참고문헌
- Choi BH, Park BY, Kong R, Son MJ, Park CS, Shin NH, Cheon HY, Yang YR, Lee JW, Jin JI, Kong IK. 2019. Effect of serum and serum free media on the developmental competence of OPU derived bovine IVP embryo. J. Anim. Reprod. Biotechnol. 34:305-310. https://doi.org/10.12750/JARB.34.4.305
- Choudhury SM, Bhuiyan MMU, Rahman MM, Rahman MM, Sharif MN, Bhattacharjee J, Bari FY, Juyena NS. 2017. Comparison between two cryo-devices for vitrification of immature oocytes of indigenous zebu cows in Bangladesh. J. Emb. Trans. 32:311-317. https://doi.org/10.12750/JET.2017.32.4.311
- Dodson MG, Minhas BS, Curtis SK, Palmer TV, Robertson JL. 1989. Spontaneous zona reaction in the mouse as a limiting factor for the time in which an oocyte may be fertilized. J. In Vitro Fert. Embryo Transf. 6:101-106. https://doi.org/10.1007/BF01130735
- Ducibella T, Duffy P, Reindollar R, Su B. 1990. Changes in the distribution of mouse oocyte cortical granules and ability to undergo the cortical reaction during gonadotropin-stimulated meiotic maturation and aging in vivo. Biol. Reprod. 43:870-876. https://doi.org/10.1095/biolreprod43.5.870
- Fang X, Qamar AY, Yoon KY, Cho J. 2018. Improved preimplantation development of porcine cloned embryos by flavone supplement as antioxidant. J. Emb. Trans. 33:255-264. https://doi.org/10.12750/JET.2018.33.4.255
- Guerin P, El Mouatassim S, Menezo Y. 2001. Oxidative stress and protection against reactive oxygen species in the preimplantation embryo and its surroundings. Hum. Reprod. Update 7:175-189. https://doi.org/10.1093/humupd/7.2.175
- Hassan BMS, Fang X, Roy PK, Shin ST, Cho JK. 2017. Effect of alpha lipoic acid as an antioxidant supplement during in Vitro maturation medium on bovine embryonic development. J. Emb. Trans. 32:123-130. https://doi.org/10.12750/JET.2017.32.3.123
- Haun F, Nakamura T, Shiu AD, Cho DH, Tsunemi T, Holland EA, La Spada AR, Lipton SA. 2013. S-nitrosylation of dynamin-related protein 1 mediates mutant huntingtin-induced mitochondrial fragmentation and neuronal injury in Huntington's disease. Antioxid. Redox Signal. 19:1173-1184. https://doi.org/10.1089/ars.2012.4928
- Hess DT and Stamler JS. 2012. Regulation by S-nitrosylation of protein post-translational modification. J. Biol. Chem. 287:4411-4418. https://doi.org/10.1074/jbc.R111.285742
- Hwang IS, Kwon DJ, Kwak TU, Lee JY, Hyung NW, Yang H, Oh KB, Ock SA, Park EW, Im GS, Hwang S. 2016. Effect of a short-term in vitro exposure time on the production of in vitro produced piglets. J. Emb. Trans. 31:117-121. https://doi.org/10.12750/JET.2016.31.2.117
- Iyer AK, Rojanasakul Y, Azad N. 2014. Nitrosothiol signaling and protein nitrosation in cell death. Nitric Oxide. 42:9-18. https://doi.org/10.1016/j.niox.2014.07.002
- Jaffrey SR, Erdjument-Bromage H, Ferris CD, Tempst P, Snyder SH. 2001. Protein S-nitrosylation: a physiological signal for neuronal nitric oxide. Nat. Cell Biol. 3:193-197. https://doi.org/10.1038/35055104
- Jeon YE, Hwangbo Y, Cheong HT, Park CK. 2019. Effects of hyaluronidase during in vitro maturation on maturation and developmental competence in porcine oocytes. J. Anim. Reprod. Biotechnol. 34:86-92. https://doi.org/10.12750/JARB.34.2.86
