Superoxide dismutase activity in gingiva in type-2 diabetes mellitus patients with chronic periodontitis

Archives of Oral Biology

Volumn 53, Issue 1, 2008, Pages 44-52

  Akalin, Ferda Alev ^a   Işiksal, Eda ^a   Baltacioǧlu, Esra ^b   Renda, Nurten ^a   Karabulut, Erdem ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b KARADENIZ TECHNICAL UNIVERSITY   (Turkey)

Author keywords

Chronic periodontitis; Diabetes mellitus; Gingiva; Superoxide dismutase

Indexed keywords

BIOLOGICAL MARKER; GLYCOSYLATED HEMOGLOBIN; LIPID; SUPEROXIDE DISMUTASE;

ADULT; AGED; ANALYSIS OF VARIANCE; ARTICLE; BLOOD; CASE CONTROL STUDY; CHRONIC DISEASE; COMPARATIVE STUDY; DIABETES MELLITUS; ENZYMOLOGY; FEMALE; GINGIVA; GLUCOSE BLOOD LEVEL; HUMAN; MALE; METABOLISM; MIDDLE AGED; NON INSULIN DEPENDENT DIABETES MELLITUS; PERIODONTITIS;

ADULT; AGED; ANALYSIS OF VARIANCE; BIOLOGICAL MARKERS; BLOOD GLUCOSE; CASE-CONTROL STUDIES; CHRONIC DISEASE; DIABETES COMPLICATIONS; DIABETES MELLITUS, TYPE 2; FEMALE; GINGIVA; HEMOGLOBIN A, GLYCOSYLATED; HUMANS; LIPIDS; MALE; MIDDLE AGED; PERIODONTITIS; SUPEROXIDE DISMUTASE;

EID: 36749012964     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2007.07.009     Document Type: Article

References (67)

