Genotoxic potential of quinolone antimicrobials in the in vitro comet assay and micronucleus test

被引:43
作者
Itoh, T
Mitsumori, K
Kawaguchi, S
Sasaki, YF
机构
[1] Tokyo Univ Agr & Technol, Lab Vet Pathol, Fac Agr, Tokyo 1838509, Japan
[2] Hachinohe Natl Coll Technol, Lab Genotoxic, Fac Chem & Biol Engn, Hachinohe, Aomori 0391192, Japan
[3] Gifu Univ, United Grad Sch Vet Sci, Gifu 5011193, Japan
关键词
quinolone; comet assay; micronucleus test; genotoxicity; single strand breaks; norfloxacin;
D O I
10.1016/j.mrgentox.2005.11.003
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
The purpose of this study was to examine the genotoxicity of quinolone antimicrobials. We investigated the genotoxic potential of eight quinolones, namely nalidixic acid (NA), pipemidic acid (PPA), oxolinic acid (OA), piromidic acid (PA), enoxacin (ENX), ofloxacin (OFLX), norfloxacin (NFLX) and ciprofloxacin (CPFX), by the in vitro alkaline single-cell gel electrophoresis (comet) assay at pH > 13. WTK-1 cells (mutant p53) were treated with each of the eight quinolones at 62.5-1000 mu g/mL for 2, 4 and 20 h. NFLX and CPFX significantly induced DNA damage concentration-dependently after 4 and 20 h treatment, but this damage was recoverable. On the other hand, DNA was not damaged in the cells treated with six other quinolones. In the cells treated with NFLX and CPFX for 20 h, DNA migration was compared by the comet assay at pH 10, 12.1 and >13. The comet assay both at pH 12.1 and >13 showed increased DNA migration, but there was no positive response in the comet assay at pH 10. In the in vitro micronucleus (MN) test, WTK-1 cells were treated with each of four quinolones (NA, PPA, NFLX and CPFX) at 15.63-125 mu g/mL for 20 h. NFLX significantly increased MNs in the cells, but no changes were noted in the cells treated with three other quinolones. These results suggest that NFLX and CPFX induced DNA single strand breaks (SSBs), and that NFLX-induced SSBs resulted in chromosome aberrations. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 144
页数:10
相关论文
共 29 条
[1]   Antibacterial activities and inhibitory effects of sitafloxacin (DU-6859a) and its optical isomers against type II topoisomerases [J].
Akasaka, T ;
Kurosaka, S ;
Uchida, Y ;
Tanaka, M ;
Sato, K ;
Hayakawa, I .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (05) :1284-1287
[2]   GENOTOXICITY OF 17 GYRASE AND 4 MAMMALIAN TOPOISOMERASE-II POISONS IN PROKARYOTIC AND EUKARYOTIC TEST SYSTEMS [J].
ALBERTINI, S ;
CHETELAT, AA ;
MILLER, B ;
MUSTER, W ;
PUJADAS, E ;
STROBEL, R ;
GOCKE, E .
MUTAGENESIS, 1995, 10 (04) :343-351
[3]  
Cai ZJ, 1999, WHO TECH REP SER, V887, P1
[4]   MECHANISM OF ACTION AND ANTITUMOR-ACTIVITY OF (S)-10-(2,6-DIMETHYL-4-PYRIDINYL)-9-FLUORO-3-METHYL-7-OXO-2,3-DIHYDRO-7H-PYRIDOL[1,2,3-DE]-[1,4]BENZOTHIAZINE-6-CARBOXYLIC ACID (WIN-58161) [J].
COUGHLIN, SA ;
DANZ, DW ;
ROBINSON, RG ;
KLINGBEIL, KM ;
WENTLAND, MP ;
CORBETT, TH ;
WAUD, WR ;
ZWELLING, LA ;
ALTSCHULER, E ;
BALES, E ;
RAKE, JB .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (01) :111-122
[5]   THE COMET ASSAY - A COMPREHENSIVE REVIEW [J].
FAIRBAIRN, DW ;
OLIVE, PL ;
ONEILL, KL .
MUTATION RESEARCH-REVIEWS IN GENETIC TOXICOLOGY, 1995, 339 (01) :37-59
[6]   MEASUREMENT OF MICRONUCLEI IN LYMPHOCYTES [J].
FENECH, M ;
MORLEY, AA .
MUTATION RESEARCH, 1985, 147 (1-2) :29-36
[7]   MUTAGENICITY OF QUINOLONE ANTIBACTERIALS [J].
FORT, FL .
DRUG SAFETY, 1992, 7 (03) :214-222
[8]   A topoisomerase II inhibitor, NK109, induces DNA single- and double-strand breaks and apoptosis [J].
Fukuda, M ;
Inomata, M ;
Nishio, K ;
Fukuoka, K ;
Kanzawa, F ;
Arioka, H ;
Ishida, T ;
Fukumoto, H ;
Kurokawa, H ;
Oka, M ;
Saijo, N .
JAPANESE JOURNAL OF CANCER RESEARCH, 1996, 87 (10) :1086-1091
[10]   Use of the alkaline comet assay for industrial genotoxicity screening:: comparative investigation with the micronucleus test [J].
Hartmann, A ;
Elhajouji, A ;
Kiskinis, E ;
Poetter, F ;
Martus, HJ ;
Fjällman, A ;
Frieauff, W ;
Suter, W .
FOOD AND CHEMICAL TOXICOLOGY, 2001, 39 (08) :843-858