Capacity of Trolox to improve the development and quality of metabolically compromised bovine oocytes and embryos in vitro during different windows of development
J. De Bie A , A. Smits B , W. F. A. Marei B C and J. L. M. R. Leroy B DA Centre for the Evaluation of Vaccination, Vaccine and Infectious Disease Institute, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium.
B Gamete Research Centre, Laboratory for Veterinary Physiology and Biochemistry, Department of Veterinary Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Wilrijk, Belgium.
C Department of Theriogenology, Faculty of Veterinary Medicine, Cairo University, Giza 12211, Egypt.
D Corresponding author. Email: jo.leroy@uantwerpen.be
Reproduction, Fertility and Development 33(4) 291-304 https://doi.org/10.1071/RD20194
Submitted: 21 August 2020 Accepted: 1 December 2020 Published: 12 February 2021
Abstract
Trials to improve oocyte developmental competence under metabolic stress by using antioxidants may start before or after oocyte maturation. In the present conceptual study, we aimed to identify the most efficient timing of antioxidant application in relation to a metabolic insult using a bovine in vitro embryo production model. Pathophysiological concentrations of palmitic acid (PA) were used to induce metabolic stress during oocyte maturation or embryo development. Trolox (TR; antioxidant) treatment prior to, during or after the PA insult was tested to evaluate the protective, neutralising and rescuing capacity of TR respectively. Changes in embryo developmental competence, mitochondrial activity, reactive oxygen species (ROS) concentrations, blastocyst cell allocation and apoptosis and cell stress-related gene expression were monitored. The improvement in developmental capacity was most obvious when oocytes were preloaded with TR before the PA insult. This protective effect could be explained by the observed combination of increased mitochondrial activity with reduced ROS production. This resulted in blastocysts with normal cell counts and apoptosis, as well as increased nuclear factor erythroid 2-related factor 2 (NRF2) expression (a marker for redox regulatory processes) and normalised the expression of the mitochondrial transcription factor A (TFAM), a marker of mitochondrial biogenesis. These results indicate that ‘pretreatment’ of oocytes with antioxidants produces embryos that seem to be more resilient to a metabolic stress insult.
Keywords: fatty acid, fertility, IVM, oxidative stress.
References
Aardema, H., Vos, P. L., Lolicato, F., Roelen, B. A., Knijn, H. M., Vaandrager, A. B., Helms, J. B., and Gadella, B. M. (2011). Oleic acid prevents detrimental effects of saturated fatty acids on bovine oocyte developmental competence. Biol. Reprod. 85, 62–69.| Oleic acid prevents detrimental effects of saturated fatty acids on bovine oocyte developmental competence.Crossref | GoogleScholarGoogle Scholar | 21311036PubMed |
Amin, A., Gad, A., Salilew-Wondim, D., Prastowo, S., Held, E., Hoelker, M., Rings, F., Tholen, E., Neuhoff, C., Looft, C., Schellander, K., and Tesfaye, D. (2014). Bovine embryo survival under oxidative-stress conditions is associated with activity of the NRF2-mediated oxidative-stress-response pathway. Mol. Reprod. Dev. 81, 497–513.
| Bovine embryo survival under oxidative-stress conditions is associated with activity of the NRF2-mediated oxidative-stress-response pathway.Crossref | GoogleScholarGoogle Scholar | 25057524PubMed |
Asadi, E., Jahanshahi, M., and Golalipour, M. J. (2012). Effect of vitamin E on oocytes apoptosis in nicotine-treated mice. Iran. J. Basic Med. Sci. 15, 880–884.
| 23493325PubMed |
Conti, M., and Franciosi, F. (2018). Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events. Hum. Reprod. Update 24, 245–266.
| Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events.Crossref | GoogleScholarGoogle Scholar | 29432538PubMed |
Cortassa, S., Sollott, S. J., and Aon, M. A. (2017). Mitochondrial respiration and ROS emission during β-oxidation in the heart: an experimental-computational study. PLOS Comput. Biol. 13, e1005588.
| Mitochondrial respiration and ROS emission during β-oxidation in the heart: an experimental-computational study.Crossref | GoogleScholarGoogle Scholar | 28598967PubMed |
Dalvit, G., Llanes, S. P., Descalzo, A., Insani, M., Beconi, M., and Cetica, P. (2005). Effect of alpha-tocopherol and ascorbic acid on bovine oocyte in vitro maturation. Reprod. Domest. Anim. 40, 93–97.
