Abstract
Over recent years there has been a rapid increase in the number of articles reporting paraoxonase-1 (PON1) alterations in diseases other than arteriosclerosis, and which involve an increased degree of oxidative stress. Chronic liver impairment is associated with decreased serum PON1 activity but with increased serum PON1 concentration; this unusual juxtaposition being explained, perhaps, by the molecular alterations related to collagen synthesis and to the inactivation of the enzyme’s active site by lipid peroxides. Polymorphisms of the PON1 gene have been shown to be associated with an increased development of several neurological diseases and to influence the organism’s capacity to protect against neurotoxins. Many infectious diseases, as HIV infection, produce a high oxidative stress, and alterations in PON1 activity and concentration may be related to the course of the disease
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Akhmedova, S.N., Yakimovsky, A.K., Schwartz, E.I., 2001, Paraoxonase 1 Met-Leu 54 polymorphism is associated with Parkinson’s disease. J. Neurol. Sci., 184: 179–82.
Alonso-Villaverde, C., Coll, B., Gomez, F., Parra, S., Camps, J., Joven, J., Masana, L., 2005, The efavirenz-induced increase in HDL-cholesterol is influenced by the multidrug resistance gene 1 C3435T polymorphism. AIDS, 19: 341–2.
Alonso-Villaverde, C., Segués, T., Coll-Crespo, B., Pérez-Bernalte, R., Rabassa, A., Gomila, M., Parra, S., González-Esteban, M.A., Jiménez-Expósito, J.M., Masana, L., 2003, High-density lipoprotein concentrations relate to the clinical course of HIV viral load in patients undergoing antiretroviral therapy. AIDS, 17: 1173–7.
Ansell, B.J., Watson, K.E., Fogelman, A.M., Navab, M., Fonarow, G.C., 2005, High-density lipoprotein function: recent advances. J. Am. Coll. Cardiol., 46: 1792–8.
Aviram, M., Hardak, E., Vaya, J., Mahmood, S., Milo, S., Hoffman, A., Billicke, S., Draganov, D., Rosenblat, M., 2000, Human serum paraoxonases (PON1) Q and R selectively decrease lipid peroxides in human coronary and carotid atherosclerotic lesions. PON1 esterase and peroxidase-like activities. Circulation, 101: 2510–7.
Aviram, M., Rosenblat, M., Billecke, S., Erogul, J., Sorenson, R., Bisgaier, C.L., Newton, R.S., La Du, B., 1999, Human serum paraoxonase (PON1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants. Free Rad Biol Med, 26: 892–904.
Benmoyal-Segal, L., Vander, T., Shifman, S., Bryk, B., Ebstein, R., Marcus, E.L., Stessman, J., Darvasi, A., Herishanu,Y., Friedman, A., Soreq, H., 2005, Acetylcholinesterase/paraoxonase interactions increase the risk of insecticide-induced Parkinson’s disease. FASEB J., 19: 452–454.
Bowcock, A.M., Crandall, J., Daneshvar, L., Lee, G.M., Young, B., Zunzunegui, V., Craik, C., Cavalli-Sforza, L.L., King, M.C., 1986, Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families. Am J Hum Genet, 39: 699–706.
Buchwald, M., Zsiga, M., Markiewicz, D., Plavsic, N., Kennedy, D., Zengerling, S., Willard, H.F., Tsipouras, P., Schmiegelow, K., Schwartz, M., et al., 1986, Linkage of cystic fibrosis to the pro alpha 2(I) collagen gene, COL1A2, on chromosome 7. Cytogenet Cell Genet, 41: 234–9.
Burlina, A., Galzigna, L., 1974, Serum arylesterase isoenzymes in chronic hepatitis. Clin Biochem, 7(3): 202–5.
Burlina, A., Michielin, E., Galzigna, L., 1977, Characteristics and behaviour of arylesterase in human serum and liver. Eur J Clin Invest, 7(1): 17–20.
Carmine A., Buervenich, S., Sydow, O., Anvret, M., Olson, L., 2002, Further evidence for association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson’s disease. Mov. Disord.,17: 764–6.
Clarimon, J., Eerola, J., Hellström, O., Tienari, P.J., Singleton, A., 2004, Paraoxonase 1 (PON1) gene polymorphisms and Parkinson’s disease in a Finnish population. Neurosci. Lett., 367: 168–70.
Coll, B., Alonso-Villaverde, C., Parra, S., Montero, M., Tous, M., Joven, J., Masana, L., 2005, The stromal derived factor-1 mutated allele (SDF1-3′A) is associated with a lower incidence of atherosclerosis in HIV-infected patients. AIDS, 19: 1877–83.
