Abstract
Our purpose was to investigate associations between adenosine deaminase (ADA), superoxide dismutase (SOD), and catalase (CAT) activities and H. pylori.Ninety-nine patients were studied. Eight antral mucosal biopsies were taken for biochemical assessment of ADA, CAT, AND SOD activity and histological assessment. H. pyloridensity wAS evaluated according to the updated Sydney system. Patients were divided into three groups according to Sydney classification. ADA activity was found to be higher in patients having H. pyloriin the present study. Also, ADA activity was higher in patients with a severe density of H. pylori. SOD level was found to be significantly higher with increased H. pyloridensity in our study (P< 0.05). In addition, SOD activity was higher in it H. Pylori-positive than H. pylori-negative patients. We did not find CAT activity in some antral tissue specimens. The significantly high levels of ADA activity in patients with H. pyloriinfection may reflect the regulator role of ADA in acid secretion. The higher ADA level with increased H. pyloridensity and H. pyloripositivity indicate the probable malign lymphoid process of the stomach. But these findings must be confirmed with larger studies that include different gastric lesions.
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References
Bruer T, Malaty HM, Graham DY: The epidemiology of H pylori associated gastroduodenal disease. In The Immunobiology of H. pylori: From Pathogenesis to Prevention. Ernst PB, Michetti P, Smith PD (eds). Philadelphia, Lippincott–Raven, 1997, pp 1–14
Chen XY, Liu WZ, Shi Y, Zhang DZ, Xiao SD, Tytgat GNJ: Helicobacter pylori associated gastric diseases and lymphoid tissue hyperplasia in gastric antral mucosa. J Clin Pathol 55:133–137, 2002
Wothespoon A. Doglionil C, Diss T, et al.: Regression of primary low-grade B-cell gastric lymphoma of mucosa-associated lymphoid tissue type after eradication of Helicobacter pylori. Lancet 342:575–579, 1993
Bagchi D, McGinn TR, Ye X, Bagchi M, Krohn RL, Chatterjee A, Stohs SJ: Helicobacter pylori-induced oxidative stress and DNA damage in a primary culture of human gastric mucosal cells. Dig Dis Sci 47:1405–1412, 2002
Mazzucchelli L Blaser A, Kappeler A, et al.: BCA-1 higly expressed in helicobacter pylori-induced mucosa-associated lymphoid tissue and gastric lymphoma. J Clin Invest 104:R49–R54, 1999
Piras MA, Gakis C, Budroni M, Andreoni G: Adenosine deaminase activity in pleural effusions: an aid to differential diagnosis. Br Med J 2:1751–1752, 1987
Biberfeld G, Biberfeld P, Sterner G: Cell-mediated immune response following Mycoplasma pneumoniae infection in man. I. Lymphocyte stimulation. Clin Exp Immunol 17:29–41, 1974
Young E, Taylor HR: Immune mechanisms in chlamydial eye infections: cellular immune responses in chronic and acute dizease. J Infect Dis 150:745–751, 1984
Querol JM, Barbe F, Manresa F, Esteban C, Canete C: Low value of adenosine deaminase in tuberculous pleural effusions. Eur Respir J 3:586–587, 1990
Durak I, Perk H, Kavutcu M, Canbolat O, Akyol O, Beduk Y: Adenosine deaminase, 5′ nucleotidase, xanthine oxidase, superoxide dismutase, and catalase activities in cancerous and noncancerous human bladder tissues. Free Rad Biol Med 16(6):825–831, 1994
Cristalli G, Costanzi S, Lambertucci C, Lupidi G, Vittori S, Volpini R, Camaioni E: Adenosine deaminase: Functional implications and different classes of inhibitors. Med Res Rev 21:105–128, 2001
Asahi M, Azuma T, Ito S, Ito Y, Suto H, Nagai Y, Tsubokawa M, Tohyama Y, Maeda S, Omata M, Suzuki T, Sasakawa C: Helicobacter pylori CagA protein can be tyrosine phosphorylated in gastric epithelial cells. J Exp Med 191:593–602, 2000
Bamba N, Nakajima S, Andoh A, Bamba M, Sugihara H, Bamba T, Hattori T: Stem cell factor expressed in human gastric mucosa in relation to mast cell increase in Helicobacter pylori–infected gastritis. Dig Dis Sci 47:274–282, 2002
