참고문헌
- Agarwal A, Aponte-Mellado A, Premkumar B J, Shaman A and Gupta S. 2012. The effects of oxidative stress on female reproduction: a review, Reprod Biol Endocrinol, 10:49. https://doi.org/10.1186/1477-7827-10-49
- Appeltant R, Somfai T, Santos E C S, Dang-Nguyen T Q, Nagai T and Kikuchi K. 2017. Effects of vitrification of cumulus-enclosed porcine oocytes at the germinal vesicle stage on cumulus expansion, nuclear progression and cytoplasmic maturation, Reprod Fertil Deve, 29:2419-2429. https://doi.org/10.1071/RD16386
- Babayev E, Wang T, Szigeti-Buck K, Lowther K, Taylor H S, Horvath T and Seli E. 2016. Reproductive aging is associated with changes in oocyte mitochondrial dynamics, function, and mtDNA quantity, Maturitas, 93:121-130. https://doi.org/10.1016/j.maturitas.2016.06.015
- Beyer E C and Berthoud V M. 2018. Gap junction gene and protein families: Connexins, innexins, and pannexins, Biochim Biophys Acta Biomembr, 1860:5-8. https://doi.org/10.1016/j.bbamem.2017.05.016
- Chen Z, Zuo X, Li H, Hong R, Ding B, Liu C, Gao D, Shang H, Cao Z, Huang W, Zhang X and Zhang Y. 2017. Effects of melatonin on maturation, histone acetylation, autophagy of porcine oocytes and subsequent embryonic development, Anim Sci J, 88:1298-1310. https://doi.org/10.1111/asj.12779
- Covarrubias L, Hernandez-Garcia D, Schnabel D, Salas-Vidal E and Castro-Obregon S. 2008. Function of reactive oxygen species during animal development: passive or active?, Dev Biol, 320:1-11. https://doi.org/10.1016/j.ydbio.2008.04.041
- Dalton C M, Szabadkai G and Carroll J. 2014. Measurement of ATP in single oocytes: impact of maturation and cumulus cells on levels and consumption, J Cell Physiol, 229:353-361. https://doi.org/10.1002/jcp.24457
- Fogg V C, Lanning N J and Mackeigan J P. 2011. Mitochondria in cancer: at the crossroads of life and death, Chin J Cancer, 30:526-539. https://doi.org/10.5732/cjc.011.10018
- Huang Z, Pang Y, Hao H, Du W, Zhao X and Zhu H. 2018. Effects of epigallocatechin-3-gallate on bovine oocytes matured in vitro, Asian-Australas J Anim Sci, 31:1420-1430. https://doi.org/10.5713/ajas.17.0880
- Ikeda S and Yamada M. 2014. Midkine and cytoplasmic maturation of mammalian oocytes in the context of ovarian follicle physiology, Br J Pharmacol, 171:827-836. https://doi.org/10.1111/bph.12311
- Kim S H, Kim S H, Lee J H, Lee B H, Yoon H J, Shin D H, Park S S, Jang S B, Park J S and Jee Y K. 2015. Superoxide Dismutase Gene (SOD1, SOD2, and SOD3) Polymorphisms and Antituberculosis Drug-induced Hepatitis, Allergy Asthma Immunol Res, 7:88-91. https://doi.org/10.4168/aair.2015.7.1.88
- Lu X, Wu Z, Wang M and Cheng W. 2018. Effects of vitamin C on the outcome of in vitro fertilization-embryo transfer in endometriosis: A randomized controlled study, J Int Med Res, 46:4624-4633. https://doi.org/10.1177/0300060518786918
- Matsunaga R and Funahashi H. 2017. Supplementation with cumulus cell masses improves the in vitro meiotic competence of porcine cumulus-oocytes complexes derived from small follicles, Reprod Domest Anim, 52:672-679. https://doi.org/10.1111/rda.12967
- Mlynarcikova A, Nagyova E, Fickova M and Scsukova S. 2009. Effects of selected endocrine disruptors on meiotic maturation, cumulus expansion, synthesis of hyaluronan and progesterone by porcine oocyte-cumulus complexes, Toxicol In Vitro, 23:371-377. https://doi.org/10.1016/j.tiv.2008.12.017
- Ni R, Cao T, Xiong S, Ma J, Fan G C, Lacefield J C, Lu Y, Le Tissier S and Peng T. 2016. Therapeutic inhibition of mitochondrial reactive oxygen species with mito-TEMPO reduces diabetic cardiomyopathy, Free Radic Biol Med, 90:12-23. https://doi.org/10.1016/j.freeradbiomed.2015.11.013
- Okon I S, Coughlan K A, Zhang M, Wang Q and Zou M H. 2015. Gefitinib-mediated reactive oxygen specie (ROS) instigates mitochondrial dysfunction and drug resistance in lung cancer cells, J Biol Chem, 290:9101-9110. https://doi.org/10.1074/jbc.M114.631580
- Ozawa M, Nagai T, Somfai T, Nakai M, Maedomari N, Fahrudin M, Karja N W, Kaneko H, Noguchi J, Ohnuma K, Yoshimi N, Miyazaki H and Kikuchi K. 2008. Comparison between effects of 3-isobutyl-1-methylxanthine and FSH on gap junctional communication, LH-receptor expression, and meiotic maturation of cumulus-oocyte complexes in pigs, Mol Reprod Dev, 75:857-866. https://doi.org/10.1002/mrd.20820
- Park H J, Park S Y, Kim J W, Yang S G, Kim M J, Jegal H G, Kim I S, Choo Y K and Koo D B. 2018. Melatonin Improves Oocyte Maturation and Mitochondrial Functions by Reducing Bisphenol A-Derived Superoxide in Porcine Oocytes In Vitro, Int J Mol Sci, 19.
