Araştırma Makalesi
BibTex RIS Kaynak Göster

Akut Bronşiolitli Çocuklarda Human Paraoksonaz-1 Aktivitesi

Yıl 2020, Cilt: 18 Sayı: 3, 336 - 345, 18.12.2020

Öz

GİRİŞ ve AMAÇ: Human paraoksonaz-1 (PON1), oksidatif strese karşı çalışan endojen antioksidan moleküllerden biridir. Bu çalışmada akut bronşiolitli çocuklarda serum PON1 aktivitesini araştırmayı amaçladık.

YÖNTEM ve GEREÇLER: Akut bronşiyolitli 3-21 aylık 29 çocuk ile yaş uyumlu 35 sağlıklı kontrol çalışmaya dahil edildi. Bronşiolit hastaları hafif (% 65) ve orta (% 35) olarak sınıflandırıldı. Akut bronşiolitli hastalar ile kontrol grubu arasında PON1'in paraoksonaz ve arilesteraz aktiviteleri karşılaştırıldı.

BULGULAR: Akut bronşiyolitli çocukların paraoksonaz aktivitesi sağlıklı kontrollere göre daha düşüktü, ancak fark anlamlı değildi (127.53 ± 64.17 U / L'ye karşı 153.95 ± 74.40 U / L) (p = 0.13). Hafif ve orta derecede bronşiyolitli çocuklarda arilesteraz aktivitesi kontrol grubuna göre anlamlı olarak daha azdı (142.43 ± 56.60 kU / L ve 103.05 ± 26.03 kU / L'ye karşılık 201.09 ± 57.26 kU / L) (p <0.001).

TARTIŞMA ve SONUÇ: Akut bronşiolitli çocuklarda serum PON1 aktivitesi kontrol grubuna göre daha düşüktü. Antioksidan kapasitenin arttırılması, viral kaynaklı akciğer hastalığında etkili bir tedavi aracı olabilir

