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Effect of Alpha Lipoic Acid as an Antioxidant Supplement during In Vitro Maturation Medium on Bovine Embryonic Development

  • Hassan, Bahia M.S. (College of Veterinary Medicine, Chungnam National University) ;
  • Fang, Xun (College of Veterinary Medicine, Chungnam National University) ;
  • Roy, Pantu Kumar (College of Veterinary Medicine, Chungnam National University) ;
  • Shin, Sang Tae (College of Veterinary Medicine, Chungnam National University) ;
  • Cho, Jong Ki (College of Veterinary Medicine, Chungnam National University)
  • Received : 2017.09.14
  • Accepted : 2017.09.26
  • Published : 2017.09.30

Abstract

This study was conducted to investigate the effects of alpha-lipoic acid (aLA) as an antioxidant that decrease the reactive oxygen species (ROS) in bovine embryonic development. Slaughterhouse derived bovine immature oocytes were collected and 4 different concentrations (0, 5, 10 and 20 mM) of aLA was supplemented in bovine in vitro maturation (IVM) medium. After 20 hrs of IVM, maturation rates, levels of ROS and glutathione (GSH), and further embryonic development after parthenogenetic activation (PA) and in vitro fertilization (IVF) was investigated according to aLA concentrations. Maturation rate was significantly higher in 10 mM group than other groups (80.5% vs. 62.9, 73.9, 64.2%; P<0.05). In the levels of ROS and GSH in matured oocytes as an indicator of oocyte quality, significantly better results were shown in 5 and 10 mM groups compared with other 2 groups. After IVM, significantly higher rates of blastocyst formation were shown in 10 mM groups in both of PA (27.9% vs. 18.8, 22.3, 14.2%; P<0.05) and IVF (32.6% vs. 23.9, 27.3, 16.2%; P<0.05) embryos. In addition, significantly more cell total cell number and higher inner cell mass ratio in 10 mM PA and IVP blastocysts showed developmental competence in 10 uM groups. Therefore, based on the entire data from this study, using $10{\mu}M$ of aLA confirmed to be the optimal concentration for bovine oocyte maturation and embryonic development.