- Kikuchi K, Naito K, Noguchi J, Kaneko H, Tojo H. 2002. Maturation/M-phase promoting factor regulates aging of porcine oocytes matured in vitro. Cloning Stem Cells 4:211-222. https://doi.org/10.1089/15362300260339494
- Kim SY, Lin T, Lee JB, Lee JE, Shin HY, Jin DI. 2019. Expression pattern of early transcription factors in porcine oocytes and embryos. J. Anim. Reprod. Biotechnol. 34:123-129. https://doi.org/10.12750/JARB.34.2.123
- Lee HJ, Park BJ, Jeon RH, Jang SJ, Son YB, Lee SL, Rho GJ, Kim SJ, Lee WJ. 2019a. Alteration of apoptosis during differentiation in human dental pulp-derived mesenchymal stem cell. J. Anim. Reprod. Biotechnol. 34:2-9. https://doi.org/10.12750/jarb.34.1.2
- Lee SY, Park CJ, Nam YK. 2019b. Assessment of suitable reference genes for RT-qPCR normalization with developmental samples in pacific abalone Haliotis discus hannai. J. Anim. Reprod. Biotechnol. 34:280-291. https://doi.org/10.12750/JARB.34.4.280
- Lee TH, Lee MS, Huang CC, Tsao HM, Lin PM, Ho HN, Shew JY, Yang YS. 2013. Nitric oxide modulates mitochondrial activity and apoptosis through protein S-nitrosylation for preimplantation embryo development. J. Assist. Reprod. Genet. 30:1063-1072. https://doi.org/10.1007/s10815-013-0045-7
- Li Q and Cui LB. 2016. Combined inhibitory effects of low temperature and N-acetyl-l-cysteine on the postovulatory aging of mouse oocytes. Zygote 24:195-205. https://doi.org/10.1017/S0967199415000039
- Liang QX, Lin YH, Zhang CH, Sun HM, Zhou L, Schatten H, Sun QY, Qian WP. 2018. Resveratrol increases resistance of mouse oocytes to postovulatory aging in vivo. Aging (Albany NY) 10:1586-1596. https://doi.org/10.18632/aging.101494
- Liu J, Liu M, Ye X, Liu K, Huang J, Wang L, Ji G, Liu N, Tang X, Baltz JM, Keefe DL, Liu L. 2012. Delay in oocyte aging in mice by the antioxidant N-acetyl-L-cysteine (NAC). Hum. Reprod. 27:1411-1420. https://doi.org/10.1093/humrep/des019
- Lord T and Aitken RJ. 2013. Oxidative stress and ageing of the post-ovulatory oocyte. Reproduction 146:R217-R227. https://doi.org/10.1530/REP-13-0111
- Lord T, Nixon B, Jones KT, Aitken RJ. 2013. Melatonin prevents postovulatory oocyte aging in the mouse and extends the window for optimal fertilization in vitro. Biol. Reprod. 88:67. https://doi.org/10.1095/biolreprod.112.106450
- Nakamura T and Lipton SA. 2011. Redox modulation by S-nitrosylation contributes to protein misfolding, mitochondrial dynamics, and neuronal synaptic damage in neurodegenerative diseases. Cell Death Differ. 18:1478-1486. https://doi.org/10.1038/cdd.2011.65
- Nasr-Esfahani MH, Aitken JR, Johnson MH. 1990. Hydrogen peroxide levels in mouse oocytes and early cleavage stage embryos developed in vitro or in vivo. Development 109:501-507. https://doi.org/10.1242/dev.109.2.501
- Park SH, Jeon Y, Yu IJ. 2017. Effects of antioxidants supplement in porcine sperm freezing on in vitro fertilization and the glutathione and reactive oxygen species level of presumptive zygotes. J. Emb. Trans. 32:337-342. https://doi.org/10.12750/JET.2017.32.4.337
- Pendergrass W, Wolf N, Poot M. 2004. Efficacy of MitoTracker GreenTM and CMXRosamine to measure changes in mitochondrial membrane potentials in living cells and tissues. Cytometry A 61:162-169. https://doi.org/10.1002/cyto.a.20033
