Research Article
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Year 2021, Volume: 49 Issue: 1, 69 - 78, 01.01.2021
https://doi.org/10.15671/hjbc.728686

Abstract

References

  • 1. D.J. Shogilev, N. Duus, S.R. Odom, N.I. Shapiro, Diagnosing appendicitis: Evidence-based review of the diagnostic approach in 2014, West. J. Emerg. Med., 15 (2014) 859-871.
  • 2. Y. Albayrak, A. Albayrak, M. Celik, I. Gelincik, I. Demiryilmaz, R. Yildirim, B. Ozogul, High mobility group box protein-1 (HMGB-1) as a new diagnostic marker in patients with acute appendicitis, Scand. J. Trauma. Resusc. Emerg. Med., 20 (2011) 19-27.
  • 3. Y. Albayrak, A. Albayrak, F. Albayrak, R. Yildirim, B. Aylu, A. Uyanik, E. Kabalar, I.C. Güzel, Mean platelet volume: A new predictor in confirming acute appendicitis diagnosis, Clin. Appl. Thromb., 17 (2011) 362-366.
  • 4. M.L. Nance, W.T. Adamson, H.L. Hedrick, Appendicitis in the young child: A continuing diagnostic challenge, Pediatr. Emerg. Care., 16 (2000) 160–162.
  • 5. D.R. Flum, T. Koepsell, The clinical and economic correlates of misdiagnosed appendicitis: Nationwide analysis, Arch. Surg., 137 (2002) 799–804.
  • 6. F.M. Yilmaz, G. Yilmaz, M.F. Erol, S. Köklü, D. Yücel, Nitric oxide, lipid peroxidation and total thiol levels in acute appendicitis, J. Clin. Lab. Anal., 24 (2010) 63–66.
  • 7. H. SIES, Strategies of antioxidant defense, Eur. J. Biochem., 215 (1993) 213–219.
  • 8. V. Stojiljković, A. Todorović, N. Radlović, S. Pejić, M. Mladenović, J. Kasapović, S.B. Pajović, Antioxidant enzymes, glutathione and lipid peroxidation in peripheral blood of children affected by coeliac disease, Ann. Clin. Biochem., 44 (2007) 537-543.
  • 9. J.E. Klaunig, Y. Xu, J.S. Isenberg, S. Bachowski, K.L. Kolaja, J. Jiang, D.E. Stevenson, E.F. Walborg, The role of oxidative stress in chemical carcinogenesis, in: Environ. Health Perspect., 44 (1998) 239–267.
  • 10. S.L. de Oliveira Machado, M.D. Bagatini, P. da Costa, J. Baldissarelli, K.P. Reichert, L.S. de Oliveira, J.G. Lemos, T. Duarte, M.R. Chitolina Schetinger,. V.M. Morsch, Evaluation of mediators of oxidative stress and inflammation in patients with acute appendicitis, Biomarkers., 21 (2016) 530-537.
  • 11. C. Espinosa-Diez, V. Miguel, D. Mennerich, T. Kietzmann, P. Sánchez-Pérez, S. Cadenas, S. Lamas, Antioxidant responses and cellular adjustments to oxidative stress, Redox Biol., 6 (2015) 183-197.
  • 12. M.M. Işgör, Ş. Beydemir, Some cardiovascular therapeutics inhibit paraoxonase 1 (PON1) from human serum, Eur. J. Pharmacol., 645 (2010) 135-142.
  • 13. H. Paşaoǧlu, B. Sancak, N. Bukan, Lipid peroxidation and resistance to oxidation in patients with type 2 diabetes mellitus, Tohoku J. Exp. Med., 203 (2004) 211–218.
  • 14. M. Kaya, M.E. Boleken, T. Kanmaz, O. Erel, S. Yucesan, Total antioxidant capacity in children with acute appendicitis, Eur. J. Pediatr. Surg., 16 (2006) 34–38.
  • 15. P.M. Reddy YN, Murthy S, Krishna DR, Role of free radicals and antioxidants in tuberculosis patients., Indian J Tuberc., 51 (2004) 213–218. 16. A.S. Veskoukis, M.G. Nikolaidis, A. Kyparos, D. Kokkinos, C. Nepka, S. Barbanis, D. Kouretas, Effects of xanthine oxidase inhibition on oxidative stress and swimming performance in rats, Appl. Physiol. Nutr. Metab., 33 (2008) 1140–1154.
  • 17. J.W. Harvey, E. Beutler, Binding of heme by glutathione S-transferase: A possible role of the erythrocyte enzyme, Blood., 60 (1982) 1227–1230.
  • 18. M. Gubandru, D. Margina, C. Tsitsimpikou, N. Goutzourelas, K. Tsarouhas, M. Ilie, A.M. Tsatsakis, D. Kouretas, Alzheimer’s disease treated patients showed different patterns for oxidative stress and inflammation markers, Food Chem. Toxicol., 61 (2013) 209-214.
  • 19. F. Renault, E. Chabrière, J.P. Andrieu, B. Dublet, P. Masson, D. Rochu, Tandem purification of two HDL-associated partner proteins in human plasma, paraoxonase (PON1) and phosphate binding protein (HPBP) using hydroxyapatite chromatography, J. Chromatogr. B Anal. Technol. Biomed. Life Sci., 836 (2006) 15–21.
