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Effect of Alpha-Linolenic Acid on Oocyte Maturation and Embryo Development in Pigs

  • Lee, Ji-Eun (College of Animal Life Sciences, Kangwon National University) ;
  • Hwangbo, Yong (College of Animal Life Sciences, Kangwon National University) ;
  • Kim, Hwa-Young (College of Animal Life Sciences, Kangwon National University) ;
  • Lee, Won-Hee (College of Animal Life Sciences, Kangwon National University) ;
  • Cheong, Hee-Tae (College of Veterinary Medicine, Kangwon National University) ;
  • Yang, Boo-Keun (College of Animal Life Sciences, Kangwon National University) ;
  • Park, Choon-Keun (College of Animal Life Sciences, Kangwon National University)
  • Received : 2017.05.27
  • Accepted : 2017.06.02
  • Published : 2017.06.30

Abstract

The aim of this study was to determine the effect of additional alpha-linolenic acid (ALA) supplementation during in vitro maturation (IVM) and culture (IVC) on nucleic maturation and embryo development of pigs. Cumulus-oocyte complexes (COCs) were incubated in IVM medium containing different concentration of ALA (25, 50 and $100{\mu}M$) for 44 h. After in vitro maturation, nuclear maturation of oocytes were evaluated by aceto-orcein stain. Mature oocytes with $50{\mu}M$ ALA were fertilized and cultured in IVC medium with ALA (25, 50 and $100{\mu}M$) during early-embryogenesis (48 hours after fertilization). Then, embryos were cultured with $25{\mu}M$ ALA during early embryogenesis and/or late embryogenesis (120 hours after early-embryogenesis). In results, oocyte maturation were significantly increased by $50{\mu}M$ ALA treatment groups compared with control groups (p<0.05). Treatment of $25{\mu}M$ ALA during early-embryogenesis enhanced cleavage rate of embryo compared with other groups (p<0.05), whereas formation and total cell number of blastocyst had no significant difference. Similarly, cleavage rate of embryos were increased by $25{\mu}M$ ALA supplement during early- or late-embryogenesis than ALA treatment both stage of embryogenesis (p<0.05), but did not influence to blastocyst formation. Interestingly, total cell number of blastocyst were enhanced in ALA treatment group during early-embryogenesis. These findings indicated that ALA supplement enhance the nuclear maturation of oocyte and embryo development, however, excessive ALA could negatively influence. Therefore, we suggest that ALA is used for improvement of in vitro production of mammalian embryo and further study regarding with functional mechanism of ALA is needed.

