Shankarram V, Narayanan M. D. S. L, Sudhakar M. D. S. U, Moses M. D. S. J, Selvan M. D. S. T, Parthiban M. D. S. S. Detection of Oxidative Stress in Periodontal Disease and Oral Cancer. Biomed Pharmacol J 2015;8(2)
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V. Shankarram1, M.D.S. Lakshmi Narayanan2, M.D.S. Uma Sudhakar3, M.D.S. Joyson Moses3, M.D.S. Tamil Selvan4 and M.D.S. S. Parthiban1

1Department of periodontics., Thai moogambigai dental college, Chennai.600107  MOBILE 9444071251,994071251. 2Department of endodontics., Thai moogambigai dental college, Golden George nagar, Chennai 600107. 3Department of periodontics., Thai moogambigai dental college, Golden George nagar, Chennai 600107. 4Department of Oralpathology., Sree Ramachandra Dental College. Chennai.    

DOI : https://dx.doi.org/10.13005/bpj/819

Abstract

The oral cavity is an entry of other systems of the body; it should not be viewed as an isolated area. Diseases that it lays down can have systemic scope and significantly affect the quality of life of  individuals who suffer them. Periodontal disease is one of the oral health problems that most often affect the global population, lack of treatment leads to loss of tooth organs and consequently alters the digestion and nutrition, without considering other relevant aspects as phonation, aesthetics and social or emotional impact. The importance of periodontal disease has raised possible bidirectional relationships with systemic diseases such as diabetes, metabolic syndrome and cardiovascular disease. We address herein the role of oxidative stress in the pathogenicity of periodontal disease. In the same context, another disease that has become relevant in our days is the oral cancer .Detection of the reactive oxygen species in the periodontitis patients  and oral cancer patients reveal the relationship between the oxidative stress in periodontitis and oral cancer patients

Keywords

Detection;  cavity; systems; periodontitis

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Shankarram V, Narayanan M. D. S. L, Sudhakar M. D. S. U, Moses M. D. S. J, Selvan M. D. S. T, Parthiban M. D. S. S. Detection of Oxidative Stress in Periodontal Disease and Oral Cancer. Biomed Pharmacol J 2015;8(2)

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Shankarram V, Narayanan M. D. S. L, Sudhakar M. D. S. U, Moses M. D. S. J, Selvan M. D. S. T, Parthiban M. D. S. S. Detection of Oxidative Stress in Periodontal Disease and Oral Cancer. Biomed Pharmacol J 2015;8(2). Available from: http://biomedpharmajournal.org/?p=3737

Introduction

Oxidative stress is the systemic  disturbance caused by the increased Reactive oxygen species a biological system’s ability to readily detoxify the reactive intermediates or to repair the resulting damage. Disturbances in the normal redox state of cells can cause toxic effects through the production of peroxides and free radicals that damage all components of the cell, including proteins, lipids, and DNA. Oxidative stress from oxidative metabolism causes base damage, as well as strand breaks in DNA. Base damage is mostly indirect and caused by reactive oxygen species (ROS) generated, e.g. O2− (superoxide radical), OH (hydroxyl radical) and H2O2 (hydrogen peroxide)1.In humans, oxidative stress is thought to be involved in the development of Asperger syndrome,2 ADHD,3cancer,4Parkinson’s disease,5 Lafora disease,6 Alzheimer’s disease,7,8 atherosclerosis,9 heart failure,10myocardial infarction,11,12 fragile X syndrome,13 Sickle Cell Disease,14 lichen planus,15vitiligo,16autism,17 infection,18  chronic fatigue syndrome.19,Periodontitis20. Epidemiological data show that the incidence of this neoplasm has been increasing in several countries. The impact of oral cancer on patients, who suffer it, is devastating. The role of oxidative stress in the development of this disease and some alternatives for its treatment, are topics addressed in this brief . Periodontitis and oral cancer are two oral diseases are a sample of the plethora of effects that oxidative stress may have at local and systemic level. So this study  find the reactive oxygen species in saliva samples  there by their role in periodontitis and oral cancer

Objectives

The study  has following ojectives

  1. To detect the oxidative stress in periodontitis patients and oral cancer patients
  2. To compare the oxidative stress between oral cancer patients and periodontitis