1. Chapple IL, Matthews JB. The role of reactive oxygen and antioxidant species in periodontal tissue destruction. Periodontol 2000 2007;43:160-232 (review).
2. Chapple I.L. Reactive oxygen species and antioxidants in inflammatory diseases. J Clin Periodontol 24 (1997) 287-296
3. Waddington R.J., Moseley R., and Embery G. Reactive oxygen species: a potential role in the pathogenesis of periodontal diseases. Oral Dis 6 (2000) 138-151
4. Maxwell S.R. Prospects for the use of antioxidant therapies. Drugs 49 (1995) 345-361
5. Bauer V., and Bauer F. Reactive oxygen species as mediators of tissue protection and injury. Gen Physiol Biophys 18 (1999) 7-14
6. Halliwell B. Mechanisms involved in the generation of free radicals. Pathol Biol 44 (1996) 6-13
7. McCord J.M. Human disease, free radicals, and the oxidant/antioxidant balance. Clin Biochem 26 (1993) 351-357
8. Seymour G.J., Whyte G.J., and Powell R.N. Chemiluminesence in the assessment of polymorphonuclear leukocyte function in chronic inflammatory periodontal disease. J Oral Pathol 15 (1986) 125-131
9. Gustafsson A., and Asman B. Increased release of free oxygen radicals from peripheral neutrophils in adult periodontitis after Fc delta-receptor stimulation. J Clin Periodontol 23 (1996) 38-44
10. Panjamurthy K., Manoharan S., and Ramachandran C.R. Lipid peroxidation and antioxidant status in patients with periodontitis. Cell Mol Biol Lett 10 (2005) 255-264
11. Komatsu T., Lee M.C., Miyagi A., Shoji H., Yoshino F., Maehata Y., et al. Reactive oxygen species generation in gingival fibroblasts of Down syndrome patients detected by electron spin resonance spectroscopy. Redox Rep 11 (2006) 71-77
12. Akali{dotless}n F.A., Baltaci{dotless}oǧlu E., Alver A., and Karabulut E. Lipid peroxidation levels and total oxidant status in serum, saliva and gingival crevicular fluid in patients with chronic periodontitis. J Clin Periodontol 34 (2007) 558-565
13. Matthews J.B., Wright H.J., Roberts A., Cooper P.R., and Chapple I.L. Hyperactivity and reactivity of peripheral blood neutrophils in chronic periodontitis. Clin Exp Immunol 147 (2007) 255-264
14. Brock G.R., Butterworth C.J., Matthews J.B., and Chapple I.L. Local and systemic total antioxidant capacity in periodontitis and health. J Clin Periodontol 31 (2004) 515-521
15. Mashayekhi F., Aghahoseini F., Rezaie A., Zamani M.J., Khorasani R., and Abdollahi M. Alteration of cyclic nucleotides levels and oxidative stress in saliva of human subjects with periodontitis. J Contemp Dent Pract 15 6 (2005) 46-53
16. Tsai C.C., Chen H.S., Chen S.L., Ho Y.P., Ho K.Y., Wu Y.M., et al. Lipid peroxidation: a possible role in the induction and progression of chronic periodontitis. J Periodontal Res 40 (2005) 378-384
17. Baltaci{dotless}oǧlu E., Akali{dotless}n F.A., Alver A., Balaban F., Ünsal M., and Karabulut E. Total antioxidant capacity and superoxide dismutase activity levels in serum and gingival crevicular fluid in postmenopausal women with chronic periodontitis. J Clin Periodontol 33 (2006) 385-392
18. Chapple I.L., Brock G.R., Milward M.R., Ling N., and Matthews J.B. Compromised GCF total antioxidant capacity in periodontitis: cause or effect?. J Clin Periodontol 34 (2007) 103-110
19. Jacoby B.H., and Davis W.L. The electron microscopic immunolocalization of a copper-zinc superoxide dismutase in association with collagen fibers of periodontal soft tissues. J Periodontol 62 (1991) 413-420
20. Skaleric U., Manthey C.M., Mergenhagen S.E., Gaspirc B., and Wahl S.M. Superoxide release and superoxide dismutase expression by human gingival fibroblasts. Eur J Oral Sci 108 (2000) 130-135
21. Tulunoǧlu O., Alaçam A., Baştuǧ M., and Yavuzer S. Superoxide dismutase activity in healthy and inflamed pulp tissues of permanent teeth in children. J Clin Pediatr Dent 22 (1998) 341-345
22. Marton I.J., Balla G., Hegedus C., Redi P., Szilagyi Z., Karmazsin L., et al. The role of reactive oxygen intermediates in the pathogenesis of chronic apical periodontitis. Oral Microbiol Immunol 8 (1993) 254-257
