Hostname: page-component-78c5997874-t5tsf Total loading time: 0 Render date: 2024-11-13T03:58:39.821Z Has data issue: false hasContentIssue false

Effect of insulin–transferrin–selenium (ITS) and l-ascorbic acid (AA) during in vitro maturation on in vitro bovine embryo development

Published online by Cambridge University Press:  17 October 2016

A.L.S. Guimarães
Affiliation:
School of Agriculture and Veterinary Medicine, University of Brasilia, Brasília – DF, Brazil.
S.A. Pereira
Affiliation:
Institute of Biology, University of Brasília, Brasília – DF, Brazil.
M. N. Diógenes
Affiliation:
School of Agriculture and Veterinary Medicine, University of Brasilia, Brasília – DF, Brazil.
M.A.N. Dode*
Affiliation:
Parque Estação Biológica, Final Av. W5/N, Prédio PBI, 70770–900, Brasília – DF, Brazil. School of Agriculture and Veterinary Medicine, University of Brasilia, Brasília – DF, Brazil. Embrapa-Genetic Resources and Biotechnology, Brasília – DF, Brazil.
*
All correspondence to: Margot Alves Nunes Dode. Parque Estação Biológica, Final Av. W5/N, Prédio PBI, 70770–900, Brasília – DF, Brazil. Tel.: +55 61 34484659. Fax: +55 61 3340 3658. E-mail: margot.dode@embrapa.br

