Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive

Yıl: 2019 Cilt: 26 Sayı: 7 Sayfa Aralığı: 1420 - 1425 Metin Dili: İngilizce DOI: 10.5455/annalsmedres.2019.05.236 İndeks Tarihi: 08-01-2020

Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive

Öz:
Aim: In this study we aimed to compare glutathione (GSH), adenosine deaminase(ADA), nitric oxide (NO) and malondialdehyde(MDA) values between the patients with and without different parasitic infections.Material and Methods: MDA, NO, ADA and GSH levels were studied in the serums of the patients group with T. gondii and cyst hydatidseropositivity and E. vermicularis and E. coli positive and the control group, while ADA levels alone were studied in G. intestinalis andDemodex spp.Results: There was a statistically significant difference between the groups in terms of the amounts of ADA, GSH, MDA, and NOaccording to results of the variance analysis (p<0.001).Conclusion: Given the change in the levels of GSH and ADA activities and MDA and NO levels observed in patients with parasiticinfection, over production of active neutrophils, macrophages, reactive oxygen radicals and reactive nitrogen species may be anindicator of accelerated oxidative stress and lipid peroxidation in these patients. Increased serum ADA activity in the group infectedby E. coli might be resulted from fight of the immune system with parasites. Low serum ADA activity in the other parasitic infectiongroups may be explained by suppression of lymphocyte proliferation by macrophages that were activated by sporozoite antigensin the late period of the infection. Accordingly, determination of the levels of MDA, NO, ADA and GSH may be important in treatmentfollow up and control of parasitic infections.
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  • 1. Kaya S, Sesli Çetin E, Akçam Z, et al. Entamoeba coli ve Blastocystis hominis saptanan olgularda klinik semptomlar. Türkiye Parazitol Derg 2005;29:229-31.
  • 2. Kuman A, Altıntaş N. Protozoon Hastalıkları. 1. baskı. İzmir: Ege Üniversitesi Basımevi, 1996.
  • 3. Kang K, Lee G, Lee J, et al. Effects of İNOS inhibitor on IFN-γ production and apoptosis of splenocytes in genetically different strains of mice infected with Toxoplasma gondii. Korean J Parasitol 2004;42:175-83.
  • 4. Nishikawa Y, Kawasa O, Vielemeyer O, et al. Toxoplasma gondii infection induces apoptosis in noninfected macrophages: role of nitric oxide and other soluble factors. Parasite Immunol 2007;29:375-85.
  • 5. Jareno EJ, Roma J, Romero B, et al. Serum malondialdehyde correlates with the rapeutice fficiency of high activity anti retroviral therapies (HAART) in HIV-1 infected children. Free Radic Res 2002;36:341-44.
  • 6. Hökelek M, Arıkoolu H. Biochemical, physiological properties and molecular biology of Echinococcus species. In: Altıntas N, Tınar R, Coker A, eds. Echinococcosis. 1st editon. Izmir: Hidatidol Association Publication; 2004. p. 87-106.
  • 7. Yildirim S, Nursal TZ, Tarim A, et al. A rare cause of acuteappendicitis: parasitic infection. Scand J Infect Dis 2005;37:757-9.
  • 8. Baima B, Sticherling M. Demodicidosis revisited. Acta DermVenereol 2002;82:3-6.
  • 9. Pena GP, Filho JSA. Is demodex really non-pathogenic? Rev Inst Med Trop Sao Paulo 2000;42:171-3.
  • 10. Akilov OE, Mumcuoglu KY. Immune response in demodicosis. J EurAcad Dermatol Venereol 2004;18:440-4.
  • 11. Kurt Ö, Ok ÜZ, Ertan P, Yüksel H. Antioksidan Maddeler ve Sıtma. Türkiye Parazitol Derg 2002;26:108-12.
  • 12. Markel EK, Voge M. Sings and symptoms of parasitic disease In: John DT, eds. Markel and Voge’s Medical Parasitology. 7st edition. Philedelphia, WB Sounders; 1992. p. 380-93.
  • 13. Amanvermez R, Çelik C. The superoxide dismutase in the hydatid cyst, glutathione, vitamin C, total antioxidant and total thiol levels. T Klin J Med Sci 2004;24:213-8.