Coll, B., Parra, S., Alonso-Villaverde, C., de Groot, E., Aragonés, G., Montero, M., Tous, M., Camps, J., Joven, J., Masana, L., 2006, HIV-infected patients with lypodystrophy have higher rates of carotid atherosclerosis: the role of monocyte chemoattractant protein-1. Cytokine, 34: 51–5.
Costa, L.G., Cole, T.B., Vitalone, C.E., Furlong, C.E., 2005, Measurement of paraoxonase (PON1) status as a potential biomarker of susceptibility to organophosphorate toxicity. Clin. Chim. Acta, 352: 37–47.
Costa, L.G., Vitalone, A., Cole, T.B., Furlong, C.E., 2005, Modulation of paraoxonase (PON1) activity. Biochem Pharmacol, 69: 541–50.
Deakin, S., Leviev, I., Brulhart-Meynet, M.C., James, R.W., 2003a, Paraoxonase-1 promoter haplotypes and serum paraoxonase: a predominant allele for polymorphic position – 107, implicating the Sp1 transcription factor. Biochem J, 372: 643–9.
Deakin, S., Leviev, I., Guernier, S., James, R.W., 2003b, Simvastatin modulates expression of the PON1 gene and increases serum paraoxonase. A role for sterol regulatory elementbinding protein-2. Arterioscler Thromb Vasc Biol, 23: 2083–9.
Erlich, P.M., Lunetta, K.L., Cupples, L.A., Huyck, M., Green, R.C., Baldwin, C.T., Farrer, L.A., 2006, Polymprphisms in the PON gene cluster are associated with Alzheimer disease. Hum. Mol. Genet., 15: 77–85.
Farrer, L.A., 1997, Genetics and the dementia patient. Neurologist, 3: 13–30.
Ferrari, A., Maretto, S., Girotto, D., Volpin, D., Bressan, G.M., 2004, SREBP contributes to induction of collagen VI transcription by serum starvation. Biochem Biophys Res Commun, 313: 600–5.
Ferré, N., Camps, J., Cabre, M., Paul, A., Joven, J., 2001, Hepatic paraoxonase activity alterations and free radical production in rats with experimental cirrhosis. Metabolism, 50(9): 997–1000.
Ferré, N., Camps, J., Prats, E., Vilella, E., Paul, A., Figuera, L., Joven, J., 2002, Serum paraoxonase activity: a new additional test for the improved evaluation of chronic liver damage. Clin Chem, 48(2): 261–8.
Ferré, N., Marsillach, J., Camps, J., Mackness, B., Mackness, M., Riu, F., Coll, B., Tous, M., Joven, J., 2006, Paraoxonase-1 is associated with oxidative stress, fibrosis and FAS expression in chronic liver diseases. J Hepatol, 45(1): 51–9.
Ferré, N., Marsillach, J., Camps, J., Rull, A., Coll, B., Tous, M., Joven, J., 2005, Genetic association of paraoxonase-1 polymorphisms and chronic hepatitis C virus infection. Clin Chim Acta, 361(1–2): 206–10.
García-Ruiz, I., de la Torre, P., Díaz, T., Esteban, E., Fernandez, I., Munoz-Yague, T., Solis-Herruzo, J.A., 2002, Sp1 and Sp3 transcription factors mediate malondialdehyde-induced collagen α1(I) gene expression in cultured hepatic stellate cells. J Biol Chem, 277: 30551–8.
Gil, F., Pla, A., Gonzalvo, M.C., Hernandez, A.F., Villanueva, E., 1993, Rat liver paraoxonase: subcellular distribution and characterization. Chem Biol Interact., 87(1–3): 149–54.
Gonzalvo, M.C., Gil, F., Hernandez, A.F., Rodrigo, L., Villanueva, E., Pla, A., 1998, Human liver paraoxonase (PON1): subcellular distribution and characterization. J Biochem Mol Toxicol., 12(1): 61–9.
Hassett, C., Richter, R.J., Humbert, R., Chapline, C., Crabb, J.W., Omiecinski, C.J., Furlong, C.E., 1991, Characterization of cDNA clones encoding rabbit and human serum paraoxonase: the mature protein retains its signal sequence. Biochemistry, 30(42): 10141–9.
He, X.M., Zhang, Z.X., Zhang, J.W., Zhou, Y.T., Tang, M.N., Wu, C.B., Hong, Z., 2006, Gln192Arg polymorphism in paraoxonase 1 gene is associated with Alzheimer disease in a Chinese Han ethnic population. Chin. Med. J., 119: 1204–9.
