Skip to main content
Log in

Prediction of oocyte developmental competence in ovine using glucose-6-phosphate dehydrogenase (G6PDH) activity determined at retrieval time

  • Gamete Biology
  • Published:
Journal of Assisted Reproduction and Genetics Aims and scope Submit manuscript

Abstract

Purpose

To determine whether G6PDH-activity measured by Brilliant Cresyl Blue known as BCB dye, predicts developmental competence within cohorts of ovine oocytes.

Methods

Ovine oocytes were exposed to BCB staining and categorized into two groups: BCB+ (blue cytoplasm, low G6PDH-activity) and BCB- (colorless cytoplasm, high G6PDH-activity). After maturation in vitro, oocytes were subjected to fertilization followed by in vitro embryo culture.

Results

We observed a significant difference in oocyte diameter considering BCB+ and BCB- oocytes. BCB+ and Control groups showed significantly higher maturation rates compared to BCB- group. There were significantly more cleaved embryos in BCB+ and control groups than in BCB- group. Blastocyst rate was significantly higher for BCB+ group compared to control and BCB- groups with control group being significantly higher than BCB- group.

Conclusion

G6PDH-activity is a strong predictive marker of oocyte competence and may be useful in identifying oocytes with a good prognosis for further develop.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  1. Ebner T, Moser M, Sommergruber M, Tews G. Selection based on morphological assessment of oocytes and embryos at different stages of preimplantation development: a review. Hum Reprod Update. 2003;9:251–62.

    Article  PubMed  CAS  Google Scholar 

  2. Hammadeh ME, Fischer-Hammadeh C, Ali KR. Assisted hatching in assisted reproduction: a state of the art. J Assist Reprod Genet. 2011;28:119–28.

    Article  PubMed  Google Scholar 

  3. Rhodes TL, McCoy TP, Higdon 3rd HL, Boone WR. Factors affecting assisted reproductive technology (ART) pregnancy rates: a multivariate analysis. J Assist Reprod Genet. 2005;22:335–46.

    Article  PubMed  Google Scholar 

  4. Borini A, Cattoli M, Bulletti C, Coticchio G. Clinical efficiency of oocyte and embryo cryopreservation. Ann N Y Acad Sci. 2008;1127:49–58.

    Article  PubMed  Google Scholar 

  5. Wang Q, Sun QY. Evaluation of oocyte quality: morphological, cellular and molecular predictors. Reprod Fertil Dev. 2007;19:1–12.

    Article  PubMed  Google Scholar 

  6. de Matos DG, Gasparrini B, Pasqualini SR, Thompson JG. Effect of glutathione synthesis stimulation during in vitro maturation of ovine oocytes on embryo development and intracellular peroxide content. Theriogenology. 2002;57:1443–51.

    Article  PubMed  Google Scholar 

  7. El Shourbagy SH, Spikings EC, Freitas M, St John JC. Mitochondria directly influence fertilisation outcome in the pig. Reproduction. 2006;131:233–45.

    Article  PubMed  Google Scholar 

  8. Koester M, Mohammadi-Sangcheshmeh A, Montag M, Rings F, Schimming T, Tesfaye D, et al. Evaluation of bovine zona pellucida characteristics in polarized light as a prognostic marker for embryonic developmental potential. Reproduction. 2011;141:779–87.

    Article  PubMed  CAS  Google Scholar 

  9. Wang WH, Day BN. Development of porcine embryos produced by IVM/IVF in a medium with or without protein supplementation: effects of extracellular glutathione. Zygote. 2002;10:109–15.

    Article  PubMed  CAS  Google Scholar 

  10. Ambruosi B, Lacalandra GM, Iorga AI, De Santis T, Mugnier S, Matarrese R, et al. Cytoplasmic lipid droplets and mitochondrial distribution in equine oocytes: implications on oocyte maturation, fertilization and developmental competence after ICSI. Theriogenology. 2009;71:1093–104.

