Gardner D K, Lane M
Centre for Early Human Development, Monash Medical Centre, Clayton, Melbourne, Victoria, Australia.
Biol Reprod. 1993 Feb;48(2):377-85. doi: 10.1095/biolreprod48.2.377.
The regulation of 1-cell mouse embryo development in culture by amino acids was investigated. When the 20 amino acids in Eagle's medium were present, blastocyst formation at 72 h (9%; p < 0.01), and blastocyst cell number (66; p < 0.05) and hatching (45%; p < 0.05) after 96 h of culture were significantly increased, compared to control embryos grown in the absence of amino acids (0%, 60, and 23%, respectively). The beneficial effect of Eagle's amino acids was attributed primarily to the non-essential group. In the presence of non-essential amino acids, blastocyst formation (54%; p < 0.001) and cell number after 72 h of culture (33; p < 0.05), and blastocyst cell number (69; p < 0.01) and hatching (68%; p < 0.01) after 96 h of culture were all significantly greater than for embryos cultured with all amino acids (9%, 26, 66, and 45%, respectively). In the absence of glutamine, essential amino acids significantly reduced blastocyst cell number after 96 h (53; p < 0.05). Continual culture in the presence of amino acids reduced the cleavage rate after around 72 h of in vitro culture; this decrease was not observed in the absence of amino acids. Transfer of embryos to fresh medium after 48-72 h of culture resulted in increases in the percentage of blastocysts formed and in blastocyst cell numbers. These data are consistent with the build-up of an inhibitory compound in the medium, possibly ammonium, an end-product of amino acid metabolism.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了氨基酸对体外培养的单细胞小鼠胚胎发育的调节作用。当伊格尔培养基中的20种氨基酸存在时,与在无氨基酸条件下培养的对照胚胎相比(分别为0%、60和23%),培养72小时时囊胚形成率(9%;p<0.01)、培养96小时后囊胚细胞数量(66;p<0.05)和孵化率(45%;p<0.05)均显著增加。伊格尔氨基酸的有益作用主要归因于非必需氨基酸组。在非必需氨基酸存在的情况下,培养72小时时的囊胚形成率(54%;p<0.001)和细胞数量(33;p<0.05),以及培养96小时后的囊胚细胞数量(69;p<0.01)和孵化率(68%;p<0.01)均显著高于用所有氨基酸培养的胚胎(分别为9%、26、66和45%)。在缺乏谷氨酰胺的情况下,必需氨基酸显著降低了培养96小时后的囊胚细胞数量(53;p<0.05)。在氨基酸存在的情况下持续培养会降低体外培养约72小时后的分裂率;在无氨基酸的情况下未观察到这种下降。培养48 - 72小时后将胚胎转移到新鲜培养基中,会导致形成的囊胚百分比和囊胚细胞数量增加。这些数据与培养基中一种抑制性化合物(可能是铵,氨基酸代谢的终产物)的积累一致。(摘要截断于250字)