James, R.W., Deakin, S.P., 2004, The importance of high-density lipoproteins for paraoxonase-1 secretion, stability, and activity. Free Radic Biol Med, 37(12): 1986–94.
Janel, N., Christophe, O., Yayha-Graison, E.A., Hamelet, J., Paly, E., Prieur, M., Delezoïde, A.L., Delabar, J.M., 2006, Paraoxonase-1expression is up-regulated in Down Syndromefetal liver. Biochem. Biophys. Res. Commun., 346: 1303–6.
Kalback, W., Esh, C., Castano, E.M., Rahman, E., Kokjohn, T., Luehrs, D.C., Sue, L., Cisneros, R., Gerber, F., Richardson, C., 2004, Atherosclerosis, vascular amyloidosis and brain hypoperfusion in the pathogenesis of sporadic Alzheimer’s disease. Neurol. Res., 26: 525–39.
Kawai, H., Sakamoto, F., Inoue, Y., 1990, Improved specific assay for serum arylesterase using a water-soluble substrate. Clin Chim Acta, 188(2): 177–82.
Kelada, S.N., Costa-Mallen, P., Checkoway, H., Viernes, H.A., Farin, F.M., Smith-Weller, T., Franklin, G.M., Costa, L.G., 2003, Paraoxonase 1 promoter and coding region polymorphisms in Parkinson’s disease. J. Neurol. Neurosurg. Psychiatry, 74: 545–8.
Kilic, S.S., Aydin, S., Kilic, N., Erman, F., Aydin, S., Celik, I., 2005, Serum arylesterase and paraoxonase activity in patients with chronic hepatitis. World J Gastroenterol, 11(46): 7351–4.
Lee, H.G., Castellani, R.J., Zhu, X., Perry, G., Smith, M.A., 2005, Amyloid-beta in Alzheimer’s disease: the horse or the cart? Pathogenic or protective? Int. J. Exp. Pathol., 86: 133–8.
Liao, Z., Graham, D.R., Hildreth, J.E., 2003, Lipid rafts and HIV pathogenesis: virion-associated cholesterol is required for fusion and infection of susceptible cells. AIDS Res. Hum. Retroviruses, 19: 675–87.
Mackness, M.I., Durrington, P.N., 1995, HDL, its enzyme and its potential to influence lipid peroxidation. Atherosclerosis, 115: 243–253.
Marsillach, J., Ferré, N., Vila, M.C., Lligoña, A., Mackness, B., Mackness, M., Deulofeu, R., Solá, R., Parés, A., Pedro-Botet, J., Joven, J., Camps, J., 2007, Serum paraoxonase-1 in chronic alcoholics: Relationship with liver disease. Clin Biochem, 40: 645–50.
Matsunaga, T., Iguchi, K., Nakajima, T., Koyama, I., Miyazaki, T., Inoue, I., Kawai, S., Katayama, S., Hirano, K., Hokari, S., Komoda, T., 2001, Glycated high-density lipoprotein induces apoptosis of endothelial cells via a mitochondrial dysfunction. Biochem Biophys Res Commun, 287(3): 714–20.
Mohs, R.C., 2005, The clinical syndrome of Alzheimer’s disease: aspects particularly relevant to clinical trials. Genes Brain Behav., 15: 129–33.
Nguyen, D.H., Hildreth, J.E., 2000, Evidence for budding of human immunodeficiency virus type I selectively from glycolipid-enriched membrane lipid rafts. J. Virol., 3264–72.
Nofer, J.R., Kehrel, B., Fobker, M., Levkau, B., Assman, G., von Eckardstein, A., 2002, HDL and arteriosclerosis: beyond reverse cholesterol transport. Atherosclerosis, 161: 1–16.
Owens, B., J., Anantharamaiah, G.M., Kahlin, J.B., Srinivas, R.V., Compans, R.W., Segrast, J.P., 1990, Apolipoprotein A-I and its amphipathic helix peptide analogues inhibit human immunodeficiency virus-induced syncytium formation. J. Clin. Invest., 86: 1142–50.
Paragh, G., Balla, P., Katona, E., Seres, I., Egerhazi, A., Degrell, I., 2002, Serum paraoxonase activity changes in patients with Alzheimer’s disease and vascular dementia. Eur. Arch. Psychiatry Clin. Neurosci., 252: 63–7.
