Antioxidant enzymatic defense in salivary glands of streptozotocin-induced diabetic rats: A temporal study

Cell Biochemistry and Function

Volumn 28, Issue 6, 2010, Pages 503-508

  Ibuki, Flavia Kazue ^a   Simoes, Alyne ^a   Nogueira, Fernando Neves ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Antioxidant; Antioxidant enzymes; Diabetes; Salivary glands

Indexed keywords

CATALASE; GLUTATHIONE PEROXIDASE; MALONALDEHYDE; PROTEIN; STREPTOZOCIN; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; LIPID PEROXIDATION; MALE; NONHUMAN; PAROTID GLAND; PRIORITY JOURNAL; RAT; SALIVARY GLAND; STREPTOZOCIN DIABETES; SUBMANDIBULAR GLAND;

ANIMALS; ANTIOXIDANTS; CATALASE; DIABETES MELLITUS, EXPERIMENTAL; GLUTATHIONE PEROXIDASE; LIPID PEROXIDATION; MALE; MALONDIALDEHYDE; RATS; RATS, WISTAR; SALIVARY GLANDS; SUPEROXIDE DISMUTASE;

ANIMALIA; RATTUS;

EID: 77956856652     PISSN: 02636484     EISSN: 10990844     Source Type: Journal    
DOI: 10.1002/cbf.1683     Document Type: Article

References (35)

