Bastias M C, McGee-Belser S T, Bryan S H, Vasquez J M
Department of Obstetrics and Gynecology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
Fertil Steril. 1993 Nov;60(5):876-80. doi: 10.1016/s0015-0282(16)56290-6.
To determine whether hypoxanthine in Ham's Nutrient Mixture F-10 (GIBCO, Grand Island, NY) culture medium affects murine embryo development or the outcome of patients undergoing IVF-ET.
For the two-cell embryo bioassay, embryos from each female were equally distributed and incubated in Ham's F-10 with or without hypoxanthine supplementation for up to 72 hours. To assess the effect of hypoxanthine in human IVF-ET, oocytes, sperm, and embryos were cultured in Ham's F-10 medium with or without hypoxanthine. Fertilization and embryo cleavage were assessed at 18 and 40 hours, respectively, after insemination.
University medical research laboratory.
PATIENTS, PARTICIPANTS: Nine couples undergoing IVF-ET.
Two-cell mouse embryos incubated for 24 hours without hypoxanthine developed 40% to morula, compared with 6.5% for the hypoxanthine group. At 72 hours, 99.5% of the embryos without hypoxanthine reached the expanded blastocyst stage with 65% of them exhibiting hatching, compared with 72% and 19.5%, respectively, for the group with hypoxanthine. Human oocytes cultured in Ham's F-10 without hypoxanthine showed higher fertilization rates than the group incubated in the presence of hypoxanthine (69% versus 53%). The proportion of cleaved embryos was not different between the two culture media; however, the rate of embryos cleaving without cytoplasmic fragments was significantly higher in the group without hypoxanthine (75% versus 35%).
Ham's F-10 medium containing hypoxanthine significantly reduced embryo development in the two-cell mouse embryo bioassay. Hypoxanthine in culture medium for IVF-ET may have a deleterious effect on human gametes, leading to decreased fertilization and increased incidence of cytoplasmic fragments in the conceptuses.
确定哈姆氏F-10营养混合物(GIBCO,纽约州大岛)培养基中的次黄嘌呤是否会影响小鼠胚胎发育或体外受精-胚胎移植(IVF-ET)患者的治疗结果。
在双细胞胚胎生物测定中,将每只雌性小鼠的胚胎平均分配,并在添加或不添加次黄嘌呤的哈姆氏F-10培养基中培养长达72小时。为评估次黄嘌呤在人类IVF-ET中的作用,将卵母细胞、精子和胚胎在添加或不添加次黄嘌呤的哈姆氏F-10培养基中培养。授精后分别在18小时和40小时评估受精和胚胎分裂情况。
大学医学研究实验室。
患者、参与者:9对接受IVF-ET的夫妇。
在无次黄嘌呤的情况下培养24小时的双细胞小鼠胚胎,40%发育为桑椹胚,而次黄嘌呤组为6.5%。72小时时,无次黄嘌呤组99.5%的胚胎发育到扩张囊胚阶段,其中65%孵化,而次黄嘌呤组分别为72%和19.5%。在无次黄嘌呤的哈姆氏F-10培养基中培养的人类卵母细胞,其受精率高于在有次黄嘌呤培养基中培养的组(69%对53%)。两种培养基中分裂胚胎的比例无差异;然而,无次黄嘌呤组无细胞质碎片的胚胎分裂率显著更高(75%对35%)。
在双细胞小鼠胚胎生物测定中,含次黄嘌呤的哈姆氏F-10培养基显著降低了胚胎发育。IVF-ET培养基中的次黄嘌呤可能对人类配子有有害影响,导致受精率降低和胚胎中细胞质碎片发生率增加。