Keywords

References

  1. Aitken RJ, Wingate JK, De Iuliis GN, Koppers AJ, Mc-Laughlin EA (2006) Cis-unsaturated fatty acids stimulate reactive oxygen species generation and lipid peroxidation in human spermatozoa. J Clin Endocrinol Metab 91:4154-4163. https://doi.org/10.1210/jc.2006-1309
  2. Al-Gubory KH, Fowler PA, Garrel C (2010) The role of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol 42:1634-1650. https://doi.org/10.1016/j.biocel.2010.06.001
  3. Ambrose DJ, Kastelic JP, Corbett R, Pitney PA, Petit HV, Small JA, Zalkovic P (2006) Lower pregnancy losses in lactating dairy cows fed a diet enriched in alpha-linolenic acid. J Dairy Sci 89:3066-3074. https://doi.org/10.3168/jds.S0022-0302(06)72581-4
  4. Bilby TR, Block J, do Amaral BC, Sa Filho O, Silvestre FT, Hansen PJ, Staples CR, Thatcher WW (2006) Effects of dietary unsaturated fatty acids on oocyte quality and follicular development in lactating dairy cows in summer. J Dairy Sci 89:3891-3903. https://doi.org/10.3168/jds.S0022-0302(06)72432-8
  5. Elahi F, Lee H, Lee Y, Park B, Lee J, Hyun SH, Lee E (2016) Cilostazol improves developmental competence of pig oocytes by increasing intraoocyte cyclic adenosine monophosphate level and delaying meiotic resumption. Reprod Domest Anim 51:220-226. https://doi.org/10.1111/rda.12669
  6. Fouladi-Nashta AA, Wonnacott KE, Gutierrez CG, Gong JG, Sinclair KD, Garnsworthy PC, Webb R (2009) Oocyte quality in lactating dairy cows fed on high levels of n-3 and n-6 fatty acids. Reproduction 138:771-781. https://doi.org/10.1530/REP-08-0391
  7. Guerin P, El Mouatassim S, Menezo Y (2001) Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings. Hum Reprod 7:175-189. https://doi.org/10.1093/molehr/7.2.175
  8. Homa ST, Brown CA (1992) Changes in linoleic acid during follicular development and inhibition of spontaneous breakdown of germinal vesicles in cumulus-free bovine oocytes. J Reprod Fertil 94:153-160. https://doi.org/10.1530/jrf.0.0940153
  9. Katska-Ksiazkiewicz L (2006) Pig embryo production by in vitro maturation and fertilization of ovarian oocytes. A review. J Anim Feed Sci 15:525-542. https://doi.org/10.22358/jafs/66923/2006
  10. Khalil WA, Marei WF, Khalid M (2013) Protective effects of antioxidants on linoleic acid-treated bovine oocytes during maturation and subsequent embryo development. Theriogenology, 80:161-168. https://doi.org/10.1016/j.theriogenology.2013.04.008
  11. Khandoker M, Tsujii H (1998). Metabolism of exogenous fatty acids by preimplantation rabbit embryos. Jpn J Fertil Steril 43:195-201.
  12. Kim CH, Cheon YP, Lee YJ, Lee KH, Kim SH, Chae DH, Kang BM (2013) The effect of fibroblast co-culture on in vitro maturation of mouse preantral follicles. Dev Reprod 17:269-274. https://doi.org/10.12717/DR.2013.17.3.269
  13. Kitagawa Y, Suzuki K, Yoneda A, Watanabe T (2004) 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 62:1186-1197. https://doi.org/10.1016/j.theriogenology.2004.01.011
  14. Kowaltowski AJ, Vercesi AE (1999) Mitochondrial dam-age induced by conditions of oxidative stress. Free Radic Biol Med 26:463-71. https://doi.org/10.1016/S0891-5849(98)00216-0
  15. Lee S, Park EJ, Moon JH, Kim SJ, Song K, Lee BC (2015) Sequential treatment with resveratrol-trolox improves development of porcine embryos derived from parthenogenetic activation and somatic cell nuclear transfer. Theriogenology 84:145-154. https://doi.org/10.1016/j.theriogenology.2015.02.021
  16. Lee Y, Lee H, Park B, Elahi J, Lee J, Lee ST, Park CK, Hyun SH, Lee E (2016) Alpha-linolenic acid treatment during oocyte maturation enhances embryonic development by influencing mitogen-activated protein ki-nase activity and intraoocyte glutathione content in pigs. J Anim Sci 94:3255-3263. https://doi.org/10.2527/jas.2016-0384
  17. Lin L, Kragh PM, Purup S, Kuwayama M, Du Y, Zhang X, Yang H, Bolund L, Callesen H, Vajta G (2009) Osmotic stress induced by sodium chloride, sucrose or trehalose improves cryotolerance and developmental competence of porcine oocytes. Reprod Fertil Dev 21:338-344. https://doi.org/10.1071/RD08145
  18. Marei WF, Wathes DC, Fouladi-Nashta AA (2009) The effect of linolenic acid on bovine oocyte maturation and development. Biol Reprod 81:1064-1072. https://doi.org/10.1095/biolreprod.109.076851
  19. Marei WF, Wathes DC, Fouladi-Nashta AA (2012) Differ-ential effects of linoleic and alpha-linolenic fatty acids on spatial and temporal mitochondrial distribution and activity in bovine oocytes. Reprod Fertil Dev 24:679-690. https://doi.org/10.1071/RD11204
  20. McKeegan PJ, Sturmey RG (2011) The role of fatty acids. in oocyte and early embryo development. Reprod Fertil Dev 24:59-67.
  21. Nagai T (2001) The improvement of in vitro maturation systems for bovine and porcine oocytes. Theriogenology, 55:1291-1301. https://doi.org/10.1016/S0093-691X(01)00483-6
  22. Pratt SL, Sherrer ES, Reeves DE, Stice SL (2006) Factors influencing the commercialisation of cloning in the pork industry. J Reprod Fertil Suppl 62:303-315.
  23. Sturmey RG, Reis A, Leese HJ, McEvoy TG (2009) Role of fatty acids in energy provision during oocyte maturation and early embryo development. Reprod Domest Anim 44:50-58. https://doi.org/10.1111/j.1439-0531.2009.01402.x
  24. Takahashi M (2012) Oxidative stress and redox regulation on in vitro development of mammalian embryos. J Reprod Dev 58:1-9. https://doi.org/10.1262/jrd.11-138N
  25. Wakefield SL, Lane M, Schulz SJ, Hebart ML, Thompson JG, Mitchell M (2007) Maternal supply of omega-3 polyunsaturated fatty acids alter mechanisms involved in oocyte and early embryo development in mouse. Am J Physiol Endocrinol Metab 294:E425-E434.
  26. Wathes DC, Abayasekara DRE, Aitken RJ (2007) Polyun-saturated fatty acids in male and female reproduction. Biol Reprod 77:190-201.
  27. Wonnacott KE, Kwong WY, Hughes J, Salter AM, Lea RG, Garnsworthy PC, Sinclair KD (2010) Dietary omega-3 and-6 polyunsaturated fatty acids affect the composition and development of sheep granulosa cells, oocytes and embryos. Reproduction 139:57-69. https://doi.org/10.1530/REP-09-0219
  28. Wu Y, Zhang N, Li YH, Zhao L, Yang M, Jin Y, Xu YN, Guo H (2017) Citrinin exposure affects oocytes maturation and embryo development by inducing oxidative stress-mediated apoptosis. Oncotarget 8:34525-34533.