SciELO - Scientific Electronic Library Online

SciELO - Scientific Electronic Library Online

Article References

FERREIRO-BARROS, Claudia Cristina; SUGAWARA, Eduardo Kinio  and  SANCHES, Livia Rentas. Determination of a method for extraction of coenzyme Q10 in human plasma: optimization of the use of surfactants and other variables. Einstein (São Paulo) [online]. 2012, vol.10, n.2, pp.203-208. ISSN 1679-4508.

    1. Rahman S, Clarke C., Hirano M. 176th ENMC International Workshop: Diagnosis and treatment of coenzyme Q10 deficiency. Neuromus Disord. 2012;22(1):76-86. [ Links ]

    2. Turunen M, Olsson J, Dallner G. Metabolism and function of coenzyme Q. Biochim Biophys Acta. 2004;1660(1-2):171-99. Review. [ Links ]

    3. Quinzii CM, DiMauro S, Hirano M. Human coenzyme Q10 deficiency. Neurochem Res. 2007;32(4-5):723-7. [ Links ]

    4. Ogasahara S, Engel AG, Frens D, Mack D. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy. Proc Natl Acad Sci U S A. 1989; 86(7):2379-82. [ Links ]

    5. Musumeci O, Naini A, Slonim AE, Skavin N, Hadjigeorgiou GL, Krawiecki N, ET al. Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Neurology. 2001;56(7):849-55. [ Links ]

    6. Montero R, Pineda M, Aracil A, Vilaseca MA, Briones P, Sánchez-Alcázar JA, ET al. Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency. Cerebellum. 2007;6(2):118-22. [ Links ]

    7. Salviati L, Sacconi S, Murer L, Zacchello G, Franceschini L, Laverda AM, et al.Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition. Neurology. 2005;65(4):606-8. [ Links ]

    8. Gironi M, Lamperti C, Nemni R, Moggio M, Comi G, Guerini FR, et al. Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency. Neurology. 2004;62(5):818-20. [ Links ]

    9. Lagier-Tourenne C, Tazir M, López LC, Quinzii CM, Assoum M, Drouot N, et al. ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency. Am J Hum Genet. 2008;82(3):661-72. [ Links ]

    10. Gin P, Clarke CF. Genetic evidence for a multi-subunit complex in coenzyme Q biosynthesis in yeast and the role of the Coq1 hexaprenyl diphosphate synthase. J Biol Chem. 2005;280(4):2676-81. [ Links ]

    11. Tzagoloff A, Dieckmann CL. PET genes of Saccharomyces cerevisiae. Microbiol Rev. 1990;54(3):211-25. [ Links ]

    12. Johnson A, Gin P, Marbois BN, Hsieh EJ, Wu M, Barros MH, et al. COQ9, a new gene required for the biosynthesis of coenzyme Q in Saccharomyces cerevisiae. J Biol Chem. 2005;280(36):31397-404. [ Links ]

    13. Barros MH, Johnson A, Gin P, Marbois BN, Clarke CF, Tzagoloff A. The Saccharomyces cerevisiae COQ10 gene encodes a START domain protein required for function of coenzyme Q in respiration. Biol Chem. 2005;280(52): 42627-35. [ Links ]

    14. Quinzii C, Naini A, Salviati L, Trevisson E, Navas P, Dimauro S, et al. A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency. Am J Hum Genet. 2006;78(2):345-9. [ Links ]

    15. Salviati L, Trevisson E, Rodriguez Hernandez MA, Casarin A, Pertegato V, Doimo M, et al. Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. J Med Genet. 2012;49(3):187-91. [ Links ]

    16. Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, et al. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest. 2011;121(5):2013-24. [ Links ]

    17. Mollet J, Delahodde A, Serre V, Chretien D, Schlemmer D, Lombes A, et al. CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. Am J Hum Genet. 2008;82(3):623-30. [ Links ]

    18. Duncan AJ, Bitner-Glindzicz M, Meunier B, Costello H, Hargreaves IP, López LC, et al. A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease. Am J Hum Genet. 2009;84(5):558-66. [ Links ]

    19. Mollet J, Giurgea I, Schlemmer D, Dallner G, Chretien D, Delahodde A, et al. Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. J Clin Invest. 2007;117(3):765-72. [ Links ]