  • 14. Maizel RM, Pearce EJ, Artis D, et al. Regulation of pathogenesis and immunity in helminth infections. JExp Med 2009;206:2059-66.
  • 15. Wilson MS1, Maizels RM. Regulation of allergy and autoimmunity in helminth infection. Clin Rev Allergy Immunol 2004;26:35-50.
  • 16. Ateş Y, Ergün H, Tüzün A, et al. The lymphocyte subgroups and serum adenonise deaminase levels in the patients with familial Mediterranean fever. Ankara Aca J Gastroent 2005;4:112-6.
  • 17. Del Rio D, Stewart AJ, Pellegrini N. A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stres. Nutrit Metabolism Cardiovascular Diseases 2005;5:316-28.
  • 18. Kolb H, Kolb-Bachofen V. Nitricoxide: a pathogenetic factor in autoimmunity. Immunol Today 1992;13:157-60.
  • 19. Liew FY. The role of nitric oxide in parasitic diseases. Ann Trop Med Parasitol 1993;87:637-42.
  • 20. Green H, Ishii K. On the existence of a guanine nucleotide trap. The role of adenosine kinase and a possible cause of excessive purine production in mammalian cells. J. Cell Sci 1972;11:173-7.
  • 21. Hasko G, Cronstein BN. Adenosine: an endogenous regulator of innate immunity. Trend Immunol 2004;25:33-9.
  • 22. Pisoschi AM, Pop A. The role of antioxidants in the chemistry of oxidative stress:Areview. Eur J Med Chem 2015;97: 55-74.
  • 23. Uchiyama M, Mihara M. Determination of malonaldehyde precursor in tissues by thiobarbituricacid test. Anal Biochem 1978; 34:271-8.
  • 24. Fairbanks V, Klee GG. Biochemical aspects of hematology. In: Tietz NW. Eds. Textbook of Clinical Chemistry. Philadelphia: WB Saunders, 1986. p. 1532-4.
  • 25. Cortas NK, Wakid NW. Determination of inorganic nitrate in serum andurineby a kinetic cadmium reduction method. Clin Chem 1990;36:1440-3.
  • 26. Ellis G, Goldberg DM. A reduced nicotinamide adenine dinucleotide-linked kinetic assay for adenosine deaminase activity. J Lab Clin Med 1970;76:507-17.
  • 27. Engin AB, Dogruman-Al F, Ercin U, Oxidative stres and tryptophan degradation pattern of acute Toxoplasma gondii infection in mice. Parasitol Res 2012;111:1725-30.
  • 28. Marchioroa AA, Collib CM, Zangari de Souza C, et al. Analysis of cytokines IFN-γ, TNF-α, TGF-β and nitricoxide in amniotic fluid and serum of pregnant women with toxoplasmosis in southern Brazil. Cytokine 2018;106:35-9.
  • 29. Xu X, He L, Zhang A, et al. Toxoplasma gondii isolate with genotype Chinese 1 triggers trophoblast apoptosis through oxidative stress and mitochondrialdys function in mice. Exp Parasitol 2015;154:51-61.
  • 30. Cınar M, Aydenizöz M, Gokpınar S, et al. Evaluation of biochemical parameters and oxidative stress in sheep naturally infected with Dicrocoelium dendriticum and hydatid cysts. Turkish J Veterinary Animal Sci 2018;42:423- 8.
  • 31. Chandramathi S, SureshK, Anita ZB, et al. Elevated levels of urinary hydrogen peroxide, advanced oxidative protein product (AOPP) and malondialdehyde in humans infected with intestinal parasites. Parasitol 2009;136:359-63.
  • 32. Al-Kennany ER. Pathological Study on the capability of Toxoplasma gondii to ınduce oxidative stres and initiation a primary lesion of atherosclerosis experimentally in broiler chickens. J Animal Veterinary Advances 2007;6:938-42.
  • 33. Jafari M, Salehi M, Shirbazou S, Abasian L, Talebi-Meymand F. Evaluation of gender-related differences in response to oxidative stress in toxoplasma gondii positive serum. Ann Military Health Sci Res 2014;12:64-9.