Summary

The aim of this study was to evaluate the effect of adding a combination of insulin, transferrin and selenium (ITS) and l-ascorbic acid (AA) during in vitro maturation (IVM) and in vitro culture (IVC) on in vitro embryo production. To verify the effect of the supplements, cleavage and blastocyst rates, embryo size and total cell number were performed. Embryonic development data, embryo size categorization and kinetics of maturation were analyzed by chi-squared test, while the total cell number was analyzed by a Kruskal–Wallis test (P < 0.05). When ITS was present during IVM, IVC or the entire culture, all treatments had a cleavage and blastocyst rates and embryo quality, similar to those of the control group (P < 0.05). Supplementation of IVM medium with ITS and AA for 12 h or 24 h showed that the last 12 h increased embryo production (51.6%; n = 220) on D7 compared with the control (39.5%; n = 213). However, no improvement was observed in blastocyst rate when less competent oocytes, obtained from 1–3 mm follicles, were exposed to ITS + AA for the last 12 h of IVM, with a blastocyst rate of 14.9% (n = 47) compared with 61.0% (n = 141) in the control group. The results suggest that the addition of ITS alone did not affect embryo production; however, when combined with AA in the last 12 h of maturation, there was improvement in the quantity and quality of embryos produced. Furthermore, the use of ITS and AA during IVM did not improve the competence of oocytes obtained from small follicles.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Agarwal, A., Durairajanayagam, D. & du Plessis, S.S. (2014). Utility of antioxidants during assisted reproductive techniques: an evidence based review. Reprod. Biol. Endocrinol. 12, 112.Google Scholar
Alberio, R. & Palma, G. (1998). Development of bovine oocytes matured in a defined medium supplemented with a low concentration of rhFSH. Theriogenology 49, 195.CrossRefGoogle Scholar
Augustin, R., Pocar, P., Wrenzycki, C., Niemann, H. & Fischer, B. (2003). Mitogenic and anti-apoptotic activity of insulin on bovine embryos produced in vitro . Reproduction 126, 91–9.CrossRefGoogle ScholarPubMed
Bessa, I.R., Nishimura, R.C., Franco, M.M. & Dode, M.A. (2013). Transcription profile of candidate genes for the acquisition of competence during oocyte growth in cattle. Reprod. Domest. Anim. 48, 781–9.Google Scholar
Blondin, P., Guilbault, L.A. & Sirard, M.A. (1997). The time interval between FSH-P administration and slaughter can influence the developmental competence of beef heifer oocytes. Theriogenology 48, 803–13.CrossRefGoogle ScholarPubMed
Bu, S., Xie, H., Tao, Y., Wang, J. & Xia, G. (2004). Nitric oxide influences the maturation of cumulus cell-enclosed mouse oocytes cultured in spontaneous maturation medium and hypoxanthine-supplemented medium through different signaling pathways. Mol. Cell. Endocrinol. 223, 8593.Google Scholar
Caixeta, E., Ripamonte, P., Franco, M., Junior, J. & Dode, M. (2009). Effect of follicle size on mRNA expression in cumulus cells and oocytes of Bos indicus: an approach to identify marker genes for developmental competence. Reprod. Fertil. Dev. 21, 655–64.CrossRefGoogle ScholarPubMed
Cerri, R.L., Rutigliano, H.M., Lima, F.S., Araujo, D.B. & Santos, J.E. (2009). Effect of source of supplemental selenium on uterine health and embryo quality in high-producing dairy cows. Theriogenology 71, 1127–37.CrossRefGoogle ScholarPubMed
Chwa, M., Atilano, S.R., Reddy, V., Jordan, N., Kim, D.W. & Kenney, M.C. (2006). Increased stress-induced generation of reactive oxygen species and apoptosis in human keratoconus fibroblasts. Invest. Ophthalmol. Vis. Sci. 47, 1902–10.Google Scholar
Córdova, B., Morató, R., Izquierdo, D., Paramio, T. & Mogas, T. (2010). Effect of the addition of insulin–transferrin–selenium and/or l-ascorbic acid to the in vitro maturation of prepubertal bovine oocytes on cytoplasmic maturation and embryo development. Theriogenology 74, 1341–8.Google Scholar
Dalvit, G., Llanes, S.P., Descalzo, A., Insani, M., Beconi, M. & Cetica, P. (2005). Effect of alpha-tocopherol and ascorbic acid on bovine oocyte in vitro maturation. Reprod. Domest. Anim. 40, 93–7.CrossRefGoogle ScholarPubMed
Dode, M.A., Dufort, I., Massicotte, L. & Sirard, M.A. (2006). Quantitative expression of candidate genes for developmental competence in bovine two-cell embryos. Mol. Reprod. Dev. 73, 288–97.Google Scholar
Dode, M.A.N. & Adona, P.R. (2001). Developmental capacity of Bos indicus oocytes after inhibition of meiotic resumption by 6-dimethylaminopurine. Anim. Reprod. Sci., 65, 171–80.Google Scholar
Dode, M.A.N., Rodovalho, N.C., Ueno, V.G. & de Oliveira Alves, R.G. (2000). Efeito do tamanho do folículo na maturação nuclear e citoplasmática de ovócitos de fêmeas zebuínas. [Effect of follicle size in nuclear and cytoplasmic maturation of oocytes from zebu cows] Pesquisa Agropecuária Brasileira 35, 207–14.CrossRefGoogle Scholar
Eppig, J.J., Hosoe, M., O'Brien, M.J., Pendola, F.M., Requena, A. & Watanabe, S. (2000). Conditions that affect acquisition of developmental competence by mouse oocytes in vitro: FSH, insulin, glucose and ascorbic acid. Mol. Cell. Endocrinol. 163, 109–16.Google Scholar
George, F., Daniaux, C., Genicot, G., Verhaeghe, B., Lambert, P. & Donnay, I. (2008). Set up of a serum-free culture system for bovine embryos: embryo development and quality before and after transient transfer. Theriogenology 69, 612–23.Google Scholar