Keywords

References

  1. Agarwal A, Durairajanayagam D, Du Plessis SS. 2014. Utility of antioxidants during assisted reproductive techniques: an evidence based review. Reproductive Biology and Endocrinology 12:112. https://doi.org/10.1186/1477-7827-12-112
  2. Amudha G, Josephine A, and Varalakshmi P. 2006. Role of lipoic acid in reducing the oxidative stress induced by cyclosporine A. Clinica chimica acta 372:134-139. https://doi.org/10.1016/j.cca.2006.03.036
  3. Bilska A, and Wlodek L. 2005. Lipoic acid-the drug of the future. Pharmacol. Rep. 57:570-577.
  4. Cakatay U. 2006. Pro-oxidant actions of ${\alpha}$-lipoic acid and dihydrolipoic acid. Medical hypotheses 66:110-117. https://doi.org/10.1016/j.mehy.2005.07.020
  5. Choi J-Y, Kang J-T, Park S-J et al. 2013. Effect of 7, 8-dihydroxyflavone as an antioxidant on in vitro maturation of oocytes and development of parthenogenetic embryos in pigs. Journal of Reproduction and Development 59:450-456. https://doi.org/10.1262/jrd.2012-134
  6. Crosier AE, Farin PW, Dykstra MJ et al. 2000. Ultrastructural morphometry of bovine compact morulae produced in vivo or in vitro. Biology of reproduction 62:1459-1465. https://doi.org/10.1095/biolreprod62.5.1459
  7. Crosier AE, Farin PW, Dykstra MJ et al. 2001. Ultrastructural morphometry of bovine blastocysts produced in vivo or in vitro. Biology of reproduction 64:1375-1385. https://doi.org/10.1095/biolreprod64.5.1375
  8. Dehghani-Mohammadabadi M, Salehi M, Farifteh F et al. 2014. Melatonin modulates the expression of BCL-xl and improve the development of vitrified embryos obtained by IVF in mice. Journal of assisted reproduction and genetics 31:453-461. https://doi.org/10.1007/s10815-014-0172-9
  9. Dennery PA. 2007. Effects of oxidative stress on embryonic development. Birth Defects Research Part C: Embryo Today: Reviews 81:155-162. https://doi.org/10.1002/bdrc.20098
  10. Fleming TP, Kwong WY, Porter R et al. 2004. The embryo and its future. Biology of Reproduction 71:1046-1054. https://doi.org/10.1095/biolreprod.104.030957
  11. Gardiner CS, Salmen JJ, Brandt CJ et al. 1998. Glutathione is present in reproductive tract secretions and improves development of mouse embryos after chemically induced glutathione depletion. Biology of reproduction 59:431-436. https://doi.org/10.1095/biolreprod59.2.431
  12. Gupta VK, and Sharma SK. 2006. Plants as natural antioxidants.
  13. Kably AA, Ruiz AJ, Carballo ME et al. 2004. Correlation between follicle levels of superoxide dismutase and oocyte quality, fertilization rates and embryo development. Ginecologia y obstetricia de Mexico 72:335-344.
  14. Kwak S-S, Cheong S-A, Jeon Y et al. 2012. The effects of resveratrol on porcine oocyte in vitro maturation and subsequent embryonic development after parthenogenetic activation and in vitro fertilization. Theriogenology 78:86-101. https://doi.org/10.1016/j.theriogenology.2012.01.024
  15. Lampiao F. 2012. Free radicals generation in an in vitro fertilization setting and how to minimize them.
  16. Lee S, Kim E, and Hyun SH. 2014. Toxicity evaluation of ethanol treatment during in vitro maturation of porcine oocytes and subsequent embryonic development following parthenogenetic activation and in vitro fertilization. International journal of molecular medicine 34:1372-1380. https://doi.org/10.3892/ijmm.2014.1924
  17. Lonergan P, Fair T, Corcoran D et al. 2006. Effect of culture environment on gene expression and developmental characteristics in IVF-derived embryos. Theriogenology 65:137-152. https://doi.org/10.1016/j.theriogenology.2005.09.028
  18. Machado G, Carvalho J, Siqueira Filho E et al. 2009. Effect of Percoll volume, duration and force of centrifugation, on in vitro production and sex ratio of bovine embryos. Theriogenology 71:1289-1297. https://doi.org/10.1016/j.theriogenology.2009.01.002
  19. Maitra I, Serbinova E, Trischler H et al. 1995. ${\alpha}$-Lipoic acid prevents buthionine sulfoximine-induced cataract formation in newborn rats. Free Radical Biology and Medicine 18:823-829. https://doi.org/10.1016/0891-5849(94)00195-P
  20. Marsh S, Pat B, Gobe G et al. 2005. Evidence for a non-antioxidant, dose-dependent role of ${\alpha}$-lipoic acid in caspase-3 and ERK2 activation in endothelial cells. Apoptosis 10:657-665. https://doi.org/10.1007/s10495-005-1901-4
  21. Packer L, Witt EH, and Tritschler HJ. 1995. Alpha-lipoic acid as a biological antioxidant. Free radical biology and medicine 19:227-250. https://doi.org/10.1016/0891-5849(95)00017-R
  22. Rakhit M, Gokul SR, Agarwal A et al. 2013. Antioxidant strategies to overcome OS in IVF-Embryo transfer. In: Studies on Women's Health. Springer. pp. 237-262.
  23. Rizos D, Gutierrez-Adan A, Perez-Garnelo S et al. 2003. Bovine embryo culture in the presence or absence of serum: implications for blastocyst development, cryotolerance, and messenger RNA expression. Biology of reproduction 68:236-243. https://doi.org/10.1095/biolreprod.102.007799
  24. Rosini M, Simoni E, Bartolini M et al. 2011. Exploiting the lipoic acid structure in the search for novel multitarget ligands against Alzheimer's disease. European journal of medicinal chemistry 46:5435-5442. https://doi.org/10.1016/j.ejmech.2011.09.001
  25. Ruder EH, Hartman TJ, Blumberg J et al. 2008. Oxidative stress and antioxidants: exposure and impact on female fertility. Human reproduction update 14:345-357. https://doi.org/10.1093/humupd/dmn011
  26. Selokar N, Saha A, Saini M et al. 2012. A protocol for differential staining of inner cell mass and trophectoderm of embryos for evaluation of health status. CURRENT SCIENCE 102:1256-1257.
  27. Sen CK, and Packer L. 2000. Thiol homeostasis and supplements in physical exercise. The American journal of clinical nutrition 72:653s-669s. https://doi.org/10.1093/ajcn/72.2.653S
  28. Sen CK, Roy S, Han D et al. 1997. Regulation of cellular thiols in human lymphocytes by ${\alpha}$-lipoic acid: A flow cytometric analysis. Free Radical Biology and Medicine 22:1241-1257. https://doi.org/10.1016/S0891-5849(96)00552-7
  29. Simbula G, Columbano A, Ledda-Columbano G et al. 2007. Increased ROS generation and p53 activation in ${\alpha}$-lipoic acid-induced apoptosis of hepatoma cells. Apoptosis 12:113-123. https://doi.org/10.1007/s10495-006-0487-9
  30. Talebi A, Zavareh S, Kashani MH et al. 2012. The effect of alpha lipoic acid on the developmental competence of mouse isolated preantral follicles. Journal of assisted reproduction and genetics 29:175-183. https://doi.org/10.1007/s10815-011-9706-6
  31. Van Langendonckt A, Donnay I, Schuurbiers N et al. 1997. Effects of supplementation with fetal calf serum on development of bovine embryos in synthetic oviduct fluid medium. Journal of reproduction and fertility 109:87-93. https://doi.org/10.1530/jrf.0.1090087
  32. Wenzel U, Nickel A, and Daniel H. 2005. ${\alpha}$-lipoic acid induces apoptosis in human colon cancer cells by increasing mitochondrial respiration with a concomitant O 2-. -generation. Apoptosis 10:359-368. https://doi.org/10.1007/s10495-005-0810-x
  33. Yamasaki M, Kawabe A, Nishimoto K et al. 2009. Dihydro-alpha-lipoic acid has more potent cytotoxicity than alpha-lipoic acid. In Vitro Cellular & Developmental Biology-Animal 45:275-280. https://doi.org/10.1007/s11626-008-9164-3
  34. Zavareh S, Karimi I, Salehnia M et al. 2016. Effect of in vitro maturation technique and alpha lipoic acid supplementation on oocyte maturation rate: focus on oxidative status of oocytes. International journal of fertility & sterility 9:442.
  35. Zhang H, Wu B, Liu H et al. 2013. Improving development of cloned goat embryos by supplementing ${\alpha}$-lipoic acid to oocyte in vitro maturation medium. Theriogenology 80:228-233. https://doi.org/10.1016/j.theriogenology.2013.03.027
  36. Zuelke KA, Jeffay SC, Zucker RM et al. 2003. Glutathione (GSH) concentrations vary with the cell cycle in maturing hamster oocytes, zygotes, and pre-implantation stage embryos. Molecular reproduction and development 64:106-112. https://doi.org/10.1002/mrd.10214