    Article  PubMed  CAS  Google Scholar 

  11. Spikings EC, Alderson J, St John JC. Regulated mitochondrial DNA replication during oocyte maturation is essential for successful porcine embryonic development. Biol Reprod. 2007;76:327–35.

    Article  PubMed  CAS  Google Scholar 

  12. Torner H, Ghanem N, Ambros C, Holker M, Tomek W, Phatsara C, et al. Molecular and subcellular characterisation of oocytes screened for their developmental competence based on glucose-6-phosphate dehydrogenase activity. Reproduction. 2008;135:197–212.

    Article  PubMed  CAS  Google Scholar 

  13. Wu YG, Liu Y, Zhou P, Lan GC, Han D, Miao DQ, et al. Selection of oocytes for in vitro maturation by brilliant cresyl blue staining: a study using the mouse model. Cell Res. 2007;17:722–31.

    Article  PubMed  CAS  Google Scholar 

  14. Alm H, Torner H, Lohrke B, Viergutz T, Ghoneim IM, Kanitz W. Bovine blastocyst development rate in vitro is influenced by selection of oocytes by brillant cresyl blue staining before IVM as indicator for glucose-6-phosphate dehydrogenase activity. Theriogenology. 2005;63:2194–205.

    Article  PubMed  CAS  Google Scholar 

  15. Tiffin GJ, Rieger D, Betteridge KJ, Yadav BR, King WA. Glucose and glutamine metabolism in pre-attachment cattle embryos in relation to sex and stage of development. J Reprod Fertil. 1991;93:125–32.

    Article  PubMed  CAS  Google Scholar 

  16. Pawlak P, Pers-Kamczyc E, Renska N, Kubickova S, Lechniak D. Disturbances of nuclear maturation in BCB positive oocytes collected from peri-pubertal gilts. Theriogenology. 2011;75:832–40.

    Article  PubMed  CAS  Google Scholar 

  17. Pawlak P, Renska N, Pers-Kamczyc E, Warzych E, Lechniak D. The quality of porcine oocytes is affected by sexual maturity of the donor gilt. Reprod Biol. 2011;11:1–18.

    PubMed  Google Scholar 

  18. Ghanem N, Holker M, Rings F, Jennen D, Tholen E, Sirard MA, et al. Alterations in transcript abundance of bovine oocytes recovered at growth and dominance phases of the first follicular wave. BMC Dev Biol. 2007;7:90.

    Article  PubMed  Google Scholar 

  19. Bhojwani S, Alm H, Torner H, Kanitz W, Poehland R. Selection of developmentally competent oocytes through brilliant cresyl blue stain enhances blastocyst development rate after bovine nuclear transfer. Theriogenology. 2007;67:341–5.

    Article  PubMed  CAS  Google Scholar 

  20. Manjunatha BM, Gupta PS, Devaraj M, Ravindra JP, Nandi S. Selection of developmentally competent buffalo oocytes by brilliant cresyl blue staining before IVM. Theriogenology. 2007;68:1299–304.

    Article  PubMed  CAS  Google Scholar 

  21. Mota GB, Batista RI, Serapiao RV, Boite MC, Viana JH, Torres CA, et al. Developmental competence and expression of the MATER and ZAR1 genes in immature bovine oocytes selected by brilliant cresyl blue. Zygote.18: 209–16.

  22. Pujol M, Lopez-Bejar M, Paramio MT. Developmental competence of heifer oocytes selected using the brilliant cresyl blue (BCB) test. Theriogenology. 2004;61:735–44.

    Article  PubMed  Google Scholar 

  23. Rodriguez-Gonzalez E, Lopez-Bejar M, Izquierdo D, Paramio MT. Developmental competence of prepubertal goat oocytes selected with brilliant cresyl blue and matured with cysteamine supplementation. Reprod Nutr Dev. 2003;43:179–87.

    Article  PubMed  CAS  Google Scholar 

  24. Thompson JG, Gardner DK, Pugh PA, McMillan WH, Tervit HR. Lamb birth weight is affected by culture system utilized during in vitro pre-elongation development of ovine embryos. Biol Reprod. 1995;53:1385–91.