  • 20. M.L. Hu, Measurement of protein thiol groups and glutathione in plasma, Methods Enzymol., 233 (1994) 381–385.
  • 21. M.B. Grisham, Oxidants and free radicals in inflammatory bowel disease, Lancet., 344 (1994) 859–861.
  • 22. T. Grune, M.M. Berger, Markers of oxidative stress in ICU clinical settings: Present and future, Curr. Opin. Clin. Nutr. Metab. Care., 10 (2007) 712-717.
  • 23. R. Aktimur, A.K. Gokakin, K. Deveci, M. Atabey, O. Topcu, Oxidative stress markers in laparoscopic vs. open appendectomy for acute appendicitis: A double-blind randomized study, J. Minim. Access Surg., 12 (2016) 143-147.
  • 24. J.N. Moloney, T.G. Cotter, ROS signalling in the biology of cancer, Semin. Cell Dev. Biol., 80 (2018) 50–64.
  • 25. K. Yamamoto, P. Zhang, F. Miake, N. Kashige, Y. Aso, Y. Banno, H. Fujii, Cloning, expression and characterization of theta-class glutathione S-transferase from the silkworm, Bombyx mori, Comp. Biochem. Physiol. - B Biochem. Mol. Biol., 141 (2005) 340–346.
  • 26. J.L. Hearne, R.F. Colman, Contribution of the mu loop to the structure and function of rat glutathione transferase M1-1, Protein Sci., 15 (2006) 1277–1289.
  • 27. J. Han, E.J. Won, D.S. Hwang, J.S. Rhee, I.C. Kim, J.S. Lee, Effect of copper exposure on GST activity and on the expression of four GSTs under oxidative stress condition in the monogonont rotifer, Brachionus koreanus, Comp. Biochem. Physiol. - C Toxicol. Pharmacol., 158 (2013) 91–100.
  • 28. M. Sohail, A. Kaul, M. Raziuddin, T. Adak, Decreased glutathione-S-transferase activity: Diagnostic and protective role in vivax malaria, Clin. Biochem., 40 (2007) 377–382.
  • 29. M. Işık, Ş. Beydemir, A. Yılmaz, M.E. Naldan, H.E. Aslan, İ. Gülçin, Oxidative stress and mRNA expression of acetylcholinesterase in the leukocytes of ischemic patients, Biomed. Pharmacother., 87 (2017) 561-567.
  • 30. A. Canales, F.J. Sánchez-Muniz, Paraoxonase, something more than an enzyme?, Med. Clin. (Barc)., 121 (2003) 537-548. 31. H. Koksal, S. Kurban, Total oxidant status, total antioxidant status, and paraoxonase and arylesterase activities during laparoscopic cholecystectomy, Clinics., 65 (2010) 285-290.
  • 32. R. Esen, M. Aslan, M.E. Kucukoglu, A. Cıkman, U. Yakan, M. Sunnetcioglu, S. Selek, Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis, Wien. Klin. Wochenschr., 127 (2015) 427-433.
  • 33. E.G. Dumlu, M. Tokaç, B. Bozkurt, M.B. Yildirim, M. Ergin, A. Yalçin, M. Kiliç, Correlation between the serum and tissue levels of oxidative stress markers and the extent of inflammation in acute appendicitis, Clinics., 69 (2014) 677-682.
  • 34. H. Koksal, Total oxidant status, total antioxidant status, and paraoxonase activity in acute appendicitis, Turkish J. Trauma Emerg. Surg., 21 (2015) 139-42.
  • 35. M. Işık, Y. Demir, M. Kırıcı, R. Demir, F. Şimşek, Ş. Beydemir, Changes in the anti-oxidant system in adult epilepsy patients receiving anti-epileptic drugs, Arch. Physiol. Biochem., 121 (2015) 97-102.
  • 36. E.M.M. Ali, H.H. Shehata, R. Ali-Labib, L.M. Esmail Zahra, Oxidant and antioxidant of arylesterase and paraoxonase as biomarkers in patients with hepatitis C virus, Clin. Biochem., 42 (2009) 1394-1400.
  • 37. U. Koltuksuz, E. Uz, S. Özen, M. Aydinç, A. Karaman, Ö. Akyol, Plasma superoxide dismutase activity and malondialdehyde level correlate with the extent of acute appendicitis, Pediatr. Surg. Int., 16 (2000) 559-561.
  • 38. M. Abu-Hilal, M.J.W. McPhail, L. Marchand, C.D. Johnson, Malondialdehyde and superoxide dismutase as potential markers of severity in acute pancreatitis, J. Pancreas., 7 (2006) 185-192.
  • 39. C. Sen Tanrikulu, Y. Tanrikulu, M. Zafer Sabuncuoglu, M. Akif Karamercan, N. Akkapulu, F. Coskun, Mean platelet volume and red cell distribution width as a diagnostic marker in acute appendicitis, Iran. Red Crescent Med. J., 16 (2014) 10211.

