User menu

Pyruvate prevents peroxide-induced injury of in vitro preimplantation bovine embryos.

Bibliographic reference Morales, H ; Tilquin, P ; Rees, Jean-François ; Massip, Alban ; Dessy, Franz ; et. al. Pyruvate prevents peroxide-induced injury of in vitro preimplantation bovine embryos.. In: Molecular reproduction and development, Vol. 52, no. 2, p. 149-57 (1999)
Permanent URL
  1. Andrae Ulrich, Singh Jaswanth, Ziegler-Skylakakis Kyriakoula, Pyruvate and related α-ketoacids protect mammalian cells in culture against hydrogen peroxide-induced cytotoxicity, 10.1016/0378-4274(85)90015-3
  2. Barnett Deborah K., Bavister Barry D., What is the relationship between the metabolism of preimplantation embryos and their developmental competence?, 10.1002/(sici)1098-2795(199601)43:1<105::aid-mrd13>;2-4
  3. Buc, J Pharm Belg, 43, 390 (1988)
  4. Butcher Liza, Coates Alison, Martin Karen L., Rutherford Anthony J., Leese Henry J., Metabolism of Pyruvate by the Early Human Embryo1, 10.1095/biolreprod58.4.1054
  5. Chun Y.S., Kim J.H., Lee H.T., Chung K.S., Effect of superoxide dismutase on the development of preimplantation mouse embryos, 10.1016/0093-691x(94)90087-y
  6. Dagnelie 1975. Les méthodes de l'inférence statistique. In: Théories et méthodes statistiques. Gembloux, Belgium: Gembloux Agronomic Press. p 213-240.
  7. de Lamirande, J Androl, 13, 379 (1992)
  8. Dorland, J Reprod Fertil, Abstr Ser, 9 (1992)
  9. Ealy A D, Howell J L, Monterroso V H, Aréchiga C F, Hansen P J, Developmental changes in sensitivity of bovine embryos to heat shock and use of antioxidants as thermoprotectants., 10.2527/1995.7351401x
  10. Ellington J.E., Farrell P.B., Foote R.H., Comparison of six-day bovine embryo development in uterine tube (oviduct) epithelial cell co-culture versus in vivo development in the cow, 10.1016/0093-691x(90)90555-8
  11. Gardner David K., Changes in requirements and utilization of nutrients during mammalian preimplantation embryo development and their significance in embryo culture, 10.1016/s0093-691x(97)00404-4
  12. Giandomenico Albert R, Cerniglia George E, Biaglow John E, Stevens Craig W, Koch Cameron J, The Importance of Sodium Pyruvate in Assessing Damage Produced by Hydrogen Peroxide, 10.1016/s0891-5849(97)00113-5
  13. Gómez E., Acetoacetate and β-d-hydroxybutyrate as energy substrates during early bovine embryo development in vitro, 10.1016/s0093-691x(97)00191-x
  14. Goto Yasuo, Noda Yoichi, Mori Takahide, Nakano Minoru, Increased generation of reactive oxygen species in embryos cultured in vitro, 10.1016/0891-5849(93)90126-f
  15. Guérin Pierre, Ménézo Yves, Hypotaurine and taurine in gamete and embryo environments: de novo synthesis via the cysteine sulfinic acid pathway in oviduct cells, 10.1017/s0967199400002768
  16. 1989. Free radicals in biology and medicine. New York: Oxford University Press.