    Article  PubMed  CAS  Google Scholar 

  25. Shirazi A, Sadeghi N. The effect of ovine oocyte diameter on nuclear maturation. Small Rumin Res. 2007;69:103–7.

    Article  Google Scholar 

  26. Wan PC, Hao ZD, Zhou P, Wu Y, Yang L, Cui MS, et al. Effects of SOF and CR1 media on developmental competence and cell apoptosis of ovine in vitro fertilization embryos. Anim Reprod Sci. 2009;114:279–88.

    Article  PubMed  CAS  Google Scholar 

  27. Roca J, Martinez E, Vazquez JM, Lucas X. Selection of immature pig oocytes for homologous in vitro penetration assays with the brilliant cresyl blue test. Reprod Fertil Dev. 1998;10:479–85.

    Article  PubMed  CAS  Google Scholar 

  28. Rodrigues BA, Rodriguez P, Silva AE, Cavalcante LF, Feltrin C, Rodrigues JL. Preliminary study in immature canine oocytes stained with brilliant cresyl blue and obtained from bitches with low and high progesterone serum profiles. Reprod Domest Anim. 2009;44 Suppl 2:255–8.

    Article  PubMed  Google Scholar 

  29. Rodriguez-Gonzalez E, Lopez-Bejar M, Velilla E, Paramio MT. Selection of prepubertal goat oocytes using the brilliant cresyl blue test. Theriogenology. 2002;57:1397–409.

    Article  PubMed  CAS  Google Scholar 

  30. Griffin J, Emery BR, Huang I, Peterson CM, Carrell DT. Comparative analysis of follicle morphology and oocyte diameter in four mammalian species (mouse, hamster, pig, and human). J Exp Clin Assist Reprod. 2006;3:2.

    Article  PubMed  Google Scholar 

  31. Antosik P, Kempisty B, Bukowska D, Jackowska M, Wlodarczyk R, Budna J, et al. Follicular size is associated with the levels of transcripts and proteins of selected molecules responsible for the fertilization ability of oocytes of puberal gilts. J Reprod Dev. 2009;55:588–93.

    Article  PubMed  CAS  Google Scholar 

  32. Sirard MA, Richard F, Blondin P, Robert C. Contribution of the oocyte to embryo quality. Theriogenology. 2006;65:126–36.

    Article  PubMed  Google Scholar 

  33. Egerszegi I, Alm H, Ratky J, Heleil B, Brussow KP, Torner H. Meiotic progression, mitochondrial features and fertilisation characteristics of porcine oocytes with different G6PDH activities. Reprod Fertil Dev. 2010;22:830–8.

    Article  PubMed  CAS  Google Scholar 

  34. Bettegowda A, Lee KB, Smith GW. Cytoplasmic and nuclear determinants of the maternal-to-embryonic transition. Reprod Fertil Dev. 2008;20:45–53.

    Article  PubMed  CAS  Google Scholar 

  35. Kempisty B, Jackowska M, Piotrowska H, Antosik P, Wozna M, Bukowska D, et al. Zona pellucida glycoprotein 3 (pZP3) and integrin beta2 (ITGB2) mRNA and protein expression in porcine oocytes after single and double exposure to brilliant cresyl blue test. Theriogenology. 2011;75:1525–35.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors thank the members of their own laboratories for their helpful discussions. We are also indebted to Miss Lida Langroudi for editing the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Abdollah Mohammadi-Sangcheshmeh.

Additional information

Capsule Glucose-6-phosphate dehydrogenase activity in ovine oocytes prior to in vitro maturation is associated with oocyte diameter, meiotic competence and developmental capacity to the blastocyst stage in vitro.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mohammadi-Sangcheshmeh, A., Soleimani, M., Deldar, H. et al. Prediction of oocyte developmental competence in ovine using glucose-6-phosphate dehydrogenase (G6PDH) activity determined at retrieval time. J Assist Reprod Genet 29, 153–158 (2012). https://doi.org/10.1007/s10815-011-9625-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10815-011-9625-6

Keywords

Navigation