  • 34. Al-Hadraawy MKA. Role of Glutathione in male infected with giardiasis. Magazin of Al-Kufa University for Biology 2014;6:1-6.
  • 35. Doleski PH, Leal DBR, Machado VS, et al. Diphenyldiselenide modulates nucleotidases, reducing inflammatory responses in the liver of Toxoplasma gondii-infected mice. Purinergic Signalling 2017;13:489-96.
  • 36. Pfefferkorn ER, Pfefferkorn LC. The biochemical basis for resistance to adenine arabinoside in a mutant of Toxoplasma gondii. J. Parasitol 1978;64:486-92.
  • 37. Doleski PH, Ten Catena MV, Passos DV, et al. Chronic toxoplasmosis treatment with diphenyldiselenide in infected mice modulates the activity of purinergic enzymes and reduces inflammation in spleen. Exp Parasitol 2017;181:7- 13.
  • 38. Azma F, Razavi SM, Nazifi S, et al. A study on the status of inflammatory systems in camels naturally infected with Toxoplasma gondii. Trop Anim Health Prod 2015;47:909-14.
  • 39. Vakılı A, Azımzadeh K, Rasouli S. Determination of potential biomarker among plasma sphingosine-1-phosphate, total sialic acid and adenosine deaminase in cattle with naturally ınfected liver cystic echinococcosis. Kafkas Univ Vet Fak Derg 2016;22:179-83. 1425
APA KIRAN T, koloren z, KAŞKO ARICI Y, YILDIZ S (2019). Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. , 1420 - 1425. 10.5455/annalsmedres.2019.05.236
Chicago KIRAN Tuğba Raika,koloren zeynep,KAŞKO ARICI YELİZ,YILDIZ Sevgi Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. (2019): 1420 - 1425. 10.5455/annalsmedres.2019.05.236
MLA KIRAN Tuğba Raika,koloren zeynep,KAŞKO ARICI YELİZ,YILDIZ Sevgi Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. , 2019, ss.1420 - 1425. 10.5455/annalsmedres.2019.05.236
AMA KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. . 2019; 1420 - 1425. 10.5455/annalsmedres.2019.05.236
Vancouver KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. . 2019; 1420 - 1425. 10.5455/annalsmedres.2019.05.236
IEEE KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S "Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive." , ss.1420 - 1425, 2019. 10.5455/annalsmedres.2019.05.236
ISNAD KIRAN, Tuğba Raika vd. "Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive". (2019), 1420-1425. https://doi.org/10.5455/annalsmedres.2019.05.236
APA KIRAN T, koloren z, KAŞKO ARICI Y, YILDIZ S (2019). Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. Annals of Medical Research, 26(7), 1420 - 1425. 10.5455/annalsmedres.2019.05.236
Chicago KIRAN Tuğba Raika,koloren zeynep,KAŞKO ARICI YELİZ,YILDIZ Sevgi Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. Annals of Medical Research 26, no.7 (2019): 1420 - 1425. 10.5455/annalsmedres.2019.05.236
MLA KIRAN Tuğba Raika,koloren zeynep,KAŞKO ARICI YELİZ,YILDIZ Sevgi Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. Annals of Medical Research, vol.26, no.7, 2019, ss.1420 - 1425. 10.5455/annalsmedres.2019.05.236
AMA KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. Annals of Medical Research. 2019; 26(7): 1420 - 1425. 10.5455/annalsmedres.2019.05.236
Vancouver KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive. Annals of Medical Research. 2019; 26(7): 1420 - 1425. 10.5455/annalsmedres.2019.05.236
IEEE KIRAN T,koloren z,KAŞKO ARICI Y,YILDIZ S "Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive." Annals of Medical Research, 26, ss.1420 - 1425, 2019. 10.5455/annalsmedres.2019.05.236
ISNAD KIRAN, Tuğba Raika vd. "Comparison of malondialdehyde, nitric oxide, adenosine deaminase and glutathione levels in patients with Entamoeba coli, Enterobius vermicularis, Giardia intestinalis, Demodex spp. positive, hydatid cyst and Toxoplasma gondii serum positive". Annals of Medical Research 26/7 (2019), 1420-1425. https://doi.org/10.5455/annalsmedres.2019.05.236