1. bookVolume 22 (2022): Edition 3 (July 2022)
Détails du magazine
License
Format
Magazine
eISSN
2300-8733
Première parution
25 Nov 2011
Périodicité
4 fois par an
Langues
Anglais
Accès libre

Effect of enzymatic pro-oxidant and antioxidant systems on bovine oocyte in vitro maturation

Publié en ligne: 19 Jul 2022
Volume & Edition: Volume 22 (2022) - Edition 3 (July 2022)
Pages: 923 - 929
Reçu: 01 Jun 2021
Accepté: 29 Sep 2021
Détails du magazine
License
Format
Magazine
eISSN
2300-8733
Première parution
25 Nov 2011
Périodicité
4 fois par an
Langues
Anglais

Aitken R.J. (2020). Impact of oxidative stress on male and female germ cells: implications for fertility. Reproduction, 159: R189–R201. Search in Google Scholar

Ali A.A., Bilodeau J.F., Sirard M.A. (2003). Antioxidant requirements for bovine oocytes varies during in vitro maturation, fertilization and development. Theriogenology, 59: 939–949. Search in Google Scholar

Ali I., Liu H.X., Zhong-Shu L., Dong-Xue M., Xu L., Shah S.Z.A., Ullah O., Nan-Zhu F. (2018). Reduced glutathione alleviates tunicamycin-induced endoplasmic reticulum stress in mouse preimplantation embryos. J. Reprod. Dev., 64: 15–24. Search in Google Scholar

Altenhöfer S., Radermacher K.A., Kleikers P.W.M., Wingler K., Schmidt H.H.H.W. (2015). Evolution of NADPH oxidase inhibitors: Selectivity and mechanisms for target engagement. Antioxid. Redox Sign., 23: 406–427. Search in Google Scholar

Alvarez G., Morado S., Soto M., Dalvit G., Cetica P. (2015). The control of reactive oxygen species influences porcine oocyte in vitro maturation. Reprod. Domest. Anim., 50: 200–205. Search in Google Scholar

Bienert G.P., Schjoerring J.K., Jahn T.P. (2006). Membrane transport of hydrogen peroxide. Biochim. Biophys. Acta - Biomembr., 1758: 994–1003. Search in Google Scholar

Blondin P., Coenen K., Sirard M.A. (1997). The impact of reactive oxygen species on bovine sperm fertilizing ability and oocyte maturation. J. Androl., 18: 454–460. Search in Google Scholar

Buck T., Hack C.T., Berg D., Berg U., Kunz L., Mayerhofer A. (2019). The NADPH oxidase 4 is a major source of hydrogen peroxide in human granulosa-lutein and granulosa tumor cells. Sci. Rep., 9: 1–11. Search in Google Scholar

Carbone M.C., Tatone C., Delle Monache S., Marci R., Caserta D., Colonna R., Amicarelli F. (2003). Antioxidant enzymatic defences in human follicular fluid: Characterization and age-dependent changes. Mol. Hum. Reprod., 9: 639–643. Search in Google Scholar

Cetica P.D., Dalvit G.C., Beconi M.T. (1999). Study of evaluation criteria used for in vitro bovine oocyte selection and maturation. Biocell, 23: 125–133. Search in Google Scholar

Cetica P.D., Pintos L.N., Dalvit G.C., Beconi M.T. (2001). Antioxidant enzyme activity and oxidative stress in bovine oocyte in vitro maturation. IUBMB Life, 51: 57–64. Search in Google Scholar

Christou-Kent M., Dhellemmes M., Lambert E., Ray P.F., Arnoult C. (2020). Diversity of RNA-binding proteins modulating post-transcriptional regulation of protein expression in the maturing mammalian oocyte. Cells, 9: 662. Search in Google Scholar

Combelles C.M.H., Holick E.A., Paolella L.J., Walker D.C., Wu Q. (2010). Profiling of superoxide dismutase isoenzymes in compartments of the developing bovine antral follicles. Reproduction, 139: 871–881. Search in Google Scholar

