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Published in: American Journal of Cardiovascular Drugs 4/2004

01-07-2004 | Leading Article

The Role of Paraoxonase 1 Activity in Cardiovascular Disease

Potential for Therapeutic Intervention

Authors: Dr Michael I. Mackness, Paul N. Durrington, Bharti Mackness

Published in: American Journal of Cardiovascular Drugs | Issue 4/2004

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Abstract

The antioxidant activity of high density lipoprotein (HDL) is largely due to the paraoxonase (PON) 1 located on it. Experiments with transgenic PON1 knockout mice indicate the potential for PON1 to protect against atherogenesis. This effect of HDL in decreasing low density lipoprotein (LDL) lipid peroxidation is maintained for longer than that of antioxidant vitamins and could therefore be more protective. Several important advances in the field of PON research have occurred recently, not least the discovery that two other members of the PON gene family — PON2 and PON3 — may also have important antioxidant properties. Significant advances have been made in understanding the basic biochemical function of PON1 and the discovery of possible modulators of its activity.
Case-control studies of PON1 activity and coronary heart disease (CHD) have shown a clear association between CHD and low serum PON1 activity. This relationship has been further strengthened by the publication of the first prospective study showing low serum PON1 activity to be an independent predictor of new CHD events. Furthermore, decreased CHD risk has been revealed by meta-analysis to be associated with the polymorphisms of PON1, which are most active in lipid peroxide hydrolysis. Although this is likely to be an underestimate of the true contribution of PON1 to CHD (because these polymorphisms explain only a small component of the variation in PON1 activity), it is important because genetic influences are unlikely to be confounded by other factors linked with both CHD and diminished PON1 activity. PON1 is being extensively researched and it is hoped that therapeutic approaches will emerge to increase its activity. Clinical trials of these, if successful, will not only provide a novel means of preventing atherosclerosis, but also provide a more satisfactory means of testing the oxidant hypothesis of atherosclerosis than antioxidant vitamin supplementation has proved to be.
Footnotes
1
The use of trade names is for identification purposes only and does not imply endorsement.
 
Literature
1.
go back to reference Miller GJ, Miller NE. Plasma high-density lipoprotein concentration and the development of ischaemic heart disease. Lancet 1975; I: 16–9CrossRef Miller GJ, Miller NE. Plasma high-density lipoprotein concentration and the development of ischaemic heart disease. Lancet 1975; I: 16–9CrossRef
2.
go back to reference Castelli WP, Garrison RJ, Wilson PW, et al. Incidence of coronary heart disease and lipoprotein cholesterol levels: the Framingham Study. JAMA 1986; 256: 2835–8PubMedCrossRef Castelli WP, Garrison RJ, Wilson PW, et al. Incidence of coronary heart disease and lipoprotein cholesterol levels: the Framingham Study. JAMA 1986; 256: 2835–8PubMedCrossRef
3.
go back to reference Tanne D, Yaari S, Goldbourt U. High-density lipoprotein cholesterol and risk of ischaemic stroke mortality: a 21 year follow-up of 8586 men from the Israeli Ischaemic Heart Disease Study. Stroke 1997; 21: 83–7CrossRef Tanne D, Yaari S, Goldbourt U. High-density lipoprotein cholesterol and risk of ischaemic stroke mortality: a 21 year follow-up of 8586 men from the Israeli Ischaemic Heart Disease Study. Stroke 1997; 21: 83–7CrossRef
4.
go back to reference Assmann G, Schulte H, von Eckardstein A, et al. High density lipoprotein cholesterol as a predictor of coronary heart disease risk: the PROCAM experience and pathophysiological implications for reverse cholesterol transport. Atherosclerosis 1996; 124: S11–20PubMedCrossRef Assmann G, Schulte H, von Eckardstein A, et al. High density lipoprotein cholesterol as a predictor of coronary heart disease risk: the PROCAM experience and pathophysiological implications for reverse cholesterol transport. Atherosclerosis 1996; 124: S11–20PubMedCrossRef
5.
go back to reference Primo-Parma SL, Sorenson RC, Teiber J, et al. The human serum paraoxonase/ arylesterase gene (PON1) is one member of a multigene family. Genomics 1996; 33: 498–509CrossRef Primo-Parma SL, Sorenson RC, Teiber J, et al. The human serum paraoxonase/ arylesterase gene (PON1) is one member of a multigene family. Genomics 1996; 33: 498–509CrossRef
6.
go back to reference La Du BN, Aviram M, Billecke S, et al. On the physiological role(s) of the paraoxonases. Chem Biol Interact 1999; 119-120: 379–88PubMedCrossRef La Du BN, Aviram M, Billecke S, et al. On the physiological role(s) of the paraoxonases. Chem Biol Interact 1999; 119-120: 379–88PubMedCrossRef
7.
