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在HEPES缓冲的培养基中对小鼠卵子进行体外受精(IVF)。

In vitro fertilization (IVF) of mouse ova in HEPES-buffered culture media.

作者信息

Behr B R, Stratton C J, Foote W D, Knutzen V, Sher G

机构信息

Northern Nevada Fertility Center, Reno 89503.

出版信息

J In Vitro Fert Embryo Transf. 1990 Feb;7(1):9-15. doi: 10.1007/BF01133877.

Abstract

Some major drawbacks of a bicarbonate-buffered culture medium include the requirement of an elaborate incubator system able to maintain a 5% CO2 environment and the inability of the culture medium to maintain a physiological pH range (pH 7.3-7.4) in room air (0.03% CO2). This work resulted in the development of IVF culture media, BB (modified T6) and Hams-HEPES, which use HEPES-buffered systems not requiring the specialized CO2 environment to maintain a physiological pH range in room air. These media generate above-average cleavage rates in in vitro fertilized, superovulated B6CBAF1 mice ova. The effect of heparin and HEPES on cleavage was studied and neither had a significant effect at the concentrations used. Cleavage rates of nonfertilized ova (parthenogenic division) were 9 to 13%. There was no significant difference in parthenogenesis between any of the culture media and it appears to be a function of the strain of mice and the timing between human chorionic gonadotropin (hCG) injection and ovum collection. These results emphasize the need to account for parthenogenesis when determining cleavage rates of in vitro fertilized mouse ova. Also, the results suggest that because of individual mouse differences in cleavage rates, it is important to use an adequate number of mice per group to determine an accurate, average cleavage rate.

摘要

碳酸氢盐缓冲培养基的一些主要缺点包括需要一个能够维持5%二氧化碳环境的精密培养箱系统,以及该培养基在室内空气(0.03%二氧化碳)中无法维持生理pH范围(pH 7.3 - 7.4)。这项工作促成了体外受精培养基BB(改良的T6)和哈姆氏-HEPES的开发,它们使用HEPES缓冲系统,不需要特殊的二氧化碳环境就能在室内空气中维持生理pH范围。这些培养基在体外受精的超排卵B6CBAF1小鼠卵子中产生高于平均水平的卵裂率。研究了肝素和HEPES对卵裂的影响,在所使用的浓度下两者均无显著影响。未受精卵(孤雌生殖分裂)的卵裂率为9%至13%。任何一种培养基之间的孤雌生殖均无显著差异,这似乎是小鼠品系以及人绒毛膜促性腺激素(hCG)注射与卵子采集之间时间间隔的函数。这些结果强调在确定体外受精小鼠卵子的卵裂率时需要考虑孤雌生殖。此外,结果表明,由于小鼠个体在卵裂率上存在差异,每组使用足够数量的小鼠以确定准确的平均卵裂率很重要。

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