Kaynakça

  • 1. 1. Carroll KN, Gebretsadik T, Griffin MR, et al. Increasing burden and risk factors for bronchiolitis-related medical visits in infants enrolled in a state health care insurance plan. Pediatrics 2008;122:58-64.
  • 2. 2. Ali S, Plint AC, Klassen TP. 2012. Bronchiolitis; in Wilmott RW, Boat TF, Bush A, Chernick V, Deterding RR, Ratjen F (eds). Kendig and Chernick’s Disorders of the Respiratory Tract in Children; 2012. pp. 443–52.
  • 3. 3. Ciencewicki J, Trivedi S, Kleeberger SR. Oxidants and the pathogenesis of lung diseases. J Allergy Clin Immunol 2008; 122:456-68.
  • 4. 4. Park HS, Kim SR, Lee YC. Impact of oxidative stress on lung diseases. Respirology 2009;14:27-38.
  • 5. 5. Owen S, Pearson D, Suarez-Mendez V, et al. Evidence of free-radical activity in asthma. N Engl J Med 1991;325:586-7.
  • 6. 6. Cemek M, Caksen H, Bayiroğlu F, et al. Oxidative stress and enzymic-non-enzymic antioxidant responses in children with acute pneumonia. Cell Biochem Funct 2006;24:269-73.
  • 7. 7. Hosakote YM, Jantzi PD, Esham DL, et al. Viral-mediated inhibition of antioxidant enzymes contributes to the pathogenesis of severe respiratory syncytial virus bronchiolitis. Am J Respir Crit Care Med 2011;183:1550-60.
  • 8. 8. Gurkan F, Atamer Y, Ece A, et al. Relationship among serum selenium levels, lipid peroxidation, and acute bronchiolitis in infancy. Biol Trace Elem Res 2004;100:97-104.
  • 9. 9. Halliwell B. Antioxidants in human health and disease. Annu Rev Nutr 1996;16: 33-50.
  • 10. 10. Van Himbergen TM, Van Tits LJ, Roest M, et al. The story of PON1: how an organophosphate-hydrolysing enzyme is becoming a player in cardiovascular medicine. Neth J Med 2006;64;34-8.
  • 11. 11. Blatter MC, James RW, Messmer S, et al. Identification of a distinct human high-density lipoprotein subspe¬cies defined by a lipoprotein-associated protein, K-45. Identity of K-45 with paraoxonase. Eur J Biochem 1993;211:871–9.
  • 12. 12. Rodrigo L, Hernández AF, López-Caballero JJ, et al. 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 2001;137:123-37.
  • 13. 13. Apostolou F, Gazi IF, Lagos K, et al. Acute infection with Epstein-Barr virus is associated with atherogenic lipid changes. Atherosclerosis 2010;212:607-13.
  • 14. 14. Selek S, Cosar N, Kocyigit A, et al. PON1 activity and total oxidant status in patients with active pulmonary tuberculosis. Clin Biochem 2008;41:140-4.
  • 15. 15. Aslan M, Nazligul Y, Horoz M, et al. Serum paraoxonase-1 activity in Helicobacter pylori infected subjects. Atherosclerosis 2008;196:270-4.
  • 16. 16. Górnicka G, Bełtowski J, Wójcicka G, et al. Serum paraoxonase activity, total antioxidant potential and lipid peroxidation products in children with bronchial asthma exacerbation. Wiad Lek 2002;55:257-63.
  • 17. 17. Koc S, Aksoy N, Bilinc H, et al. Paraoxonase and arylesterase activity and total oxidative/ anti-oxidative status in patients with chronic adenotonsillitis. Int J Pediatr Otorhinolaryngol 2011;75:1364-7.
  • 18. 18 Lakhanpaul M, Armon K, Eccleston P, et al. An evidence based guideline for the management of children presenting with acute breathing difficulty. Nottingham University, Available from; http://www.nottingham.ac.uk/paediatric-guideline/breathingguideline.pdf Accessed, 15 March 2019.
  • 19. 19. Ozturk E, Balat O, Dikensoy E, et al. No association between serum paraoxonase, arylesterase activities, and hydatidiform mole. Int J Gynecol Cancer 2011;21:149- 52.
  • 20. 20. Mackness MI, Arrol S, Abbot C, et al. Protection of low-density lipoprotein against oxidative modification by high-density lipoprotein associated paraoxonase. Atherosclerosis 1993;104:129-35.
  • 21. 21. Aviram M, Rosenblat M. Paraoxonases 1, 2, and 3, oxidative stress, and macrophage foam cell formation during atherosclerosis development. Free Radic Biol Med 2004;37:1304-16.
  • 22. 22. Van Lenten BJ, Wagner AC, Nayak DP, et al. High-density lipoprotein loses its anti-inflammatory properties during acute influenza A infection. Circulation 2001;103:2283-8.
  • 23. 23. Campbell LA, Yaraei K, Van Lenten B. The acute phase reactant response to respiratory infection with Chlamydia pneumoniae: implications for the pathogenesis of atherosclerosis. Microbes Infect 2010;12:598-606.
  • 24. 24. Rosenblat M, Gaidukov L, Khersonsky O, et al. The catalytic histidine dyad of high density lipopro¬tein-associated serum paraoxonase-1 (PON1) is essential for PON1-mediated inhibition of low density lipoprotein oxidation and stimu¬lation of macrophage cholesterol efflux. J Biol Chem 2006;281:7657–65.
  • 25. 25. Khersonsky O, Tawfik DS. Structure-reactivity studies of serum paraoxonase PON1 suggest that its native activity is lactonase. Biochemistry 2005;44:6371-82.
  • 26. 26. Camps J, Pujol I, Ballester F, et al. Paraoxonases as potential antibiofilm agents: their relationship with quorum-sensing signals in Gram-negative bacteria. Antimicrob Agents Chemother 2011;55:1325-31.
  • 27. 27. Nguyen SD, Sok DE. Oxidative inactivation of paraoxonase 1, an antioxidant protein and its effect on antioxidant action. Free Radic Res 2003;37:1319-30.
  • 28. 28. James RW, Deakin SP. The importance of high-density lipoproteins for paraoxonase-1 secretion, stability, and activity. Free Radic Biol Med 2004;37:1986-94.
  • 29. 29. Gruber M, Christ-Crain M, Stolz D, et al. Prognostic impact of plasma lipids in patients with lower respiratory tract infections - an observational study. Swiss Med Wkly 2009;139:166-72.
  • 30. 30. Novak F, Vavrova L, Kodydkova J, et al. Decreased paraoxonase activity in critically ill patients with sepsis. Clin Exp Med 2010;10:21-5.
  • 31. 31. Aviram M, Rosenblat M, Billecke S, et al. Human serum paraoxonase (PON1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants. Free Radic Biol Med 1999;26:892-904.
  • 32. 32. Da Costa LA, Badawi A, El-Sohemy A. Nutrigenetics and modulation of oxidative stress. Ann Nutr Metab 2012; 60 Suppl 3:27-36. Epub 2012 May 15.
  • 33. 33. Kunes JP, Cordero-Koning KS, Lee LH, Lynch SM. Vitamin C attenuates hypochlorite-mediated loss of paraoxonase-1 activity from human plasma. Nutr Res 2009;29:114-22.
  • 34. 34. Bose KS, Agrawal BK. Effect of lycopene from cooked tomatoes on serum antioxidant enzymes, lipid peroxidation rate and lipid profile in coronary heart disease. Singapore Med J 2007;48:415-20.

Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis

Yıl 2020, Cilt: 18 Sayı: 3, 336 - 345, 18.12.2020

Öz

INTRODUCTION: Human paraoxonase-1 (PON1) is one of the endogenous antioxidant molecules working against oxidative stress. We aimed to investigate serum PON1 activity in children with acute bronchiolitis.

MATERIALS and METHODS: A total of 29 children aged between 3-21 months with acute bronchiolitis and 35 age-matched healthy controls were included in the study. Bronchiolitis patients were further classified as mild (65%) and moderate (35%). Paraoxonase and arylesterase activities of PON1 were compared between patients with acute bronchiolitis and the control group.

RESULTS: Paraoxonase activity of children with acute bronchiolitis was lower than healthy controls but the difference was not significant (127.53 ± 64.17 U/L versus 153.95 ± 74.40 U/L) (p=0.13). Arylesterase activity was significantly decreased in children with mild and moderate bronchiolitis in comparison to the control group (142.43± 56.60 kU/L and 103.70± 26.03 kU/L versus 201.09± 57.26 kU/L) (p<0.001).

CONCLUSIONS: Serum PON1 activity was lower in children with acute bronchiolitis compared to controls. Increasing antioxidant capacity may be an effective means of therapy in viral induced lung disease.

Kaynakça

  • 1. 1. Carroll KN, Gebretsadik T, Griffin MR, et al. Increasing burden and risk factors for bronchiolitis-related medical visits in infants enrolled in a state health care insurance plan. Pediatrics 2008;122:58-64.
  • 2. 2. Ali S, Plint AC, Klassen TP. 2012. Bronchiolitis; in Wilmott RW, Boat TF, Bush A, Chernick V, Deterding RR, Ratjen F (eds). Kendig and Chernick’s Disorders of the Respiratory Tract in Children; 2012. pp. 443–52.
  • 3. 3. Ciencewicki J, Trivedi S, Kleeberger SR. Oxidants and the pathogenesis of lung diseases. J Allergy Clin Immunol 2008; 122:456-68.
  • 4. 4. Park HS, Kim SR, Lee YC. Impact of oxidative stress on lung diseases. Respirology 2009;14:27-38.
  • 5. 5. Owen S, Pearson D, Suarez-Mendez V, et al. Evidence of free-radical activity in asthma. N Engl J Med 1991;325:586-7.
  • 6. 6. Cemek M, Caksen H, Bayiroğlu F, et al. Oxidative stress and enzymic-non-enzymic antioxidant responses in children with acute pneumonia. Cell Biochem Funct 2006;24:269-73.
  • 7. 7. Hosakote YM, Jantzi PD, Esham DL, et al. Viral-mediated inhibition of antioxidant enzymes contributes to the pathogenesis of severe respiratory syncytial virus bronchiolitis. Am J Respir Crit Care Med 2011;183:1550-60.
  • 8. 8. Gurkan F, Atamer Y, Ece A, et al. Relationship among serum selenium levels, lipid peroxidation, and acute bronchiolitis in infancy. Biol Trace Elem Res 2004;100:97-104.
  • 9. 9. Halliwell B. Antioxidants in human health and disease. Annu Rev Nutr 1996;16: 33-50.
  • 10. 10. Van Himbergen TM, Van Tits LJ, Roest M, et al. The story of PON1: how an organophosphate-hydrolysing enzyme is becoming a player in cardiovascular medicine. Neth J Med 2006;64;34-8.
  • 11. 11. Blatter MC, James RW, Messmer S, et al. Identification of a distinct human high-density lipoprotein subspe¬cies defined by a lipoprotein-associated protein, K-45. Identity of K-45 with paraoxonase. Eur J Biochem 1993;211:871–9.
  • 12. 12. Rodrigo L, Hernández AF, López-Caballero JJ, et al. 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 2001;137:123-37.
  • 13. 13. Apostolou F, Gazi IF, Lagos K, et al. Acute infection with Epstein-Barr virus is associated with atherogenic lipid changes. Atherosclerosis 2010;212:607-13.
  • 14. 14. Selek S, Cosar N, Kocyigit A, et al. PON1 activity and total oxidant status in patients with active pulmonary tuberculosis. Clin Biochem 2008;41:140-4.
  • 15. 15. Aslan M, Nazligul Y, Horoz M, et al. Serum paraoxonase-1 activity in Helicobacter pylori infected subjects. Atherosclerosis 2008;196:270-4.