The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis

Year 2021, Volume: 49 Issue: 1, 69 - 78, 01.01.2021
https://doi.org/10.15671/hjbc.728686

Abstract

It is known that free radicals, their products and reactive oxygen species (ROS) are associated with many diseases. The study focuses on both some changes in oxidative stress factors in patients with acute appendicitis (AA) and the changes of GST and PON1 enzyme activities in the metabolism. This study involved control group (n = 31) and the study group (n = 52). In the groups, some changes in oxidative stress factors and GST and PON1 enzyme activities which play an important role in metabolism were determined. There are changes in GST activity between study and control groups. The activity of the enzyme were significantly higher in AA groups (p < 0.01) than control. Malondialdehyde (MDA) levels in acute perforated appendicitis (PeA) groups were found significantly higher than control (p <0.01). There is a negative correlation between mean platelet volume (MPV) and lipid peroxidation in AA patients (r=-0.654, p<0.01). An increase in GSH production and GST activity provides an important defense mechanism against the oxidation of some macromolecules and may prevent oxidative stress in patients with appendicitis to some extent.

References

  • 1. D.J. Shogilev, N. Duus, S.R. Odom, N.I. Shapiro, Diagnosing appendicitis: Evidence-based review of the diagnostic approach in 2014, West. J. Emerg. Med., 15 (2014) 859-871.
  • 2. Y. Albayrak, A. Albayrak, M. Celik, I. Gelincik, I. Demiryilmaz, R. Yildirim, B. Ozogul, High mobility group box protein-1 (HMGB-1) as a new diagnostic marker in patients with acute appendicitis, Scand. J. Trauma. Resusc. Emerg. Med., 20 (2011) 19-27.
  • 3. Y. Albayrak, A. Albayrak, F. Albayrak, R. Yildirim, B. Aylu, A. Uyanik, E. Kabalar, I.C. Güzel, Mean platelet volume: A new predictor in confirming acute appendicitis diagnosis, Clin. Appl. Thromb., 17 (2011) 362-366.
  • 4. M.L. Nance, W.T. Adamson, H.L. Hedrick, Appendicitis in the young child: A continuing diagnostic challenge, Pediatr. Emerg. Care., 16 (2000) 160–162.
  • 5. D.R. Flum, T. Koepsell, The clinical and economic correlates of misdiagnosed appendicitis: Nationwide analysis, Arch. Surg., 137 (2002) 799–804.
  • 6. F.M. Yilmaz, G. Yilmaz, M.F. Erol, S. Köklü, D. Yücel, Nitric oxide, lipid peroxidation and total thiol levels in acute appendicitis, J. Clin. Lab. Anal., 24 (2010) 63–66.
  • 7. H. SIES, Strategies of antioxidant defense, Eur. J. Biochem., 215 (1993) 213–219.
  • 8. V. Stojiljković, A. Todorović, N. Radlović, S. Pejić, M. Mladenović, J. Kasapović, S.B. Pajović, Antioxidant enzymes, glutathione and lipid peroxidation in peripheral blood of children affected by coeliac disease, Ann. Clin. Biochem., 44 (2007) 537-543.
  • 9. J.E. Klaunig, Y. Xu, J.S. Isenberg, S. Bachowski, K.L. Kolaja, J. Jiang, D.E. Stevenson, E.F. Walborg, The role of oxidative stress in chemical carcinogenesis, in: Environ. Health Perspect., 44 (1998) 239–267.