go back to reference Durrington PN, Mackness B, Mackness MI. Paraoxonase and atherosclerosis. Arterioscler Thromb Vasc Biol 2001; 21: 473–80PubMedCrossRef Durrington PN, Mackness B, Mackness MI. Paraoxonase and atherosclerosis. Arterioscler Thromb Vasc Biol 2001; 21: 473–80PubMedCrossRef
8.
go back to reference Mackness MI, Abbott CA, Arrol S, et al. The role of high density lipoprotein and lipid-soluble antioxidant vitamins in inhibiting low-density lipoprotein oxidation. Biochem J 1993; 294: 829–35PubMed Mackness MI, Abbott CA, Arrol S, et al. The role of high density lipoprotein and lipid-soluble antioxidant vitamins in inhibiting low-density lipoprotein oxidation. Biochem J 1993; 294: 829–35PubMed
9.
go back to reference Mackness MI, Arrol S, Durrington PN. Paraoxonase prevents accumulation of lipoperoxides in low-density lipoprotein. FEBS Letts 1991; 286: 152–4CrossRef Mackness MI, Arrol S, Durrington PN. Paraoxonase prevents accumulation of lipoperoxides in low-density lipoprotein. FEBS Letts 1991; 286: 152–4CrossRef
10.
go back to reference Watson AD, Berliner JA, Hama SY, et al. Protective effect of high density lipoprotein associated paraoxonase: inhibition of the biological activity of minimally oxidised low-density lipoprotein. J Clin Invest 1995; 96: 2882–91PubMedCrossRef Watson AD, Berliner JA, Hama SY, et al. Protective effect of high density lipoprotein associated paraoxonase: inhibition of the biological activity of minimally oxidised low-density lipoprotein. J Clin Invest 1995; 96: 2882–91PubMedCrossRef
11.
go back to reference Aviram M, Billecke S, Sorenson R, et al. Paraoxonase active site required for protection against LDL oxidation involves its free sulphydryl group and is different from that required for its arylesterase/paraoxonase activities: selective action of human paraoxonase alloenzymes Q and R. Arterioscl Thromb Vasc Biol 1998; 10: 1617–24CrossRef Aviram M, Billecke S, Sorenson R, et al. Paraoxonase active site required for protection against LDL oxidation involves its free sulphydryl group and is different from that required for its arylesterase/paraoxonase activities: selective action of human paraoxonase alloenzymes Q and R. Arterioscl Thromb Vasc Biol 1998; 10: 1617–24CrossRef
12.
go back to reference Arrol S, Mackness MI, Durrington PN. High-density lipoprotein associated enzymes and the prevention of low-density lipoprotein oxidation. Eur J Lab Med 1996; 4: 33–8 Arrol S, Mackness MI, Durrington PN. High-density lipoprotein associated enzymes and the prevention of low-density lipoprotein oxidation. Eur J Lab Med 1996; 4: 33–8
13.
go back to reference Mackness MI, Arrol S, Abbott CA, et al. Protection of low-density lipoprotein against oxidative modification by high-density lipoprotein associated paraoxonase. Atherosclerosis 1993; 104: 129–35PubMedCrossRef Mackness MI, Arrol S, Abbott CA, et al. Protection of low-density lipoprotein against oxidative modification by high-density lipoprotein associated paraoxonase. Atherosclerosis 1993; 104: 129–35PubMedCrossRef
14.
go back to reference Rodrigo L, Mackness B, Durrington PN, et al. Hydrolysis of platelet-activating factor by human serum paraoxonase. Biochem J 2001; 354: 1–7PubMedCrossRef Rodrigo L, Mackness B, Durrington PN, et al. Hydrolysis of platelet-activating factor by human serum paraoxonase. Biochem J 2001; 354: 1–7PubMedCrossRef
15.
go back to reference Mackness MI, Durrington PN. High density lipoprotein, its enzymes and its potential to influence lipid peroxidation. Atherosclerosis 1995; 115: 243–53PubMedCrossRef Mackness MI, Durrington PN. High density lipoprotein, its enzymes and its potential to influence lipid peroxidation. Atherosclerosis 1995; 115: 243–53PubMedCrossRef
16.
go back to reference Packard CJ, O’Reilly DSJ, Caslake MJ, et al. Lipoprotein-associated phospholipase A2 as an independent predictor of coronary heart disease. N Engl J Med 2000; 343: 1148–55PubMedCrossRef Packard CJ, O’Reilly DSJ, Caslake MJ, et al. Lipoprotein-associated phospholipase A2 as an independent predictor of coronary heart disease. N Engl J Med 2000; 343: 1148–55PubMedCrossRef
17.
