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多胺合成抑制剂对体外激活滞育小鼠囊胚的影响。

Effect of inhibitors of polyamine synthesis on activation of diapausing mouse blastocysts in vitro.

作者信息

Van Winkle L J, Campione A L

出版信息

J Reprod Fertil. 1983 Jul;68(2):437-44. doi: 10.1530/jrf.0.0680437.

Abstract

Diapausing mouse blastocysts were cultured in vitro with inhibitors of polyamine synthesis and/or the polyamines, putrescine, spermidine and/or spermine. Attachment of blastocysts to the culture dish, the onset of trophoblastic outgrowth and the extent of outgrowth were retarded by methylornithine (10 mM) or methylglyoxal bis(guanylhydrazone) (50 or 200 microM) and apparently blocked by a combination of these inhibitors. The embryos appeared to make no progress towards activation in the presence of both inhibitors but became active and grew normally when transferred to inhibitor-free medium. The inhibition of growth was also reversed when polyamines (10(-5) M) were supplied in the medium along with the inhibitors (P less than 0.01). These results suggest that polyamine synthesis is required for activation, growth and development of diapausing blastocysts in vitro.

摘要

将滞育的小鼠囊胚与多胺合成抑制剂和/或多胺(腐胺、亚精胺和/或精胺)一起进行体外培养。甲基鸟氨酸(10 mM)或甲基乙二醛双(胍腙)(50或200 μM)会延迟囊胚与培养皿的附着、滋养层生长的起始以及生长的程度,而这两种抑制剂的组合显然会阻止这些过程。在两种抑制剂存在的情况下,胚胎似乎在激活方面没有进展,但转移到无抑制剂的培养基中时会变得活跃并正常生长。当培养基中同时添加抑制剂和多胺(10^(-5) M)时,生长抑制也会被逆转(P < 0.01)。这些结果表明,多胺合成是滞育囊胚在体外激活、生长和发育所必需的。

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