, preformed lipid hydroperoxides, and cholesterol as predictors of the susceptibility of human LDL to metal ion-dependent and -independent oxidation. , 1993, Journal of lipid research.
[27] S. Adkins,et al. Studies on human serum paraoxonase/arylesterase. , 1993, Chemico-biological interactions.
[28] S. Adkins,et al. Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes. , 1993, American journal of human genetics.
[29] M. Aviram,et al. Phospholipase A2-modified LDL is taken up at enhanced rate by macrophages. , 1992, Biochemical and biophysical research communications.
[30] P. Winocour,et al. Serum paraoxonase activity in familial hypercholesterolaemia and insulin-dependent diabetes mellitus. , 1991, Atherosclerosis.
[31] A. Smolen,et al. PURIFICATION OF HUMAN SERUM PARAOXONASE/ARYLESTERASE , 1991 .
[32] H. Esterbauer,et al. A spectrophotometric assay for lipid peroxides in serum lipoproteins using a commercially available reagent. , 1989, Journal of lipid research.
[33] C. Walker,et al. Distribution of paraoxon hydrolytic activity in the serum of patients after myocardial infarction. , 1986, Clinical chemistry.
[34] B. La Du,et al. The human serum paraoxonase polymorphism: identification of phenotypes by their response to salts. , 1983, American journal of human genetics.
[35] S. Aust,et al. Microsomal lipid peroxidation. , 1978, Methods in enzymology.
[36] O. Lamm,et al. Enzymatic Hydrolysis of Organophosphorus Compounds. VI. Effect of Metallic Ions on the Phosphorylphosphatases of Human Serum and Swine Kidney. , 1955 .