Gonadotropin releasing hormone antagonists and cryopreservation outcome: A review

被引:3
作者
Nikolettos N. [1 ]
Asimakopoulos B. [1 ]
Simopoulou M. [1 ]
Al-Hasani S. [2 ]
Diedrich K. [2 ]
机构
[1] Lab. of Reproductive Physiology-IVF, Faculty of Medicine, Democritus University of Thrace, 68100 Dragana, Alexandroupolis
[2] Department of Obstetrics, Medical University Lübeck, 23538 Lübeck
关键词
Cryopreservation; GnRH-agonist; GnRH-antagonist; In-vitro fertilisation;
D O I
10.1007/s00404-003-0597-3
中图分类号
学科分类号
摘要
Review: The outcome of freeze-thaw cycles with pronuclear stage oocytes or embryos, derived from collecting cycles stimulated with gonadotropin-releasing hormone (GnRH)-antagonists' protocols, was reviewed. Conclusion: The viability of cryopreserved pronuclear stage oocytes and embryos, the quality of transferred embryos and the pregnancy rates of the freeze-thaw cycles seem to be satisfactory regardless of the type and dose of GnRH-antagonist.
引用
收藏
页码:69 / 73
页数:4
相关论文
共 52 条
[41]  
Olivennes F., Fanchin R., Bouchard P., De Ziegler D., Taieb J., Selva J., Frydman R., The single or dual administration of the gonadotrophin-releasing hormone antagonist Cetrorelix in an in vitro fertilization-embryo transfer programme, Fertil Steril, 62, pp. 468-476, (1994)
[42]  
Olivennes F., Fanchin R., Bouchard P., Taieb J., Selva J., Frydman R., Scheduled administration of a gonadotrophin-releasing hormone antagonist (Cetrorelix) on day 8 of in vitro fertilization cycles: A pilot study, Hum Reprod, 10, pp. 1382-1386, (1995)
[43]  
Olivennes F., Belaisch-Allart J., Emperaire J.C., Dechaud H., Alvarez S., Moreau L., Nicollet B., Zorn J.R., Bouchard P., Frydman R., Prospective, randomized, controlled study of in-vitro fertilization-embryo transfer with a single dose of a luteinizing hormone-releasing hormone (LHRH) antagonist (Cetrorelix) or a depot formula of an LH-RH agonist (Triptoreline), Fertil Steril, 73, pp. 314-320, (2000)
[44]  
Ortmann O., Diedrich K., Pituitary and extrapituitary actions of gonadotrophin-releasing hormone and its analogues, Hum Reprod, 14, SUPPL. 1, pp. 194-206, (1999)
[45]  
Ortmann O., Weiss J.M., Diedrich K., Embryo implantation and GnRH antagonists. Ovarian actions of GnRH antagonists, Hum Reprod, 16, pp. 608-611, (2001)
[46]  
Pinski J., Reile H., Halmos G., Groot K., Schally A.V., Inhibitory effects of analogs of luteinizing hormone-releasing hormone on the growth of the androgen-independent dunning R-3327-AT-1 rat prostate cancer, Int J Cancer, 59, pp. 51-55, (1994)
[47]  
Reissmann T., Felberbaum R., Diedrich K., Engel J., Comaru-Schally A.M., Schally A.V., Development and applications of luteinizing hormone-releasing hormone antagonists in the treatment of infertility: An overview, Hum Reprod, 10, pp. 1974-1981, (1995)
[48]  
Sadler S.E., Type III phosphodiesterase plays a necessary role in the growth-promoting actions of insulin, IGF-I and Ha p21ras in Xenopus laevis oocytes, Mol Endocrinol, 5, pp. 1939-1946, (1991)
[49]  
Seelig A.S., Al-Hasani S., Katalinic A., Schopper B., Sturm R., Diedrich K., Ludwig M., Comparison of cryopreservation outcome with gonadotropin-releasing hormone agonists or antagonists in the collecting cycle, Fertil Steril, 77, pp. 472-475, (2002)
[50]  
Shirahige Y., Cook C.B., Pinski J., Et al., Treatment with luteinizing hormone-releasing hormone antagonist SB-75 decreases levels of epidermal growth factor receptor and its mRNA in OV-1063 human epithelial ovarian cancer xenografts in nude mice, Int J Oncol, 5, pp. 3052-3060, (1994)