Ain R, Seshagiri P B
Center for Reproductive Biology and Molecular Endocrinology, Indian Institute of Science, Bangalore, India.
Mol Reprod Dev. 1997 Aug;47(4):440-7. doi: 10.1002/(SICI)1098-2795(199708)47:4<440::AID-MRD11>3.0.CO;2-#.
The in vitro development of hamster preimplantation embryos is supported by non-glucose energy substrates. To investigate the importance of embryonic metabolism, influence of succinate and malate on the development of hamster 8-cell embryos to blastocysts was examined using a chemically defined protein-free modified hamster embryo culture medium-2 (HECM-2m). There was a dose-dependent influence of succinate on blastocyst development; 0.5 mM succinate was optimal (85.1% +/- 3.9 vs. 54.5% +/- 3.5). In succinate-supplemented HECM-2m, blastocyst development was reduced by omission of lactate (68.5% +/- 7.2), but not pyruvate (85.8% +/- 6.2) or glutamine (84.1% +/- 2.1). Succinate along with either glutamine or lactate or pyruvate poorly supported blastocyst development (28%-58%). Malate also stimulated blastocyst development; 0.01 mM malate was optimal (86.3% +/- 2.8). Supplementation of both succinate and malate to HECM-2m supported maximal (100%) blastocyst development, which was inhibited 4-fold by the addition of glucose/phosphate. The mean cell numbers (MCN) of blastocysts cultured in succinate-supplemented HECM-2m was higher (28.3 +/- 1.1) than it was for those cultured in the absence of glutamine or pyruvate (range 20-24). The MCN was the highest (33.4 +/- 1.6) for blastocysts cultured in succinate-malate-supplemented HECM-2m followed by those in succinate (28.3 +/- 1.1) or malate (24.7 +/- 0.5) supplemented HECM-2m. Embryo transfer experiments showed that 29.8% (+/- 4.5) of transferred blastocysts cultured in succinate-malate-supplemented HECM-2m produced live births, similar (P > 0.1) to the control transfers of freshly recovered 8-cells (33.5% +/- 2.0) or blastocysts (28.9% +/- 3.0). These data show that supplementation of succinate and malate to HECM-2m supports 100% development of hamster 8-cell embryos to high quality viable blastocysts and that non-glucose oxidizable energy substrates are the most preferred components in hamster embryo culture medium.
仓鼠植入前胚胎的体外发育由非葡萄糖能量底物支持。为了研究胚胎代谢的重要性,使用化学限定的无蛋白改良仓鼠胚胎培养基 -2(HECM - 2m)研究了琥珀酸和苹果酸对仓鼠8细胞胚胎发育至囊胚的影响。琥珀酸对囊胚发育有剂量依赖性影响;0.5 mM琥珀酸是最佳浓度(85.1% +/- 3.9对54.5% +/- 3.5)。在添加琥珀酸的HECM - 2m中,省略乳酸会降低囊胚发育率(68.5% +/- 7.2),但省略丙酮酸(85.8% +/- 6.2)或谷氨酰胺(84.1% +/- 2.1)则不会。琥珀酸与谷氨酰胺或乳酸或丙酮酸一起对囊胚发育的支持作用较差(28% - 58%)。苹果酸也能刺激囊胚发育;0.01 mM苹果酸是最佳浓度(86.3% +/- 2.8)。在HECM - 2m中同时添加琥珀酸和苹果酸可支持最大(100%)的囊胚发育,添加葡萄糖/磷酸盐会使其受到4倍抑制。在添加琥珀酸的HECM - 2m中培养的囊胚平均细胞数(MCN)更高(28.3 +/- 1.1),高于在无谷氨酰胺或丙酮酸条件下培养的囊胚(范围为20 - 24)。在添加琥珀酸 - 苹果酸的HECM - 2m中培养的囊胚MCN最高(33.4 +/- 1.6),其次是在添加琥珀酸(28.3 +/- 1.1)或苹果酸(24.7 +/- 0.5)的HECM - 2m中培养的囊胚。胚胎移植实验表明,在添加琥珀酸 - 苹果酸的HECM - 2m中培养的移植囊胚有29.8%(+/- 4.5)产生活仔,与新鲜回收的8细胞(33.5% +/- 2.0)或囊胚(28.9% +/- 3.0)的对照移植相似(P > 0.1)。这些数据表明,在HECM - 2m中添加琥珀酸和苹果酸可支持仓鼠8细胞胚胎100%发育为高质量的有活力囊胚,并且非葡萄糖可氧化能量底物是仓鼠胚胎培养基中最优选的成分。