Browse > Article
http://dx.doi.org/10.12750/JET.2017.32.4.337

Effects of Antioxidants Supplement in Porcine Sperm Freezing on in vitro Fertilization and the Glutathione and Reactive Oxygen Species Level of Presumptive Zygotes  

Park, Sang-Hyoun (Department of Theriogenology and Reproductive Biotechnology, College of Veterinary Medicine and Bio-safety Research Institute, Chonbuk National University)
Jeon, Yubyoel (Department of Theriogenology and Reproductive Biotechnology, College of Veterinary Medicine and Bio-safety Research Institute, Chonbuk National University)
Yu, Il-Jeoung (Department of Theriogenology and Reproductive Biotechnology, College of Veterinary Medicine and Bio-safety Research Institute, Chonbuk National University)
Publication Information
Journal of Embryo Transfer / v.32, no.4, 2017 , pp. 337-342 More about this Journal
Abstract
The present study was aimed to determine the effects of green tea extract (GTE) and beta-mercaptoethanol (${\beta}-ME$) supplementation in boar sperm freezing extender on in vitro fertilization (IVF) and reactive oxygen species (ROS) and glutathione (GSH) levels of presumptive zygotes (PZs). Experimental groups were allocated into lactose egg yolk (LEY) without antioxidant (control), GTE (1,000 mg/l in LEY) and ${\beta}-ME$ ($50{\mu}M$ in LEY). In freezing, spermatozoa extended with LEY were cooled to $5^{\circ}C$ for 3 h and then kept at $5^{\circ}C$ for 30 min following dilution with LEY containing 9% glycerol and 1.5% Equex STM. The final sperm concentration was $1{\times}10^8/ml$. Spermatozoa were loaded into straws and frozen in nitrogen vapor for 20 min. For IVF, oocytes were matured in NCSU-23 medium and co-cultured with spermatozoa following thawing at $37^{\circ}C$ for 25 sec. At 12 h following IVF, IVF parameters (sperm penetration and monospermy) were evaluated. In addition, GSH and ROS levels of PZs were determined by Cell Tracker Blue CMF2HC and DCHFDA, respectively. IVF parameters did not show any significant difference among the experimental groups. GSH and ROS levels of PZs were not significantly different between groups. In conclusion, antioxidant supplementation in boar sperm freezing could not influence IVF parameters, ROS and GSH levels of PZs.
Keywords
Beta-mercaptoethanol; Boar spermatozoa; Green tea extract; Glutathione; Reactive oxygen species;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
연도 인용수 순위
1 Abeydeera LR, Wang WH, Cantley TC, Prather RS and Day BN. 1998. Presence of beta-mercaptoethanol can increase the glutathione content of pig oocytes matured in vitro and the rate of blastocyst development after in vitro fertilization. Theriogenology 50: 747-756.   DOI
2 Watson PF. 1995. Recent developments and concepts in the cryopreservation of spermatozoa and the assessment of their ost-thawing function. Reprod. Fertil. Dev. 7: 871-891.   DOI
3 Waterhouse KE, Gjeldnes A, Tverdal A, De Angelis PM, Farstad W, Haard M & Kommisrud, E. 2010. Alterations of sperm DNA integrity during cryopreservation procedure and in vitro incubation of bull semen. Anim. Reprod. Sci. 117: 34-42.   DOI
4 Agarwal A, Saleh RA and Bedaiwy MA. 2003. Role of reactive oxygen species in the pathophysiology of human reproduction. Fertil. Steril. 79: 829-843.   DOI
5 Bailey JL, Bilodeau JF and Cormier N. 2000. Semen cryopreservation in domestic animals: a damaging and capacitating phenomenon. J. Androl. 21: 1-7.
6 Chatterjee S and Gagnon C. 2001. Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing. Mol. Reprod. Dev. 59: 451-458.   DOI
7 Dalvit G, Llanes SP, 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.   DOI
8 Dufresne CJ and Farnworth ER. 2001. A review of latest research findings on the health promotion properties of tea. J. Nutr. Biochem. 12: 404-421.   DOI
9 Funahashi H, Cantley TC, Stumpf TT, Terlouw SL and Day BN. 1994: Use of low-salt culture medium for in vitro maturation of porcine oocytes is associated with elevated oocyte glutathione levels and enhanced male pronuclear formation after in vitro fertilization. Biol. Reprod. 51:633-639.   DOI
10 Gil MA, Alminana C, Cuello C, Parrilla I, Roca J, Vazquez JM and Martinez EA. 2007. Brief coincubation of gametes in porcine in vitro fertilization: role of sperm: oocyte ratio and post-coincubation medium. Theriogenology 67: 620-626.   DOI
11 de Lamirande E and Gagnon C. 1992. Reactive oxygen species and human spermatozoa. I. Effects on the motility of intact spermatozoa and on sperm axonemes. J. Androl. 13: 368-378.