go back to reference Klimov AN, Kozhevnikova KA, Kuzmin AA, et al. On the ability of high density lipoproteins to remove phospholipid peroxidation products from erythrocyte membranes. Biochemistry (Mosc) 2001; 66: 300–4CrossRef Klimov AN, Kozhevnikova KA, Kuzmin AA, et al. On the ability of high density lipoproteins to remove phospholipid peroxidation products from erythrocyte membranes. Biochemistry (Mosc) 2001; 66: 300–4CrossRef
18.
go back to reference Shih DM, Gu L, Xia Y-R, et al. Mice lacking serum paraoxonase are susceptible to organophosphate toxicity and atherosclerosis. Nature 1998; 394: 284–7PubMedCrossRef Shih DM, Gu L, Xia Y-R, et al. Mice lacking serum paraoxonase are susceptible to organophosphate toxicity and atherosclerosis. Nature 1998; 394: 284–7PubMedCrossRef
19.
go back to reference Mackness B, Durrington PN, Mackness MI. Lack of protection against oxidative modification of LDL by avian HDL. Biochem Biophys Res Commun 1998; 247: 443–6PubMedCrossRef Mackness B, Durrington PN, Mackness MI. Lack of protection against oxidative modification of LDL by avian HDL. Biochem Biophys Res Commun 1998; 247: 443–6PubMedCrossRef
20.
go back to reference Tward A, Xia YR, Wang XP, et al. Decreased atherosclerotic lesion formation in human serum paraoxonase transgenic mice. Circulation 2002; 106: 484–90PubMedCrossRef Tward A, Xia YR, Wang XP, et al. Decreased atherosclerotic lesion formation in human serum paraoxonase transgenic mice. Circulation 2002; 106: 484–90PubMedCrossRef
21.
go back to reference Witztum JL, Steinberg D. Role of oxidized low density lipoprotein in atherogenesis. J Clin Invest 1991; 88: 1785–92PubMedCrossRef Witztum JL, Steinberg D. Role of oxidized low density lipoprotein in atherogenesis. J Clin Invest 1991; 88: 1785–92PubMedCrossRef
22.
go back to reference Hessler JR, Robertson AL, Chisholm GM. LDL-induced cytotoxicity and its inhibition by HDL in human vascular smooth muscle and endothelial cells in culture. Atherosclerosis 1979; 32: 213–29PubMedCrossRef Hessler JR, Robertson AL, Chisholm GM. LDL-induced cytotoxicity and its inhibition by HDL in human vascular smooth muscle and endothelial cells in culture. Atherosclerosis 1979; 32: 213–29PubMedCrossRef
23.
go back to reference Parthasarathy S, Barnett J, Fong LG. High-density lipoprotein inhibits the oxidative modification of low-density lipoprotein. Biochim Biophys Acta 1990; 1044: 275–83PubMedCrossRef Parthasarathy S, Barnett J, Fong LG. High-density lipoprotein inhibits the oxidative modification of low-density lipoprotein. Biochim Biophys Acta 1990; 1044: 275–83PubMedCrossRef
24.
go back to reference Navab M, Imes SS, Hama SY, et al. Monocyte transmigration induced by modification of low density lipoprotein in cocultures of human aortic wall cells is due to induction of monocyte chemotactic protein 1 synthesis and is abolished by high density lipoprotein. J Clin Invest 1991; 88: 2039–46PubMedCrossRef Navab M, Imes SS, Hama SY, et al. Monocyte transmigration induced by modification of low density lipoprotein in cocultures of human aortic wall cells is due to induction of monocyte chemotactic protein 1 synthesis and is abolished by high density lipoprotein. J Clin Invest 1991; 88: 2039–46PubMedCrossRef
25.
go back to reference Aviram M, Rosenblat M, Bisgaier CL, et al. Paraoxonase inhibits high-density lipoprotein and preserves its functions. J Clin Invest 1998; 101: 1581–90PubMedCrossRef Aviram M, Rosenblat M, Bisgaier CL, et al. Paraoxonase inhibits high-density lipoprotein and preserves its functions. J Clin Invest 1998; 101: 1581–90PubMedCrossRef
26.
go back to reference Steinbrecher UP, Lougheed M, Kwan W-C, et al. Recognition of oxidised low density lipoprotein by the scavenger receptor of macrophages results from derivatisation of apolipoprotein B by products of fatty acid peroxidation. J Biol Chem 1989; 264: 15216–23PubMed Steinbrecher UP, Lougheed M, Kwan W-C, et al. Recognition of oxidised low density lipoprotein by the scavenger receptor of macrophages results from derivatisation of apolipoprotein B by products of fatty acid peroxidation. J Biol Chem 1989; 264: 15216–23PubMed
27.
go back to reference Sangvanich P, Mackness B, Gaskill S, et al. The effect of HDL on the formation of lipid/protein conjugates during in vitro oxidation of LDL. Biochem Biophys Res Commun 2002; 300: 501–6CrossRef Sangvanich P, Mackness B, Gaskill S, et al. The effect of HDL on the formation of lipid/protein conjugates during in vitro oxidation of LDL. Biochem Biophys Res Commun 2002; 300: 501–6CrossRef
28.
