Behavior of Selenium and Selenium-Dependent Glutathione Peroxidase Activity in Cystic Fibrosis

Authors

DOI:

https://doi.org/10.33448/rsd-v9i4.2689

Keywords:

Glutathione peroxidase; Selenium; Cystic fibrosis.

Abstract

To investigate in the literature the behavior of different levels of selenium and the activity of glutathione peroxidase (GPx-Se) observed in patients with cystic fibrosis. This is an integrative literature review, carried out by searching for original articles, with no year limit, in English and Portuguese, indexed in the PubMed, Scopus and Web of Science databases. 56 articles were retrieved, of which 16.1% (n = 9) were included in this review, for reading the full text. It was observed that of the studies compiled, 33.3% (n=3) identified a reduction in the selenium concentrations, as well as in the GPx activity, although 11.1% (n=1) reported an increase only in the plasma concentrations of the mineral, and another 22.2% (n=2), added by GPx. On the other hand, 33.3% (n=3) of the studies did not find any significant differences regarding these parameters compared between the control group and the group with cystic fibrosis. It is concluded that the levels of selenium and the activity of the enzyme Glutathione Peroxidase Dependent on Selenium (GPx-Se) can present different behaviors in conditions of Cystic Fibrosis (CF), however, the fragile reasoning, which justify controversial and little results consistent, reinforces the need for further studies to deepen the theme.

References

Athanazio, R. A., Silva Filho, L. V. R. F., Vergara, A. A., Ribeiro, A. F., Riedi, C. A., Procianoy, E. D. F. A., ... & Fuccio, M. B. D. (2017). Diretrizes brasileiras de diagnóstico e tratamento da fibrose cística. Jornal brasileiro de pneumologia, 43(3), 219-245.

Benabdeslam, H., Abidi, H., Garcia, I., Bellon, G., Gilly, R., & Revol, A. (1999). Lipid peroxidation and antioxidant defenses in cystic fibrosis patients. Clinical chemistry and laboratory medicine, 37(5), 511-516.

Bernardi, D. M., Ribeiro, A. F., Mazzola, T. N., Vilela, M. M., & Sgarbieri, V. C. (2013). O impacto da fibrose cística no perfil imunológico de pacientes pediátricos. Jornal de Pediatria, 89(1), 40-47.

Brasil. (2017). Fibrose cística. Ministério da Saúde. Recuperado de http://www.saude.gov.br/acoes-e-programas/programa-nacional-da-triagem-neonatal/fibrose-cistica-fc.

Carmagnol, F., Sinet, P. M., Lenoir, G., Nicole, A., Rapin, J., & Jerome, H. (1983). Absence of modifications of the enzyme defense system against oxygen toxicity in cystic fibrosis. Pediatric research, 17(3), 181-182.

Castillo, R., Landon, C., Eckhardt, K., Morris, V., Levander, O., & Lewiston, N. (1981). Selenium and vitamin E status in cystic fibrosis. The Journal of pediatrics, 99(4), 583-585.

Ciofu, O., & Lykkesfeldt, J. (2014). Antioxidant supplementation for lung disease in cystic fibrosis. Cochrane Database of Systematic Reviews, (8).

Dworkin, B. R. A. D., Newman, L. J., Berezin, S., Rosenthal, W. S., Schwarz, S. M., & Weiss, L. (1987). Low blood selenium levels in patients with cystic fibrosis compared to controls and healthy adults. Journal of Parenteral and Enteral Nutrition, 11(1), 38-41.

De Cássia Firmida, M., & Lopes, A. J. (2011). Aspectos epidemiológicos da fibrose cística. Revista Hospital Universitário Pedro Ernesto, 10(4).

Galli, F., Battistoni, A., Gambari, R., Pompella, A., Bragonzi, A., Pilolli, F., ... & Cabrini, G. (2012). Oxidative stress and antioxidant therapy in cystic fibrosis. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, 1822(5), 690-713.

Grupo Brasileiro De Estudos De Fibrose Cística. (2014). Registro Brasileiro de Fibrose Cística 2014. Recuperado de http://portalgbefc.org.br/wpcontent/uploads/2016/11/Registro2014_v09.pdf.

Heinrich, H. C., Gabbe, E. E., Bartels, H., Oppitz, K. H., Bender-Götze, C., & Pfau, A. A. (1977). Bioavailability of food iron-(59 Fe), vitamin B 12-(60 Co) and protein bound selenomethionine-(75 Se) in pancreatic exocrine insufficiency due to cystic fibrosis. Klinische Wochenschrift, 55(12), 595-601.

Homnick, D. N., Cox, J. H., DeLoof, M. J., & Ringer, T. V. (1993). Carotenoid levels in normal children and in children with cystic fibrosis. The Journal of pediatrics, 122(5), 703-707.

Jardilino, J. R.; Rossi, G.; & Santos, G. T. (2000). Orientações Metodológicas para elaboração de trabalhos acadêmicos. São Paulo: Gion.

Lloyd-Still, J. D., & Ganther, H. E. (1980). Selenium and glutathione peroxidase levels in cystic fibrosis. Pediatrics, 65(5), 1010-1012.

