Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-22T09:17:16.710Z Has data issue: false hasContentIssue false

Effects of changing culture medium on preimplantation embryo development in rabbit

Published online by Cambridge University Press:  29 September 2021

Haixia Wang
Affiliation:
Qinghai Drug Purchasing Center, Xining, Qinghai Province, China Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Wenbin Cao
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Huizhong Hu
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Chenglong Zhou
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Ziyi Wang
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Naqash Alam
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Pengxiang Qu*
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
Enqi Liu*
Affiliation:
Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, Xi’an, 710061, Shaanxi Province, China
*
Authors for correspondence: Dr Pengxiang Qu and Professor Liu Enqi, Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, No. 76 Yanta West Road, Xi’an, 710061, Shaanxi Province, China. E-mail: [email protected] and [email protected]
Authors for correspondence: Dr Pengxiang Qu and Professor Liu Enqi, Laboratory Animal Center, Xi’an Jiaotong University Health Science Center, No. 76 Yanta West Road, Xi’an, 710061, Shaanxi Province, China. E-mail: [email protected] and [email protected]

Summary

Many studies have focused on the optimization of the composition of embryo culture medium; however, there are few studies involving the effect of a culture medium changing procedure on the preimplantation development of embryos. In this study, three groups were designed: a non-renewal group, a renewal group and a half-renewal group. The levels of reactive oxygen species (ROS), apoptotic index, blastocyst ratio and blastocyst total cell number were analyzed in each group. The results showed that the ROS level and the apoptotic index of blastocyst in the non-renewal group were significantly higher than in the renewal group and the half-renewal group (P < 0.05). The blastocyst ratio and blastocyst total cell number were significantly higher in the half-renewal group than that in non-renewal group and the renewal group (P < 0.05). These results demonstrated that the procedure of changing the culture medium influenced ROS level, apoptotic index, blastocyst ratio and total cell number of blastocysts. In addition, the result suggested that changing the culture medium may lead to a loss of important regulatory factors for embryos, while not changing the culture medium may lead to the accumulation of toxic substances. Half-renewal can alleviate the defects of both no renewal and renewal, and benefit embryo development. This study will be of high value as a reference for the optimization of embryo culture in vitro, and is very significant for assisted reproduction.

Type
Research Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press

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.)

Footnotes

*

These authors contributed equally to this work.