23. Ellis S.D., Tucci M.A., Serio F.G., and Johnson R.B. Factors for progression of periodontal diseases. J Oral Pathol Med 27 (1998) 101-105
24. Akali{dotless}n F.A., Toklu E., and Renda N. Analysis of superoxide dismutase activity levels in gingiva and gingival crevicular fluid in patients with chronic periodontitis and periodontally healthy controls. J Clin Periodontol 32 (2005) 238-243
25. Cianciola L.J., Park B.H., Bruck E., Mosovich L., and Genco R.J. Prevalence of periodontal disease in insulin-dependent diabetes mellitus (juvenile diabetes). J Am Dent Assoc 104 (1982) 653-660
26. Papapanou P.N. Periodontal diseases: epidemiology. Ann Periodontol 1 (1996) 1-36
27. Löe H. Periodontal disease. The sixth complication of diabetes mellitus. Diabetes Care 16 (1993) 329-334
28. Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature 13 414 (2001) 813-820
29. Brownlee M. A radical explanation for glucose-induced beta cell dysfunction. J Clin Invest 112 (2003) 1788-1790
30. Southerland J.H., Taylor G.W., Moss K., Beck J.D., and Offenbacher S. Commonality in chronic inflammatory diseases: periodontitis, diabetes, and coronary artery disease. Periodontol 2000 40 (2006) 130-143
31. Howard B.V. Lipoprotein metabolism in diabetes mellitus. J Lipid Res 28 (1987) 613-628
32. Dutta-Roy A.K. Lipid metabolism. Curr Opin Lipidol 5 (1994) U9-U16
33. Cutler C.W., Machen R.L., Jotwani R., and Iacopino A.M. Heightened gingival inflammation and attachment loss in type 2 diabetics with hyperlipidemia. J Periodontol 70 (1999) 1313-1321
34. Iacopino A.M., and Cutler C.W. Pathopyhsiological relationships between periodontitis and systemic disease: recent concepts involving serum lipids. J Periodontol 71 (2000) 1375-1384
35. Lösche W., Karapetow F., Pohl A., Pohl C., and Kocher T. Plasma lipid and blood glucose levels in patients with destructive periodontal disease. J Clin Periodontol 27 (2000) 537-541
36. Krause S., Pohl A., Pohl C., Liebrenz A., Rühling K., and Lösche W. Increased generation of reactive oxygen species in mononuclear blood cells from hypercholesterolemic patients. Thromb Res 71 (1993) 237-240
37. Nath N., Chari S.N., and Rathi A.B. Superoxide dismutase in diabetic polymorphonuclear leukocytes. Diabetes 33 (1984) 586-589
38. Giugliano D., Ceriello A., and Paolisso G. Oxidative stress and diabetic vascular complications. Diabetes Care 19 (1996) 257-267
39. Karima M., Kantarci{dotless} A., Ohira T., Hasturk H., Jones V.L., Nam B.H., et al. Enhanced superoxide release and elevated protein kinase C activity in neutrophils from diabetic patients: association with periodontitis. J Leukoc Biol 78 (2005) 862-870
40. Schmidt A.M., Weidman E., Lalla E., Yan S.D., Hori O., Cao R., et al. Advanced glycation endproducts (AGEs) induce oxidant stress in the gingiva: a potential mechanism underlying accelerated periodontal disease associated with diabetes. J Periodontal Res 31 (1996) 508-515
41. Lalla E., Lamster I.B., Drury S., Fu C., and Schmidt A.M. Hyperglycemia, glycoxidation and receptor for advanced glycation endproducts: potential mechanisms underlying diabetic complications, including diabetes-associated periodontitis. Periodontol 2000 23 (2000) 50-62
42. Szaleczky E., Prechl J., Feher J., and Somogyi A. Alterations in enzymatic antioxidant defence in diabetes mellitus-a rational approach. Postgrad Med J 75 (1999) 13-17
43. Wohaieb S.A., and Godin D.V. Starvation-related alterations in free radical tissue defense mechanisms in rats. Diabetes 36 (1987) 169-173
44. Sechi L.A., Ceriello A., Griffin C.A., Catena C., Amstad P., Schambelan M., et al. Renal antioxidant enzyme mRNA levels are increased in rats with experimental diabetes mellitus. Diabetologia 40 (1997) 23-29
45. Ali{dotless}ci{dotless}güzel Y., Özen I., Aslan M., and Karayalçi{dotless}n U. Activities of xanthine oxidoreductase and antioxidant enzymes in different tissues of diabetic rats. J Lab Clin Med 142 (2003) 172-177