  17. Herz Herman, Blake David R., Grootveld Martin, Multicomponent Investigations of the Hydrogen Peroxide- and Hydroxyl Radical-Scavenging Antioxidant Capacities of Biofluids: The Roles of Endogenous Pyruvate and Lactate Relevance to Inflammatory Joint Diseases, 10.3109/10715769709097781
  18. Holleman A. F., Notice sur l'action de l'eau oxygénée sur les acides α-cétoniques et sur les dicétones 1. 2, 10.1002/recl.19040230504
  19. Johnson Martin H., Nasresfahani Mohammad H., Radical solutions and cultural problems: Could free oxygen radicals be responsible for the impaired development of preimplantation mammalian embryos invitro?, 10.1002/bies.950160105
  20. Kim Jong-Heung, Niwa Koji, Lim Jeong-Mook, Okuda Kiyoshi, Effects of Phosphate, Energy Substrates, and Amino Acids on Development of in Vitro-Matured, in Vitro-Fertilized Bovine Oocytes in a Chemically Defined, Protein-Free Culture Medium1, 10.1095/biolreprod48.6.1320
  21. Leese, Oxford Rev Reprod Biol, 13, 35 (1991)
  22. Legge Michael, Sellens Martin H., Free radical scavengers ameliorate the 2-cell block in mouse embryo culture, 10.1093/oxfordjournals.humrep.a137442
  23. Lim J.M., Liou S.S., Hansel W., Intracytoplasmic glutathione concentration and the role of β-mercaptoethanol in preimplantation development of bovine embryos, 10.1016/0093-691x(96)00165-3
  24. Lindner Gary M., Wright Raymond W., Bovine embryo morphology and evaluation, 10.1016/0093-691x(83)90201-7
  25. Liu Zishu, Foote Robert H., Development of Bovine Embryos in KSOM with Added Superoxide Dismutase And Taurine and with Five and Twenty Percent 021, 10.1095/biolreprod53.4.786
  26. Luvoni Gaia C., Keskintepe Levent, Brackett Benjamin G., Improvement in bovine embryo production in vitro by glutathione-containing culture media, 10.1002/(sici)1098-2795(199604)43:4<437::aid-mrd5>;2-q
  27. Maral J., Puget K., Michelson A.M., Comparative study of superoxide dismutase, catalase and glutathione peroxidase levels in erythrocytes of different animals, 10.1016/s0006-291x(77)80151-4
  28. Massip Alban, Mermillod Pascal, Dinnyes Andras, Morphology and biochemistry of in-vitro produced bovine embryos: implications for their cryopreservation, 10.1093/oxfordjournals.humrep.a135837
  29. Nakayama T., Noda Y., Goto Y., Mori T., Effects of visible light and other environmental factors on the production of oxygen radicals by hamster embryos, 10.1016/0093-691x(94)90086-x
  30. Nasr-Esfahani, Development, 109, 501 (1990)
  31. Nasr-Esfahani M. H., Johnson M. H., How does transferrin overcome the in vitro block to development of the mouse preimplantation embryo?, 10.1530/jrf.0.0960041
  32. Nath, Am J Physiol, 264, f306 (1993)
  33. Nath Karl A., Enright Helen, Nutter Louise, Fischereder Michael, Zou Jing-nan, Hebbel Robert P., Effect of pyruvate on oxidant injury to isolated and cellular DNA, 10.1038/ki.1994.20
  34. Nathan C., Tumor cell anti-oxidant defenses. Inhibition of the glutathione redox cycle enhances macrophage-mediated cytolysis, 10.1084/jem.153.4.766
  35. Díaz A. Navas, Sánchez F. García, García J. A. GonzáLez, Enhancement and inhibition of luminol chemiluminescence by phenolic acids, 10.1002/bio.1170100306
  36. Noda, Assisted Reprod Rev, 2, 9 (1992)
  37. O'Donnell-Tormey J, DeBoer C J, Nathan C F, Resistance of human tumor cells in vitro to oxidative cytolysis., 10.1172/jci111981
  38. O'Donnell-Tormey J., Secretion of pyruvate. An antioxidant defense of mammalian cells, 10.1084/jem.165.2.500
