참고문헌
- Apa, R., Lanzone, A., Mastrandrea, M., Miceli, F., Macchione, E., Fulghesu, A.M., Caruso, A., Canipari, R., 1997. Effect of pituitary adenylate cyclase-activating peptide on meiotic maturation in follicle-enclosed, cumulus-enclosed, and denuded rat oocytes. Biology of reproduction 57, 1074-1079. https://doi.org/10.1095/biolreprod57.5.1074
- Arimura, A., 1998. Perspectives on pituitary adenylate cyclase activating polypeptide (PACAP) in the neuroendocrine, endocrine, and nervous systems. The Japanese journal of physiology 48, 301-331. https://doi.org/10.2170/jjphysiol.48.301
- Arimura, A., 2007. PACAP: the road to discovery, Elsevier.
- Cecconi, S., Rossi, G., Barberi, M., Scaldaferri, L., Canipari, R., 2004. Effect of pituitary adenylate cyclase-activating polypeptide and vasoactive intestinal polypeptide on mouse preantral follicle development in vitro. Endocrinology 145, 2071-2079. https://doi.org/10.1210/en.2003-1004
- Chen, L., Wert, S.E., Hendrix, E.M., Russell, P.T., Cannon, M., Larsen, W.J., 1990. Hyaluronic acid synthesis and gap junction endocytosis are necessary for normal expansion of the cumulus mass. Molecular reproduction and development 26, 236-247. https://doi.org/10.1002/mrd.1080260307
- Cheng, T., Huang, C., Huang, L., Chen, C., Lee, M., Liu, J., 2004. Evaluation of mouse blastocyst implantation rate by morphology grading. Chinese Journal of Physiology 47, 43.
- Combelles, C.M., Gupta, S., Agarwal, A., 2009. Could oxidative stress influence the in-vitro maturation of oocytes? Reproductive biomedicine online 18, 864-880. https://doi.org/10.1016/S1472-6483(10)60038-7
- Conti, M., Andersen, C.B., Richard, F., Mehats, C., Chun, S.-Y., Horner, K., Jin, C., Tsafriri, A., 2002. Role of cyclic nucleotide signaling in oocyte maturation. Molecular and cellular endocrinology 187, 153-159. https://doi.org/10.1016/S0303-7207(01)00686-4
- Coy, P., Romar, R., Ruiz, S., Canovas, S., Gadea, J., Vazquez, F.G., Matas, C., 2005. Birth of piglets after transferring of in vitro-produced embryos pre-matured with R-roscovitine. Reproduction 129, 747-755. https://doi.org/10.1530/rep.1.00691
- Dieci, C., Lodde, V., Franciosi, F., Lagutina, I., Tessaro, I., Modina, S.C., Albertini, D.F., Lazzari, G., Galli, C., Luciano, A.M., 2013. The effect of cilostamide on gap junction communication dynamics, chromatin remodeling, and competence acquisition in pig oocytes following parthenogenetic activation and nuclear transfer. Biology of reproduction 89.
- Edwards, R., 1965. Maturation in vitro of mouse, sheep, cow, pig, rhesus monkey and human ovarian oocytes. Nature 208, 349-351. https://doi.org/10.1038/208349a0
- Eppig, J.J., Freter, R.R., Ward-Bailey, P.F., Schultz, R.M., 1983. Inhibition of oocyte maturation in the mouse: participation of cAMP, steroid hormones, and a putative maturation-inhibitory factor. Developmental biology 100, 39-49. https://doi.org/10.1016/0012-1606(83)90198-7
- Findlay, J.K., 2012. Molecular biology of the female reproductive system. Elsevier.
- Gutnisky, C., Dalvit, G.C., Pintos, L.N., Thompson, J.G., Beconi, M.T., Cetica, P.D., 2007. Influence of hyaluronic acid synthesis and cumulus mucification on bovine oocyte in vitro maturation, fertilisation and embryo development. Reproduction, Fertility and Development 19, 488-497. https://doi.org/10.1071/RD06134
- Isaac, E.R., Sherwood, N.M., 2008. Pituitary adenylate cyclase-activating polypeptide (PACAP) is important for embryo implantation in mice. Molecular and cellular endocrinology 280, 13-19. https://doi.org/10.1016/j.mce.2007.09.003
- Ko, C., Park-Sarge, O.-K., 2000. Progesterone receptor activation mediates LH-induced type-I pituitary adenylate cyclase activating polypeptide receptor (PAC1) gene expression in rat granulosa cells. Biochemical and biophysical research communications 277, 270-279. https://doi.org/10.1006/bbrc.2000.3667
- Koppan, M., Varnagy, A., Reglodi, D., Brubel, R., Nemeth, J., Tamas, A., Mark, L., Bodis, J., 2012. Correlation between oocyte number and follicular fluid concentration of pituitary adenylate cyclase-activating polypeptide (PACAP) in women after superovulation treatment. Journal of Molecular Neuroscience 48, 617-622. https://doi.org/10.1007/s12031-012-9743-3
- Kwak, S.-S., Jang, S.-H., Jeong, S.-H., Jeon, Y., Biswas, D., Hyun, S.-H., 2012. The Effects of 3-Isobutyl-1-methylxanthine (IBMX) on Nuclear and Cytoplasmic Maturation of Porcine Oocytes In Vitro. Journal of Embryo Transfer 27, 163-169.