| Effect of alpha-tocopherol and ascorbic acid on bovine oocyte in vitro maturation.Crossref | GoogleScholarGoogle Scholar | 15819954PubMed |
De Bie, J., Langbeen, A., Verlaet, A. A. J., Florizoone, F., Immig, I., Hermans, N., Fransen, E., Bols, P. E. J., and Leroy, J. L. M. R. (2016). The effect of a negative energy balance status on β-carotene availability in serum and follicular fluid of nonlactating dairy cows. J. Dairy Sci. 99, 5808–5819.
| The effect of a negative energy balance status on β-carotene availability in serum and follicular fluid of nonlactating dairy cows.Crossref | GoogleScholarGoogle Scholar | 27157583PubMed |
De Bie, J., Marei, W. F., Maillo, V., Jordaens, L., Gutierrez-Adan, A., Bols, P. E., and Leroy, J. L. (2017). Differential effects of high and low glucose concentrations during lipolysis-like conditions on bovine in vitro oocyte quality, metabolism and subsequent embryo development. Reprod. Fertil. Dev. 29, 2284–2300.
| Differential effects of high and low glucose concentrations during lipolysis-like conditions on bovine in vitro oocyte quality, metabolism and subsequent embryo development.Crossref | GoogleScholarGoogle Scholar | 28390473PubMed |
Desmet, K. L. J., Van Hoeck, V., Gagné, D., Fournier, E., Thakur, A., O’Doherty, A. M., Walsh, C. P., Sirard, M. A., Bols, P. E. J., and Leroy, J. L. M. R. (2016). Exposure of bovine oocytes and embryos to elevated non-esterified fatty acid concentrations: integration of epigenetic and transcriptomic signatures in resultant blastocysts. BMC Genomics 17, 1004.
| Exposure of bovine oocytes and embryos to elevated non-esterified fatty acid concentrations: integration of epigenetic and transcriptomic signatures in resultant blastocysts.Crossref | GoogleScholarGoogle Scholar |
Dobbelaar, P., Bouwstra, R. J., Goselink, R. M., Jorritsma, R., van den Borne, J. J., and Jansen, E. H. (2010). Effects of vitamin E supplementation on and the association of body condition score with changes in peroxidative biomarkers and antioxidants around calving in dairy heifers. J. Dairy Sci. 93, 3103–3113.
| Effects of vitamin E supplementation on and the association of body condition score with changes in peroxidative biomarkers and antioxidants around calving in dairy heifers.Crossref | GoogleScholarGoogle Scholar | 20630228PubMed |
Forrest, V. J., Kang, Y.-H., McClain, D. E., Robinson, D. H., and Ramakrishnan, N. (1994). Oxidative stress-induced apoptosis prevented by trolox. Free Radic. Biol. Med. 16, 675–684.
| Oxidative stress-induced apoptosis prevented by trolox.Crossref | GoogleScholarGoogle Scholar | 8070670PubMed |
Goossens, K., Van Poucke, M., Van Soom, A., Vandesompele, J., Van Zeveren, A., and Peelman, L. J. (2005). Selection of reference genes for quantitative real-time PCR in bovine preimplantation embryos. BMC Dev. Biol. 5, 27.
| Selection of reference genes for quantitative real-time PCR in bovine preimplantation embryos.Crossref | GoogleScholarGoogle Scholar | 16324220PubMed |
Gruber, I., and Klein, M. (2011). Embryo culture media for human IVF: which possibilities exist? J. Turk. Ger. Gynecol. Assoc. 12, 110–117.
| Embryo culture media for human IVF: which possibilities exist?Crossref | GoogleScholarGoogle Scholar | 24591972PubMed |
Hamad, I., Arda, N., Pekmez, M., Karaer, S., and Temizkan, G. (2010). Intracellular scavenging activity of Trolox (6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid) in the fission yeast, Schizosaccharomyces pombe. J. Nat. Sci. Biol. Med. 1, 16–21.
| Intracellular scavenging activity of Trolox (6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid) in the fission yeast, Schizosaccharomyces pombe.Crossref | GoogleScholarGoogle Scholar | 22096330PubMed |
Han, L., Wang, H., Li, L., Li, X., Ge, J., Reiter, R. J., and Wang, Q. (2017). Melatonin protects against maternal obesity-associated oxidative stress and meiotic defects in oocytes via the SIRT3–SOD2-dependent pathway. J. Pineal Res. 63, e12431.
