Micronuclei are induced in rat spermatids in vitro by 1,2,3,4-diepoxybutane but not by 1,2-epoxy-3-butene and 1,2-dihydroxy-3,4-epoxybutane

被引:12
|
作者
Sjoblom, T
Lahdetie, J
机构
[1] Institute of Biomedicine, Department of Medical Genetics, University of Turku, FIN-20520 Turku
关键词
D O I
10.1093/mutage/11.5.525
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The genotoxic effects of three 1,3-butadiene metabolites, 1,2-epoxy-3-butene (monoepoxide, EB), 1,2,3,4-diepoxybutane (diepoxide, DEB) and 1,2-dihydroxy-3,4-epoxybutane (diolepoxide, DiolEB), on male rat germ cells were studied by the meiotic micronucleus method in vitro. Seminiferous tubular segments from stages XII to XIII containing late pachytene-diakinetic spermatocytes were cultivated in the presence of the test chemical for 4 days, During the culture, spermatocytes passed through meiotic divisions and developed into early spermatids in which micronuclei could be scored, DEB was found to be a very potent micronucleus inducer in rat meiosis, All concentrations tested (5-20 mu M) were able to cause a statistically significantly higher frequency of micronuclei (P < 0.05) compared with controls and a linear dose-dependent trend for micronucleus induction was seen (P < 0.01), However, EB and DiolEB caused no increase in micronucleus frequencies in spermatids at the concentrations tested (100-1000 mu M for EB and 10-100 mu M for DiolEB) and at higher concentrations cytotoxic effects were seen upon dividing cells causing a significant reduction in the number of spermatids. According to these results DEB is the most genotoxic butadiene metabolite in rat germ cells during meiosis.
引用
收藏
页码:525 / 528
页数:4
相关论文
共 50 条
  • [1] Physiologically based pharmacokinetic modeling of 1,3-butadiene, 1,2-epoxy-3-butene, and 1,2:3,4-diepoxybutane toxicokinetics in mice and rats
    Sweeney, LM
    Schlosser, PM
    Medinsky, MA
    Bond, JA
    CARCINOGENESIS, 1997, 18 (04) : 611 - 625
  • [2] Flow cytometric analysis of micronucleus induction in rat bone marrow polychromatic erythrocytes by 1,2;3,4-diepoxybutane, 3,4-epoxy-1-butene, and 1,2-epoxybutane-3,4-diol
    Lahdetie, J
    Grawe, J
    CYTOMETRY, 1997, 28 (03): : 228 - 235
  • [3] Comparison of cytogenetic effects of 3,4-epoxy-1-butene and 1,2:3,4-diepoxybutane in mouse, rat and human lymphocytes following in vitro G0 exposures
    Kligerman, AD
    DeMarini, DM
    Doerr, CL
    Hanley, NM
    Milholland, VS
    Tennant, AH
    MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 439 (01) : 13 - 23
  • [4] Hepatic and pulmonary glutathione conjugation of 1,2:3,4-diepoxybutane in human, rat, and mouse in vitro
    Boogaard, PJ
    Sumner, SCJ
    Turner, MJ
    Bond, JA
    TOXICOLOGY, 1996, 113 (1-3) : 297 - 299
  • [5] Hemoglobin adduct levels in rat and mouse treated with 1,2:3,4-diepoxybutane
    Fred, C
    Kautiainen, A
    Athanassiadis, L
    Törnqvist, M
    CHEMICAL RESEARCH IN TOXICOLOGY, 2004, 17 (06) : 785 - 794
  • [6] OXIDATION OF 1,2-EPOXY-3-BUTENE TO 1,2-3,4-DIEPOXYBUTANE BY CDNA-EXPRESSED HUMAN CYTOCHROMES P450 2E1 AND 3A4 AND HUMAN, MOUSE AND RAT-LIVER MICROSOMES
    SEATON, MJ
    FOLLANSBEE, MH
    BOND, JA
    CARCINOGENESIS, 1995, 16 (10) : 2287 - 2293
  • [7] Synthesis of diols from 1,2-epoxy-3-butene
    Mel'nik, L. V.
    Srednev, S. S.
    Rybina, G. V.
    Meshechkina, A. E.
    Shevchuk, A. S.
    Danilova, A. S.
    PETROLEUM CHEMISTRY, 2007, 47 (03) : 201 - 204
  • [8] METHOD FOR DETERMINING 1,2:3,4-DIEPOXYBUTANE IN WORKPLACE AIR
    Kowalska, Joanna
    Jezewska, Anna
    MEDYCYNA PRACY, 2016, 67 (05) : 645 - 652
  • [9] Synthesis of diols from 1,2-epoxy-3-butene
    L. V. Mel’nik
    S. S. Srednev
    G. V. Rybina
    A. E. Meshechkina
    A. S. Shevchuk
    A. S. Danilova
    Petroleum Chemistry, 2007, 47 : 201 - 204
  • [10] Glutathione conjugation of 1,2:3,4-diepoxybutane in human liver and rat and mouse liver and lung in vitro
    Boogaard, PJ
    Sumner, SCJ
    Bond, JA
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 136 (02) : 307 - 316