46. Dohi T., Kawamura K., Morita K., Okamoto H., and Tsujimoto A. Alterations of the plasma selenium concentrations and the activities of tissue peroxide metabolism enzymes in streptozotocin-induced diabetic rats. Horm Metab Res 20 (1988) 671-675
47. Armitage G.C. Development of a classification system for periodontal diseases and conditions. Ann Periodontol 4 1 (1999) 1-6
48. Committee Report. American Diabetes Association Expert Committee on the diagnosis and classification of diabetes mellitus. Diabetes Care 2001;24(Suppl 1):5-20.
49. Löe H., and Silness J. Periodontal disease in pregnancy. Prevalance and severity. Acta Odontol Scand 21 (1963) 533-555
50. Nowicki D., Vogel R.I., Melcer S., and Deasy M.J. The gingival bleeding time index. J Periodontol 52 (1981) 260-262
51. Silness J., and Löe H. Periodontal disease in pregnancy. II. Correlation between oral hygiene and periodontal condition. Acta Odontol Scand 22 (1964) 121-135
52. Golub L.M., Ciancio S., Ramamamurthy N.S., Leung M., and McNamara T.F. Low-dose doxycycline therapy: effect on gingival and crevicular fluid collagenase activity in humans. J Periodontal Res 25 (1990) 321-330
53. Gorska R., Gregorek H., Kowalski J., Laskus-Perendyk A., Syczewska M., and Madalinski K. Relationship between clinical parameters and cytokine profiles in inflamed gingival tissue and serum samples from patients with chronic periodontitis. J Clin Periodontol 30 (2003) 1046-1052
54. Sun Y., Oberley L.W., and Li Y. A simple method for clinical assay of superoxide dismutase. Clin Chem 34 (1988) 497-500
55. Lowry O.H., Rosebrough N.J., Farr A.L., and Randall R.J. Protein measurement with the folin phenol reagent. J Biol Chem 193 (1951) 265-275
56. Bartold P.M., Wiebkin O.W., and Thonard J.C. The effect of oxygen-derived free radicals on gingival proteoglycans and hyaluronic acid. J Periodontal Res 19 (1984) 390-400
57. Chapple I.L., Mason G.I., Garner I., Matthews J.B., Thorpe G.H., Maxwell S.R., et al. Enhanced chemiluminescent assay for measuring the total antioxidant capacity of serum, saliva and crevicular fluid. Ann Clin Biochem 34 (1997) 412-421
58. Muchova J., Liptakova A., Orszaghova Z., Garaiova I., Tison P., Carsky J., et al. Antioxidant systems in polymorphonuclear leukocytes of type 2 diabetes mellitus. Diabet Med 16 (1999) 74-78
59. Cutler C.W., Shinedling E.A., Nunn M., Jotwani R., Kim B.O., Nares S., et al. Association between periodontitis and hyperlipidemia: cause or effect?. J Periodontol 70 (1999) 1429-1434
60. Akkuş I., Kalak S., Vural H., Caglayan O., Menekse E., Can G., et al. Leukocyte lipid peroxidation, superoxide dismutase, glutathione peroxidase and serum and leukocyte vitamin C levels of patients with type 2 diabetes mellitus. Clin Chim Acta 31 244 (1996) 221-227
61. Ross R. The pathogenesis of atherosclerosis: a perspective for the 1990s. Nature 29 362 (1993) 801-809
62. Guo Z., Van Remmen H., Yang H., Chen X., Mele J., Vijg J., et al. Changes in expression of antioxidant enzymes affect cell-mediated LDL oxidation and oxidized LDL-induced apoptosis in mouse aortic cells. Arterioscler Thromb Vasc Biol 21 (2001) 1131-1138
63. Reilly P.M., Schiller H.J., and Bulkley G.B. Pharmacologic approach to tissue injury mediated by free radicals and other reactive oxygen metabolites. Am J Surg 161 (1991) 488-503
64. Ansell B.J., Fonarow G.C., Navab M., and Fogelman A.M. Modifying the anti-inflammatory effects of high-density lipoprotein. Curr Atheroscler Rep 9 (2007) 57-63
65. Kontush A., and Chapman M.J. Functionally defective high-density lipoprotein: a new therapeutic target at the crossroads of dyslipidemia, inflammation, and atherosclerosis. Pharmacol Rev 58 (2006) 342-374
66. Ansell B.J., Fonarow G.C., and Fogelman A.M. High-density lipoprotein: is it always atheroprotective?. Curr Atheroscler Rep 8 (2006) 405-411
67. American Academy of Periodontology. The pathogenesis of periodontal diseases (informational paper). J Periodontol 1999;70:457-70.