  • 16. 16. Górnicka G, Bełtowski J, Wójcicka G, et al. Serum paraoxonase activity, total antioxidant potential and lipid peroxidation products in children with bronchial asthma exacerbation. Wiad Lek 2002;55:257-63.
  • 17. 17. Koc S, Aksoy N, Bilinc H, et al. Paraoxonase and arylesterase activity and total oxidative/ anti-oxidative status in patients with chronic adenotonsillitis. Int J Pediatr Otorhinolaryngol 2011;75:1364-7.
  • 18. 18 Lakhanpaul M, Armon K, Eccleston P, et al. An evidence based guideline for the management of children presenting with acute breathing difficulty. Nottingham University, Available from; http://www.nottingham.ac.uk/paediatric-guideline/breathingguideline.pdf Accessed, 15 March 2019.
  • 19. 19. Ozturk E, Balat O, Dikensoy E, et al. No association between serum paraoxonase, arylesterase activities, and hydatidiform mole. Int J Gynecol Cancer 2011;21:149- 52.
  • 20. 20. Mackness MI, Arrol S, Abbot C, et al. Protection of low-density lipoprotein against oxidative modification by high-density lipoprotein associated paraoxonase. Atherosclerosis 1993;104:129-35.
  • 21. 21. Aviram M, Rosenblat M. Paraoxonases 1, 2, and 3, oxidative stress, and macrophage foam cell formation during atherosclerosis development. Free Radic Biol Med 2004;37:1304-16.
  • 22. 22. Van Lenten BJ, Wagner AC, Nayak DP, et al. High-density lipoprotein loses its anti-inflammatory properties during acute influenza A infection. Circulation 2001;103:2283-8.
  • 23. 23. Campbell LA, Yaraei K, Van Lenten B. The acute phase reactant response to respiratory infection with Chlamydia pneumoniae: implications for the pathogenesis of atherosclerosis. Microbes Infect 2010;12:598-606.
  • 24. 24. Rosenblat M, Gaidukov L, Khersonsky O, et al. The catalytic histidine dyad of high density lipopro¬tein-associated serum paraoxonase-1 (PON1) is essential for PON1-mediated inhibition of low density lipoprotein oxidation and stimu¬lation of macrophage cholesterol efflux. J Biol Chem 2006;281:7657–65.
  • 25. 25. Khersonsky O, Tawfik DS. Structure-reactivity studies of serum paraoxonase PON1 suggest that its native activity is lactonase. Biochemistry 2005;44:6371-82.
  • 26. 26. Camps J, Pujol I, Ballester F, et al. Paraoxonases as potential antibiofilm agents: their relationship with quorum-sensing signals in Gram-negative bacteria. Antimicrob Agents Chemother 2011;55:1325-31.
  • 27. 27. Nguyen SD, Sok DE. Oxidative inactivation of paraoxonase 1, an antioxidant protein and its effect on antioxidant action. Free Radic Res 2003;37:1319-30.
  • 28. 28. James RW, Deakin SP. The importance of high-density lipoproteins for paraoxonase-1 secretion, stability, and activity. Free Radic Biol Med 2004;37:1986-94.
  • 29. 29. Gruber M, Christ-Crain M, Stolz D, et al. Prognostic impact of plasma lipids in patients with lower respiratory tract infections - an observational study. Swiss Med Wkly 2009;139:166-72.
  • 30. 30. Novak F, Vavrova L, Kodydkova J, et al. Decreased paraoxonase activity in critically ill patients with sepsis. Clin Exp Med 2010;10:21-5.
  • 31. 31. Aviram M, Rosenblat M, Billecke S, et al. Human serum paraoxonase (PON1) is inactivated by oxidized low density lipoprotein and preserved by antioxidants. Free Radic Biol Med 1999;26:892-904.
  • 32. 32. Da Costa LA, Badawi A, El-Sohemy A. Nutrigenetics and modulation of oxidative stress. Ann Nutr Metab 2012; 60 Suppl 3:27-36. Epub 2012 May 15.
  • 33. 33. Kunes JP, Cordero-Koning KS, Lee LH, Lynch SM. Vitamin C attenuates hypochlorite-mediated loss of paraoxonase-1 activity from human plasma. Nutr Res 2009;29:114-22.
  • 34. 34. Bose KS, Agrawal BK. Effect of lycopene from cooked tomatoes on serum antioxidant enzymes, lipid peroxidation rate and lipid profile in coronary heart disease. Singapore Med J 2007;48:415-20.
Toplam 34 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular İç Hastalıkları
Bölüm Research Article
Yazarlar