Cui M.S., Wang X.L., Tang D.W., Zhang J., Liu Y., Zeng S.M. (2011). Acetylation of H4K12 in porcine oocytes during in vitro aging: Potential role of ooplasmic reactive oxygen species. Theriogenology, 75: 638–646. Search in Google Scholar

Egea J., Fabregat I., Frapart Y.M., Ghezzi P., Görlach A., Kietzmann T., Kubaichuk K., Knaus U.G., et al. (2017). European contribution to the study of ROS: A summary of the findings and prospects for the future from the COST action BM1203 (EU-ROS). Redox Biol., 13: 94–162. Search in Google Scholar

El-Shahat K.H., Kandil M. (2012). Antioxidant capacity of follicular fluid in relation to follicular size and stage of estrous cycle in buffaloes. Theriogenology, 77: 1513–1518. Search in Google Scholar

García-Martínez T., Vendrell-Flotats M., Martínez-Rodero I., Ordóñez-León E.A., Álvarez-Rodríguez M., López-Béjar M., Yeste M., Mogas T. (2020). Glutathione ethyl ester protects in vitro-maturing bovine oocytes against oxidative stress induced by subsequent vitrification/warming. Int. J. Mol. Sci., 21: 1–26. Search in Google Scholar

Goud A.P., Goud P.T., Diamond M.P., Gonik B., Abu-Soud H.M. (2008). Reactive oxygen species and oocyte aging: Role of superoxide, hydrogen peroxide, and hypochlorous acid. Free Radic. Biol. Med., 44: 1295–1304. Search in Google Scholar

Gupta S., Choi A., Yu H.Y., Czerniak S.M., Holick E.A., Paolella L.J., Agarwal A., Combelles C.M.H. (2011). Fluctuations in total antioxidant capacity, catalase activity, and hydrogen peroxide levels of follicular fluid during bovine folliculogenesis. Reprod. Fertil. Dev., 23: 673–680. Search in Google Scholar

Gutnisky G., Morado S., Gadze T., Donato A., Alvarez G., Dalvit G., Cetica P. (2020) Morphological, biochemical and functional studies to evaluate bovine oocyte vitrification. Theriogenology, 143: 18–26.10.1016/j.theriogenology.2019.11.037 Search in Google Scholar

Hancock J.T., Desikan R., Neill S.J. (2001). Role of reactive oxygen species in cell signalling pathways. Biochem. Soc. Trans., 29: 345–349. Search in Google Scholar

Herrick J.R., Brad A.M., Krisher R.L. (2006). Chemical manipulation of glucose metabolism in porcine oocytes: Effects on nuclear and cytoplasmic maturation in vitro. Reproduction, 131: 289–298. Search in Google Scholar

Kala M., Shaikh M.V., Nivsarkar M. (2017). Equilibrium between anti-oxidants and reactive oxygen species: a requisite for oocyte development and maturation. Reprod. Med. Biol., 16: 28–35. Search in Google Scholar

Lamirande De E., Gagnon C. (1993). A positive role for the superoxide anion in triggering hyperactivation and capacitation of human spermatozoa. Int. J. Androl., 16: 21–25. Search in Google Scholar

Leyens G., Knoops B., Donnay I. (2004 a). Expression of peroxiredoxins in bovine oocytes and embryos produced in vitro. Mol. Reprod. Dev., 69: 243–251.10.1002/mrd.20145 Search in Google Scholar

Leyens G., Verhaeghe B., Landtmeters M., Marchandise J., Knoops B., Donnay I. (2004 b). Peroxiredoxin 6 is upregulated in bovine oocytes and cumulus cells during in vitro maturation: role of intercellular communication. Biol. Reprod., 71: 1646–1651.10.1095/biolreprod.104.030155 Search in Google Scholar