- Latini, S., Chiarpotto, M., Muciaccia, B., Vaccari, S., Barberi, M., Guglielmo, M.C., Stefanini, M., Cecconi, S., Canipari, R., 2010. Inhibitory effect of pituitary adenylate cyclase activating polypeptide on the initial stages of rat follicle development. Molecular and cellular endocrinology 320, 34-44. https://doi.org/10.1016/j.mce.2010.01.040
- Li, H., Sutton-McDowall, M., Wang, X., Sugimura, S., Thompson, J., Gilchrist, R., 2016. Extending prematuration with cAMP modulators enhances the cumulus contribution to oocyte antioxidant defence and oocyte quality via gap junctions. Human Reproduction 31, 810-821. https://doi.org/10.1093/humrep/dew020
- Marchal, R., Vigneron, C., Perreau, C., Bali-Papp, A., Mermillod, P., 2002. Effect of follicular size on meiotic and developmental competence of porcine oocytes. Theriogenology 57, 1523-1532. https://doi.org/10.1016/S0093-691X(02)00655-6
- McGaughey, R.W., Montgomery, D.H., Richter, J.D., 1979. Germinal vesicle configurations and patterns of polypeptide synthesis of porcine oocytes from antral follicles of different size, as related to their competency for spontaneous maturation. Journal of Experimental Zoology Part A: Ecological Genetics and Physiology 209, 239-253.
- Morelli, M.B., Barberi, M., Gambardella, A., Borini, A., Cecconi, S., Coticchio, G., Canipari, R., 2008. Characterization, expression, and functional activity of pituitary adenylate cyclase-activating polypeptide and its receptors in human granulosa-luteal cells. The Journal of Clinical Endocrinology & Metabolism 93, 4924-4932. https://doi.org/10.1210/jc.2007-2621
- Park, B., Lee, H., Lee, Y., Elahi, F., Lee, J., Lee, S.T., Park, C.-K., Hyun, S.-H., Lee, E., 2016. Cilostamide and forskolin treatment during pre-IVM improves preimplantation development of cloned embryos by influencing meiotic progression and gap junction communication in pigs. Theriogenology 86, 757-765. https://doi.org/10.1016/j.theriogenology.2016.02.029
- Park, H.-J., Lee, J., Wang, L., Park, J.-H., Kwon, H.-B., Arimura, A., Chun, S.-Y., 2000. Stage-specific expression of pituitary adenylate cyclase-activating polypeptide type I receptor messenger ribonucleic acid during ovarian follicle development in the rat. Endocrinology 141, 702-709. https://doi.org/10.1210/endo.141.2.7322
- Richani, D., Wang, X., Zeng, H., Smitz, J., Thompson, J., Gilchrist, R., 2014. Pre maturation with cAMP modulators in conjunction with EGF like peptides during in vitro maturation enhances mouse oocyte developmental competence. Molecular reproduction and development 81, 422-435. https://doi.org/10.1002/mrd.22307
- Sherwood, N.M., Krueckl, S.L., McRory, J.E., 2000. The origin and function of the pituitary adenylate cyclase-activating polypeptide (PACAP)/glucagon superfamily. Endocrine Reviews 21, 619-670.
- Shimada, M., Hernandez-Gonzalez, I., Gonzalez-Robayna, I., Richards, J.S., 2006. Paracrine and autocrine regulation of epidermal growth factor-like factors in cumulus oocyte complexes and granulosa cells: key roles for prostaglandin synthase 2 and progesterone receptor. Molecular Endocrinology 20, 1352-1365. https://doi.org/10.1210/me.2005-0504
- Shioda, S., Takenoya, F., Wada, N., Hirabayashi, T., Seki, T., Nakamachi, T., 2016. Pleiotropic and retinoprotective functions of PACAP. Anatomical science international 91, 313-324. https://doi.org/10.1007/s12565-016-0351-0
- Vaccari, S., Latini, S., Barberi, M., Teti, A., Stefanini, M., Canipari, R., 2006. Characterization and expression of different pituitary adenylate cyclase-activating polypeptide/vasoactive intestinal polypeptide receptors in rat ovarian follicles. Journal of endocrinology 191, 287-299. https://doi.org/10.1677/joe.1.06470
- Wu, D., Cheung, Q.C.-K., Wen, L., Li, J., 2006. A growth-maturation system that enhances the meiotic and developmental competence of porcine oocytes isolated from small follicles. Biology of reproduction 75, 547-554. https://doi.org/10.1095/biolreprod.106.051300
- You, J., Kim, J., Lim, J., Lee, E., 2010. Anthocyanin stimulates in vitro development of cloned pig embryos by increasing the intracellular glutathione level and inhibiting reactive oxygen species. Theriogenology 74, 777-785. https://doi.org/10.1016/j.theriogenology.2010.04.002
- Zeng, H.-T., Richani, D., Sutton-McDowall, M.L., Ren, Z., Smitz, J.E., Stokes, Y., Gilchrist, R.B., Thompson, J.G., 2014. Prematuration with cyclic adenosine monophosphate modulators alters cumulus cell and oocyte metabolism and enhances developmental competence of in vitro-matured mouse oocytes. Biology of reproduction 91.