Hammami, S., Morató, R., Romaguera, R., Roura, M., Catalá, M.G., Paramio, M.T., Mogas, T. & Izquierdo, D. (2013). Developmental competence and embryo quality of small oocytes from pre-pubertal goats cultured in IVM medium supplemented with low level of hormones, insulin–transferrin–selenium and ascorbic acid. Reprod. Dom. Anim. 48, 339–44.Google Scholar
Holm, P., Shukri, N.N., Vajta, G., Booth, P., Bendixen, C. & Callesen, H. (1998). Developmental kinetics of the first cell cycles of bovine in vitro produced embryos in relation to their in vitro viability and sex. Theriogenology 50, 1285–99.Google Scholar
Hu, J., Ma, X., Bao, J.C., Li, W., Cheng, D., Gao, Z., Lei, A., Yang, C. & Wang, H. (2011). Insulin–transferrin–selenium (ITS) improves maturation of porcine oocytes in vitro . Zygote 19, 191–7.Google Scholar
Hyttel, P., Viuff, D., Laurincik, J., Schmidt, M., Thomsen, P.D., Avery, B., Callesen, H., Rath, D., Niemann, H., Rosenkranz, H., Schellander, K., Ochs, R.L. & Greve, T. (2000). Risks of in-vitro production of cattle and swine embryos: aberrations in chromosome numbers, ribosomal RNA gene activation and perinatal physiology. Hum. Reprod. 15, 8797.Google Scholar
Jeong, Y.W., Hossein, M.S., Bhandari, D.P., Kim, Y.W., Kim, J.H., Park, S.W., Lee, E., Park, S.M., Jeong, Y.I., Lee, J.Y., Kim, S. & Hwang, W.S. (2008). Effects of insulin–transferrin–selenium in defined and porcine follicular fluid supplemented IVM media on porcine IVF and SCNT embryo production. Anim. Reprod. Sci. 106, 1324.Google Scholar
Kere, M., Siriboon, C., Lo, N.-W., Nguyen, N.T. & Ju, J.-C. (2013). Ascorbic acid improves the developmental competence of porcine oocytes after parthenogenetic activation and somatic cell nuclear transplantation. J. Reprod. Dev. 59, 7884.Google Scholar
Keskintepe, L. & Brackett, B.G. (1996). In vitro developmental competence of in vitro-matured bovine oocytes fertilized and cultured in completely defined media. Biol. Reprod. 55, 333–9.Google Scholar
Kim, S., Lee, G.S., Lee, S.H., Kim, H.S., Jeong, Y.W., Kim, J.H., Kang, S.K., Lee, B.C. & Hwang, W.S. (2005). Embryotropic effect of insulin-like growth factor (IGF)-I and its receptor on development of porcine preimplantation embryos produced by in vitro fertilization and somatic cell nuclear transfer. Mol. Reprod. Dev. 72, 8897.Google Scholar
Lee, M.S., Kang, S.K., Lee, B.C. & Hwang, W.S. (2005). The beneficial effects of insulin and metformin on in vitro developmental potential of porcine oocytes and embryos. Biol. Reprod. 73, 1264–8.Google Scholar
Machado, G.M., Carvalho, J.O., Filho, E.S., Caixeta, E.S., Franco, M.M., Rumpf, R. & Dode, M.A. (2009). Effect of Percoll volume, duration and force of centrifugation, on in vitro production and sex ratio of bovine embryos. Theriogenology 71, 1289–97.CrossRefGoogle ScholarPubMed
Murray, A., Molinek, M., Baker, S., Kojima, F., Smith, M., Hillier, S. & Spears, N. (2001). Role of ascorbic acid in promoting follicle integrity and survival in intact mouse ovarian follicles in vitro . Reproduction 121, 8996.Google Scholar
Parrish, J.J., Krogenaes, A. & Susko-Parrish, J.L. (1995). Effect of bovine sperm separation by either swim-up or Percoll method on success of in vitro fertilization and early embryonic development. Theriogenology 44, 859–69.Google Scholar
Racedo, S.E., Wrenzycki, C., Lepikhov, K., Salamone, D., Walter, J. & Niemann, H. (2009). Epigenetic modifications and related mRNA expression during bovine oocyte in vitro maturation. Reprod. Fertil. Dev. 21, 738–48.Google Scholar
Revel, F., Mermillod, P., Peynot, N., Renard, J.P. & Heyman, Y. (1995). Low developmental capacity of in vitro matured and fertilized oocytes from calves compared with that of cows. J. Reprod. Fertil. 103, 115–20.Google Scholar
Rossetto, R., Lima-Verde, I.B., Matos, M.H., Saraiva, M.V., Martins, F.S., Faustino, L.R., Araujo, V.R., Silva, C.M., Name, K.P., Sn, S.N., Campello, C.C., Figueiredo, J.R. & Blume, H. (2009). Interaction between ascorbic acid and follicle-stimulating hormone maintains follicular viability after long-term in vitro culture of caprine preantral follicles. Domest. Anim. Endocrinol. 37, 112–23.Google Scholar
Tao, Y., Chen, H., Tian, N.N., Huo, D.T., Li, G., Zhang, Y.H., Liu, Y., Fang, F.G., Ding, J.P. & Zhang, X.R. (2010). Effects of l-ascorbic acid, α-tocopherol and co-culture on in vitro developmental potential of porcine cumulus cells free oocytes. Reprod. Domest. Anim. 45, 1925.Google Scholar
Tao, Y., Zhou, B., Xia, G., Wang, F., Wu, Z. & Fu, M. (2004). Exposure to l-ascorbic acid or α-tocopherol facilitates the development of porcine denuded oocytes from metaphase I to metaphase II and prevents cumulus cells from fragmentation. Reprod. Domest. Anim. 39, 52–7.Google Scholar
Tatemoto, H., Muto, N., Sunagawa, I., Shinjo, A. & Nakada, T. (2004). Protection of porcine oocytes against cell damage caused by oxidative stress during in vitro maturation: role of superoxide dismutase activity in porcine follicular fluid. Biol. Reprod. 71, 1150–7.Google Scholar
Tilly, J.L. & Tilly, K.I. (1995). Inhibitors of oxidative stress mimic the ability of follicle-stimulating hormone to suppress apoptosis in cultured rat ovarian follicles. Endocrinology 136, 242–52.Google Scholar
Wydooghe, E., Heras, S., Dewulf, J., Piepers, S., Van den Abbeel, E., De Sutter, P., Vandaele, L. & Van Soom, A. (2014). Replacing serum in culture medium with albumin and insulin, transferrin and selenium is the key to successful bovine embryo development in individual culture. Reprod. Fertil. Dev. 26, 717–24.Google Scholar