| Melatonin protects against maternal obesity-associated oxidative stress and meiotic defects in oocytes via the SIRT3–SOD2-dependent pathway.Crossref | GoogleScholarGoogle Scholar | 28658527PubMed |
Igosheva, N., Abramov, A. Y., Poston, L., Eckert, J. J., Fleming, T. P., Duchen, M. R., and McConnell, J. (2010). Maternal diet-induced obesity alters mitochondrial activity and redox status in mouse oocytes and zygotes. PLoS One 5, e10074.
| Maternal diet-induced obesity alters mitochondrial activity and redox status in mouse oocytes and zygotes.Crossref | GoogleScholarGoogle Scholar | 20404917PubMed |
Jordaens, L., Van Hoeck, V., De Bie, J., Berth, M., Marei, W. F. A., Desmet, K. L. J., Bols, P. E. J., and Leroy, J. (2017). Non-esterified fatty acids in early luteal bovine oviduct fluid mirror plasma concentrations: an ex vivo approach. Reprod. Biol. 17, 281–284.
| Non-esterified fatty acids in early luteal bovine oviduct fluid mirror plasma concentrations: an ex vivo approach.Crossref | GoogleScholarGoogle Scholar | 28551031PubMed |
Jorritsma, R., Cesar, M. L., Hermans, J. T., Kruitwagen, C. L., Vos, P. L., and Kruip, T. A. (2004). Effects of non-esterified fatty acids on bovine granulosa cells and developmental potential of oocytes in vitro. Anim. Reprod. Sci. 81, 225–235.
| Effects of non-esterified fatty acids on bovine granulosa cells and developmental potential of oocytes in vitro.Crossref | GoogleScholarGoogle Scholar | 14998649PubMed |
Jungheim, E. S., Louden, E. D., Chi, M. M., Frolova, A. I., Riley, J. K., and Moley, K. H. (2011). Preimplantation exposure of mouse embryos to palmitic acid results in fetal growth restriction followed by catch-up growth in the offspring. Biol. Reprod. 85, 678–683.
| Preimplantation exposure of mouse embryos to palmitic acid results in fetal growth restriction followed by catch-up growth in the offspring.Crossref | GoogleScholarGoogle Scholar | 21653893PubMed |
Komatsu, K., Iwase, A., Mawatari, M., Wang, J., Yamashita, M., and Kikkawa, F. (2014). Mitochondrial membrane potential in 2-cell stage embryos correlates with the success of preimplantation development. Reproduction 147, 627–638.
| Mitochondrial membrane potential in 2-cell stage embryos correlates with the success of preimplantation development.Crossref | GoogleScholarGoogle Scholar | 24459207PubMed |
Koyama, H., Ikeda, S., Sugimoto, M., and Kume, S. (2012). Effects of folic acid on the development and oxidative stress of mouse embryos exposed to heat stress. Reprod. Domest. Anim. 47, 921–927.
| Effects of folic acid on the development and oxidative stress of mouse embryos exposed to heat stress.Crossref | GoogleScholarGoogle Scholar | 22309244PubMed |
Leroy, J. L. M. R., Vanholder, T., Delanghe, J. R., Opsomer, G., Van Soom, A., Bols, P. E., Dewulf, J., and de Kruif, A. (2004). Metabolic changes in follicular fluid of the dominant follicle in high-yielding dairy cows early post partum. Theriogenology 62, 1131–1143.
| Metabolic changes in follicular fluid of the dominant follicle in high-yielding dairy cows early post partum.Crossref | GoogleScholarGoogle Scholar |
Leroy, J. L. M. R., Vanholder, T., Mateusen, B., Christophe, A., Opsomer, G., de Kruif, A., Genicot, G., and Van Soom, A. (2005). Non-esterified fatty acids in follicular fluid of dairy cows and their effect on developmental capacity of bovine oocytes in vitro. Reproduction 130, 485–495.
| Non-esterified fatty acids in follicular fluid of dairy cows and their effect on developmental capacity of bovine oocytes in vitro.Crossref | GoogleScholarGoogle Scholar |
Leroy, J. L. M. R., Van Hoeck, V., Clemente, M., Rizos, D., Gutierrez-Adan, A., Van Soom, A., Uytterhoeven, M., and Bols, P. E. (2010). The effect of nutritionally induced hyperlipidaemia on in vitro bovine embryo quality. Hum. Reprod. 25, 768–778.
