Genotoxic and cytotoxic effects of different types of dental cement on normal cultured human lymphocytes

被引:34
作者
Bakopoulou, A. [2 ]
Mourelatos, D. [1 ]
Tsiftsoglou, A. S. [3 ]
Giassin, N. P. [2 ]
Mioglou, E. [1 ]
Garefis, P. [2 ]
机构
[1] Aristotle Univ Thessaloniki, Sch Med, Dept Biol & Genet, Thessaloniki 54124, Greece
[2] Aristotle Univ Thessaloniki, Sch Dent, Dept Fixed & Implant Prosthodont, Thessaloniki 54124, Greece
[3] Aristotle Univ Thessaloniki, Dept Pharmaceut Sci, Pharmacol Lab, Thessaloniki 54124, Greece
关键词
Dental cements; Glass ionomers; Resin-modified glass ionomers; Dual cure resin cements; Sister chromatid exchange (SCE); Chromosomal aberrations (CAs); Proliferation rate index (PRI); GLASS-IONOMER CEMENTS; SISTER-CHROMATID EXCHANGE; IN-VITRO CYTOTOXICITY; CELL-CYCLE ARREST; CHROMOSOMAL-ABERRATIONS; RESIN MONOMERS; GLUTATHIONE DEPLETION; HUMAN-POPULATIONS; RELEASE; HEMA;
D O I
10.1016/j.mrgentox.2008.10.011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study we have investigated the genotoxic and cytotoxic effects Of eluates derived from different types of commercially available dental cements, including glass ionomer cements (GICs) (Ketac Cem/3 M ESPE and GC Fuji I/GC Corp), resin-modified glass ionomer cements (RM-GICs) (RelyX Luting/3 M ESPE and Vitrebond/3 M ESPE) and dual-cure resin cements (RCs) (Variolink II/ Ivoclar-Vivadent and Panavia F 2.0/Kuraray) on normal cultured human lymphocytes. Lymphocyte primary cultures obtained from blood samples of three healthy donors were exposed to serial dilutions of eluates derived from specimens of each material tested. Metaphases were induced with phytoliaemagglutinin, collected after 72 h treatment by use of colchicine and stained according to the fluorescence plus giemsa (FPG) procedure. Preparations were scored for sister chromatid exchange (SCE) and chromosomal aberrations (CAs), while the proliferation rate index (PRI) was also calculated. Our results show that eluates derived from the RM-GICs and RCs caused severe genotoxic effects by significantly increasing the frequencies of SCEs and CAs in cultures of peripheral blood lymphocytes and by decreasing the relevant PRI values in a dose-dependent manner, whereas the two GICs caused only minor cytogenetic effects. Eluates of the two RM-GICs (Vitrebond and RelyX) were also very cytotoxic, as the first serial dilutions of both materials caused a complete mitotic arrest in lymphocyte cultures. Overall, the degree of genotoxicity and cytoroxicity caused by dental cements decreased as follows: Viterbond > Rely X> Panavia F 2.0 > Variolink II > Ketac Cem = GC Fuji I. These results indicate that different types of dental cement differ extensively in their genotoxic and cytotoxic potential and their ability to affect chromosomal integrity, cell-cycle progression, DNA replication and repair. Although these results cannot be directly extrapolated to the clinical situation, the potential occurrence of adverse effects Caused by the RM-GICs and RCs tested in this study should be considered when making a clinical decision about dental cements. (c) 2008 Elsevier B.V. All rights reserved.
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收藏
页码:103 / 112
页数:10
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