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Karpuk I.Y.
The importance of matrix metalloproteinases-8 and -9 in the development of oral mucosa allergopathology caused by intolerance to tooth prosthetic materials
Education Establishment "Vitebsk State Order of Peoples’ Friendship Medical University", Republic of Belarus

Abstract.
Objectives. To determine the role of metalloproteinases system in the pathogenesis of an allergy to dentoprosthetic materials for broadening the notion about pathogenetic mechanisms of its formation with the purpose of the elaboration of biochemical criteria to assess the risk of the development of an allergy to dentoprosthetic materials.
Material and methods. We have established the content of matrix metalloproteinases (MMP)-8 and -9 in the oral fluid in 40 patients allergic to dentoprosthetic materials.
Results. The results of the comparative immunofermental research of the content of matrix metalloproteinases -8 and -9 in the oral fluid of people with various constructional materials of teeth and tooth alignments restorations are presented.
Proteolysis system including matrix metalloproteinases family is characterized by the increase in the activity of MMP-8 and -9 in the saliva of patients with intolerance to dentoprosthetic materials 33,3 mg/ml and 37,3 mg/ml respectively (in the control group – 9 mg/ml and 14 mg/ml).
It has been revealed that MMP-8 and-9 in the oral fluid may serve as a marker of an allergy to dentoprosthetic materials, this being proved by the correlation analysis of the obtained data between the results of the reaction of allergen-induced damage of leukocytes (RADL) and MMP-8 and MMP-9 levels. The following dependences have been found: 1) direct strong correlation of RADL (ZnCl2 0,01%) and MMP-8 levels (R=0,76; p=0,001) and MMP-9 (R=0,8; p=0,001); 2) direct moderate correlation of RADL (CrCl3 0,01%) and MMP-8 levels (R=0,49; p=0,0019) and MMP-9 (R=0,34; p=0,04); 3) direct moderate correlation of RADL (NiCl2 0,01%) and MMP-8 levels (R=0,52; p=0,001) and MMP-9 (R=0,57; p=0,001); 4) direct moderate correlation of RADL (CoCl2 0,005%) and MMP-8 levels (R=0,53; p=0,005) and MMP-9 (R=0,36; p=0,02).
Conclusion. Studying qualitative and quantitative characteristics of MMP and their inhibitors in the oral fluid is a new direction of scientific researches which will enable the elaboration of new approaches to the diagnosing, prognostication and scientific substantiation of the choice of the most informative criteria to assess individual predisposition to the development of an allergy to dentoprosthetic materials.
Key words: oral fluid, allergy, matrix metalloproteinases.

References

1. Lygre H. Prosthodontic biomaterials and adverse reactions: a critical review of the clinical and research literature. Acta Odontol Scand. 2002 Jan;60(1):1-9.
2. Maksimovskiy YuM, Grinin VM, Gorbov SI. Biosovmestimost' splavov, ispol'zuemykh v stomatologii [Biocompatibility of the alloys used in an odontology]. Stomatologiia. 2000;(4):73-5.
3. Lebedev KA, Mitronin AV, Poniakina ID. Neperenosimost' zuboproteznykh materialov [Intolerance of dentoprosthetic materials]. Moscow, RF: Librokom; 2010. 208 р.
4. Kushlinskiy NE, Karaoglanova TB, Solovykh EA, Gershtein ES, Troshin AA, Yanushevich OO. Matriksnye metalloproteinazy i ikh tkanevye ingibitory v rotovoi zhidkosti bol'nykh khronicheskim generalizovannym parodontitom s razlichnymi konstruktsionnymi materialami restavratsii zubov i zubnykh riadov [Matriksny metalproteinases and their fabric inhibitors in stomatic liquid of patients with a chronic generalized periodontal disease with various constructional materials of restorations of teeth and dentitions]. Voprosy biologicheskoi, meditsinskoi i farmatsevticheskoi khimii. 2012;(10):47-51.
5. Ardans J, Economou A, Martinson J, Zhou M, Wahl LM. Oxidised low density and high density lipoproteins regulate the production of matrix metalloproteinases 1 and 9 by activated monocytes. J. Leukoc. Biol.  2002 Jun;71(6):1012-8.
6. Bakos SR, Schwob JE, Costanzo RM. Matrix metalloproteinase-9 and -2 expression in the olfactory bulb following methyl bromide gas exposure. Chem Senses. 2010 Oct;35(8):655-61.
7. Chow AK, Cena J, Schulz R. Acute actions and novel targets of matrix metalloproteinases in the heart and vasculature. Br J Pharmacol. 2007 Sep;152(2):189-205.
8. Kiili M, Cox SW, Chen HY, Wahlgren J, Maisi P, Eley BM, Salo T, Sorsa T. Collagenase-2 (MMP-8) and collagenase-3 (MMP-13) in adult periodontitis: molecular forms and levels in gingival crevicular fluid and immunolocalisation in gingival tissue. J Clin Periodontol. 2002 Mar;29(3):224-32.
9. Maesco G, Bravo M, Bascones A. Levels of metalloproteinase-2 and -9 and tissue inhibitor of matrix metalloproteinase-1 in gingival crevicular fluid of patients with periodontitis, gingivitis, and healthy gingival. Quintessence Int. 2007 Mar;38(3):247-52.
10. Mäkelä M, Salo T, Uitto VJ, Larjava H. Matrix metalloproteinases (MMP-2 and MMP-9) of the oral cavity: cellular origin and relationship to periodontal status. J Dent Res. 1994 Aug;73(8):1397-406.
11. Pozo P, Valenzuela MA, Melej C, Zaldívar M, Puente J, Martínez B, Gamonal J. Longitudinal analysis of metalloproteinases, tissue inhibitors of metalloproteinases and clinical parameters in gingival crevicular fluid from periodontitis-affected patients. J Periodontal Res. 2005 Jun;40(3):199-207.
12. Séguier S, Gogly B, Bodineau A, Godeau G, Brousse N. Is collagen breakdown during periodontitis linked to inflammatory cells and expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in human gingival tissue? J Periodontol. 2001 Oct;72(10):1398-406.
13. Verstappen J, Von den Hoff JW. Tissue inhibitors of metalloproteinases (TIMPs): their biological functions and involvement in oral disease. J Dent Res. 2006 Dec;85(12):1074-84.
14. Novikov DK, Sergeev YuV, Novikov PD. Lekarstvennaia allergiia [Medicinal allergy]. Moscow, RF: Natsional'naia akademiia mikologii; 2001. 363 р.
15. Novikov DK, Novikova VI. Otsenka immunnogo statusa [Assessment of the immune status]. Mosсow, RF: Meditsina; 1996. 240 р.

 

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