Tooth Bleaching Increases Dentinal Protease Activity
- C. Sato1
- F.A. Rodrigues1
- D.M. Garcia1
- C.M.P. Vidal2
- D.H. Pashley3
- L. Tjäderhane4
- M.R. Carrilho5
- F.D. Nascimento6,*
- I.L.S. Tersariol1,7,*
- 1Centro Interdisciplinar de Investigação Bioquímica, UMC, Mogi das Cruzes, Brazil
- 2Department of Restorative Dentistry, Piracicaba Dental School, UNICAMP, Piracicaba, Brazil
- 3Department of Oral Biology, College of Dental Medicine, Georgia Health Sciences University, Augusta, GA, USA
- 4Institute of Dentistry, University of Oulu, Finland
- 5Schulich Dentistry, University of Western Ontario, London, Canada
- 6Biomaterials Research Group, UNIBAN, Brazil
- 7Departamento de Bioquímica, UNIFESP, São Paulo, Brazil
Abstract
Hydrogen peroxide is an oxidative agent commonly used for dental bleaching procedures. The structural and biochemical responses
                     of enamel, dentin, and pulp tissues to the in vivo
 bleaching of human (n = 20) premolars were investigated in this study. 
Atomic force microscopy (AFM) was used to observe
                     enamel nanostructure. The chemical composition of 
enamel and dentin was analyzed by infrared spectroscopy (FTIR). The 
enzymatic
                     activities of dental cathepsin B and matrix 
metalloproteinases (MMPs) were monitored with fluorogenic substrates. 
The amount
                     of collagen in dentin was measured by emission of 
collagen autofluorescence with confocal fluorescence microscopy. The 
presence
                     of Reactive Oxygen Species (ROS) in the pulp was 
evaluated with a fluorogenic 2′,7′-dichlorodihydrofluorescein diacetate 
(DCFDA)
                     probe. Vital bleaching of teeth significantly 
altered all tested parameters: AFM images revealed a corrosion of 
surface enamel
                     nanostructure; FTIR analysis showed a loss of 
carbonate and proteins from enamel and dentin, along with an increase in
 the
                     proteolytic activity of cathepsin-B and MMPs; and 
there was a reduction in the autofluorescence of collagen and an 
increase
                     in both cathepsin-B activity and ROS in pulp 
tissues. Together, these results indicate that 35% hydrogen peroxide 
used in
                     clinical bleaching protocols dramatically alters 
the structural and biochemical properties of dental hard and soft pulp 
tissue. 
 
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