Study groups

The case control study was done in department of periodontology under the ethical clearance from Dr. MGR UNIVERSITY And Research Institute three groups n=25  was selected

1.n=25  group of periodontitis

2.n=25 group of oral cancer

3.n=25 group of healthy controls

Materials and Methods

The saliva samples were collected from the three groups and stored in the plastic bottles,and the study done in regenix laboratory ,Chennai .Oxidative stress status was assessed by measuring the total antioxidant capacity (TAOC) and biomarkers of oxidative stress 8-hydroxy-2′-deoxyguanosine (8-OHdG) and malondialdehyde (MDA) in saliva and the activity of some of the main antioxidant enzymes glutathione peroxidase (GPx) and superoxide dismutase (SOD).

GPx and SOD activities and TAOC levels were determined using a competitive ELISA kit (Cayman Chemical Company; Item numbers 703102, 706002, and 709001, resp.) according to the manufacturer’s instructions. MDA levels were measured with NWLSS Malondialdehyde Assay (Northwest Life Science Specialities; Catalog number NWK-MDA01) following the manufacturer’s instructions. 8-hydroxy-2′-deoxyguanosine (8-OHdG) levels were measured with NWLSS High Sensitivity 8-OHdG ELISA (Northwest Life Science Specialities; Catalog number NWK-MDA01) following manufacturer’s instructions.

Statistical Analysis

All results shown are expressed as mean and 95% confidence interval. Statistical comparisons between groups were assessed by Mann-Whitney or Kruskal-Wallis tests. The linear trend between groups was analyzed by the Jonckheere-Terpstra test. Multivariant linear regression predictive models were made with the different oxidative stress parameters as the dependent variable. The independent variables were age, gender, smoker (as confounding variables).

Results

we obtained a highly significant elevation of all oxidative stress marker levels except for that of SOD. Periodontitis group and oral cancer denoted increased oxidative stress level. Therefore, the presence of oxidative stress in periodontitis and oral cancer is significant over healthy group

Table 1. Oxidative stress parameters and periodontal status Table 1: Oxidative stress parameters and periodontal status

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Table 2 comparison between the three groups Table 2: comparison between the three  groups

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Discussion

The pathological events which lead to the destruction of the periodontium during inflammatory periodontal disease have been related to the effect of the imbalance between oxidants and antioxidants in patients with periodontal disease 20.

ROS are generated predominantly by PMN during an inflammatory response 21 It has been suggested that the bacterial species in subgingival plaques and the PMN response are important factors in the changes in periodontal disease status. An increase in ROS leads to the destruction of periodontal tissue, and it is one of the most important causes of periodontal disease. The present study has demonstrated significative changes in oxidative stress by measuring different oxidative stress markers (8-OHdG, MDA, GPx, SOD, and TAOC) that increased with worsened periodontal status.

The involvement of free radicals in cancer development has been studied for 3 decades, and there is sufficient evidence that implicates theirs in the multistage theory of carcinogenesis Free radicals are products of the oxidation-reduction systems of the cell and its participation in cellular metabolic functions is essential for cell survival. A classic example is the electron transport chain in mitochondria. However, in what pathological conditions, free radicals can become deleterious?

In fact, what are the results of its harmful effects. They are proposed to cause diverse DNA alterations like: punctual mutations, DNA base oxidations, strand breaks, mutation of tumor suppressor genes and can induce overexpression of proto-oncogenes22. Several works explore the levels of oxidative stress in patients with oral cancer 23 most of them quantified the products of lipid-peroxidation(mainly malonilaldehyde) and contrast them with the activity of antioxidant enzymes or exogenous antioxidants levels in blood or even saliva. The results agree that there is an imbalance between the high amount of free radicals and insufficient antioxidant system activity.Added to this, some researchers haveobserved that high levels of lipid-peroxidation combined with low levels of thiols and antioxidant status, correlate with poor survival rate in patients with oral cancer 24.It should be added that oxidative protein damage participates in facilitating thedevelopment of cancer. The present study has demonstrated significative changes in oxidative stress by measuring different oxidative stress markers (8-OHdG, MDA, GPx, SOD, and TAOC) that increased in oral cancer

Our results agree partly with Canakci et al. 25. In saliva collected samples from 30 patients with chronic periodontitis and 30 periodontally healthy controls, these authors obtained higher salivary 8-OHdG and MDA levels and lower salivary antioxidant activities that seem to reflect increased oxygen radical activity during periodontal inflammation.