go back to reference Myant NB. The biology of cholesterol and related steroids. London: William Heinemann Medical Books Ltd, 1981 Myant NB. The biology of cholesterol and related steroids. London: William Heinemann Medical Books Ltd, 1981
29.
go back to reference The Heart Outcomes Prevention Evaluation Study Investigators. Vitamin E supplementation and cardiovascular events in high-risk patients. N Engl J Med 2000; 342: 154–60CrossRef The Heart Outcomes Prevention Evaluation Study Investigators. Vitamin E supplementation and cardiovascular events in high-risk patients. N Engl J Med 2000; 342: 154–60CrossRef
30.
go back to reference Arrol S, Mackness MI, Durrington PN. Vitamin E supplementation increases the resistance of both LDL and HDL to oxidation and increases cholesteryl ester transfer activity. Atherosclerosis 2000; 150: 129–34PubMedCrossRef Arrol S, Mackness MI, Durrington PN. Vitamin E supplementation increases the resistance of both LDL and HDL to oxidation and increases cholesteryl ester transfer activity. Atherosclerosis 2000; 150: 129–34PubMedCrossRef
31.
go back to reference Okamoto H, Yonemori F, Wakitani K, et al. A cholesteryl ester transfer protein inhibitor attenuates atherosclerosis in rabbits. Nature 2000; 406: 203–7PubMedCrossRef Okamoto H, Yonemori F, Wakitani K, et al. A cholesteryl ester transfer protein inhibitor attenuates atherosclerosis in rabbits. Nature 2000; 406: 203–7PubMedCrossRef
32.
go back to reference Arrol S, Mackness MI, Durrington PN. High-density lipoprotein associated enzymes and the prevention of low-density lipoprotein oxidation. Eur J Lab Med 1996; 4: 33–8 Arrol S, Mackness MI, Durrington PN. High-density lipoprotein associated enzymes and the prevention of low-density lipoprotein oxidation. Eur J Lab Med 1996; 4: 33–8
33.
go back to reference Graham A, Hassall DG, Rafique S, et al. Evidence for a paraoxonase independent inhibition of low-density lipoprotein oxidation by high-density lipoprotein. Atherosclerosis 1997; 135: 193–204PubMedCrossRef Graham A, Hassall DG, Rafique S, et al. Evidence for a paraoxonase independent inhibition of low-density lipoprotein oxidation by high-density lipoprotein. Atherosclerosis 1997; 135: 193–204PubMedCrossRef
34.
go back to reference Suehiro T, Nakamura T, Inoue M, et al. A polymorphism upstream from the human paraoxonase (PON1) gene and its association with PON1 expression. Atherosclerosis 2000; 150: 295–8PubMedCrossRef Suehiro T, Nakamura T, Inoue M, et al. A polymorphism upstream from the human paraoxonase (PON1) gene and its association with PON1 expression. Atherosclerosis 2000; 150: 295–8PubMedCrossRef
35.
go back to reference Leviev I, James RW. Promoter polymorphisms of human paraoxonase PON1 gene and serum activities and concentrations. Arterioscl Thromb Vasc Biol 2000; 20: 516–21PubMedCrossRef Leviev I, James RW. Promoter polymorphisms of human paraoxonase PON1 gene and serum activities and concentrations. Arterioscl Thromb Vasc Biol 2000; 20: 516–21PubMedCrossRef
36.
go back to reference Brophy VH, Hastings MD, Clendenning JB, et al. Polymorphisms in the human paraoxonase (PON1) promoter. Pharmacogenetics 2001; 11: 77–84PubMedCrossRef Brophy VH, Hastings MD, Clendenning JB, et al. Polymorphisms in the human paraoxonase (PON1) promoter. Pharmacogenetics 2001; 11: 77–84PubMedCrossRef
37.
go back to reference Brophy VH, Jampsa RL, Clendenning JB, et al. Effects of 5′regulatory-region polymorphisms on paraoxonase-gene (PON1) expression. Am J Hum Genet 2001; 68: 1428–36PubMedCrossRef Brophy VH, Jampsa RL, Clendenning JB, et al. Effects of 5′regulatory-region polymorphisms on paraoxonase-gene (PON1) expression. Am J Hum Genet 2001; 68: 1428–36PubMedCrossRef
38.
go back to reference Wheeler JG, Keavney BD, Watkins H, et al. Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: metaanalysis of 43 studies. Lancet 2004; 363: 689–95PubMedCrossRef Wheeler JG, Keavney BD, Watkins H, et al. Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: metaanalysis of 43 studies. Lancet 2004; 363: 689–95PubMedCrossRef
39.
