TY - JOUR
T1 - Effect of N-acetylcysteine on rat dental pulp cells cultured on mineral trioxide aggregate
AU - Minamikawa, Hajime
AU - Yamada, Masahiro
AU - Deyama, Yoshiaki
AU - Suzuki, Kuniaki
AU - Kaga, Masayuki
AU - Yawaka, Yasutaka
AU - Ogawa, Takahiro
PY - 2011/5
Y1 - 2011/5
N2 - Introduction: The purpose of this study was to evaluate the cytotoxicity of mineral trioxide aggregate (MTA) and its potential detoxification by an antioxidant amino acid, N-acetylcysteine (NAC). Methods: Rat dental pulp cells extracted from rat maxillary incisors were directly cultured on MTA with or without NAC in culture me-dium. The number of cells and their spreading behavior were both assessed 24 hours after seeding. The intracellular levels of reactive oxygen species (ROS) and glutathione (GSH) were also assessed after 24 hours of culture. Results: The number of cells attached to MTA was 60% greater when NAC was added to the culture medium. In addition, the area and perimeter of the cells were found to be 2-fold greater in the culture containing NAC. Cells cultured on MTA alone showed large ROS concentrations, which disappeared when the medium was supplemented with NAC. The intracellular GSH level, however, increased 3.5-fold with NAC addition. Conclusions: This study demonstrated that the presence of NAC in environments can substantially improve attachment and spreading behaviors of dental pulp cells on MTA. This biological effect was associated with an im-provement in the cellular redox system by NAC and warrants further exploration of NAC for determining its therapeutic value in improving the biocompatibility of MTA.
AB - Introduction: The purpose of this study was to evaluate the cytotoxicity of mineral trioxide aggregate (MTA) and its potential detoxification by an antioxidant amino acid, N-acetylcysteine (NAC). Methods: Rat dental pulp cells extracted from rat maxillary incisors were directly cultured on MTA with or without NAC in culture me-dium. The number of cells and their spreading behavior were both assessed 24 hours after seeding. The intracellular levels of reactive oxygen species (ROS) and glutathione (GSH) were also assessed after 24 hours of culture. Results: The number of cells attached to MTA was 60% greater when NAC was added to the culture medium. In addition, the area and perimeter of the cells were found to be 2-fold greater in the culture containing NAC. Cells cultured on MTA alone showed large ROS concentrations, which disappeared when the medium was supplemented with NAC. The intracellular GSH level, however, increased 3.5-fold with NAC addition. Conclusions: This study demonstrated that the presence of NAC in environments can substantially improve attachment and spreading behaviors of dental pulp cells on MTA. This biological effect was associated with an im-provement in the cellular redox system by NAC and warrants further exploration of NAC for determining its therapeutic value in improving the biocompatibility of MTA.
KW - Cytotoxicity
KW - glutathione
KW - mineral trioxide aggregate
KW - N-acetylcysteine
KW - reactive oxygen species
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U2 - 10.1016/j.joen.2011.02.012
DO - 10.1016/j.joen.2011.02.012
M3 - Article
C2 - 21496663
AN - SCOPUS:79956189454
SN - 0099-2399
VL - 37
SP - 637
EP - 641
JO - Journal of Endodontics
JF - Journal of Endodontics
IS - 5
ER -