References

Alarifi, S, Ali, D, Verma, A, Almajhdi, FN and Al-Qahtani, AA (2014). Single-walled carbon nanotubes induce cytotoxicity and DNA damage via reactive oxygen species in human hepatocarcinoma cells. In Vitro Cell Dev Biol Anim 50, 714722.CrossRefGoogle ScholarPubMed
Alexandre, H (2001). A history of mammalian embryological research. Int J Dev Biol 45, 457–67.Google ScholarPubMed
Amoushahi, M, Salehnia, M and Ghorbanmehr, N (2018). The mitochondrial DNA copy number, cytochrome c oxidase activity and reactive oxygen species level in metaphase II oocytes obtained from in vitro culture of cryopreserved ovarian tissue in comparison with in vivo-obtained oocyte. J Obstet Gynaecol Res 44, 1937–46.Google ScholarPubMed
An, QL, Peng, W, Cheng, YY, Lu, ZZ, Zhou, C, Zhang, Y and Su, JM (2019). Melatonin supplementation during in vitro maturation of oocyte enhances subsequent development of bovine cloned embryos. J Cell Physiol 234, 17370–81.CrossRefGoogle ScholarPubMed
Barratt, CLR, Björndahl, L, De Jonge, CJ, Lamb, DJ, Osorio Martini, FO, McLachlan, R, Oates, RD, van der Poel, S, St John, B, Sigman, M, Sokol, R and Tournaye, H (2017). The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance-challenges and future research opportunities. Hum Reprod Update 23, 660–80.CrossRefGoogle Scholar
Chen, S and Schoen, J (2019). Air–liquid interface cell culture: from airway epithelium to the female reproductive tract. Reprod Domest Anim 54 Supplement 3, 3845.CrossRefGoogle ScholarPubMed
De Neubourg, D, van Duijnhoven, NTL, Nelen, WLDM and D’Hooghe, TM (2012). Dutch translation of the ICMART-WHO revised glossary on ART terminology. Gynecol Obstet Invest 74, 233–48.CrossRefGoogle ScholarPubMed
Faddy, MJ, Gosden, MD and Gosden, RG (2018). A demographic projection of the contribution of assisted reproductive technologies to world population growth. Reprod Biomed Online 36, 455–8.CrossRefGoogle ScholarPubMed
Fischer, B, Chavatte-Palmer, P, Viebahn, C, Navarrete Santos, AN and Duranthon, V (2012). Rabbit as a reproductive model for human health. Reproduction 144, 110.CrossRefGoogle ScholarPubMed
Hall-Woods, ML, Krisher, RL, Lane, M, Gardner, DK and Asa, CS (2000). Comparison of Gardner’s G1/G2 sequential media and buffalo rat liver (BRL) cell go-culture for bovine in-vitro embryo production. Biol Reprod 62, 316.Google Scholar
Hicks, E, Mentler, M, Arena, HA, Current, JZ and Whitaker, BD (2020). Cyanidin improves oocyte maturation and the in vitro production of pig embryos. In Vitro Cell Dev Biol Anim 56, 577–84.CrossRefGoogle ScholarPubMed
Huang, ZQ, Pang, YW, Hao, HS, Du, WH, Zhao, XM and Zhu, HB (2018). Effects of epigallocatechin-3-gallate on bovine oocytes matured in vitro . Asian Australas J Anim Sci 31, 1420–30.CrossRefGoogle ScholarPubMed
Jia, LY, Ding, B, Shen, C, Luo, SW, Zhang, YR, Zhou, L, Ding, RK, Qu, PX and Liu, EQ (2019). Use of oocytes selected by brilliant cresyl blue staining enhances rabbit cloned embryo development in vitro . Zygote 27, 166–72.CrossRefGoogle ScholarPubMed
Jin, DI, Kim, DK, Im, KS and Choi, WS (2000). Successful pregnancy after transfer of rabbit blastocysts grown in vitro from single-cell zygotes. Theriogenology 54, 1109–16.CrossRefGoogle ScholarPubMed
de Los Santos, MJ, Gámiz, P, de Los Santos, JM, Romero, JL, Prados, N, Alonso, C, Remohí, J and Dominguez, F (2015). The metabolomic profile of spent culture media from Day-3 human embryos cultured under low oxygen tension. PLoS One 10, e0142724.CrossRefGoogle ScholarPubMed
Kim, J, Lee, J, Kim, SH and Jun, JH (2016). Coculture of preimplantation embryos with outgrowth embryos improves embryonic developmental competence in mice. Reprod Sci 23, 913–23.CrossRefGoogle ScholarPubMed
Kleijkers, SHM, van Montfoort, APA, Bekers, O, Coonen, E, Derhaag, JG, Evers, JLH and Dumoulin, JCM (2016). Ammonium accumulation in commercially available embryo culture media and protein supplements during storage at 2-8°C and during incubation at 37°C. Hum Reprod 31, 1192–9.CrossRefGoogle Scholar
Koscinski, I, Merten, M, Kazdar, N and Guéant, JL (2018). Culture conditions for gametes and embryos: which culture medium? Which impact on newborn? Gynecol Obstet Fertil Senol 46, 474–80.Google ScholarPubMed
Lee, J, Lee, H, Lee, Y, Park, B, Elahi, F, Lee, ST, Park, CK, Hyun, SH and Lee, E (2017). In vitro oocyte maturation in a medium containing reduced sodium chloride improves the developmental competence of pig oocytes after parthenogenesis and somatic cell nuclear transfer. Reprod Fertil Dev 29, 1625–34.CrossRefGoogle Scholar