12 Yamaguchi S and Funahashi H. 2012. Effect of the addition of beta-mercaptoethanol to a thawing solution supplemented with caffeine on the function of frozen-thawed boar sperm and on the fertility of sows after artificial insemination. Theriogenology 77: 926-932.   DOI
13 Yoshida M, Ishigaki K, Nagai T, Chikyu M and Pursel VG. 1993. Glutathione concentration during maturation and after fertilization in pig oocytes: relevance to the ability of oocytes to form male pronucleus. Biol. Reprod. 49: 89-94.   DOI
14 Gadea J, Matas C and Lucas X. 1998: Prediction of porcine semen fertility by homologous in vitro penetration (hIVP) assay. Anim. Reprod. Sci. 54: 95-108.   DOI
15 Gadea J, Selles E, Marco MA, Coy P, Matas C, Romar R and Ruiz S. 2004: Decrease in glutathione content in boar sperm after cryopreservation: Effect of the addition of reduced glutathione to the freezing and thawing extenders. Theriogenology 62: 690-701.   DOI
16 Hu JH, Li QW, Jiang ZL and Li WY. 2008. Effects of different extenders on DNA integrity of boar spermatozoa following freezing-thawing. Cryobiology 57: 257-262.   DOI
17 Luvoni GC, Keskintepe L and Brackett BG. 1996. Improvement in bovine embryo production in vitro by glutathione-containing culture media. Mol. Reprod. Dev. 43: 437-443.   DOI
18 Makker K, Agarwal A and Sharma R. 2009. Oxidative stress & male infertility. Indian. J. Med. Res. 129: 357-367.
19 Mammoto A, Masumoto N, Tahara M, Ikebuchi Y, Ohmichi M, Tasaka K and Miyake A. 1996. Reactive oxygen species block sperm-egg fusion via oxidation of sperm sulfhydryl proteins in mice. Biol. Reprod. 55: 1063-1068.   DOI
20 de Matos DG and Furnus CC. 2000. The importance of having high glutathione (GSH) level after bovine in vitro maturation on embryo development effect of beta-mercaptoethanol, cysteine and cystine. Theriogenology 53: 761-771.   DOI
21 Maya-Soriano MJ, Taberner E and Lopez-Bejar M. 2013. Retinol improves in vitro oocyte nuclear maturation under heat stress in heifers. Zygote 21: 377-384.   DOI
22 Park SH and Yu IJ. 2017. Effect of antioxidant supplementation in freezing extender on porcine sperm viability, motility and reactive oxygen species. J. Emb. Trans. 32: 9-15.   DOI
23 Oborna I, Wojewodka G, De Sanctis JB, Fingerova H, Svobodova M, Brezinova J, Hajduch M, Novotny J, Radova L and Radzioch D. 2010. Increased lipid peroxidation and abnormal fatty acid profiles in seminal and blood plasma of normozoospermic males from infertile couples. Hum. Reprod. 25: 308-316.   DOI
24 Olson SE and Seidel GE Jr. 2000. Culture of in vitro-produced bovine embryos with vitamin E improves development in vitro and after transfer to recipients. Biol. Reprod. 62:248-252.   DOI
25 Park SH and Yu IJ. 2015. Evaluation of Toxicity of Green Tea Extract in Chilled Boar Spermatozoa. J. Emb. Trans. 30:1-6.   DOI
26 Selles E, Gadea J, Romar R, Matas C and Ruiz S. 2003. Analysis of in vitro fertilizing capacity to evaluate the freezing procedures of boar semen and to predict the subsequent fertility. Reprod. Domest. Anim. 38: 66-72.   DOI
27 Tatemoto H, Muto N, Sunagawa I, Shinjo A and 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: 1150-1157.   DOI
28 Truong T and Gardner DK. 2017. Antioxidants improve IVF outcome and subsequent embryo development in the mouse. Hum. Reprod. Nov. 10:1-10 doi: 10.1093/humrep/ex330.