Parra, S., Alonso-Villaverde, C., Coll, B., Ferré, N., Marsillach, J., Aragonès, G., Mackness, M., Mackness, B., Masana, L., Joven, J., Camps, J., Serum paraoxonase -1 activity and concentration are influenced by HIV infection 2007, Atherosclerosis, In press.
Pellin, M.C., Moretto, A., Lotti, M., Vilanova, E., 1990, Distribution and some biochemical properties of rat paraoxonase activity. Neurotoxicol Teratol, 12(6): 611–4.
Pola, R., Flex, A., Ciaburri, M., Rovella, E., Valiani, A., Reali, G., Silveri, M.C., Bernabei, R., 2005, Responsiveness to cholinesterase inhibitors in Alzheimer’s disease: A possible role for the 192 Q/R polymorphism of the PON-1 gene. Neurosci. Lett., 382: 338–41.
Pola, R., Gaetani, E., Flex, A., Gerardino, L., Aloi, F., Flore, R., Serricchio, M., Pola, P., Bernabei, R., 2003, Lack of association between Alzheimer’s disease and Gln-Arg 192 Q/R polymorphism of the PON1 gene in an Italian population. Dement. Geriatr. Cogn. Disord., 15: 88–91.
Primo-Parmo, S.L., Sorenson, R.C., Teiber, J., La Du, B.N, 1996, The human serum paraoxonase/arylesterase gene (PON1) is one member of a multigene family. Genomics, 33(3): 498–507.
Rao, M.N., Marmillot, P., Gong, M., Palmer, D.A., Seeff, L.B., Strader, D.B., Lakshman, M.R., 2003, Light, but not heavy alcohol drinking, stimulates paraoxonase by upregulating liver mRNA in rats and humans. Metabolism, 52(10): 1287–94.
Rodrigo, L., Hernandez, A.F., Lopez-Caballero, J.J., Gil, F., Pla, A., 2001, Immunohistochemical evidence for the expression and induction of paraoxonase in rat liver, kidney, lung and brain tissue. Implications for its physiological role. Chem Biol Interact, 137(2): 123–37.
Roher, A.E., Esh, C., Rahman, A., Kokjohn, T.A., Beach, T.G., 2004, Atherosclerosis of cerebral arteries in Alzheimer disease. Stroke, 35: 2623–7.
Rose, H., Woolley, I., Hoy, J., Dart, A., Bryant, B., Mijch, A., Sviridov, D., 2006, HIV infection and high-density lipoprotein: the effect of disease vs. the effect of treatment. Metabolism, 55: 90–5.
Rosenblat, M., Vaya, J., Shih, D., Aviram, M., 2005, Paraoxonase 1 (PON1) enhances HDL-mediated macrophage cholesterol efflux via the ABCA1 transporter in association with increased HDL binding to the cells: a possible role for lysophosphatidylcholine. Atherosclerosis, 179: 69–77.
Sabesin, S.M., 1981, Lipid and lipoprotein abnormalities in alcoholic liver disease. Circulation, 64: 1172–84.
Sabesin, S.M., Hawkins, H.L., Kuiken, L., Ragland, J.B., 1997, Abnormal plasma lipoproteins and lecithin-cholesterol acyltransferase deficiency in alcoholic liver disease. Gastroenterology, 72: 510–8.
Saeed, M., Siddique, N., Hung, W.Y., Usacheva, E., Liu, E., Sufit, R.L., Heller, S.L., Haines, J.L., Pericak-Vance, M., Siddique, T., 2006, Paraoxonase cluster polymorphisms are associated with sporadic ALS. Neurology, 67: 771–6.
Scacchi, R., Gambina, G., Martini, M.C., Broggio, E., Vilardo, T., Corbo, R.M., 2003, Different pattern of association of paraoxonase Gln192-Arg polymorphism with sporadic late-onset Alzheimer’s disease and coronary artery disease. Neurosci. Lett., 339: 17–20.
Sebastiani, G., Alberti, A., 2006, Non invasive fibrosis biomarkers reduce but not substitute the need for liver biopsy. World J Gastroenterol, 12(23): 3682–94.
Shi, J., Zhang, S., Tang, M., Liu, X., Li, T., Han, H., Wang, Y., Guo, Y., Zhao, J., Li, H., Ma, C., 2004, Possible association between Cys311Ser polymorphism of paraoxonase 2 gene and late-onset Alzheimer’s disease in Chinese. Brain Res. Mol. Brain Res., 120: 201–4.