- Premkumar KV and Chaube SK. 2015. Nitric oxide signals postovulatory aging-induced abortive spontaneous egg activation in rats. Redox Rep. 20:184-192. https://doi.org/10.1179/1351000215Y.0000000003
- Raju K, Doulias PT, Evans P, Krizman EN, Jackson JG, Horyn O, Daikhin Y, Nissim I, Yudkoff M, Nissim I, Sharp KA, Robinson MB, Ischiropoulos H. 2015. Regulation of brain glutamate metabolism by nitric oxide and S-nitrosylation. Sci. Signal. 8:ra68. https://doi.org/10.1126/scisignal.aaa4312
- Rizza S, Cardaci S, Montagna C, Di Giacomo G, De Zio D, Bordi M, Maiani E, Campello S, Borreca A, Puca AA, Stamler JS, Cecconi F, Filomeni G. 2018. S-nitrosylation drives cell senescence and aging in mammals by controlling mitochondrial dynamics and mitophagy. Proc. Natl. Acad. Sci. U. S. A. 115:E3388-E3397. https://doi.org/10.1073/pnas.1722452115
- Seth D, Hess DT, Hausladen A, Wang L, Wang YJ, Stamler JS. 2018. A multiplex enzymatic machinery for cellular protein S-nitrosylation. Mol. Cell 69:451-464.e456. https://doi.org/10.1016/j.molcel.2017.12.025
- Sun J, Morgan M, Shen RF, Steenbergen C, Murphy E. 2007. Preconditioning results in S-nitrosylation of proteins involved in regulation of mitochondrial energetics and calcium transport. Circ. Res. 101:1155-1163. https://doi.org/10.1161/CIRCRESAHA.107.155879
- Tatone C, Di Emidio G, Barbaro R, Vento M, Ciriminna R, Artini PG. 2011. Effects of reproductive aging and postovulatory aging on the maintenance of biological competence after oocyte vitrification: insights from the mouse model. Theriogenology 76:864-873. https://doi.org/10.1016/j.theriogenology.2011.04.017
- Wakayama S, Thuan NV, Kishigami S, Ohta H, Mizutani E, Hikichi T, Miyake M, Wakayama T. 2004. Production of offspring from one-day-old oocytes stored at room temperature. J. Reprod. Dev. 50:627-637. https://doi.org/10.1262/jrd.50.627
- Wang T, Gao YY, Chen L, Nie ZW, Cheng W, Liu X, Schatten H, Zhang X, Miao YL. 2017. Melatonin prevents postovulatory oocyte aging and promotes subsequent embryonic development in the pig. Aging (Albany NY) 9:1552-1564. https://doi.org/10.18632/aging.101252
- Wang Y, Li L, Fan LH, Jing Y, Li J, Ouyang YC, Wang ZB, Hou Y, Sun QY. 2019. N-acetyl-L-cysteine (NAC) delays post-ovulatory oocyte aging in mouse. Aging (Albany NY) 11:2020-2030. https://doi.org/10.18632/aging.101898
- Xu Z, Abbott A, Kopf GS, Schultz RM, Ducibella T. 1997. Spontaneous activation of ovulated mouse eggs: time-dependent effects on M-phase exit, cortical granule exocytosis, maternal messenger ribonucleic acid recruitment, and inositol 1,4,5-trisphosphate sensitivity. Biol. Reprod. 57:743-750. https://doi.org/10.1095/biolreprod57.4.743
- Zhang M, ShiYang X, Zhang Y, Miao Y, Chen Y, Cui Z, Xiong B. 2019. Coenzyme Q10 ameliorates the quality of postovulatory aged oocytes by suppressing DNA damage and apoptosis. Free Radic. Biol. Med. 143:84-94. https://doi.org/10.1016/j.freeradbiomed.2019.08.002
- Zhang N, Wakai T, Fissore RA. 2011. Caffeine alleviates the deterioration of Ca(2+) release mechanisms and fragmentation of in vitro-aged mouse eggs. Mol. Reprod. Dev. 78:684-701. https://doi.org/10.1002/mrd.21366