| The effect of nutritionally induced hyperlipidaemia on in vitro bovine embryo quality.Crossref | GoogleScholarGoogle Scholar |
Leroy, J. L. M. R., Valckx, S. D., Jordaens, L., De Bie, J., Desmet, K. L., Van Hoeck, V., Britt, J. H., Marei, W. F., and Bols, P. E. (2015). Nutrition and maternal metabolic health in relation to oocyte and embryo quality: critical views on what we learned from the dairy cow model. Reprod. Fertil. Dev. 27, 693–703.
| Nutrition and maternal metabolic health in relation to oocyte and embryo quality: critical views on what we learned from the dairy cow model.Crossref | GoogleScholarGoogle Scholar |
Livak, K. J., and Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25, 402–408.
| Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method.Crossref | GoogleScholarGoogle Scholar | 11846609PubMed |
Luddi, A., Capaldo, A., Focarelli, R., Gori, M., Morgante, G., Piomboni, P., and De Leo, V. (2016). Antioxidants reduce oxidative stress in follicular fluid of aged women undergoing IVF. Reprod. Biol. Endocrinol. 14, 57.
| Antioxidants reduce oxidative stress in follicular fluid of aged women undergoing IVF.Crossref | GoogleScholarGoogle Scholar | 27604261PubMed |
Marei, W. F., Alvarez, M. A., Van Hoeck, V., Gutierrez-Adan, A., Bols, P. E., and Leroy, J. L. (2017a). Effect of nutritionally induced hyperlipidaemia on in vitro bovine embryo quality depends on the type of major fatty acid in the diet. Reprod. Fertil. Dev. 29, 1856–1867.
| Effect of nutritionally induced hyperlipidaemia on in vitro bovine embryo quality depends on the type of major fatty acid in the diet.Crossref | GoogleScholarGoogle Scholar | 27832581PubMed |
Marei, W. F., De Bie, J., Mohey-Elsaeed, O., Wydooghe, E., Bols, P. E. J., and Leroy, J. (2017b). Alpha-linolenic acid protects the developmental capacity of bovine cumulus-oocyte complexes matured under lipotoxic conditions in vitro. Biol. Reprod. 96, 1181–1196.
| Alpha-linolenic acid protects the developmental capacity of bovine cumulus-oocyte complexes matured under lipotoxic conditions in vitro.Crossref | GoogleScholarGoogle Scholar | 28520897PubMed |
Marei, W. F., Van Den Bosch, L., Pintelon, I., Mohey, O., Bols, P. E. J., and Leroy, J. L. M. (2019a). Mitochondria-targeted therapy rescues development and quality of embryos derived from metabolically compromised oocytes: a bovine in vitro model. Hum. Reprod. 34, 1984–1998.
| Mitochondria-targeted therapy rescues development and quality of embryos derived from metabolically compromised oocytes: a bovine in vitro model.Crossref | GoogleScholarGoogle Scholar | 31625574PubMed |
Marei, W. F. A., Van Raemdonck, G., Baggerman, G., Bols, P. E. J., and Leroy, J. L. M. R. (2019b). Proteomic changes in oocytes after in vitro maturation in lipotoxic conditions are different from those in cumulus cells. Sci. Rep. 9, 3673.
| Proteomic changes in oocytes after in vitro maturation in lipotoxic conditions are different from those in cumulus cells.Crossref | GoogleScholarGoogle Scholar |
Messier, E. M., Bahmed, K., Tuder, R. M., Chu, H. W., Bowler, R. P., and Kosmider, B. (2013). Trolox contributes to Nrf2-mediated protection of human and murine primary alveolar type II cells from injury by cigarette smoke. Cell Death Dis. 4, e573.
| Trolox contributes to Nrf2-mediated protection of human and murine primary alveolar type II cells from injury by cigarette smoke.Crossref | GoogleScholarGoogle Scholar | 23559007PubMed |
Mirabi, P., Chaichi, M. J., Esmaeilzadeh, S., Ali Jorsaraei, S. G., Bijani, A., Ehsani, M., and Hashemi Karooee, S. F. (2017). The role of fatty acids on ICSI outcomes: a prospective cohort study. Lipids Health Dis. 16, 18.
| The role of fatty acids on ICSI outcomes: a prospective cohort study.Crossref | GoogleScholarGoogle Scholar | 28109274PubMed |
Natarajan, R., Shankar, M. B., and Munuswamy, D. (2010). Effect of alpha-tocopherol supplementation on in vitro maturation of sheep oocytes and in vitro development of preimplantation sheep embryos to the blastocyst stage. J. Assist. Reprod. Genet. 27, 483–490.