go back to reference Ikeda Y, Suehiro T, Inoue M, et al. Serum paraoxonase activity and its relationship to diabetic complications in patients with non-insulin-dependent diabetes mellitus. Metabolism 1998; 47: 598–602PubMedCrossRef Ikeda Y, Suehiro T, Inoue M, et al. Serum paraoxonase activity and its relationship to diabetic complications in patients with non-insulin-dependent diabetes mellitus. Metabolism 1998; 47: 598–602PubMedCrossRef
40.
go back to reference James RW, Leviev K, Righetti A. Smoking is associated with reduced serum paraoxonase activity and concentration in patients with coronary artery disease. Circulation 2000; 101: 2252–7PubMedCrossRef James RW, Leviev K, Righetti A. Smoking is associated with reduced serum paraoxonase activity and concentration in patients with coronary artery disease. Circulation 2000; 101: 2252–7PubMedCrossRef
41.
go back to reference Senti M, Tomas M, Vila J, et al. Relationship of age-related myocardial infarction risk and Gln/Arg 192 variants of the human paraoxonase gene: the Regicor study. Atherosclerosis 2001; 156: 443–9PubMedCrossRef Senti M, Tomas M, Vila J, et al. Relationship of age-related myocardial infarction risk and Gln/Arg 192 variants of the human paraoxonase gene: the Regicor study. Atherosclerosis 2001; 156: 443–9PubMedCrossRef
42.
go back to reference Blatter-Garin M-C, James RW, Dussoix P, et al. Paraoxonase Polymorphism Met-Leu 54 is associated with modified serum concentrations of the enzyme. J Clin Invest 1997; 99: 62–6CrossRef Blatter-Garin M-C, James RW, Dussoix P, et al. Paraoxonase Polymorphism Met-Leu 54 is associated with modified serum concentrations of the enzyme. J Clin Invest 1997; 99: 62–6CrossRef
43.
go back to reference Salonen JT, Malin R, Toumaineu T-P, et al. Polymorphism in high density lipoprotein gene and risk of acute myocardial infarction in men: prospective nested case-control study. BMJ 1999; 319: 487–8PubMedCrossRef Salonen JT, Malin R, Toumaineu T-P, et al. Polymorphism in high density lipoprotein gene and risk of acute myocardial infarction in men: prospective nested case-control study. BMJ 1999; 319: 487–8PubMedCrossRef
44.
go back to reference Sanghera DK, Saha N, Kamboh MI. The codon 55 polymorphism of the paraoxonase 1 gene is not associated with risk of coronary heart disease in Asian Indians and Chinese. Atherosclerosis 1998; 136: 217–23PubMedCrossRef Sanghera DK, Saha N, Kamboh MI. The codon 55 polymorphism of the paraoxonase 1 gene is not associated with risk of coronary heart disease in Asian Indians and Chinese. Atherosclerosis 1998; 136: 217–23PubMedCrossRef
45.
go back to reference Arca M, Ombres D, Montali A, et al. PON1 L55M polymorphism is not a predictor of coronary atherosclerosis either alone or in combination with Q192R polymorphism in an Italian population. Eur J Clin Invest 2002; 32: 9–15PubMedCrossRef Arca M, Ombres D, Montali A, et al. PON1 L55M polymorphism is not a predictor of coronary atherosclerosis either alone or in combination with Q192R polymorphism in an Italian population. Eur J Clin Invest 2002; 32: 9–15PubMedCrossRef
46.
go back to reference Robertson KS, Hawe E, Miller GJ, et al. Northwick Park Heart Study II: human paraoxonase gene cluster polymorphisms as predictors of coronary heart disease risk in the prospective Northwick Park Heart Study II. Biochim Biophys Acta 2003; 1639: 203–12PubMedCrossRef Robertson KS, Hawe E, Miller GJ, et al. Northwick Park Heart Study II: human paraoxonase gene cluster polymorphisms as predictors of coronary heart disease risk in the prospective Northwick Park Heart Study II. Biochim Biophys Acta 2003; 1639: 203–12PubMedCrossRef
47.
go back to reference McElveen J, Mackness MI, Colley CM, et al. Distribution of paraoxon hydrolysing activity in the serum of patients after myocardial infarction. Clin Chem 1986; 32: 671–3PubMed McElveen J, Mackness MI, Colley CM, et al. Distribution of paraoxon hydrolysing activity in the serum of patients after myocardial infarction. Clin Chem 1986; 32: 671–3PubMed
48.
go back to reference Ayub A, Mackness MI, Arrol S, et al. Serum paraoxonase after myocardial infarction. Arterioscl Thromb Vasc Biol 1999; 19: 330–5PubMedCrossRef Ayub A, Mackness MI, Arrol S, et al. Serum paraoxonase after myocardial infarction. Arterioscl Thromb Vasc Biol 1999; 19: 330–5PubMedCrossRef
49.