Sierksma, A., van der Gaga, M.S., van Tol, A., James, R.W., Hendriks, F.J., 2002, Kinetics of HDL cholesterol and paraoxonase activity in moderate alcohol consumers. Alcohol Clin Exp Res, 26: 1430–5.
Sinan, S., Kockar, F., Arslan, O., 2006, Novel purification strategy for human PON1 and inhibition of the activity by cephalosporin and aminoglikozide derived antibiotics. Biochemie, 88: 565–74.
Slowik, A., Tomik, B., Wolkow, P.P., Partyka, D., Turaj, W., Malecki, M.T., Pera, J., Dziedzic, T., Szczudlik, A., Figlewicz, D.A., 2006, Paraoxonase gene polymorphisms and sporadic ALS. Neurology, 67: 766–70.
Sorenson, R.C., Bisgaier, C.L., Aviram, M., Hsu, C., Billecke, S., La Du, B.N., 1999, Human serum paraoxonase/arylesterase’s retained hydrophobic N-terminal leader sequence associates with HDL binding phospholipids: apolipoprotein A-I stabilizes activity. Arterioscler Thromb Vasc Biol, 19: 2214–25.
Sorenson, R.C., Primo-Parmo, S.L., Kuo, C.L., Adkins, S., Lockridge, O., La Du, B.N., 1995, Reconsideration of the catalytic center and mechanism of mammalian paraoxonase/arylesterase. Proc Natl Sci USA, 92: 7187–91.
Stanbridge, J.B., 2004, Pharmacotherapeutic approaches to the treatment of Alzheimer’s disease. Clin. Ther., 26: 615–30.
Sugano, M., Tsuchida, K., Makino, N., 2000, High-density lipoprotens protect endothelial cells from tumor necrosis factor-a-induced apoptosis. Biochem Biophys Res Commun, 272: 872–876.
Tahl, D.R., Ghebremedhin, E., Orantes, M., Wiestler, O.D., 2003, Vascular pathology in Alzheimer disease: correlation of cerebral amyloid angiopathy and arteriosclerosis/lipohyalinosis with cognitive decline. J. Neuropathol. Exp. Neurol., 62: 1287–301.
Tanikawa, K., Torimura, T., 2006, Studies on oxidative stress in liver diseases: important trends in liver research. Med Mol Morphol, 39: 22–7.
Turner, P., Miller, N., Chrystie, I., Coltart, J., Mistry, P., Nicoll, A., Lewis, B., 1979, Splanchnic production of discoidal plasma high-density lipoprotein in man. Lancet, 24: 645–6.
Wang, J., Liu, Z., 2000, No association between paraoxonase 1 (PON1) gene polymorphism and susceptibility to Parkinson’s disease in a Chinese population. Mov. Disord., 15: 1265–7.
Watson, A.D., Berliner, J.A., Hama, S.Y., La Du, B.N., Faull, K.F., Fogelman, A.M., Navab, M., 1995, Protective effect of high density lipoprotein associated paraoxonase. Inhibition of the biological activity of minimally oxidized low density lipoprotein. J Clin Invest, 96: 2882–2891.
Xu, G.Y., Lv, G.C., Chen, Y., Hua, Y.C., Zhu, S.M., Yang, Y.D., 2005, Monitoring the level of serum paraoxonase 1 activity in liver transplantation patients. Hepatobiliary Pancreat Dis Int, 4(2): 178–81.
Zintzaras, E., Hadjigeorgiou, G.M., 2004, Association of paraoxonase 1 gene polymorphisms with risk of Parkinson’s disease: a meta-analysis. J. Hum. Genet., 49: 474–81.
Zuliani, G., Zanca, R., Munari, M.R., Zurlo, A., Vavalle, C., Atti, A.R., Fellin, R., 2001, Genetic polymorphisms in older subjects with vascular or Alzheimer’s dementia. Acta Neurol. Scand., 103: 304–8.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2008 Springer
About this chapter
Cite this chapter
Marsillach, J. et al. (2008). Paraoxonase-1 in Chronic Liver Diseases, Neurological Diseases and HIV Infection. In: Mackness, B., Mackness, M., Aviram, M., Paragh, G. (eds) The Paraoxonases: Their Role in Disease Development and Xenobiotic Metabolism. Proteins And Cell Regulation, vol 6. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6561-3_12
Download citation
DOI: https://doi.org/10.1007/978-1-4020-6561-3_12
Publisher Name: Springer, Dordrecht
Print ISBN: 978-1-4020-6560-6
Online ISBN: 978-1-4020-6561-3
eBook Packages: MedicineMedicine (R0)