| Effect of alpha-tocopherol supplementation on in vitro maturation of sheep oocytes and in vitro development of preimplantation sheep embryos to the blastocyst stage.Crossref | GoogleScholarGoogle Scholar | 20454845PubMed |
Nonogaki, T., Noda, Y., Goto, Y., Kishi, J., and Mori, T. (1994). Developmental blockage of mouse embryos caused by fatty acids. J. Assist. Reprod. Genet. 11, 482–488.
| Developmental blockage of mouse embryos caused by fatty acids.Crossref | GoogleScholarGoogle Scholar | 7633171PubMed |
O’Gorman, A., Wallace, M., Cottell, E., Gibney, M. J., McAuliffe, F. M., Wingfield, M., and Brennan, L. (2013). Metabolic profiling of human follicular fluid identifies potential biomarkers of oocyte developmental competence. Reproduction 146, 389–395.
| Metabolic profiling of human follicular fluid identifies potential biomarkers of oocyte developmental competence.Crossref | GoogleScholarGoogle Scholar | 23886995PubMed |
Palomer, X., Pizarro-Delgado, J., Barroso, E., and Vazquez-Carrera, M. (2018). Palmitic and oleic acid: the yin and yang of fatty acids in type 2 diabetes mellitus. Trends Endocrinol. Metab. 29, 178–190.
| Palmitic and oleic acid: the yin and yang of fatty acids in type 2 diabetes mellitus.Crossref | GoogleScholarGoogle Scholar | 29290500PubMed |
Rizos, D., Ward, F., Duffy, P., Boland, M. P., and Lonergan, P. (2002). Consequences of bovine oocyte maturation, fertilization or early embryo development in vitro versus in vivo: implications for blastocyst yield and blastocyst quality. Mol. Reprod. Dev. 61, 234–248.
| Consequences of bovine oocyte maturation, fertilization or early embryo development in vitro versus in vivo: implications for blastocyst yield and blastocyst quality.Crossref | GoogleScholarGoogle Scholar | 11803560PubMed |
Rizos, D., Gutiérrez-Adán, A., Pérez-Garnelo, S., De La Fuente, J., Boland, M. P., and Lonergan, P. (2003). Bovine embryo culture in the presence or absence of serum: implications for blastocyst development, cryotolerance, and messenger RNA expression. Biol. Reprod. 68, 236–243.
| Bovine embryo culture in the presence or absence of serum: implications for blastocyst development, cryotolerance, and messenger RNA expression.Crossref | GoogleScholarGoogle Scholar | 12493719PubMed |
Robert, C., McGraw, S., Massicotte, L., Pravetoni, M., Gandolfi, F., and Sirard, M. A. (2002). Quantification of housekeeping transcript levels during the development of bovine preimplantation embryos. Biol. Reprod. 67, 1465–1472.
| Quantification of housekeeping transcript levels during the development of bovine preimplantation embryos.Crossref | GoogleScholarGoogle Scholar | 12390877PubMed |
Rooke, J. A., Watt, R. G., Ashworth, C. J., and McEvoy, T. G. (2012). Inclusion of bovine lipoproteins and the vitamin E analogue, Trolox, during in vitro culture of bovine embryos changes both embryo and fetal development. Reprod. Fertil. Dev. 24, 309–316.
| Inclusion of bovine lipoproteins and the vitamin E analogue, Trolox, during in vitro culture of bovine embryos changes both embryo and fetal development.Crossref | GoogleScholarGoogle Scholar | 22281076PubMed |
Salway, J. (1999). ‘Metabolism at a Glance.’ (Blackwell Science: Oxford, UK.)
Smits, A., De Bie, J., Bols, P. E. J., Marei, W. F., and Leroy, J. L. M. R. (2016). Effect of embryo culture conditions on developmental potential of bovine oocytes matured under lipotoxic conditions. In ‘Proceedings of the 18th International Congress on Animal Reproduction’, 26–30 June 2016, Tours, France. pp. PW552. (Elsevier.)