go back to reference Mackness B, Davies GK, Turkie W, et al. Paraoxonase status in coronary heart disease: are activity and concentration more important than genotype? Arterioscler Thromb Vasc Biol 2001; 21: 1451–7PubMedCrossRef Mackness B, Davies GK, Turkie W, et al. Paraoxonase status in coronary heart disease: are activity and concentration more important than genotype? Arterioscler Thromb Vasc Biol 2001; 21: 1451–7PubMedCrossRef
50.
go back to reference Mackness MI, Harty D, Bhatnagar D, et al. Serum paraoxonase activity in familial hypercholesterolaemia and insulin-dependent diabetes mellitus. Atherosclerosis 1991; 86: 193–9PubMedCrossRef Mackness MI, Harty D, Bhatnagar D, et al. Serum paraoxonase activity in familial hypercholesterolaemia and insulin-dependent diabetes mellitus. Atherosclerosis 1991; 86: 193–9PubMedCrossRef
51.
go back to reference Abbott CA, Mackness MI, Kumar S, et al. Serum paraoxonase activity, concentration, and phenotype distribution in diabetes mellitus and its relationship to serum lipids and lipoproteins. Arterioscler Thromb Vasc Biol 1995; 15: 1812–8PubMedCrossRef Abbott CA, Mackness MI, Kumar S, et al. Serum paraoxonase activity, concentration, and phenotype distribution in diabetes mellitus and its relationship to serum lipids and lipoproteins. Arterioscler Thromb Vasc Biol 1995; 15: 1812–8PubMedCrossRef
52.
go back to reference Mackness B, Mackness MI, Arrol S, et al. Serum paraoxonase (PON1) 55 and 192 polymorphism and paraoxonase activity and concentration in non-insulin dependent diabetes mellitus. Atherosclerosis 1998; 139: 341–9PubMedCrossRef Mackness B, Mackness MI, Arrol S, et al. Serum paraoxonase (PON1) 55 and 192 polymorphism and paraoxonase activity and concentration in non-insulin dependent diabetes mellitus. Atherosclerosis 1998; 139: 341–9PubMedCrossRef
53.
go back to reference Patel BN, Mackness MI, Harty DW, et al. Serum esterase activities and hyperlipidaemia in the streptozotocin-diabetic rat. Biochim Biophys Acta 1990; 1035: 113–6PubMedCrossRef Patel BN, Mackness MI, Harty DW, et al. Serum esterase activities and hyperlipidaemia in the streptozotocin-diabetic rat. Biochim Biophys Acta 1990; 1035: 113–6PubMedCrossRef
54.
go back to reference Hasselwander O, McMaster D, Fogarty DG, et al. Serum paraoxonase and plateletactivating factor acetylhydrolase in chronic renal failure. Clin Chem 1998; 44: 179–81PubMed Hasselwander O, McMaster D, Fogarty DG, et al. Serum paraoxonase and plateletactivating factor acetylhydrolase in chronic renal failure. Clin Chem 1998; 44: 179–81PubMed
55.
go back to reference Mackness B, Durrington P, McElduff P, et al. Low paraoxonase activity predicts coronary events in the Caerphilly Prospective Study. Circulation 2003; 107: 2775–9PubMedCrossRef Mackness B, Durrington P, McElduff P, et al. Low paraoxonase activity predicts coronary events in the Caerphilly Prospective Study. Circulation 2003; 107: 2775–9PubMedCrossRef
56.
go back to reference Mackness B, Hunt R, Durrington PN, et al. Increased immunolocalisation of paraoxonase, clusterin and apolipoprotein AI in the human artery wall with progression of atherosclerosis. Arterioscler Thromb Vasc Biol 1997; 17: 1233–8PubMedCrossRef Mackness B, Hunt R, Durrington PN, et al. Increased immunolocalisation of paraoxonase, clusterin and apolipoprotein AI in the human artery wall with progression of atherosclerosis. Arterioscler Thromb Vasc Biol 1997; 17: 1233–8PubMedCrossRef
57.
go back to reference Aviram M, Hardak E, Vaya J, et al. Human serum paraoxonase (PON1) Q and R selectively decrease lipid peroxides in human coronary and carotid atherosclerotic lesions: PON1 esterase and peroxidase-like activities. Circulation 2000; 101: 2510–7PubMedCrossRef Aviram M, Hardak E, Vaya J, et al. Human serum paraoxonase (PON1) Q and R selectively decrease lipid peroxides in human coronary and carotid atherosclerotic lesions: PON1 esterase and peroxidase-like activities. Circulation 2000; 101: 2510–7PubMedCrossRef
58.
go back to reference Jarvik GP, Tsai NT, McKinstry LA, et al. Vitamin C and E intake are associated with increased PON1 activity. Arterioscl Thromb Vasc Biol 2002; 22: 1329–33PubMedCrossRef Jarvik GP, Tsai NT, McKinstry LA, et al. Vitamin C and E intake are associated with increased PON1 activity. Arterioscl Thromb Vasc Biol 2002; 22: 1329–33PubMedCrossRef
59.