1. Committee, Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus, Diabetes Care 2002; 25 (Supplement 1): S5-S20.
2. Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature 2001; 414(6865): 813-820.
3. Giardino I, Edelstein D, Brownlee M. BCL-2 expression or antioxidants prevent hyperglycemia-induced formation of intracellular advanced glycation endproducts in bovine endothelial cells. J Clin Invest 1996; 97(6): 1422-1428.
4. Kakkar R, Kalra J, Mantha SV, Prasad K. Lipid peroxidation and activity of antioxidant enzymes in diabetic rats. Mol Cell Biochem 1995; 151(2): 113-119.
5. Gumieniczek A, Hopkala H, Wojtowicz Z, Nieradko M. Differences in antioxidant status in skeletal muscle tissue in experimental diabetes. Clin Chim Acta 2001; 314(1-2): 39-45.
6. Fridovich I. Superoxide radical and superoxide dismutases. Annu Rev Biochem 1995; 64: 97-112.
7. Nogueira FN, Carvalho AM, Yamaguti PM, Nicolau J. Antioxidant parameters and lipid peroxidation in salivary glands of streptozotocininduced diabetic rats. Clin Chim Acta 2005; 353(1-2): 133-139.
8. Simoes A, Ganzerla E, Yamaguti PM, de Paula Eduardo C, Nicolau J. Effect of diode laser on enzymatic activity of parotid glands of diabetic rats. Lasers Med Sci 2009; 24(4): 591-596.
9. Moore PA, Guggenheimer J, Etzel KR, Weyant RJ, Orchard T. Type 1 diabetes mellitus, xerostomia, and salivary flow rates. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2001; 92(3): 281-291.
10. Manfredi M, McCullough MJ, Vescovi P, Al-Kaarawi ZM, Porter SR. Update on diabetes mellitus and related oral diseases. Oral Dis 2004; 10(4): 187-200.
11. Nicolau J, Matos JA, Souza DN, Neves LB, AC L. Altered glycogen metabolism in the submandibular and parotid salivary glands of rats with streptozotocin-induced diabetes. J Oral Sci 2005; 47(2): 111-116.
12. von Bultzingslowen I, Sollecito TP, Fox PC, et al. Salivary dysfunction associated with systemic diseases: Systematic review and clinical management recommendations. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2007; 103 Suppl: P. S57 e1-15.
13. Anderson LC. Effects of diabetes and dietary manipulation on rat parotid gland secretory response to sympathetic nerve stimulation. Comp Biochem Physiol A 1991; 98(2): 363-366.
14. Pedersen AM, Bardow A, Jensen SB, Nauntofte B. Saliva and gastrointestinal functions of taste, mastication, swallowing and digestion. Oral Dis 2002; 8(3): 117-129.
15. Nicolau J, Rosa R, Fava-de-Moraes F. The effect of alloxan diabetes upon N-acetylneuraminic acid concentration in the submaxillary glands of rats. Acta Physiol Lat Am 1969; 19(2): 106-110.
16. Nicolau J, Souza DN, Nogueira FN. Activity, distribution and regulation of phosphofructokinase in salivary gland of rats with streptozotocin- induced diabetes. Braz Oral Res 2006; 20(2): 108-113.
17. Nogueira FN, Santos MF, Nicolau J. Influence of streptozotocininduced diabetes on hexokinase activity of rat salivary glands. J Physiol Biochem 2005; 61(3): 421-427.
18. Nicolau J, de Matos JA, de Souza DN, Neves LB, Lopes AC. Altered glycogen metabolism in the submandibular and parotid salivary glands of rats with streptozotocin-induced diabetes. J Oral Sci 2005; 47(2): 111-116.
19. Paoletti F, Aldinucci D, Mocali A, Caparrini A. A sensitive spectrophotometric method for the determination of superoxide dismutase activity in tissue extracts. Anal Biochem 1986; 154(2): 536-541.
20. Aebi H. Catalase in vitro. Methods Enzymol 1984; 105: 121-126.
21. Wendel A. Glutathione peroxidase. Methods Enzymol 1981; 77: 325-333.
22. Esterbauer H, Cheeseman KH. Determination of aldehydic lipid peroxidation products: Malonaldehyde and 4-hydroxynonenal. Methods Enzymol 1990; 186: 407-421.
23. Simoes A, Nicolau J, de Souza DN, et al. Effect of defocused infrared diode laser on salivary flow rate and some salivary parameters of rats. Clin Oral Invest 2008; 12(1): 25-30.
24. Greenspan FS, Gardner DG. Basic and Clinical Endocrinology, 2004; McGraw-Hill: New York, 976.
25. Freeman BA, Crapo JD. Biology of disease: Free radicals and tissue injury. Lab Invest 1982; 47(5): 412-426
26. Townsend DM, Tew KD, Tapiero H. The importance of glutathione in human disease. Biomed Pharmacother 2003; 57(3-4): 145-155.
27. West IC. Radicals and oxidative stress in diabetes. Diabet Med 2000; 17(3): 171-180.
28. Oberley LW. Free radicals and diabetes. Free Radic Biol Med 1988; 5(2): 113-124.
29. Hand AR, Weiss RE. Effect of streptozotocin-induced diabetes on the rat parotid gland. Lab Invest 1984; 51(4): 429-440.
30. Anderson LC. Effects of alloxan diabetes and insulin in vivo on rat parotid gland. Am J Physiol 1983; 245(3): G431-7.
31. Sabino-Silva R, Freitas HS, Lamers ML, Okamoto MM, Santos MF, Machado UF. Na+-glucose cotransporter SGLT1 protein in salivary glands: Potential involvement in the diabetes-induced decrease in salivary flow. J Membr Biol 2009; 228(2): 63-69.
32. Nicolau J, De Souza DN, Simoes A. Alteration of Ca(2+)-ATPase activity in the homogenate, plasma membrane and microsomes of the salivary glands of streptozotocin-induced diabetic rats. Cell Biochem Funct 2009; 27(3): 128-134.
33. Nicolau J, de Souza DN, Carrilho M. Increased glycated calmodulin in the submandibular salivary glands of streptozotocin-induced diabetic rats. Cell Biochem Funct 2009; 27(4): 193-198.
34. Nicolau J, Sassaki KT. Metabolism of carbohydrate in the major salivary glands of rats. Arch Oral Biol 1976; 21(11): 659-661.
35. Schenkels LC, Veerman EC, Nieuw Amerongen AV. Biochemical composition of human saliva in relation to other mucosal fluids. Crit Rev Oral Biol Med 1995; 6(2): 161-175.