Sutton-McDowall, M. L., Wu, L. L. Y., Purdey, M., Abell, A. D., Goldys, E. M., Macmillan, K. L., Thompson, J. G., and Robker, R. L. (2016). Nonesterified fatty acid-induced endoplasmic reticulum stress in cattle cumulus oocyte complexes alters cell metabolism and developmental competence1. Biol. Reprod. 94, 23.
| Nonesterified fatty acid-induced endoplasmic reticulum stress in cattle cumulus oocyte complexes alters cell metabolism and developmental competence1.Crossref | GoogleScholarGoogle Scholar | 26658709PubMed |
Tao, Y., Zhou, B., Xia, G., Wang, F., Wu, Z., and Fu, M. (2004). Exposure to l-ascorbic acid or alpha-tocopherol facilitates the development of porcine denuded oocytes from metaphase I to metaphase II and prevents cumulus cells from fragmentation. Reprod. Domest. Anim. 39, 52–57.
| Exposure to l-ascorbic acid or alpha-tocopherol facilitates the development of porcine denuded oocytes from metaphase I to metaphase II and prevents cumulus cells from fragmentation.Crossref | GoogleScholarGoogle Scholar | 15129922PubMed |
Valckx, S. D., Arias-Alvarez, M., De Pauw, I., Fievez, V., Vlaeminck, B., Fransen, E., Bols, P. E., and Leroy, J. L. (2014). Fatty acid composition of the follicular fluid of normal weight, overweight and obese women undergoing assisted reproductive treatment: a descriptive cross-sectional study. Reprod. Biol. Endocrinol. 12, 13.
| Fatty acid composition of the follicular fluid of normal weight, overweight and obese women undergoing assisted reproductive treatment: a descriptive cross-sectional study.Crossref | GoogleScholarGoogle Scholar | 24498875PubMed |
Valckx, S. D., De Bie, J., Michiels, E. D., Goovaerts, I. G., Punjabi, U., Ramos-Ibeas, P., Gutierrez-Adan, A., Bols, P. E., and Leroy, J. L. (2015). The effect of human follicular fluid on bovine oocyte developmental competence and embryo quality. Reprod. Biomed. Online 30, 203–207.
| The effect of human follicular fluid on bovine oocyte developmental competence and embryo quality.Crossref | GoogleScholarGoogle Scholar | 25498595PubMed |
Van Hoeck, V., Sturmey, R. G., Bermejo-Alvarez, P., Rizos, D., Gutierrez-Adan, A., Leese, H. J., Bols, P. E., and Leroy, J. L. (2011). Elevated non-esterified fatty acid concentrations during bovine oocyte maturation compromise early embryo physiology. PLoS One 6, e23183.
| Elevated non-esterified fatty acid concentrations during bovine oocyte maturation compromise early embryo physiology.Crossref | GoogleScholarGoogle Scholar | 21858021PubMed |
Van Hoeck, V., De Bie, J., Andries, S., Merckx, E., Bols, P. E. J., and Leroy, J. L. M. R. (2012). Elevated concentrations of saturated NEFA during bovine in vitro embryo culture compromise pre-implantation embryo development. In ‘Proceedings of the 28th Scientific Meeting AETE’, 11–13 September 2012, St-Malo, France. pp. 224 (AETE.)
Van Hoeck, V., Leroy, J. L. M. R., Arias-Alvarez, M., Rizos, D., Gutierrez-Adan, A., Schnorbusch, K., Bols, P. E. J., Leese, H. J., and Sturmey, R. G. (2013). Oocyte developmental failure in response to elevated non-esterified fatty acid concentrations: mechanistic insights. Reproduction 145, 33–44.
| Oocyte developmental failure in response to elevated non-esterified fatty acid concentrations: mechanistic insights.Crossref | GoogleScholarGoogle Scholar | 23108110PubMed |
Wang, H., Cheng, Q., Li, X., Hu, F., Han, L., Zhang, H., Li, L., Ge, J., Ying, X., Guo, X., and Wang, Q. (2018). Loss of TIGAR induces oxidative stress and meiotic defects in oocytes from obese mice. Mol. Cell. Proteomics 17, 1354–1364.
| Loss of TIGAR induces oxidative stress and meiotic defects in oocytes from obese mice.Crossref | GoogleScholarGoogle Scholar | 29776966PubMed |
Wu, K. C., Cui, J. Y., and Klaassen, C. D. (2011). Beneficial role of Nrf2 in regulating NADPH generation and consumption. Toxicol. Sci. 123, 590–600.
| Beneficial role of Nrf2 in regulating NADPH generation and consumption.Crossref | GoogleScholarGoogle Scholar | 21775727PubMed |