go back to reference Kleemola P, Freese R, Jauhiainen M, et al. Dietary determinants of serum paraoxonase activity in healthy humans. Atheroslcerosis 2002; 160: 425–32CrossRef Kleemola P, Freese R, Jauhiainen M, et al. Dietary determinants of serum paraoxonase activity in healthy humans. Atheroslcerosis 2002; 160: 425–32CrossRef
60.
go back to reference Kordonouri O, James RW, Bennetts JB, et al. Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with type 1 diabetes mellitus. Metabolism 2001; 50: 657–60PubMedCrossRef Kordonouri O, James RW, Bennetts JB, et al. Modulation by blood glucose levels of activity and concentration of paraoxonase in young patients with type 1 diabetes mellitus. Metabolism 2001; 50: 657–60PubMedCrossRef
61.
go back to reference Van Lenten BJ, Wagner AC, Navab M, et al. Oxidised phospholipids induce changes in hepatic paraoxonase and Apo J but not monocyte chemoattractant protein-1 via interleukin-6. J Biol Chem 2001; 276: 1923–9PubMedCrossRef Van Lenten BJ, Wagner AC, Navab M, et al. Oxidised phospholipids induce changes in hepatic paraoxonase and Apo J but not monocyte chemoattractant protein-1 via interleukin-6. J Biol Chem 2001; 276: 1923–9PubMedCrossRef
62.
go back to reference Kudchodkar BJ, Lacko AG, Dory L, et al. Dietary fat modulates serum paraoxonase 1 activity in rats. J Nutr 2000; 130: 2427–33PubMed Kudchodkar BJ, Lacko AG, Dory L, et al. Dietary fat modulates serum paraoxonase 1 activity in rats. J Nutr 2000; 130: 2427–33PubMed
63.
go back to reference Sutherland WHF, Walker RJ, de Jong SA, et al. Reduced postprandial serum paraoxonase activity after a meal rich in used cooking fat. Arterioscl Thromb Vasc Biol 1999; 19: 1340–7PubMedCrossRef Sutherland WHF, Walker RJ, de Jong SA, et al. Reduced postprandial serum paraoxonase activity after a meal rich in used cooking fat. Arterioscl Thromb Vasc Biol 1999; 19: 1340–7PubMedCrossRef
64.
go back to reference Shih DM, Gu L, Hama S, et al. Genetic-dietary regulation of serum paraoxonase expression and its role in atherogenesis in a mouse model. J Clin Invest 1996; 97: 1630–9PubMedCrossRef Shih DM, Gu L, Hama S, et al. Genetic-dietary regulation of serum paraoxonase expression and its role in atherogenesis in a mouse model. J Clin Invest 1996; 97: 1630–9PubMedCrossRef
65.
go back to reference Mackness MI, Bouiller A, Hennuyer M, et al. Paraoxonase activity is reduced by a pro-atherosclerotic diet in rabbits. Biochem Biophys Res Commun 2000; 269: 232–6PubMedCrossRef Mackness MI, Bouiller A, Hennuyer M, et al. Paraoxonase activity is reduced by a pro-atherosclerotic diet in rabbits. Biochem Biophys Res Commun 2000; 269: 232–6PubMedCrossRef
66.
go back to reference Aviram M, Dornfold L, Rosenblat M, et al. Pomegranate juice consumption reduces oxidative stress, atherogenic modification of LDL, and platelet aggregation: studies in humans and in atherosclerotic apolipoprotein E-deficient mice. Am J Clin Nutr 2000; 71: 1062–76PubMed Aviram M, Dornfold L, Rosenblat M, et al. Pomegranate juice consumption reduces oxidative stress, atherogenic modification of LDL, and platelet aggregation: studies in humans and in atherosclerotic apolipoprotein E-deficient mice. Am J Clin Nutr 2000; 71: 1062–76PubMed
67.
go back to reference van der Gaag MS, van Tol A, Scheek LM, et al. Daily moderate alcohol consumption increases serum paraoxonase activity; a diet controlled, randomised intervention study in middle-aged men. Atherosclerosis 1999; 147(2): 405–10PubMedCrossRef van der Gaag MS, van Tol A, Scheek LM, et al. Daily moderate alcohol consumption increases serum paraoxonase activity; a diet controlled, randomised intervention study in middle-aged men. Atherosclerosis 1999; 147(2): 405–10PubMedCrossRef
68.
go back to reference Sözmen EY, Mackness B, Sözmen B, et al. Effect of organophosphate intoxications on human serum paraoxonase. Hum Exp Toxicol 2002; 21(5): 247–52PubMedCrossRef Sözmen EY, Mackness B, Sözmen B, et al. Effect of organophosphate intoxications on human serum paraoxonase. Hum Exp Toxicol 2002; 21(5): 247–52PubMedCrossRef
69.