  • 10. S.L. de Oliveira Machado, M.D. Bagatini, P. da Costa, J. Baldissarelli, K.P. Reichert, L.S. de Oliveira, J.G. Lemos, T. Duarte, M.R. Chitolina Schetinger,. V.M. Morsch, Evaluation of mediators of oxidative stress and inflammation in patients with acute appendicitis, Biomarkers., 21 (2016) 530-537.
  • 11. C. Espinosa-Diez, V. Miguel, D. Mennerich, T. Kietzmann, P. Sánchez-Pérez, S. Cadenas, S. Lamas, Antioxidant responses and cellular adjustments to oxidative stress, Redox Biol., 6 (2015) 183-197.
  • 12. M.M. Işgör, Ş. Beydemir, Some cardiovascular therapeutics inhibit paraoxonase 1 (PON1) from human serum, Eur. J. Pharmacol., 645 (2010) 135-142.
  • 13. H. Paşaoǧlu, B. Sancak, N. Bukan, Lipid peroxidation and resistance to oxidation in patients with type 2 diabetes mellitus, Tohoku J. Exp. Med., 203 (2004) 211–218.
  • 14. M. Kaya, M.E. Boleken, T. Kanmaz, O. Erel, S. Yucesan, Total antioxidant capacity in children with acute appendicitis, Eur. J. Pediatr. Surg., 16 (2006) 34–38.
  • 15. P.M. Reddy YN, Murthy S, Krishna DR, Role of free radicals and antioxidants in tuberculosis patients., Indian J Tuberc., 51 (2004) 213–218. 16. A.S. Veskoukis, M.G. Nikolaidis, A. Kyparos, D. Kokkinos, C. Nepka, S. Barbanis, D. Kouretas, Effects of xanthine oxidase inhibition on oxidative stress and swimming performance in rats, Appl. Physiol. Nutr. Metab., 33 (2008) 1140–1154.
  • 17. J.W. Harvey, E. Beutler, Binding of heme by glutathione S-transferase: A possible role of the erythrocyte enzyme, Blood., 60 (1982) 1227–1230.
  • 18. M. Gubandru, D. Margina, C. Tsitsimpikou, N. Goutzourelas, K. Tsarouhas, M. Ilie, A.M. Tsatsakis, D. Kouretas, Alzheimer’s disease treated patients showed different patterns for oxidative stress and inflammation markers, Food Chem. Toxicol., 61 (2013) 209-214.
  • 19. F. Renault, E. Chabrière, J.P. Andrieu, B. Dublet, P. Masson, D. Rochu, Tandem purification of two HDL-associated partner proteins in human plasma, paraoxonase (PON1) and phosphate binding protein (HPBP) using hydroxyapatite chromatography, J. Chromatogr. B Anal. Technol. Biomed. Life Sci., 836 (2006) 15–21.
  • 20. M.L. Hu, Measurement of protein thiol groups and glutathione in plasma, Methods Enzymol., 233 (1994) 381–385.
  • 21. M.B. Grisham, Oxidants and free radicals in inflammatory bowel disease, Lancet., 344 (1994) 859–861.
  • 22. T. Grune, M.M. Berger, Markers of oxidative stress in ICU clinical settings: Present and future, Curr. Opin. Clin. Nutr. Metab. Care., 10 (2007) 712-717.
  • 23. R. Aktimur, A.K. Gokakin, K. Deveci, M. Atabey, O. Topcu, Oxidative stress markers in laparoscopic vs. open appendectomy for acute appendicitis: A double-blind randomized study, J. Minim. Access Surg., 12 (2016) 143-147.
  • 24. J.N. Moloney, T.G. Cotter, ROS signalling in the biology of cancer, Semin. Cell Dev. Biol., 80 (2018) 50–64.
  • 25. K. Yamamoto, P. Zhang, F. Miake, N. Kashige, Y. Aso, Y. Banno, H. Fujii, Cloning, expression and characterization of theta-class glutathione S-transferase from the silkworm, Bombyx mori, Comp. Biochem. Physiol. - B Biochem. Mol. Biol., 141 (2005) 340–346.