Conclusion

Certainly, the main limitation of the study has been the small sample size, but the study could confirm the possible linear correlation between markers of oxidative stress and the periodontitis and oral cancer. Further studies with larger sample size should continue this line of research. In conclusion, the determination of oxidative stress levels could be a potent tool in controlling the development of periodontitis.and tool in detection of oral cancer.

Reference

  1. Kala Chandra, Ali Syed Salman, Abid Mohd., Rajpoot Sweety, Khan Najam Ali. Protection Against FCA Induced Oxidative Stress Induced DNA Damage as a Model of Arthritis and In vitro Anti-arthritic Potential of Costus speciosus Rhizome Extract. www.ijppr.com International Journal of Pharmacognosy and Phytochemical Research 2015; 7(2); 383-389. ISSN: 0975-4873
  2. Parellada M1, Moreno C, Mac-Dowell K, Leza JC, Giraldez M, Bailón C, Castro C, Miranda-Azpiazu P, Fraguas D, Arango”Plasma antioxidant capacity is reduced in Asperger syndrome.”. J Psychiatr Res. 2012 Mar;46(3):394-401. doi: 10.1016/j.jpsychires.2011.10.004. Epub 2012 Jan 4.
  3. ” A Meta-Analysis. Mol Neurobiol. 2015 Jun;51(3):932-46. doi: 10.1007/s12035-014-8747-0. Epub 2014 May 17. Increased oxidative stress and impaired antioxidant response in Lafora disease. Romá-Mateo C1, Aguado C, García-Giménez JL, Ibáñez-Cabellos JS, Seco-Cervera M, Pallardó FV, Knecht E, Sanz P.
  4. a b Halliwell, Barry (2007). “Oxidative stress and cancer: have we moved forward?” (PDF). Biochem. J. 401 (1): 1–11. doi:10.1042/BJ20061131. PMID 17150040.
  5. “Role of Oxidative Stress in Parkinson’s Disease”. Exp Neurobiol. 2013 Mar; 22(1): 11–17. Published online 2013 Mar 31.
  6. “Increased oxidative stress and impaired antioxidant response in lafora disease Romá-Mateo C1, Aguado C, García-Giménez JL, Ibáñez-Cabellos JS, Seco-Cervera M, Pallardó FV, Knecht E, Sanz P.
  7. Valko, M., Leibfritz, D., Moncol, J., Cronin, MTD., Mazur, M., Telser, J. (August 2007). “Free radicals and antioxidants in normal physiological functions and human disease”. International Journal of Biochemistry & Cell Biology 39 (1): 44–84. doi:10.1016/j.biocel.2006.07.001. PMID 16978905.
  8. Pohanka, M (2013). “Alzheimer´s disease and oxidative stress: a review”. Current Medicinal Chemistry 21 (3): 356–364. doi:10.2174/09298673113206660258. PMID 24059239.
  9. Bonomini F1, Tengattini S, Fabiano A, Bianchi R, Rezzani R.”Atherosclerosis and oxidative stress. Histol Histopathol. 2008 Mar;23(3):381-90.
  10. Singh, N., Dhalla, A.K., Seneviratne, C., Singal, P.K. (June 1995). “Oxidative stress and heart failure”. Molecular and Cellular Biochemistry 147 (1): 77–81. doi:10.1007/BF00944786.
  11. Ramond A, Godin-Ribuot D, Ribuot C, Totoson P, Koritchneva I, Cachot S, Levy P, Joyeux-Faure M. (December 2011). “Oxidative stress mediates cardiac infarction aggravation induced by intermittent hypoxia.”. Fundam Clin Pharmacol. 27 (3): 252–261. doi:10.1111/j.1472-8206.2011.01015.x. PMID 22145601.
  12. Dean OM, van den Buuse M, Berk M, Copolov DL, Mavros C, Bush AI. (July 2011). “N-acetyl cysteine restores brain glutathione loss in combined 2-cyclohexene-1-one and D-amphetamine-treated rats: relevance to schizophrenia and bipolar disorder”. Neurosci Lett. 499 (3): 149–53. doi:10.1016/j.neulet.2011.05.027. PMID 21621586.
