QUANTITATIVE-ANALYSIS OF CELLULAR GLUTATHIONE IN EARLY PREIMPLANTATION MOUSE EMBRYOS DEVELOPING INVIVO AND INVITRO

被引:74
作者
NASRESFAHANI, MH [1 ]
JOHNSON, MH [1 ]
机构
[1] UNIV CAMBRIDGE,DOWNING ST,CAMBRIDGE CB2 3DY,ENGLAND
基金
英国医学研究理事会;
关键词
DEVELOPMENTAL BLOCK; FREE RADICALS; GLUTATHIONE; MOUSE EGGS;
D O I
10.1093/oxfordjournals.humrep.a137843
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The relative levels of reduced glutathione (GSH) have been measured fluorimetrically in individual eggs and early embryos from two mouse strains, one of which shows developmental arrest in vitro. GSH levels fell by approximately 20-25% at fertilization and by approximately 45% by the late 2-cell and early 4-cell stages. No differences were observed between strains or between embryos cultured in vitro or in vivo. Addition of exogenous H2O2 or diethylmaleate depleted GSH. GSH levels were not affected significantly after inhibition of GSH-peroxidase by mercaptosuccinate nor of catalase by aminotriazole. Mercaptosuccinate did not inhibit development but catalase inhibition caused arrest at the 2-cell stage. Addition of exogenous GSH or thioredoxin did not promote development of 'blocking' embryos through the 2-cell block. It is concluded that early embryos lack a mercaptosuccinate sensitive peroxidase activity for removing H2O2, which may be removed by catalase or the glutathione-S-transferase system. It is suggested that GSH may have a role in detoxifying peroxidated lipids. The results are consistent with a role for reactive oxygen species in the 2-cell block.
引用
收藏
页码:1281 / 1290
页数:10
相关论文
共 36 条
[1]  
Allameh A., Saxena M., Mehta L.N., Raj H.G., Comparison of pulmonary and hepatic glutathione depletion by diethyl maleate, Med. Sci. Res., pp. 957-958, (1987)
[2]  
Baird M.B., Hough J.L., Adriamycin induced oxidative stress: Evidence for strain specific protection against cardiac lipid peroxida-tion, 5Th Biennial Meeting of the International Society of Free Radicals and Medicine, 13, (1990)
[3]  
Boerjan M.L., De Boer P., The first cell cycle of zygotes of the mouse derived from oocytes and aged post-ovulation in vivo and fertilization in vivo, Zygote Development after Delayed Fertilization, pp. 17-33, (1990)
[4]  
Calvin H.I., Grosshans K., Blake E.J., Estimation and manipulation of glutathione levels in perpuberal mouse ovaries and ova: Relevance to sperm nucleus transformation in the fertilized egg, Gamete Res, 14, pp. 265-275, (1986)
[5]  
Chisholm J.C., Johnson M.H., Warren P.D., Fleming T.P., Pickering S.J., Developmental variability within and between mouse expanding blastocysts and their ICMs, J. Embryo! Exp. Morphol, 86, pp. 311-336, (1985)
[6]  
Den Boer P.J., Van Loon A., Mackenbach P., Van Der Schans G.P., Grootegoed J.A., Effect of glutathione depletion on the cytotoxicity of xenobiotics and induction of single-strand DNA breaks by ionizing radiation in isolated hamster round spermatids, J. Reprod. Fertil, 88, pp. 259-269, (1990)
[7]  
Fernandez Checa J.C., Kaplowitz N., The use of monochloro-bimane to determine hepatic GSH levels and synthesis, Anal. Biochem, 190, pp. 212-219, (1990)
[8]  
Goto Y., Noda Y., Narimoto K., Mori T., Effects of thioredoxin on mouse embryo development. 7th Annual Meeting of the ESHRE and 7th World Congress on IVF and Assisted Procrea-tion, Hum. Reprod., Abstr, (1991)
[9]  
Gutteridge J., Rowley D.A., Halliwell B., Superoxide dependent formation of hydroxy radicals in the presence of iron salts, Biochem, J, 199, pp. 263-265, (1981)
[10]  
Halliwell B., Gutteridge J., Free Radicals in Biology and Medicine, (1990)