Effect of culture condition and cell-permeable superoxide dismutase on levels of reactive oxygen species (ROS) production in " in vitro" produced sheep embryos

Small Ruminant Research

Volumn 97, Issue 1-3, 2011, Pages 88-93

  Hosseini, S Ostad ^a   Aghaee, F ^b   Hosseini, S M ^a   Hajian, M ^a   Forouzanfar, M ^c   Noorbakhshnia, M ^b   Gourabi, H ^a   Shahverdi, A H ^d   Vosough Taghi Dizaj, A ^a   Nasr Esfahani, M H ^a  

^a ROYAN INSTITUTE FOR REPRODUCTIVE BIOMEDICINE   (Iran)

^b SHAHREKORD UNIVERSITY   (Iran)

^c ISLAMIC AZAD UNIVERSITY   (Iran)

^d AVICENNA RESEARCH INSTITUTE   (Iran)

Author keywords

Embryo; In vitro; ROS; Sheep

Indexed keywords

OVIS ARIES;

EID: 79954814097     PISSN: 09214488     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.smallrumres.2011.02.010     Document Type: Article

References (28)

1. Agarwal A., Allamaneni S.S. Role of free radicals in female reproductive diseases and assisted reproduction. Reprod. Biomed. Online 2004, 9(3):338-347.
2. Agarwal A., Gupta S., Sharma R. Oxidative stress and its implications in female infertility - a clinician's perspective. Reprod. Biomed. Online 2005, 11(5):641-650.
3. Betts D.H., Madan P. Permanent embryo arrest: molecular and cellular concepts. Mol. Hum. Reprod. 2008, 4:445-453.
4. Blondin P., Coenen K., Sirard M.A. The impact of reactive oxygen species on bovine sperm fertilizing ability and oocyte maturation. Andrologia 1997, 18(4):454-460.
5. Cetica P.D., Pintos L.N., Dalvit G.C., Beconi M.T. Antioxidant enzyme activity and oxidative stress in bovine oocyte in vitro maturation. IUBMB Life 2001, 51(1):57-64.
6. Chun Y.S., Kim J.H., Lee H.T., Chung K.S. Effect of superoxide dismutase on the development of preimplantation mouse embryos. Theriogenology 1994, 41:511-520.
7. Cuzzocrea S., Costantino G., Mazzon E., De Sarro A., Caputi A.P. Beneficial effects of Mn(III)tetrakis (4-benzoic acid) porphyrin (MnTBAP), a superoxide dismutase mimetic, in zymosan-induced shock. Br. J. Pharmacol. 1999, 128(6):1241-1251.
8. Dalvit G.C., Cetica P.D., Pintos L.N., Beconi M.T. Reactive oxygen species in bovine embryo in vitro production. Biocell 2005, 29(2):209-212.
9. Eugene A., Konorev E.A., Kennedy M.C., Kalyanaraman B. Cell-permeable superoxide dismutase and glutathione peroxidase mimetics afford superior protection against doxorubicin-induced cardiotoxicity: the role of reactive oxygen and nitrogen intermediates. Arch. Biochem. Biophys. 1999, 15(368 (2)):421-428.
10. Gardner D.K., Lane M., Spitzer A., Batt P.A. Enhanced rates of cleavage and development for sheep zygotes cultured to the blastocyst stage in vitro in the absence of serum and somatic cells: amino acids, vitamins, and culturing embryos in groups stimulate development. Biol. Reprod. 1994, 994(50 (2)):390-400.
11. Goto Y., Noda Y., Mori T., Nakano M. Increased generation of reactive oxygen species in embryos cultured in vitro. Free Radic. Biol. Med. 1993, 15:69-75.
12. Guerin P., Moutassam S.E., Menezo Y. Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings. Hum. Reprod. 2001, 7:175-189.
13. Gupta S., Malhotra N., Sharma D., Chandra A., Agarwal A. Oxidative stress and its role in female infertility and assisted reproduction: clinical implications. IJFS 2009, 2(4):147-164.
14. Gupta M.K., Uhm S.J., Lee H.T. Effect of vitrification and beta-mercaptoethanol on reactive oxygen species activity and in vitro development of oocytes vitrified before or after in vitro fertilization. Fertil. Steril. 2010, 93(8):2602-2607.
15. Holm P., Booth P.J., Schmidt M.H., Greve T., Callesen H. High bovine blastocyst development in a static in vitro production system using SOFaa medium supplemented with sodium citrate and myo-inositol with or without serum-proteins. Theriogenology 1999, 52(4):683-700.
16. Johnson M.H., Nasr-Esfahani M.H. Radical solutions and cultural problems: could free oxygen radicals be responsible for the impaired development of preimplantation mammalian embryos in vitro?. Bioassays 1994, 16(1):31-38.
17. Kitagawa Y., Suzuki K., Yoneda A., Watanabe T. Effects of oxygen concentration and antioxidants on the in vitro developmental ability, production of reactive oxygen species (ROS), and DNA fragmentation in porcine embryos. Theriogenology 2004, 1(62 (7)):1186-1197.
18. Lane M., Gardner D.K. Embryo culture medium: which is the best?. Pract. Res. Clin. Obstet. Gynaecol. 2007, 21(1):83-100.
19. Lindenau A., Fischer B. Effect of oxygen concentration in the incubator's gas phase on the development of cultured preimplantation rabbit embryos. Theriogenology 1994, 41(4):889-898.
20. Malassagne B., Ferret P.J., Hammoud R., Tulliez M., Bedda S., Trebeden H., Jaffray P., Calmus Y., Weill B., Batteux F. The superoxide dismutase mimetic MnTBAP prevents Fas-induced acute liver failure in the mouse. Gastroenterology 2001, 121:1451-1459.
21. Nasr-Esfahani M.H., Aitken J.R., Johnson M.H. Hydrogen peroxide level in mouse oocytes and early cleavage stage embryos developed in vitro or in vivo. Development 1990, 109:501-507.
22. Nasr-Esfahani M.H., Johnson M.H. The origin of reactive oxygen species in mouse embryos cultured in vitro. Development 1991, 113(2):551-560.
23. Nasr-Esfahani M.H., Johnson M.H. Quantitative analysis of cellular glutathione in early preimplantation mouse embryos developing in vivo and in vitro. Hum. Reprod. 1992, 7(9):1281-1290.
24. Szeto H.H. Cell-permeable, mitochondrial-targeted, peptide antioxidants. AAPS J. 2006, 21(8 (2)):277-283.
25. Sharafi M., Forouzanfar M., Hosseini S.M., Hajian M., Ostadhosseini S. In vitro comparison of soybean lecithin based-extender with commercially available extender for ram semen cryopreservation. IJFS 2009, 3:149-152.
26. Yang H.W., Hwang K.J., Kwon H.C., Kim H.C., Choi K.W., Ohl K.S. Detection of reactive oxygen species (ROS) and apoptosis in human fragmented embryos. Hum. Reprod. 1998, 13:998-1002.
27. Zahmatkesh M., Kadkhodaee M., Moosavi S.M., Jorjani M., Kajbafzadeh A., Golestani A., Ghaznavi M. Beneficial effects of MnTBAP, a broad-spectrum reactive species scavenger, in rat renal ischemia/reperfusion injury. Clin. Exp. Nephrol. 2005, 9:212-218.
28. Zingarelli B., Day B.J., Crapo J., Salzman A.L., Szabo C. The potential involvement of peroxynitrite in the pathogenesis of endotoxic shock. Br. J. Pharmacol. 1997, 120:259-264.