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3H-胸腺嘧啶核苷对体外培养的植入前小鼠胚胎的影响。

Effects of 3H-thymidine on preimplantation mouse embryos in vitro.

作者信息

Olsen W M, Storeng R

机构信息

Department of Microbiology, Dental Faculty, University of Oslo, Norway.

出版信息

Pharmacol Toxicol. 1987 Sep;61(3):203-8. doi: 10.1111/j.1600-0773.1987.tb01804.x.

DOI:10.1111/j.1600-0773.1987.tb01804.x
PMID:3684953
Abstract

The effect of 3H-thymidine on in vitro development of preimplantation mouse embryos was studied. Two-cell and 4-8-cell embryos from B6CBA/F1 mice were continuously exposed to 3H-thymidine in medium containing 3H-thymidine in concentrations ranging from 10-500 nCi/ml. The effect of the radioactive precursor on embryo development to the blastocyst stage was studied by morphological observation, counting the blastocyst cell number and measuring 3H-thymidine incorporation. The continuous presence of 3H-thymidine significantly inhibited development of 2-cell and 4-8-cell embryos to the blastocyst stage. Embryos cultured from the 2-cell stage were more sensitive to 3H-thymidine than those exposed from the 4-8-cell stage. Even in morphologically normal blastocysts the cell number was significantly reduced. A 2 hr pulse of 100 nCi/ml 3H-thymidine at the blastocyst stage, did not affect the blastocyst formation or the blastocyst cell number and the amount of incorporated 3H-thymidine was sufficient to provide a reliable quantitation of DNA synthesis during the culture of preimplantation embryos in vitro. Continuous incubation with 3H-thymidine in order to measure DNA synthesis of preimplantation mouse embryos should be avoided when DNA synthesis is used as a means of evaluating toxic effect of an agent. Adverse radiation effects by 3H-thymidine on preimplantation mouse embryos during toxicity testing can be avoided by pulse labelling.

摘要

研究了3H-胸腺嘧啶核苷对植入前小鼠胚胎体外发育的影响。从B6CBA/F1小鼠获取的二细胞和4-8细胞胚胎,在含有浓度范围为10 - 500 nCi/ml 3H-胸腺嘧啶核苷的培养基中持续暴露。通过形态学观察、计数囊胚细胞数量和测量3H-胸腺嘧啶核苷掺入量,研究放射性前体对胚胎发育至囊胚阶段的影响。3H-胸腺嘧啶核苷的持续存在显著抑制二细胞和4-8细胞胚胎发育至囊胚阶段。从二细胞阶段开始培养的胚胎比从4-8细胞阶段开始暴露的胚胎对3H-胸腺嘧啶核苷更敏感。即使在形态正常的囊胚中,细胞数量也显著减少。在囊胚阶段给予100 nCi/ml 3H-胸腺嘧啶核苷2小时脉冲,不影响囊胚形成或囊胚细胞数量,且掺入的3H-胸腺嘧啶核苷量足以可靠地定量体外培养植入前胚胎期间的DNA合成。当将DNA合成用作评估某种试剂毒性作用的手段时,应避免用3H-胸腺嘧啶核苷持续孵育以测量植入前小鼠胚胎的DNA合成。在毒性测试期间,通过脉冲标记可避免3H-胸腺嘧啶核苷对植入前小鼠胚胎产生不利的辐射效应。

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