  13. de Diego-Otero Y, Romero-Zerbo Y, el Bekay R, Decara J, Sanchez L, Rodriguez-de Fonseca F, del Arco-Herrera I. (March 2009). “Alpha-tocopherol protects against oxidative stress in the fragile X knockout mouse: an experimental therapeutic approach for the Fmr1 deficiency.”. Neuropsychopharmacology 34 (4): 1011–26. doi:10.1038/npp.2008.152. PMID 18843266.
  14. Amer, J., Ghoti, H., Rachmilewitz, E., Koren, A., Levin, C. and Fibach, E. (January 2006). “Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants”. British Journal of Haematology 132 (1): 108–113. doi:10.1111/j.1365-2141.2005.05834.x. PMID 16371026.
  15. Aly, D. G.; Shahin, R. S. (2010). “Oxidative stress in lichen planus”. Acta dermatovenerologica Alpina, Panonica, et Adriatica 19 (1): 3–11. PMID 20372767.
  16. Arican, O.; Kurutas, EB. (Mar 2008). “Oxidative stress in the blood of patients with active localized vitiligo.”. Acta Dermatovenerol Alp Panonica Adriat 17 (1): 12–6. PMID 18454264.
  17. James, SJ.; Cutler, P.; Melnyk, S.; Jernigan, S.; Janak, L.; Gaylor, DW.; Neubrander, JA. (Dec 2004). “Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism.”. Am J Clin Nutr 80 (6): 1611–7. PMID 15585776.
  18. Pohanka, M (2013). “Role of oxidative stress in infectious diseases. A review.”. Folia Microbiologica 584 (6): 503–513. doi:10.1007/s12223-013-0239-5. PMID 23504625.
  19. Gwen Kennedy, Vance A. Spence, Margaret McLaren, Alexander Hill, Christine Underwood & Jill J. F. Belch (September 2005). “Oxidative stress levels are raised in chronic fatigue syndrome and are associated with clinical symptoms”. Free radical biology & medicine 39 (5): 584–9. doi:10.1016/j.freeradbiomed.2005.04.020. PMID 16085177.
  20. Borges Jr., E. A. M. Moreira, D. W. Filho, T. B. de Oliveira, M. B. S. da Silva, and T. S. Fröde, “Proinflammatory and oxidative stress markers in patients with periodontal disease,” Mediators of Inflammation, vol. 2007, Article ID 45794, 5 pages, 2007..
  21. R. J. Waddington, R. Moseley, and G. Embery, “Reactive oxygen species: a potential role in the pathogenesis of periodontal diseases,” Oral Diseases, vol. 6, no. 3, pp. 138–151, 2000.
  22. Halliwell, B. (2007). Oxidative stress and cancer: have we moved forward?, Biochemical Journal, 401(1), 1-11.
  23. Das, S., Mahapatra, S. K., Gautam, N., Das, A., & Roy, S. (2007). Oxidative stress in lymphocytes, neutrophils, and serum of oral cavity cancer patients: modulatory array of l-glutamine., Supportive Care in Cancer, 15(12), 1399-1405.
  24. Patel B.P, Rawal U.M, Dave T.K, Rawal R.M, Shukla S.N, Shah P.M, Patel P.S. Lipid peroxidation, total antioxidant status, and total thiol levels predict overall survival in patients with oral squamous cell carcinoma. 2007, Integrative Cancer Therapies, 6(4), 365-372.
  25. C. F. Canakci, Y. Cicek, A. Yildirim, U. Sezer, and V. Canakci, “Increased levels of 8-hydroxydeoxyguanosine and malondialdehyde and its relationship with antioxidant enzymes in saliva of periodontitis patients,” European Journal of Dentistry, vol. 3, no. 2, pp. 100–106, 2009.
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