70.
go back to reference Tomas M, Senti M, Garcia-Faria F, et al. Effect of simvastatin therapy on paraoxonase activity and related lipoproteins in familial hypercholesterolaemic patients. Arterioscler Thromb Vasc Biol 2000; 20: 2113–9PubMedCrossRef Tomas M, Senti M, Garcia-Faria F, et al. Effect of simvastatin therapy on paraoxonase activity and related lipoproteins in familial hypercholesterolaemic patients. Arterioscler Thromb Vasc Biol 2000; 20: 2113–9PubMedCrossRef
71.
go back to reference Aviram M, Rosenblat M, Bisgaier CL, et al. Atorvastatin and gemfibrozil metabolites, but not the parent drugs are potent antioxidants against lipoprotein oxidation. Atherosclerosis 1998; 138: 271–80PubMedCrossRef Aviram M, Rosenblat M, Bisgaier CL, et al. Atorvastatin and gemfibrozil metabolites, but not the parent drugs are potent antioxidants against lipoprotein oxidation. Atherosclerosis 1998; 138: 271–80PubMedCrossRef
72.
go back to reference Paragh G, Balogh Z, Seres I, et al. Effect of gemfibrozil on HDL-associated serum paraoxonase activity and lipoprotein profile in patients with hyperlipidaemia. Clin Drug Invest 2000; 19: 277–82CrossRef Paragh G, Balogh Z, Seres I, et al. Effect of gemfibrozil on HDL-associated serum paraoxonase activity and lipoprotein profile in patients with hyperlipidaemia. Clin Drug Invest 2000; 19: 277–82CrossRef
73.
go back to reference Durrington PN, Mackness MI, Bhatnagar D, et al. Effects of two different fibric acid derivatives on lipoproteins, cholesteryl ester transfer, fibrinogen, plasminogen activator inhibitor and paraoxonase activity in type IIb hyperlipoproteinaemia. Atherosclerosis 1998; 138: 217–25PubMedCrossRef Durrington PN, Mackness MI, Bhatnagar D, et al. Effects of two different fibric acid derivatives on lipoproteins, cholesteryl ester transfer, fibrinogen, plasminogen activator inhibitor and paraoxonase activity in type IIb hyperlipoproteinaemia. Atherosclerosis 1998; 138: 217–25PubMedCrossRef
74.
go back to reference Balogh Z, Fülöp P, Seres I, et al. Effect of simvastatin on serum paraoxonase activity. Clin Drug Invest 2001; 21: 505–10CrossRef Balogh Z, Fülöp P, Seres I, et al. Effect of simvastatin on serum paraoxonase activity. Clin Drug Invest 2001; 21: 505–10CrossRef
75.
go back to reference Turay J, Grniaková V, Valka J. Changes in paraoxonase and apolipoprotein A-I, B, C-III and E in subjects with combined familial hyperlipoproteinaemia treated with ciprofibrate. Drugs Exp Clin Res 2000; 26: 83–8PubMed Turay J, Grniaková V, Valka J. Changes in paraoxonase and apolipoprotein A-I, B, C-III and E in subjects with combined familial hyperlipoproteinaemia treated with ciprofibrate. Drugs Exp Clin Res 2000; 26: 83–8PubMed
76.
go back to reference Gouédard C, Koum-Besson N, Barouki R, et al. Opposite regulation of the human paraoxonase-1 gene PON1 by fenofibrate and statins. Mol Pharmacol 2003; 63: 945–56PubMedCrossRef Gouédard C, Koum-Besson N, Barouki R, et al. Opposite regulation of the human paraoxonase-1 gene PON1 by fenofibrate and statins. Mol Pharmacol 2003; 63: 945–56PubMedCrossRef
77.
go back to reference Calabresi L, Villa B, Canavesi M, et al. An omega-3 polyunsaturated fatty acid concentrate increases plasma high-density lipoprotein 2 cholesterol and paraoxonase levels in patients with familial combined hyperlipidemia. Metabolism 2004; 53(2): 153–8PubMedCrossRef Calabresi L, Villa B, Canavesi M, et al. An omega-3 polyunsaturated fatty acid concentrate increases plasma high-density lipoprotein 2 cholesterol and paraoxonase levels in patients with familial combined hyperlipidemia. Metabolism 2004; 53(2): 153–8PubMedCrossRef
Metadata
Title
The Role of Paraoxonase 1 Activity in Cardiovascular Disease
Potential for Therapeutic Intervention
Authors
Dr Michael I. Mackness
Paul N. Durrington
Bharti Mackness
Publication date
01-07-2004
Publisher
Springer International Publishing
Published in
American Journal of Cardiovascular Drugs / Issue 4/2004
Print ISSN: 1175-3277
Electronic ISSN: 1179-187X
DOI
https://doi.org/10.2165/00129784-200404040-00002

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