- Prochazka R, Petlach M, Nagyova E and Nemcova L. 2011. Effect of epidermal growth factor-like peptides on pig cumulus cell expansion, oocyte maturation, and acquisition of developmental competence in vitro: comparison with gonadotropins, Reproduction, 141:425-435. https://doi.org/10.1530/REP-10-0418
- Redza-Dutordoir M and Averill-Bates D A. 2016. Activation of apoptosis signalling pathways by reactive oxygen species, Biochim Biophys Acta, 1863:2977-2992. https://doi.org/10.1016/j.bbamcr.2016.09.012
- Schieber M and Chandel N S. 2014. ROS function in redox signaling and oxidative stress, Curr Biol, 24:R453-462. https://doi.org/10.1016/j.cub.2014.03.034
- Shaeib F, Khan S N, Ali I, Thakur M, Saed M G, Dai J, Awonuga A O, Banerjee J and Abu-Soud H M. 2016. The Defensive Role of Cumulus Cells Against Reactive Oxygen Species Insult in Metaphase II Mouse Oocytes, Reprod Sci, 23:498-507. https://doi.org/10.1177/1933719115607993
- Slominski A T, Zmijewski M A, Semak I, Kim T K, Janjetovic Z, Slominski R M and Zmijewski J W. 2017. Melatonin, mitochondria, and the skin, Cell Mol Life Sci, 74:3913-3925. https://doi.org/10.1007/s00018-017-2617-7
- Sturmey R G and Leese H J. 2003. Energy metabolism in pig oocytes and early embryos, Reproduction, 126:197-204. https://doi.org/10.1530/rep.0.1260197
- Vaka V R, McMaster K M, Cunningham M W, Jr., Ibrahim T, Hazlewood R, Usry N, Cornelius D C, Amaral L M and LaMarca B. 2018. Role of Mitochondrial Dysfunction and Reactive Oxygen Species in Mediating Hypertension in the Reduced Uterine Perfusion Pressure Rat Model of Preeclampsia, Hypertension, 72:703-711. https://doi.org/10.1161/HYPERTENSIONAHA.118.11290
- Wang H W, Zhao W P, Liu J, Tan P P, Zhang C and Zhou B H. 2017. Fluoride-induced oxidative stress and apoptosis are involved in the reducing of oocytes development potential in mice, Chemosphere, 186:911-918. https://doi.org/10.1016/j.chemosphere.2017.08.068
- Wang T, Gao Y Y, Chen L, Nie Z W, Cheng W, Liu X, Schatten H, Zhang X and Miao Y L. 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 W, Zhang Y, Lu W and Liu K. 2015. Mitochondrial reactive oxygen species regulate adipocyte differentiation of mesenchymal stem cells in hematopoietic stress induced by arabinosylcytosine, PLoS One, 10:e0120629. https://doi.org/10.1371/journal.pone.0120629
- Yang M, Tao J, Chai M, Wu H, Wang J, Li G, He C, Xie L, Ji P, Dai Y, Yang L and Liu G. 2017. Melatonin Improves the Quality of Inferior Bovine Oocytes and Promoted Their Subsequent IVF Embryo Development: Mechanisms and Results, Molecules, 22.
- Yang S G, Park H J, Kim J W, Jung J M, Kim M J, Jegal H G, Kim I S, Kang M J, Wee G, Yang H Y, Lee Y H, Seo J H, Kim S U and Koo D B. 2018. Mito-TEMPO improves development competence by reducing superoxide in preimplantation porcine embryos, Sci Rep, 8:10130. https://doi.org/10.1038/s41598-018-28497-5
- Zhang J, Wang Q, Xu C, Lu Y, Hu H, Qin B, Wang Y, He D, Li C, Yu X, Wang S and Liu J. 2017. MitoTEMPO Prevents Oxalate Induced Injury in NRK-52E Cells via Inhibiting Mitochondrial Dysfunction and Modulating Oxidative Stress, Oxid Med Cell Longev, 2017:7528090.
- Zhou C J, Wu S N, Shen J P, Wang D H, Kong X W, Lu A, Li Y J, Zhou H X, Zhao Y F and Liang C G. 2016. The beneficial effects of cumulus cells and oocyte-cumulus cell gap junctions depends on oocyte maturation and fertilization methods in mice, PeerJ, 4:e1761. https://doi.org/10.7717/peerj.1761
- Zorov D B, Juhaszova M and Sollott S J. 2014. Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release, Physiol Rev, 94:909-950. https://doi.org/10.1152/physrev.00026.2013