Ufuk Erenberk Bu kişi benim 0000-0002-5481-8356

Feyza Ustabaş Kahraman

Mehmet Emin Özkaya 0000-0003-4553-819X

Mustafa Atilla Nursoy Bu kişi benim 0000-0003-0520-1082

Ayşegül Doğan Demir Bu kişi benim 0000-0002-2536-1422

Özden Türel Bu kişi benim 0000-0002-6535-4147

Yayımlanma Tarihi 18 Aralık 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 18 Sayı: 3

Kaynak Göster

APA Erenberk, U., Ustabaş Kahraman, F., Özkaya, M. E., Nursoy, M. A., vd. (t.y.). Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis. Güncel Pediatri, 18(3), 336-345. https://doi.org/10.32941/pediatri.841417
AMA Erenberk U, Ustabaş Kahraman F, Özkaya ME, Nursoy MA, Doğan Demir A, Türel Ö. Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis. Güncel Pediatri. 18(3):336-345. doi:10.32941/pediatri.841417
Chicago Erenberk, Ufuk, Feyza Ustabaş Kahraman, Mehmet Emin Özkaya, Mustafa Atilla Nursoy, Ayşegül Doğan Demir, ve Özden Türel. “Human Paraoxonase-1 Activity in Children With Acute Bronchiolitis”. Güncel Pediatri 18, sy. 3 t.y.: 336-45. https://doi.org/10.32941/pediatri.841417.
EndNote Erenberk U, Ustabaş Kahraman F, Özkaya ME, Nursoy MA, Doğan Demir A, Türel Ö Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis. Güncel Pediatri 18 3 336–345.
IEEE U. Erenberk, F. Ustabaş Kahraman, M. E. Özkaya, M. A. Nursoy, A. Doğan Demir, ve Ö. Türel, “Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis”, Güncel Pediatri, c. 18, sy. 3, ss. 336–345, doi: 10.32941/pediatri.841417.
ISNAD Erenberk, Ufuk vd. “Human Paraoxonase-1 Activity in Children With Acute Bronchiolitis”. Güncel Pediatri 18/3 (t.y.), 336-345. https://doi.org/10.32941/pediatri.841417.
JAMA Erenberk U, Ustabaş Kahraman F, Özkaya ME, Nursoy MA, Doğan Demir A, Türel Ö. Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis. Güncel Pediatri.;18:336–345.
MLA Erenberk, Ufuk vd. “Human Paraoxonase-1 Activity in Children With Acute Bronchiolitis”. Güncel Pediatri, c. 18, sy. 3, ss. 336-45, doi:10.32941/pediatri.841417.
Vancouver Erenberk U, Ustabaş Kahraman F, Özkaya ME, Nursoy MA, Doğan Demir A, Türel Ö. Human Paraoxonase-1 Activity in Children with Acute Bronchiolitis. Güncel Pediatri. 18(3):336-45.