Assessment of 1,2-propanediol (PrOH) genotoxicity on mouse oocytes by comet assay

被引:21
作者
Berthelot-Ricou, Anais [3 ]
Perrin, Jeanne [2 ,3 ]
di Giorgio, Carole [3 ]
de Meo, Michel [3 ]
Botta, Alain [3 ]
Courbiere, Blandine [1 ,3 ]
机构
[1] AP HM Concept, Pole Gynecol Obstet & Reprod, Pr Gamerre, F-13005 Marseille, France
[2] AP HM Concept, CECOS Lab Biol Reprod, Pr Grillo, F-13005 Marseille, France
[3] Univ Mediterranee, Fac Med & Pharm, Federat Rech CNRS ECCOREV 3098, Lab Biogenotoxicol & Mutagenese Environm, Marseille, France
关键词
1,2-Propanediol; PrOH; cryoprotectant; mouse; oocytes; genotoxicity; DNA damage; comet assay; ETHYLENE-GLYCOL; DNA-DAMAGE; ONGOING PREGNANCIES; DIMETHYL-SULFOXIDE; MEIOTIC SPINDLE; IN-VITRO; VITRIFICATION; CRYOPRESERVATION; SLOW; PERMEABILITY;
D O I
10.1016/j.fertnstert.2011.07.1106
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To assess the genotoxicity of 1,2-propanediol (PrOH) on mouse oocytes by comet assay. Design: In vitro assay using murine model. Setting: Biogenotoxicology research laboratory. Animal(s): CD1 female mice. Intervention(s): Three 40-oocyte groups were exposed to different PrOH concentrations (5%, 7.5%, and 15%). Each concentration was tested during both long and short exposures (1-2 hours and 1-5 minutes) in comparison with control groups. DNA damage was evaluated by a single-cell gel electrophoresis assay, also called "comet assay," and analyzed with Komet software. Main Outcome Measure(s): DNA damage was quantified as Olive tail moment (OTM). Interpretation was done on OTM with the use of chi(2). Result(s): High PrOH concentrations (7.5% and 15%) induced significant DNA damage on mouse oocytes. The OTM c 2 values were 4.16 +/- 0.40 and 6.80 +/- 0.4 with 7.5% PrOH at 1 and 2 hours, respectively, 24.35 +/- 1.60 with 15% at 1 hour, and for 2h at 15% the DNA damage was too drastic to calculate OTM chi(2). After 1 and 5 minutes, the OTM chi(2) values were, respectively, 5.19 perpendicular to 0.26 and 6.06 perpendicular to 0.42 with 7.5%, and 7.53 perpendicular to 0.33 and 16.81 perpendicular to 0.67 with 15%. Conclusion(s): High concentrations of PrOH (7.5% and 15%) induced significant DNA damage on mouse oocytes, whatever the exposure duration. These results should be interpreted with caution, because additional data are needed to evaluate PrOH genotoxicity and DNA oocyte reparation after exposure to high PrOH concentrations. (Fertil Steril (R) 2011; 96: 1002-7. (C) 2011 by American Society for Reproductive Medicine.)
引用
收藏
页码:1002 / 1007
页数:6
相关论文
共 45 条
  • [1] SFTG international collaborative study on in vitro micronucleus test - III. Using CHO cells
    Aardema, Marilyn J.
    Snyder, Ronald D.
    Spicer, Carol
    Divi, Katyayini
    Morita, Takeshi
    Mauthe, Robert J.
    Gibson, David P.
    Soelter, Sandra
    Curry, Patrick T.
    Thybaud, Veronique
    Lorenzon, Giocondo
    Marzin, Daniel
    Lorge, Elisabeth
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2006, 607 (01) : 61 - 87
  • [2] Cryotop vitrification of human oocytes results in high survival rate and healthy deliveries
    Antinori, Monica
    Licata, Emanuele
    Dani, Gianluca
    Ceerusico, Fabrizio
    Versaci, Caterina
    Antinori, Severino
    [J]. REPRODUCTIVE BIOMEDICINE ONLINE, 2007, 14 (01) : 72 - 79
  • [3] Assessment of the genotoxicity of three cryoprotectants used for human oocyte vitrification: Dimethyl sulfoxide, ethylene glycol and propylene glycol
    Aye, M.
    Di Giorgio, C.
    De Mo, M.
    Botta, A.
    Perrin, J.
    Courbiere, B.
    [J]. FOOD AND CHEMICAL TOXICOLOGY, 2010, 48 (07) : 1905 - 1912
  • [4] A randomized controlled study of human Day 3 embryo cryopreservation by slow freezing or vitrification: vitrification is associated with higher survival, metabolism and blastocyst formation
    Balaban, B.
    Urman, B.
    Ata, B.
    Isiklar, A.
    Larman, M. G.
    Harnilton, R.
    Gardner, D. K.
    [J]. HUMAN REPRODUCTION, 2008, 23 (09) : 1976 - 1982
  • [5] The distribution of the tail moments in single cell gel electrophoresis (comet assay) obeys a chi-square (χ2) not a gaussian distribution
    Bauer, E
    Recknagel, RD
    Fiedler, U
    Wollweber, L
    Bock, C
    Greulich, KO
    [J]. MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 398 (1-2) : 101 - 110
  • [6] Comet assay on mouse oocytes: an improved technique to evaluate genotoxic risk on female germ cells
    Berthelot-Ricou, Anais
    Perrin, Jeanne
    Di Giorgio, Carole
    De Meo, Michel
    Botta, Alain
    Courbiere, Blandine
    [J]. FERTILITY AND STERILITY, 2011, 95 (04) : 1452 - 1457
  • [7] Boldt J, 2010, REPROD BIOMED O 1213
  • [8] Effects of UVA and Visible Light on the Photogenotoxicity of Benzo[a]pyrene and Pyrene
    Botta, Celine
    Di Giorgio, Carole
    Sabatier, Anne-Sophie
    De Meo, Michel
    [J]. ENVIRONMENTAL TOXICOLOGY, 2009, 24 (05) : 492 - 505
  • [9] The in vivo comet assay:: use and status in genotoxicity testing
    Brendler-Schwaab, S
    Hartmann, A
    Pfuhler, S
    Speit, G
    [J]. MUTAGENESIS, 2005, 20 (04) : 245 - 254
  • [10] Fourth International Workgroup on Genotoxicity Testing: Results of the in vivo Comet assay workgroup
    Burlinson, Brian
    Tice, Raymond R.
    Speit, Gunter
    Agurell, Eva
    Brendler-Schwaab, Susanne Y.
    Collins, Andrew R.
    Escobar, Patricia
    Honma, Masamitsu
    Kumaravel, Tirukalikundram S.
    Nakajima, Madoka
    Sasaki, Yu F.
    Thybaud, Veronique
    Uno, Yoshifumi
    Vasquez, Marie
    Hartmann, Andreas
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2007, 627 (01) : 31 - 35