Li W., Young J.F., Sun J. (2018). NADPH oxidase-generated reactive oxygen species in mature follicles are essential for Drosophila ovulation. Proc. Natl. Acad. Sci., 115: 7765–7770. Search in Google Scholar

Lopes A., Lane M., Thompson J.G. (2010). Oxygen consumption and ROS production are increased at the time of fertilization and cell cleavage in bovine zygotes. Human Reprod., 25: 2762–2773. Search in Google Scholar

Von Mengden L., Klamt F., Smitz J. (2020). Redox biology of human cumulus cells: basic concepts, impact on oocyte quality, and potential clinical use. Antioxid. Redox Sign., 32: 522–535. Search in Google Scholar

Morado S.A., Cetica P.D., Beconi M.T., Dalvit G. C. (2009). Reactive oxygen species in bovine oocyte maturation in vitro. Reprod. Fert. Develop., 21: 608–614. Search in Google Scholar

Morado S., Cetica P., Beconi M., Thompson J.G., Dalvit G. (2013). Reactive oxygen species production and redox state in parthenogenetic and sperm-mediated bovine oocyte activation. Reproduction, 145: 471–478. Search in Google Scholar

Mouatassim El S., Guérin P., Ménézo Y. (1999). Expression of genes encoding antioxidant enzymes in human and mouse oocytes during the final stages of maturation. Mol. Hum. Reprod., 5: 720–725. Search in Google Scholar

Mourot M., Dufort I., Gravel C., Algriany O., Dieleman S., Sirard M.-A. (2006). The influence of follicle size, FSH-enriched maturation medium, and early cleavage on bovine oocyte maternal mRNA levels. Mol. Reprod. Dev., 73: 1367–1379. Search in Google Scholar

Nishihara T., Matsumoto K., Hosoi Y., Morimoto Y. (2018). Evaluation of antioxidant status and oxidative stress markers in follicular fluid for human in vitro fertilization outcome. Reprod. Med. Biol., 17: 481–486. Search in Google Scholar

O’Flaherty C., Breininger E., Beorlegui N., Beconi M.T. (2005). Acrosome reaction in bovine spermatozoa: Role of reactive oxygen species and lactate dehydrogenase C4. Biochim. Biophys. Acta - Gen. Subj., 1726: 96–101. Search in Google Scholar

Pandey A.N., Chaube S. K. (2014). A moderate increase of hydrogen peroxide level is beneficial for spontaneous resumption of meiosis from diplotene arrest in rat oocytes cultured in vitro. Biores. Open Access, 3: 183–191. Search in Google Scholar

Song B.S., Jeong P.S., Lee J.H., Lee M.H., Yang H.J., Choi S.A., Lee H.Y., Yoon S.B., Park Y.H., et al., (2018). The effects of kinase modulation on in vitro maturation according to different cumulus oocyte complex morphologies. PLoS One, 13: 1–20. Search in Google Scholar

Takahashi Y., First N.L. (1992) In vitro development of bovine one-cell embryos: influence of glucose, lactate, pyruvate, amino acids and vitamins. Theriogenology, 37: 963–978.10.1016/0093-691X(92)90096-A Search in Google Scholar

Vandaele L., Thys M., Bijttebier J., Van Langendonckt A., Donnay I., Maes D., Meyer E., Van Soom A. (2010). Short-term exposure to hydrogen peroxide during oocyte maturation improves bovine embryo development. Reproduction, 139: 505–511. Search in Google Scholar

Velez-Pardo C., Tarazona Morales A., Jimenez Del Rio M., Olivera-Angel M. (2007). Endogenously generated hydrogen peroxide induces apoptosis via mitochondrial damage independent of NF-κB and p53 activation in bovine embryos. Theriogenology, 67: 1285–1296. Search in Google Scholar

van der Vliet A. (2008). NADPH oxidases in lung biology and pathology: Host defense enzymes, and more. Free Radic. Biol. Med., 44: 938–955. Search in Google Scholar

Articles recommandés par Trend MD