    20. López LC, Schuelke M, Quinzii CM, Kanki T, Rodenburg RJ, Naini A, et al. Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations. Am J Hum Genet. 2006; 79(6):1125-9. [ Links ]

    21. Lamperti C, Naini AB, Lucchini V, Prelle A, Bresolin N, Moggio M, et al. Muscle coenzyme Q10 level in statin-related myopathy. Arch Neurol. 2005; 62(11):1709-12. [ Links ]

    22. Molyneux SL, Young JM, Florkowski CM, Lever M, George PM. Coenzyme q10: is there a clinical role and a case for measurement? Clin Biochem Rev. 2008;29(2):71-82. [ Links ]

    23. Ernster, L., Dallner, G. Biochemical, physiological and medical aspects of ubiquinone function. Biochim Biophys Acta. 1995;1271(1):195-204. [ Links ]

    24. Dimauro S, Rustin P. A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases. Biochim Biophys Acta. 2009;1792(12):1159-67. [ Links ]

    25. Kaikkonen J, Nyyssönen K, Salonen JT. Measurement and stability of plasma reduced, oxidized and total coenzyme Q10 in humans. Scand J Clin Lab Invest. 1999;59(6):457-66. [ Links ]

    26. Edlund PO. Determination of coenzyme Q10, alpha-tocopherol and cholesterol in biological samples by coupled-column liquid chromatography with coulometric and ultraviolet detection. J Chromatogr. 1988;425(1):87-97. [ Links ]

    27. Tang PH, Miles MV, DeGrauw A, Hershey A, Pesce A.HPLC analysis of reduced and oxidized coenzyme Q(10) in human plasma. Clin Chem. 2001;47(2):256-65. [ Links ]

    28. Littarru GP, Mosca F, Fattorini D, Bompadre S, Battino M. Assay of coenzyme Q10 in plasma by a single dilution step. Methods Enzymol. 2004;378:170-6. Review. [ Links ]

    29. Okamoto T, Fukunaga Y, Ida Y, Kishi T. Determination of reduced and total ubiquinones in biological materials by liquid chromatography with electrochemical detection. J Chromatogr. 1988;430(1):11-9. [ Links ]

    30. Kommuru TR, Khan MA, Ashraf M, Kattenacker R, Reddy IK. A simplified chromatographic method for quantitative determination of coenzyme Q10 in dog plasma. J Pharm Biomed Anal. 1998;16(6):1037-40. [ Links ]

    31. Takada M, IKenoya S,Yuzuriha T, Katayama K. Simultaneous determination of reduced and oxidezed coenzyme Q10 in human plasma. Methods Enzymol. 1984;105:147-55. [ Links ]

    32. Yamashita S, Yamamoto Y. Simultaneous detection of ubiquinol and ubiquinone in human plasma as a marker of oxidative stress. Anal Biochem. 1997;250(1):66-73. [ Links ]

    33. Wang Q, Lee BL, Ong CN. Automated high-performance liquid chromatographic method with precolumn reduction for the determination of ubiquinol and ubiquinone in human plasma. J Chromatogr B Biomed Sci Appl. 1999;726(1-2):297-302. [ Links ]

    34. Karpińska J, Mikołuć B, Motkowski R, Piotrowska-Jastrzebska J. HPLC method for simultaneous determination of retinol, alpha-tocopherol and coenzyme Q10 in human plasma. J Pharm Biomed Anal. 2006;42(2):232-6. [ Links ]

    35. Alleva R, Tomasetti M, Bompadre S, Littarru GP. Oxidation of LDL and their subfractions: kinetic aspects and CoQ10 content. Mol Aspects Med. 1997;18 Suppl:S105-12. [ Links ]

    36. Menke T, Niklowitz P, de Sousa G, Reinehr T, Andler W. Comparison of coenzyme Q10 plasma levels in obese and normal weight children. Clin Chim Acta. 2004;349(1-2):121-7. [ Links ]

    37. Hirota K, Kawase M, Kishie T. Effect of sodium dodecyl sulphate on the extraction of ubiquinone-10 in the determination of plasma samples. J Chromatogr. 1984;310(1):204-7. [ Links ]

    38. González-Mañas JM, Virto MD, Gurtubay JI, Goñi FM. The interaction of Triton X-100 with purple membranes. Detergent binding, spectral changes and membrane solubilization.Eur J Biochem. 1990;188(3):673-8. [ Links ]