Li, ZC, Gu, RH, Lu, XW, Zhao, S, Feng, Y and Sun, YJ (2018). Preincubation with glutathione ethyl ester improves the developmental competence of vitrified mouse oocytes. J Assist Reprod Genet 35, 1169–78.CrossRefGoogle ScholarPubMed
Lin, T, Lee, JE, Oqani, RK, Kim, SY, Cho, ES, Jeong, YD, Baek, JJ and Jin, DI (2016). Tauroursodeoxycholic acid improves pre-implantation development of porcine SCNT embryo by endoplasmic reticulum stress inhibition. Reprod Biol 16, 269–78.CrossRefGoogle ScholarPubMed
Lin, XY, Beckers, E, McCafferty, S, Gansemans, Y, Szymanska, KJ, Pavani, KC, Catani, JP, Van Nieuwerburgh, F, Deforce, D, De Sutter, P, Van Soom, A and Peelman, L (2019). Bovine embryo-secreted microRNA-30c is a potential non-invasive biomarker for hampered preimplantation developmental competence. Front Genet 10, 15.CrossRefGoogle ScholarPubMed
Liu, Z, Foote, RH and Yang, X (1995). Development of early bovine embryos in co-culture with KSOM and taurine, superoxide dismutase or insulin. Theriogenology 44, 741–50.CrossRefGoogle ScholarPubMed
Mani, S and Mainigi, M (2018). Embryo culture conditions and the epigenome. Seminars in Reprod Med 36, 211–20.CrossRefGoogle ScholarPubMed
Men, H, Stone, BJ and Bryda, EC (2020). Media optimization to promote rat embryonic development to the blastocyst stage in vitro . Theriogenology 151, 81–5.CrossRefGoogle Scholar
Pang, YW, Jiang, XL, Wang, YC, Wang, YY, Hao, HS, Zhao, SJ, Du, WH, Zhao, XM, Wang, L and Zhu, HB (2019). Melatonin protects against paraquat-induced damage during in vitro maturation of bovine oocytes. J Pineal Res 66, e12532.CrossRefGoogle ScholarPubMed
Pantaleon, M, Ryan, JP, Gil, M and Kaye, PL (2001). An unusual subcellular localization of GLUT1 and link with metabolism in oocytes and preimplantation mouse embryos. Biol Reprod 64, 1247–54.CrossRefGoogle ScholarPubMed
Qu, P, Wang, Y, Zhang, C and Liu, E (2020a). Insights into the roles of sperm in animal cloning. Stem Cell Res Ther 11, 65.CrossRefGoogle ScholarPubMed
Qu, PX, Luo, SW, Du, Y, Zhang, YR, Song, XJ, Yuan, XT, Lin, ZJ, Li, YH and Liu, EQ (2020b). Extracellular vesicles and melatonin benefit embryonic develop by regulating reactive oxygen species and 5-methylcytosine. J Pineal Res 68, e12635.CrossRefGoogle ScholarPubMed
Rossi, G, Di Nisio, V, Macchiarelli, G, Nottola, S A, Halvaei, I, De Santis, L and Cecconi, S (2019). Technologies for the production of fertilizable mammalian oocytes. Appl Sci 9, 17.CrossRefGoogle Scholar
Sanches, BV, Pontes, JHF, Basso, AC, Ferreira, CR, Perecin, F and Seneda, MM (2013). Comparison of synthetic oviductal fluid and G1/G2 medium under Low-1 oxygen atmosphere on embryo production and pregnancy rates in Nelore (Bos indicus) cattle. Reprod Domest Anim 48, e79.CrossRefGoogle ScholarPubMed
Sekirina, GG and Neganova, IE (1995). The microenvironment created by non-blocking embryos in aggregates may rescue blocking embryos via cell-embryo adherent contacts. Zygote 3, 313–24.CrossRefGoogle ScholarPubMed
Shohael, AM, Ali, MB, Yu, KW, Hahn, EJ, Islam, R and Paek, KY (2006). Effect of light on oxidative stress, secondary metabolites and induction of antioxidant enzymes in Eleutherococcus senticosus somatic embryos in bioreactor. Process Biochem 41, 1179–85.CrossRefGoogle Scholar
Simonstein, F, Mashiach-Eizenberg, M, Revel, A and Younis, JS (2014). Assisted reproduction policies in Israel: a retrospective analysis of in vitro fertilization-embryo transfer. Fertil Steril 102, 1301–6.CrossRefGoogle ScholarPubMed
Takahashi, M (2012). Oxidative stress and redox regulation on in vitro development of mammalian embryos. J Reprod Dev 58, 19.CrossRefGoogle ScholarPubMed
Thouas, GA, Jones, GM and Trounson, AO (2003). The ‘GO’ system – a novel method of microculture for in vitro development of mouse zygotes to the blastocyst stage. Reproduction 126, 161–9.CrossRefGoogle Scholar
Yang, B, Zhu, W, Zheng, Z, Chai, R, Ji, S, Ren, G, Liu, T, Liu, Z, Song, T, Li, F, Liu, S and Li, G (2017). Fluctuation of ROS regulates proliferation and mediates inhibition of migration by reducing the interaction between DLC1 and CAV-1 in breast cancer cells. In Vitro Cell Dev Biol Anim 53, 354–62.CrossRefGoogle ScholarPubMed
Yang, Y, Wang, LQ, Chen, C, Qi, HB, Baker, PN, Liu, XQ, Zhang, H and Han, TL (2020). Metabolic changes of maternal uterine fluid, uterus, and plasma during the peri-implantation period of early pregnancy in mice. Reprod Sci 27, 488502.CrossRefGoogle ScholarPubMed
Zhu, BK, Walker, SK and Maddocks, S (2004). Optimisation of in vitro culture conditions in B6CBF1 mouse embryos. Reprod Nutr Dev 44, 219–31.CrossRefGoogle ScholarPubMed