  • 26. J.L. Hearne, R.F. Colman, Contribution of the mu loop to the structure and function of rat glutathione transferase M1-1, Protein Sci., 15 (2006) 1277–1289.
  • 27. J. Han, E.J. Won, D.S. Hwang, J.S. Rhee, I.C. Kim, J.S. Lee, Effect of copper exposure on GST activity and on the expression of four GSTs under oxidative stress condition in the monogonont rotifer, Brachionus koreanus, Comp. Biochem. Physiol. - C Toxicol. Pharmacol., 158 (2013) 91–100.
  • 28. M. Sohail, A. Kaul, M. Raziuddin, T. Adak, Decreased glutathione-S-transferase activity: Diagnostic and protective role in vivax malaria, Clin. Biochem., 40 (2007) 377–382.
  • 29. M. Işık, Ş. Beydemir, A. Yılmaz, M.E. Naldan, H.E. Aslan, İ. Gülçin, Oxidative stress and mRNA expression of acetylcholinesterase in the leukocytes of ischemic patients, Biomed. Pharmacother., 87 (2017) 561-567.
  • 30. A. Canales, F.J. Sánchez-Muniz, Paraoxonase, something more than an enzyme?, Med. Clin. (Barc)., 121 (2003) 537-548. 31. H. Koksal, S. Kurban, Total oxidant status, total antioxidant status, and paraoxonase and arylesterase activities during laparoscopic cholecystectomy, Clinics., 65 (2010) 285-290.
  • 32. R. Esen, M. Aslan, M.E. Kucukoglu, A. Cıkman, U. Yakan, M. Sunnetcioglu, S. Selek, Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis, Wien. Klin. Wochenschr., 127 (2015) 427-433.
  • 33. E.G. Dumlu, M. Tokaç, B. Bozkurt, M.B. Yildirim, M. Ergin, A. Yalçin, M. Kiliç, Correlation between the serum and tissue levels of oxidative stress markers and the extent of inflammation in acute appendicitis, Clinics., 69 (2014) 677-682.
  • 34. H. Koksal, Total oxidant status, total antioxidant status, and paraoxonase activity in acute appendicitis, Turkish J. Trauma Emerg. Surg., 21 (2015) 139-42.
  • 35. M. Işık, Y. Demir, M. Kırıcı, R. Demir, F. Şimşek, Ş. Beydemir, Changes in the anti-oxidant system in adult epilepsy patients receiving anti-epileptic drugs, Arch. Physiol. Biochem., 121 (2015) 97-102.
  • 36. E.M.M. Ali, H.H. Shehata, R. Ali-Labib, L.M. Esmail Zahra, Oxidant and antioxidant of arylesterase and paraoxonase as biomarkers in patients with hepatitis C virus, Clin. Biochem., 42 (2009) 1394-1400.
  • 37. U. Koltuksuz, E. Uz, S. Özen, M. Aydinç, A. Karaman, Ö. Akyol, Plasma superoxide dismutase activity and malondialdehyde level correlate with the extent of acute appendicitis, Pediatr. Surg. Int., 16 (2000) 559-561.
  • 38. M. Abu-Hilal, M.J.W. McPhail, L. Marchand, C.D. Johnson, Malondialdehyde and superoxide dismutase as potential markers of severity in acute pancreatitis, J. Pancreas., 7 (2006) 185-192.
  • 39. C. Sen Tanrikulu, Y. Tanrikulu, M. Zafer Sabuncuoglu, M. Akif Karamercan, N. Akkapulu, F. Coskun, Mean platelet volume and red cell distribution width as a diagnostic marker in acute appendicitis, Iran. Red Crescent Med. J., 16 (2014) 10211.
There are 37 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Articles
Authors

