SIMULTANEOUS MICRONUCLEUS AND CHROMOSOME ABERRATION ASSESSMENT IN THE RAT

被引:34
作者
KRISHNA, G
KROPKO, ML
CIARAVINO, V
THEISS, JC
机构
[1] Molecular Toxicology Section, Departrnent of Pathology and Experirnental Toxicology, Parke-Davis Pharmaceutical Research Division, Ann Arbor, MI 48105, Warner-Lambert Cornpany
来源
MUTATION RESEARCH | 1991年 / 264卷 / 01期
关键词
MICRONUCLEUS ASSAY; CHROMOSOME ABERRATION TEST; CYCLOPHOSPHAMIDE; SEX COMPARISON; (RAT);
D O I
10.1016/0165-7992(91)90042-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Using a cellulose column fractionation procedure to eliminate nucleated cells for micronucleus assessment, micronucleus and chromosome aberration endpoints in the same animal were compared in male and female rats following i.p. injection with cyclophosphamide (CP). Groups of 5 Wistar rats per sex were given single doses of CP at 0, 20, or 40 mg/kg. Two hours prior to sacrifice, animals were given colchicine (4 mg/kg) to arrest cells in metaphase. One femur from each animal was used for micronucleus assessment and the other for chromosome aberration assessment. In the micronucleus assessment, 2000 polychromatic erythrocytes (PCEs) per animal and in the chromosome aberration assessment, 50 metaphase cells per animal were scored. This experiment was repeated once. In both experiments, significant increases in micronucleated PCEs and chromosome aberrations were noted at both doses of CP in both sexes. In general, the clastogenic effects of CP were more pronounced in males than females. Both doses of CP caused a decrease in the proportion of PCEs and in mitotic index in both experiments, indicating toxicity of CP to the bone marrow. These results show the usefulness of this rat model for simultaneous evaluation of two cytogenetic endpoints in the same animal and indicate that assessment of MNPCE frequency in the bone marrow of male rats may be an appropriate model for screening test substances for in vivo clastogenic activity in this species.
引用
收藏
页码:29 / 35
页数:7
相关论文
共 29 条
[1]   THE CYTONUCLEUS TEST IN THE RAT - A COMBINED METAPHASE AND MICRONUCLEUS ASSAY [J].
ALBANESE, R .
MUTATION RESEARCH, 1987, 182 (06) :309-321
[2]   SPECIES-SPECIFIC RESPONSE TO THE RODENT CARCINOGENS 1,2-DIMETHYLHYDRAZINE AND 1,2-DIBROMO-3-CHLOROPROPANE IN RODENT BONE-MARROW MICRONUCLEUS ASSAYS [J].
ALBANESE, R ;
MIRKOVA, E ;
GATEHOUSE, D ;
ASHBY, J .
MUTAGENESIS, 1988, 3 (01) :35-38
[3]   MICRONUCLEI - ORIGINS, APPLICATIONS AND METHODOLOGIES - A WORKSHOP SPONSORED BY THE HEALTH-AND-SAFETY-EXECUTIVE HELD IN MANCHESTER, MAY 23-25, 1988 [J].
ARLETT, CF ;
ASHBY, J ;
FIELDER, RJ ;
SCOTT, D .
MUTAGENESIS, 1989, 4 (06) :482-485
[4]   SLIDE PREPARATION AND SAMPLING AS A MAJOR SOURCE OF VARIABILITY IN THE MOUSE MICRONUCLEUS ASSAY [J].
ASHBY, J ;
MOHAMMED, R .
MUTATION RESEARCH, 1986, 164 (04) :217-235
[5]   KINETICS OF MICRONUCLEUS FORMATION IN RELATION TO CHROMOSOMAL-ABERRATIONS IN MOUSE BONE-MARROW [J].
HAYASHI, M ;
SOFUNI, T ;
ISHIDATE, M .
MUTATION RESEARCH, 1984, 127 (02) :129-137
[6]   THE INDUCTION OF MICRONUCLEI AS A MEASURE OF GENOTOXICITY - A REPORT OF THE UNITED-STATES ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
HEDDLE, JA ;
HITE, M ;
KIRKHART, B ;
MAVOURNIN, K ;
MACGREGOR, JT ;
NEWELL, GW ;
SALAMONE, MF .
MUTATION RESEARCH, 1983, 123 (01) :61-118
[7]   INVIVO AND INVIVO INVITRO KINETICS OF CYCLOPHOSPHAMIDE-INDUCED SISTER-CHROMATID EXCHANGES IN MOUSE BONE-MARROW AND SPLEEN-CELLS [J].
KRISHNA, G ;
NATH, J ;
PETERSEN, M ;
ONG, T .
MUTATION RESEARCH, 1988, 204 (02) :297-305
[8]   CYCLOPHOSPHAMIDE-INDUCED CYTOGENETIC EFFECTS IN MOUSE BONE-MARROW AND SPLEEN-CELLS IN INVIVO AND INVIVO INVITRO ASSAYS [J].
KRISHNA, G ;
NATH, J ;
PETERSEN, M ;
ONG, T .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1987, 7 (02) :183-195
[9]   INVIVO CYTOGENETIC STUDIES ON MICE EXPOSED TO ETHYLENE DIBROMIDE [J].
KRISHNA, G ;
XU, J ;
NATH, J ;
PETERSEN, M ;
ONG, T .
MUTATION RESEARCH, 1985, 158 (1-2) :81-87
[10]  
KRISHNA G, 1990, Environmental and Molecular Mutagenesis Supplement, V15, P32