Comparison of melatonin levels in saliva in individuals with healthy periodontium, generalized chronic gingivitis and generalized chronic periodontitis
Keywords:
melatonin, ELISA, Hormone, gingivitis, periodontitis, healthy periodontiumAbstract
Introduction: Melatonin, is a hormone secreted by the pineal gland which activates several elements of the immune system that reduce tissue destruction during the inflammatory response, either directly by scavenging free radical, reactive oxygen species and reactive nitrogen species or indirectly by modulating the action of agents such as cytokines and adhesion molecules, which contribute to the advance of cell damage. Aim: The aim of the present study was to compare and evaluate melatonin levels in saliva in individuals with healthy periodontium, generalized chronic gingivitis and generalized chronic periodontitis. Materials and method: A total of 60 patients were examined and assessed and divided into 3 groups; Group 1: 20 individuals with healthy periodontium, Group 2: 20 individuals with generalised chronic gingivitis and Group 3: 20 individuals with generalised chronic periodontitis. Saliva samples were collected from each sample and melatonin levels were assessed using ELISA, a competitive immunoassay using a capture antibody technique. Results: Melatonin levels in saliva was highest in individuals with healthy periodontium when compared to gingivitis and periodontitis group which was highly significant and inversely proportional correlation was observed between periodontal index and melatonin levels which was statically significant.
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Robert J. Genco. Current View of Risk Factors for Periodontal Diseases. J Periodontol 1996;67:1041–1049.
Newman M (2001) Genotype and clinical management of periodontitis. Compend Contin Educ Dent 22: 12-16
Tatakis DN, Trombelli L (2004) Modulation of clinical expression ofplaque-induced gingivitis. I. Background review and rationale. J ClinPeriodontol 31: 229-238.
Kinane DF (2000) Aetiology and pathogenesis of periodontal disease.Ann R Australas Coll Dent Surg 15: 42-50.
Warwas M, Kaczmarek U, Golab K (2000) The role of cysteineprotease and cystatin in pathogenesis and laboratory diagnosis ofperiodontal disease. PostepyHig Med Dosw 54: 879-894.
Zambon JJ, Reynolds H, Fisher JG, Shlossman M, Dunford R, et al. (1988) Microbiological and immunological studies of adult periodontitis in patients with noninsulin-dependent diabetes mellitus. J Periodontol 59: 23-31.
Kimura S, Yonemura T, Kaya H (1993) Increased oxidative product formation by peripheral blood polymorphonuclear leukocytes in human periodontal diseases. J Periodontal Res 28: 197-203.
Halliwell B (1994) Free radicals, antioxidants, and human disease: curiosity, cause, or consequence? Lancet 34: 721-724.
Battino M, Bullon P, Wilson M, Newman H (1999) Oxidative injury and inflammatory periodontal diseases: the challenge of antioxidants to free radicals and reactive oxygen species. Crit Rev Oral Biol Med 10: 458-476.
Brennan R, Jan JE, Lyons CJ. Light, dark, and melatonin: emerging evidence for the importance of melatonin in ocular physiology. Eye (Lond) 2007;21:901– 909.
Cutando A, Gomez-Moreno G, Arana C, Acuna-Castroviejo D, Reiter RJ (2007a) Melatonin: potential functions in the oral cavity. J Periodontol 78: 1094-1102.
Yazıcı C, Köse K (2004) Melatonin: the antioxidant power of darkness. Health Sci 13: 56-65.
Laakso ML, Porkka-Heiskanen T, Alila A, Stenberg D, Johansson G. Correlation between salivary and serum melatonin: dependence on serum melatonin levels. J Pineal Res 1990;9:39–50.
Hattori A, Migitaka H, Iigo M, et al. Identification of melatonin in plants and its effects on plasma melatonin levels and binding to melatonin receptors in vertebrates. Biochem Mol Biol Int 1995;35: 627–634.
Iguichi H, Kato KI, Ibayashi H. Agedependent reduction in serum melatonin concentrations in healthy human subjects. J Clin Endocrinol Metab 1982;55: 27–29.
Czesnikiewicz-Guzik M, Konturek SJ, Loster B, Wisniewska G, Majewski S. Melatonin and its role in oxidative stress related diseases of oral cavity. J PhysiolPharmacol 2007;58:5–19.
Poon AM, Liu ZM, Pang CS, Brown GM, Pang SF. Evidence for a direct action of melatonin on the immune system. Biol Signals 1994;3:107–117.
Reiter RJ, Calvo JR, Karbownik M, Qi W, Tan DX. Melatonin and its relation to the immune system and inflammation. Ann N Y Acad Sci 2000;917:376–386. Bergstrom WH, Hakanson DO. Melatonin: the dark force. Adv Pediatr 1998; 45:91–106.
Bergstrom WH, Hakanson DO. Melatonin: the dark force. Adv Pediatr 1998; 45:91–106.
Allegra M, Reiter RJ, Tan DX, Gentile C, Tesoriere L, Livrea MA. The chemistry of melatonin’s interaction with reactive species. J Pineal Res 2003;34:1–10.
Srinath R, Acharya AB, Thakur SL. Salivary and gingival crevicular fluid melatonin in periodontal health and disease. J Periodontol 2010;81:277–283.
Kennaway D. Re: salivary and gingival crevicular fluid melatonin in periodontal health and disease. J Periodontol 2010;81:1102.
Khaled M. Salama et al. liver enzymes in children with beta thalassemia major: Correlation with Iron overload and viral hepatitis .open access maced J med Sci, 2015 Jun ; 13 (2);287-292
Suryasa, I. W., Rodríguez-Gámez, M., & Koldoris, T. (2022). Post-pandemic health and its sustainability: Educational situation. International Journal of Health Sciences, 6(1), i-v. https://doi.org/10.53730/ijhs.v6n1.5949
Kumar Subramanian, Aravind & Thangavelu, Lakshmi. (2011). Efficacy of natural products in fixed orthodontic appliances (FOA) treatment -A dental note. International Journal of Drug Development and Research. 3. 1-2.
Cho CM, You HK, Jeong SN. The clinical assessment of aggressive periodontitis patients. J Periodontal Implant Sci 2011;41:143–148.
Sies, H. Oxidative stress: Oxidants and antioxidants. Exp. Physiol. 1997, 82, 291–295.
Najeeb, S.; Khurshid, Z.; Zohaib, S.; Zafar, M.S. Therapeutic potential of melatonin in oral medicine and periodontology. Kachsiung J. Med. Sci. 2016, 32, 391–396.
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