Ayetullah Temiz 0000-0003-2178-3369

Mesut Işık 0000-0002-4677-8104

Yavuz Albayrak 0000-0002-2535-4329

Hatice Esra Duran 0000-0003-2080-0091

Adem Aslan 0000-0002-9083-9306

Yeliz Demir 0000-0003-3216-1098

Ayse Albayrak 0000-0002-5133-0793

Mesut Işık 0000-0002-5480-1140

Şükrü Beydemir 0000-0003-3667-6902

Publication Date January 1, 2021
Acceptance Date October 27, 2020
Published in Issue Year 2021 Volume: 49 Issue: 1

Cite

APA Temiz, A., Işık, M., Albayrak, Y., Duran, H. E., et al. (2021). The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis. Hacettepe Journal of Biology and Chemistry, 49(1), 69-78. https://doi.org/10.15671/hjbc.728686
AMA Temiz A, Işık M, Albayrak Y, Duran HE, Aslan A, Demir Y, Albayrak A, Işık M, Beydemir Ş. The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis. HJBC. January 2021;49(1):69-78. doi:10.15671/hjbc.728686
Chicago Temiz, Ayetullah, Mesut Işık, Yavuz Albayrak, Hatice Esra Duran, Adem Aslan, Yeliz Demir, Ayse Albayrak, Mesut Işık, and Şükrü Beydemir. “The Role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis”. Hacettepe Journal of Biology and Chemistry 49, no. 1 (January 2021): 69-78. https://doi.org/10.15671/hjbc.728686.
EndNote Temiz A, Işık M, Albayrak Y, Duran HE, Aslan A, Demir Y, Albayrak A, Işık M, Beydemir Ş (January 1, 2021) The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis. Hacettepe Journal of Biology and Chemistry 49 1 69–78.
IEEE A. Temiz, M. Işık, Y. Albayrak, H. E. Duran, A. Aslan, Y. Demir, A. Albayrak, M. Işık, and Ş. Beydemir, “The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis”, HJBC, vol. 49, no. 1, pp. 69–78, 2021, doi: 10.15671/hjbc.728686.
ISNAD Temiz, Ayetullah et al. “The Role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis”. Hacettepe Journal of Biology and Chemistry 49/1 (January 2021), 69-78. https://doi.org/10.15671/hjbc.728686.
JAMA Temiz A, Işık M, Albayrak Y, Duran HE, Aslan A, Demir Y, Albayrak A, Işık M, Beydemir Ş. The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis. HJBC. 2021;49:69–78.
MLA Temiz, Ayetullah et al. “The Role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis”. Hacettepe Journal of Biology and Chemistry, vol. 49, no. 1, 2021, pp. 69-78, doi:10.15671/hjbc.728686.
Vancouver Temiz A, Işık M, Albayrak Y, Duran HE, Aslan A, Demir Y, Albayrak A, Işık M, Beydemir Ş. The role of the Cellular Antioxidant Defense System on Oxidative Stress in Acute Appendicitis. HJBC. 2021;49(1):69-78.

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