  39. O'Fallon J.V., Wright R.W., Pyruvate revisited: A non-metabolic role for pyruvate in preimplantation embryo development, 10.1016/0093-691x(95)92442-c
  40. Olson S.E., Seidel G.E., Vitamin E improves development of bovine embryos produced in vitro, 10.1016/0093-691x(95)92443-d
  41. Pabon Julio E., Findley William E., Gibbons William E., The toxic effect of short exposures to the atmospheric oxygen concentration on early mouse embryonic development, 10.1016/s0015-0282(16)60688-x
  42. Parchment, In Vivo, 5, 493 (1991)
  43. Payne SR, Munday R, Thompson JG, Addition of superoxide dismutase and catalase does not necessarily overcome developmental retardation of one-cell mouse embryos during in-vitro culture , 10.1071/rd9920167
  44. Pierce G. Barry, Parchment Ralph E., Lewellyn Andrea L., Hydrogen peroxide as a mediator of programmed cell death in the blastocyst, 10.1111/j.1432-0436.1991.tb00880.x
  45. Pursel V.G., Wall R.J., Rexroad C.E., Hammer R.E., Brinster R.L., A rapid whole-mount staining procedure for nuclei of mammalian embryos, 10.1016/0093-691x(85)90167-0
  46. Reitzer, J Biol Chem, 254, 2669 (1979)
  47. Rieger D., Guay P., Measurement of the metabolism of energy substrates in individual bovine blastocysts, 10.1530/jrf.0.0830585
  48. Rieger D, Loskutoff NM, Betteridge KJ, Developmentally related changes in the uptake and metabolism of glucose, glutamine and pyruvate by cattle embryos produced in vitro, 10.1071/rd9920547
  49. Rosenkrans C. F., Zeng G. Q., McNamara G. T., Schoff P. K., First N. L., Development of Bovine Embryos in Vitro as Affected by Energy Substrates1, 10.1095/biolreprod49.3.459
  50. Salahudeen A K, Clark E C, Nath K A, Hydrogen peroxide-induced renal injury. A protective role for pyruvate in vitro and in vivo., 10.1172/jci115511
  51. SAS Institute Inc 1989. SAS/STAT user's guide, version 6, 4th edition. Cary, NC: SAS Institute Inc.
  52. SAS Institute Inc 1996. SAS/STAT software: changes and enhancements through release 6.11. Cary, NC: SAS Institute Inc.
  53. Spragg R G, Hinshaw D B, Hyslop P A, Schraufstätter I U, Cochrane C G, Alterations in adenosine triphosphate and energy charge in cultured endothelial and P388D1 cells after oxidant injury., 10.1172/jci112126
  54. Takahashi Y., First N.L., In vitro development of bovine one-cell embryos: Influence of glucose, lactate, pyruvate, amino acids and vitamins, 10.1016/0093-691x(92)90096-a
  55. Takahashi Masashi, Nagai Taku, Hamano Seizo, Kuwayama Masashige, Okamura Naomichi, Okano Akira, Effect of Thiol Compounds on in Vitro Development and Intracellular Glutathione Content of Bovine Embryos, 10.1095/biolreprod49.2.228
  56. Thomas Craig E., Reed Donald J., Radical-induced inactivation of kidney Na+,K+-ATPase: Sensitivity to membrane lipid peroxidation and the protective effect of vitamin E, 10.1016/0003-9861(90)90418-x
  57. Thompson J. G., Partridge R. J., Houghton F. D., Cox C. I., Leese H. J., Oxygen uptake and carbohydrate metabolism by in vitro derived bovine embryos, 10.1530/jrf.0.1060299
  58. Vajta, Cryo-Lett, 18, 191 (1997)
  59. Van Langendonckt A., Donnay I., Schuurbiers N., Auquier P., Carolan C., Massip A., Dessy F., Effects of supplementation with fetal calf serum on development of bovine embryos in synthetic oviduct fluid medium, 10.1530/jrf.0.1090087
  60. Whitehead T.P., Thorpe G.H.G., Maxwell S.R.J., Enhanced chemiluminescent assay for antioxidant capacity in biological fluids, 10.1016/0003-2670(92)85052-8