Mahan, L. K., & Escott-Stump, S. (2018). Krause, alimentos, nutrição & dietoterapia (14a ed.). São Paulo: Roca.

Mendes, K. D. S.; Silveira, R. C. C. P.; & Galvao, C. M. (2008). Revisão integrativa: método de pesquisa para a incorporação de evidências na saúde e na enfermagem. Texto contextoenferm, 17(4), 758-764.4.

Martin, S. L., Saint-Criq, V., Hwang, T. C., & Csanády, L. (2018). Ion channels as targets to treat cystic fibrosis lung disease. Journal of Cystic Fibrosis, 17(2), S22-S27.

Mowbray, P. K., Wilkinson, A., & Tse, H. H. (2015). An integrative review of employee voice: Identifying a common conceptualization and research agenda. International Journal of Management Reviews, 17(3), 382-400.

Neve, J., Geffel, R. V., Hanocq, M., & Molle, L. (1983). Plasma and erythrocyte zinc, copper and selenium in cystic fibrosis. Acta Paediatrica, 72(3), 437-440.

Pereira, A. S., Shitsuka, D. M., Parreira, F. J., & Shitsuka, R. (2018). Metodologia da pesquisa científica.[e-book]. Santa Maria. Ed. UAB/NTE/UFSM. Disponível em: https://repositorio. ufsm. br/bitstream/handle/1/15824/Lic_Computacao_Metodologia-Pesquisa-Cientifica. pdf.

Portal, B., Richard, M. J., Ducros, V., Aguilaniu, B., Brunel, F., Faure, H., ... & Favier, A. (1993). Effect of double-blind crossover selenium supplementation on biological indices of selenium status in cystic fibrosis patients. Clinical chemistry, 39(6), 1023-1028.

Portal, B. C., Richard, M. J., Faure, H. S., Hadjian, A. J., & Favier, A. E. (1995). Altered antioxidant status and increased lipid peroxidation in children with cystic fibrosis. The American journal of clinical nutrition, 61(4), 843-847.

Rover Júnior, L., Höehr, N. F., Vellasco, A. P., & Kubota, L. T. (2001). Sistema antioxidante envolvendo o ciclo metabólico da glutationa associado a métodos eletroanalíticos na avaliação do estresse oxidativo. Química Nova, 24(1), 112-119.

Santos, C. M. D. C., Pimenta, C. A. D. M., & Nobre, M. R. C. (2007). A estratégia PICO para a construção da pergunta de pesquisa e busca de evidências. Revista Latino-Americana de Enfermagem, 15(3), 508-511.

Sagel, S. D., Khan, U., Jain, R., Graff, G., Daines, C. L., Dunitz, J. M., ... & Clancy, J. P. (2018). Effects of an antioxidant-enriched multivitamin in cystic fibrosis. a randomized, controlled, multicenter Clinical trial. American journal of respiratory and critical care medicine, 198(5), 639-647.

Thomas, A. G., Miller, V., Shenkin, A., Fell, G. S., & Taylor, F. (1994). Selenium and glutathione peroxidase status in paediatric health and gastrointestinal disease. Journal of pediatric gastroenterology and nutrition, 19(2), 213-219.

Van Caillie‐Bertrand, M., De Biéville, F., Neijens, H., Kerrebijn, K., Fernandes, J., & Degenhart, H. (1982). Trace metals in cystic fibrosis. Acta Pædiatrica, 71(2), 203-207.

Winklhofer-Roob, B. M., Tiran, B., Tuchschmid, P. E., van’t Hof, M. A., & Shmerling, D. H. (1998). Effects of pancreatic enzyme preparations on erythrocyte glutathione peroxidase activities and plasma selenium concentrations in cystic fibrosis. Free Radical Biology and Medicine, 25(2), 242-249.

Winklhofer‐Roob, B. M. (1994). Oxygen free radicals and antioxidants in cystic fibrosis: the concept of an oxidant‐antioxidant imbalance. Acta Paediatrica, 83, 49-57.

Wood, L. G., Fitzgerald, D. A., Lee, A. K., & Garg, M. L. (2003). Improved antioxidant and fatty acid status of patients with cystic fibrosis after antioxidant supplementation is linked to improved lung function. The American journal of clinical nutrition, 77(1), 150-159.

Wood, L. G., Fitzgerald, D. A., Gibson, P. G., Cooper, D. M., & Garg, M. L. (2002). Increased plasma fatty acid concentrations after respiratory exacerbations are associated with elevated oxidative stress in cystic fibrosis patients. The American journal of clinical nutrition, 75(4), 668-675.

Published

20/03/2020

How to Cite

SILVA, A. G. S.; DANTAS, L. S. A.; NOGUEIRA, T. R.; FREITAS, B. de J. e S. de A. Behavior of Selenium and Selenium-Dependent Glutathione Peroxidase Activity in Cystic Fibrosis. Research, Society and Development, [S. l.], v. 9, n. 4, p. e86942689, 2020. DOI: 10.33448/rsd-v9i4.2689. Disponível em: https://rsdjournal.org/index.php/rsd/article/view/2689. Acesso em: 22 dec. 2024.

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Section

Review Article