Genotoxicity of nitric oxide produced from sodium nitroprusside

被引:23
作者
Lin, WC [1 ]
Xue, HW [1 ]
Liu, SY [1 ]
He, YQ [1 ]
Fu, JL [1 ]
Zhou, ZC [1 ]
机构
[1] Beijing Med Univ, Dept Toxicol, Beijing 100083, Peoples R China
关键词
nitric oxide; sodium nitroprusside; g12; cell; genotoxicity;
D O I
10.1016/S1383-5718(98)00014-X
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
Induction of mutation and micronucleus (MN) formation by nitric oxide (NO) was investigated in mammalian cells using sodium nitroprusside (SNP) as a drug donor of NO. Results showed that the concentration of NO; in the tested solution rose according to time- and concentration-exposure to SNP. The treatment of SNP (0.5-8 mu mol/ml with S9 or 2-8 mu mol/ml without S9) induced a concentration-dependent increase in the mutation frequency at the gpt gene locus in g12 cells and caused a 13- (-S9) to 25- (+S9) fold increase above the background level at the highest concentration. A statistically significant increase in the number of micronucleated binucleated cells (MNBN) was also observed in treated groups. MNBN parts per thousand, MN parts per thousand and the proportion of the multiple micronuleated cells increased in a concentration-dependent manner in the concentration range of SNP (0.5-4 mu mol/ml with S9 or 2-8 mu mol/ml without S9). Our results indicate that SNP, an NO releasing drug, is genotoxic in g12 cells. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 27 条
[11]   BIOSYNTHESIS AND METABOLISM OF ENDOTHELIUM-DERIVED NITRIC-OXIDE [J].
IGNARRO, LJ .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1990, 30 :535-560
[12]  
ISHEDATE M, 1988, MUTAT RES, V195, P151
[13]   INDUCTION OF MUTATIONS AND CHROMOSOME-ABERRATIONS IN LUNG-CELLS FOLLOWING INVIVO EXPOSURE OF RATS TO NITROGEN-OXIDES [J].
ISOMURA, K ;
CHIKAHIRA, M ;
TERANISHI, K ;
HAMADA, K .
MUTATION RESEARCH, 1984, 136 (02) :119-125
[14]   COMPARATIVE-STUDIES ON RADIATION-INDUCED MICRONUCLEI AND CHROMOSOMAL-ABERRATIONS IN V79 CELLS [J].
KESHAVA, C ;
ONG, T ;
NATH, J .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 328 (01) :63-71
[15]   THE SALMONELLA-TYPHIMURIUM MAMMALIAN MICROSOMAL ASSAY - A REPORT OF THE UNITED-STATES-ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
KIER, LE ;
BRUSICK, DJ ;
AULETTA, AE ;
VONHALLE, ES ;
BROWN, MM ;
SIMMON, VF ;
DUNKEL, V ;
MCCANN, J ;
MORTELMANS, K ;
PRIVAL, M ;
RAO, TK ;
RAY, V .
MUTATION RESEARCH, 1986, 168 (02) :69-240
[16]   TRANSGENIC CHINESE HAMSTER V79 CELL-LINES WHICH EXHIBIT VARIABLE LEVELS OF GPT MUTAGENESIS [J].
KLEIN, CB ;
ROSSMAN, TG .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1990, 16 (01) :1-12
[17]   A REVIEW AND ANALYSIS OF THE CHINESE-HAMSTER OVARY HYPOXANTHINE GUANINE PHOSPHORIBOSYL TRANSFERASE ASSAY TO DETERMINE THE MUTAGENICITY OF CHEMICAL-AGENTS - A REPORT OF PHASE-III OF THE UNITED-STATES ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
LI, AP ;
GUPTA, RS ;
HEFLICH, RH ;
WASSOM, JS .
MUTATION RESEARCH, 1988, 196 (01) :17-36
[18]   POTENTIAL GENOTOXICITY OF CHRONICALLY ELEVATED NITRIC-OXIDE - A REVIEW [J].
LIU, RH ;
HOTCHKISS, JH .
MUTATION RESEARCH-REVIEWS IN GENETIC TOXICOLOGY, 1995, 339 (02) :73-89
[19]   MUTAGENICITY OF GLYCERYL TRINITRATE (NITROGLYCERIN) IN SALMONELLA-TYPHIMURIUM [J].
MARAGOS, CM ;
ANDREWS, AW ;
KEEFER, LK ;
ELESPURU, RK .
MUTATION RESEARCH, 1993, 298 (03) :187-195
[20]   NITRIC-OXIDE AS A SECRETORY PRODUCT OF MAMMALIAN-CELLS [J].
NATHAN, C .
FASEB JOURNAL, 1992, 6 (12) :3051-3064