The origin of reactive oxygen species in mouse embryos cultured in vitro.

The increase in production of reactive oxygen species such as H2O2 at the G2/M phase of the second cell cycle may be related to the in vitro block to development of mouse 2-cell embryos. The occurrence of the H2O2 rise is independent of the activation of the embryonic genome and of passage through the S, G2 and M phases of the first cell cycle and G1 and M phases of the second cell cycle, but does require the activation of the unfertilized oocyte. The H2O2 is produced via dismutation of superoxide by the enzyme superoxide dismutase. Production of superoxide via mitochondrial, NADPH-oxidase and xanthine/xanthine oxidase systems has been investigated. The evidence suggests that superoxide, and thereby H2O2, is produced by the xanthine/xanthine oxidase system, but an involvement of the other superoxide generating systems has not been excluded. The relation between H2O2 and development in vitro is discussed.

[1]  J. Kishi,et al.  Involvement of superoxide radicals in the mouse two‐cell block , 1991, Molecular reproduction and development.

[2]  E. Wallach,et al.  Effect of inhibition of oxygen free radical on ovulation and progesterone production by the in-vitro perfused rabbit ovary. , 1991, Journal of reproduction and fertility.

[3]  R. Aitken,et al.  The effect of iron and iron chelators on the in-vitro block to development of the mouse preimplantation embryo: BAT6 a new medium for improved culture of mouse embryos in vitro. , 1990, Human reproduction.

[4]  A. Nureddin,et al.  Purines inhibit the development of mouse embryos in vitro. , 1990, Journal of reproduction and fertility.

[5]  L. Kobzik,et al.  Selective down-regulation of alveolar macrophage oxidative response to opsonin-independent phagocytosis. , 1990, Journal of immunology.

[6]  M. Johnson,et al.  Hydrogen peroxide levels in mouse oocytes and early cleavage stage embryos developed in vitro or in vivo. , 1990, Development.

[7]  G. Schultz,et al.  Transition from maternal to embryonic control in early mammalian development: A comparison of several species , 1990, Molecular reproduction and development.

[8]  Gregor Rothe,et al.  Flow Cytometric Analysis of Respiratory Burst Activity in Phagocytes With Hydroethidine and 2′,7′‐Dichlorofluorescin , 1990, Journal of leukocyte biology.

[9]  L. Kobzik,et al.  Oxidative Metabolism in the Alveolar Macrophage: Analysis by Flow Cytometry , 1990, Journal of leukocyte biology.

[10]  S. Pickering,et al.  A technique for quantifying the amount of macromolecule injected into cells of the early mouse embryo. , 1990, Journal of reproduction and fertility.

[11]  A. Cross,et al.  Purification and some properties of the 45 kDa diphenylene iodonium-binding flavoprotein of neutrophil NADPH oxidase. , 1990, The Biochemical journal.

[12]  E. Wallach,et al.  In vivo administration of allopurinol affects ovulation and early embryonic development in rabbits. , 1989, American journal of obstetrics and gynecology.

[13]  W. Hall,et al.  Inhibition of xanthine oxidase by 4-hydroxy-6-mercaptopyrazolo[3,4-d]pyrimidine. , 1989, Biochemical pharmacology.

[14]  J. Lewis,et al.  An improved culture medium supports development of random-bred 1-cell mouse embryos in vitro. , 1989, Journal of reproduction and fertility.

[15]  T. Bloom The effects of phorbol ester on mouse blastomeres: a role for protein kinase C in compaction? , 1989, Development.

[16]  B. Shapiro,et al.  Respiratory burst oxidase of fertilization. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[17]  S. Aust,et al.  The role of iron in oxygen radical mediated lipid peroxidation. , 1989, Chemico-biological interactions.

[18]  J. Lambeth Introduction: Respiratory burst oxidase and its regulation , 1988, Journal of bioenergetics and biomembranes.

[19]  C. Hegele-hartung,et al.  Potential risk of light and room temperature exposure to preimplantation embryos. , 1988, Fertility and sterility.

[20]  J. Jackson,et al.  Hypoxia increases glutathione redox cycle and protects rat lungs against oxidants. , 1988, Journal of applied physiology.

[21]  H. Pratt,et al.  Cycling cytoplasmic factors that promote mitosis in the cultured 2-cell mouse embryo. , 1988, Development.

[22]  T. Spector Oxypurinol as an inhibitor of xanthine oxidase-catalyzed production of superoxide radical. , 1988, Biochemical pharmacology.

[23]  D. Loutradis,et al.  Hypoxanthine causes a 2-cell block in random-bred mouse embryos. , 1987, Biology of reproduction.

[24]  B. Halliwell,et al.  Allopurinol and oxypurinol are hydroxyl radical scavengers , 1987, FEBS letters.

[25]  J. Levy,et al.  The timing of compaction: control of a major developmental transition in mouse early embryogenesis. , 1986, Journal of embryology and experimental morphology.

[26]  S. Howlett A set of proteins showing cell cycle dependent modification in the early mouse embryo , 1986, Cell.

[27]  R. W. Wright,et al.  Quantitative determination of the pentose phosphate pathway in preimplantation mouse embryos. , 1986, Biology of reproduction.

[28]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[29]  J. C. Chisholm,et al.  Developmental variability within and between mouse expanding blastocysts and their ICMs. , 1985, Journal of embryology and experimental morphology.

[30]  S. Pickering,et al.  Changes in actin distribution during fertilization of the mouse egg. , 1984, Journal of embryology and experimental morphology.

[31]  M. Johnson,et al.  The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo. , 1984, Journal of embryology and experimental morphology.

[32]  Matthew H. Kaufman,et al.  Early mammalian development : parthenogenetic studies , 1985 .

[33]  M. Goddard,et al.  Control of events during early cleavage of the mouse embryo: an analysis of the '2-cell block'. , 1983, Journal of embryology and experimental morphology.

[34]  P. Braude,et al.  The transition from maternal to embryonic control in the 2‐cell mouse embryo. , 1982, The EMBO journal.

[35]  R Yanagimachi,et al.  Detrimental effect of visible light on meiosis of mammalian eggs in vitro. , 1978, The Journal of experimental zoology.

[36]  B. Halliwell Superoxide‐dependent formation of hydroxyl radicals in the presence of iron chelates , 1978, FEBS letters.

[37]  JOSEPH C. DANIEL,et al.  Cleavage of Mammalian Ova inhibited by Visible Light , 1964, Nature.