Variation of mouse oocyte sensitivity to griseofulvin‐induced aneuploidy and meiotic delay during the first meiotic division

The effects of varying the time of chemical treatment on the induction of areuploidy and meiotic delay in metaphase II (Mll) oocytes were studied by administering 1,500 mg/kg griseofulvin (GF) at 0, 2, 4, 6, or 8 hr after on injection of human chorionic gonadotrophin (HCG). The results show that the oocytes have a different sensitivity to GF‐induced aneuploidy and meiotic delay during the course of meiotic maturation. Although not restricted to a particular period of meiotic maturation, the frequency of aneuploidy was highest (P < 0.05) when GF was given at 2, 4, or 6 hr after HCG. The maximum frequency of hyperploidy (42.4%) occurred at the 4‐hr treatment time. Also, GF treatment resulted in the induction of meiotic delay as demonstrated by ovulated metaphase I (Ml) and polyploid Mll oocytes. The meiotic delay data depict a period of relative resistance between two periods of sensitivity in that the percentages of ovulated Ml oocytes were 53.3, 21.3, 3.5, 6.7, and 25.7 when GF was given at 0, 2, 4, 6, and 8 hr after HCG, respectively. Also, at these treatment times the percentages of polyploid oocytes were 0.6, 1.7, 7.7, 20.1, and 15.4, respectively. Therefore, the oocytes seem to be more sensitive to GF‐induced meiotic delay during the periods preceding and following meiotic spindle assembly. In conclusion, the results demonstrate that the time of chemical treatment influences the frequency of aneuploidy and the degree of meiotic delay. Also, the results emphasize that to thoroughly characterize the aneugenic potential of a specific chemical several treatment times may be needed. © 1994 Wiley‐Liss, Inc.

[1]  F. Marchetti,et al.  The Relationship Between Chemically-Induced Meiotic Delay and Aneuploidy in Mouse Oocytes and Zygotes , 1993 .

[2]  M. Aardema,et al.  Griseofulvin-induced aneuploidy and meiotic delay in mouse oocytes: effect of dose and harvest time. , 1993, Mutation research.

[3]  M. Gaulden Maternal age effect: the enigma of Down syndrome and other trisomic conditions. , 1992, Mutation research.

[4]  M. Aardema,et al.  Benomyl-induced aneuploidy in mouse oocytes. , 1992, Mutagenesis.

[5]  F. Marchetti,et al.  Griseofulvin-induced aneuploidy and meiotic delay in female mouse germ cells. II. Cytogenetic analysis of one-cell zygotes. , 1992, Mutation research.

[6]  F. Marchetti,et al.  Griseofulvin-induced aneuploidy and meiotic delay in female mouse germ cells. I. Cytogenetic analysis of metaphase II oocytes. , 1992, Mutation research.

[7]  M. Aardema,et al.  Cytogenetic analysis of mouse oocytes and one-cell zygotes as a potential assay for heritable germ cell aneuploidy. , 1990, Mutation research.

[8]  A. Russo,et al.  Meiotic arrest and aneuploidy induced by vinblastine in mouse oocytes. , 1988, Mutation research.

[9]  J. B. Mailhes,et al.  Cytogenetic technique for mouse metaphase II oocytes. , 1987, Gamete research.

[10]  Z. Polański In-vivo and in-vitro maturation rate of oocytes from two strains of mice. , 1986, Journal of reproduction and fertility.

[11]  S. Malawista,et al.  Griseofulvin: association with tubulin and inhibition of in vitro microtubule assembly. , 1982, Biochemical and biophysical research communications.

[12]  R. Keates Griseofulvin at low concentration inhibits the rate of microtubule polymerization in vitro. , 1981, Biochemical and biophysical research communications.

[13]  A. Leonard,et al.  Mutagenicity tests with griseofulvin. , 1979, Mutation research.

[14]  G. Borisy,et al.  Role of tubulin-associated proteins in microtubule nucleation and elongation. , 1977, Journal of molecular biology.

[15]  K. Weber,et al.  Interaction of griseofulvin with microtubules, microtubule protein and tubulin. , 1977, Journal of molecular biology.

[16]  K. Gull,et al.  Evidence that griseofulvin binds to a microtubule associated protein , 1977, FEBS letters.

[17]  I. Hansmann,et al.  Chromosome aberrations in metaphase II oocytes of Chinese hamster (Cricetulus griseus). I. The sensitivity of the pre-ovulatory phase to triaziquone. , 1974, Mutation research.

[18]  R. Donahue Maturation of the mouse oocyte in vitro. I. Sequence and timing of nuclear progression. , 1968, The Journal of experimental zoology.

[19]  R. Edwards,et al.  Timing of the stages of the maturation divisions, ovulation, fertilization and the first cleavage of eggs of adult mice treated with gonadotrophins. , 1959, The Journal of endocrinology.

[20]  J. B. Mailhes,et al.  Differential sensitivity of mouse oocytes to colchicine‐induced aneuploidy , 1987, Environmental and molecular mutagenesis.

[21]  C. Tease,et al.  Oocytes from young and old female mice respond differently to colchicine. , 1986, Mutation research.

[22]  E. Hook The impact of aneuploidy upon public health: mortality and morbidity associated with human chromosome abnormalities. , 1985, Basic life sciences.

[23]  E. Hummler,et al.  Preferential nondisjunction of specific bivalents in oocytes from Djungarian hamsters (Phodopus sungorus) following colchicine treatment. , 1985, Cytogenetics and cell genetics.