Stein M, Rappuoli R, Covacci A: Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation. Proc Natl Acad Sci USA 97:1263–1268, 2000
Dunn BE, Cohen H, Blaser MJ: Helicobacter pylori. Clin Microbiol Rev 10:720–741, 1997
Blaser MJ, Berg DE: Helicobacter pylori genetic diversity and risk of human dizease. J Clin Invest 107:767–773, 2001
Ito Y, Azuma T, Ito S, Suto H, Miyaji H, Yamazaki Y, Kato T, Kohli Y, Keida Y, Kuriyama M: Sequence analysis and clinical significance of the iceA gene from Helicobacter pylori strains in Japan. J Clin Microbiol 38:483–488, 2000
Giusti G: Adenosine deaminase. In Methods of Enzymatic Analysis, 2nd ed. Bergmeyer MV (ed). New York, Academic Press, 1974, pp 1092–1098
Beutler E: Red Cell Metabolism, 2nd ed. New York, Grune and Stratton, 1975, pp 261–265
Fridovich I: Superoxide dismutase. Adv Enzymol 41:35–97, 1974
Lowry OH, Rosebrough NJ, Farr A, Randall R: Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275, 1951
Genta RM, Robason Go, Graham DY: Simultaneous visualization of Helicobacter pylori and gastric morphology: a new stain. Hum Pathol 25:221–226, 1994
Ota H, Genta RM: Morphological characterization of the gastric mucosa during infection with H Pylori. In The Immunobiolology of H pylori: From Pathogenesis to Prevention. Ernst PB, Michetti P, Smith PD (eds). Philadelphia, Lippincott–Raven, 1977, pp 15–28
Xiang Z, Bugndi M, Rappuoli: Helicobacter pylori host responses in peptic ulceration. Lancet 342:900–901, 1993
Wyatt JI, Rathbone BJ: Immune response of the gastric mucosa to Campylobacter pylori. Scand J Gastroenterol 142:44–49, 1988
Eidt S, Stolte M: Prevalence of lymphoid follicles and aggregates in Helicobacter pylori gastritis in antral and body mucosa. J Clin Pathol 46:832–835, 1993
Genta RM, Hammer HW, Graham DY: Gastric lymphoid follicles in Helicobacter pylori infection: frequency, distribution, and response to triple therapy. Hum Pathol 24:577–583, 1993
Ren Z, Pang G, Lee R: Circulating T-cell response to helicobacter pylori infection in chronic gastritis. Helicobacter 5:135–141, 2000
Xia Y, Khatchikian G, Zweier JL: Adenosine deaminase inhibition prevents free radical mediated injury in the postischemic heart. J Biol Chem 271:10096–10102, 1996
Namiot Z, Rutkiewicz J, Stasiewicz J, Gorski J: Adenosine deaminase activity in the human gastric mucosa in relation to acid secretion. Digestion 45:172–175, 1990
Kojima O, Majima T, Uehara Y, Yamane T, Fujita Y, Takahashi T, Majima S: Alteration of adenosine deaminase activity in peripheral blood lymphocytes of patients with gastric cancer. Jpn J Surg 15:130–133, 1986
Durak I, Ormeci N, Akyol O, Canbolat O, Kavutcu M, Bulbul M: Adenosine deaminase, 5′-nucleotidase, xanthine oxidase, superoxide dismutase, and catalase activities in gastric juices from patients with gastric cancer, ulcer, and atrophic gastritis. Dig Dis Sci 39:721–728, 1994
Mori M, Suziki H, Suzuki M, Kai A, Miura S, Ishii H: Catalase and SOD secreted from Helicobacter pylori. Free Radic Res 24:439–450, 1996
Farkas R, Selmeci L, Tulassay Z, Pronai L: Superoxide-dismutase activity of the gastric mucosa in patients with Helicobacter pylori infection. Anticancer Res 23:4309–4312, 2003
Vo TKO, Druez C, Delzenne N, Taper HS, Poberfroid M: Analysis of antioxidant defence systems during rat hepatocarcinogenesis. Carcinogenesis 9:2009–2013, 1988
Goldstein BD, Czerniecki B, Witz G: The role of free radicals in tumor promotion. Environ Health Perspect 81:55–57, 1989
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Bulbuloglu, E., Inanc, F., Bakaris, S. et al. Association of Adenosine Deaminase, Superoxide Dismutase, and Catalase Activities with Helicobacter pylori . Dig Dis Sci 50, 2296–2299 (2005). https://doi.org/10.1007/s10620-005-3050-6
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DOI: https://doi.org/10.1007/s10620-005-3050-6