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α-鹅膏蕈碱对猪卵母细胞核成熟的体外影响。

Effects of alpha-amanitin on nuclear maturation of porcine oocytes in vitro.

作者信息

Meinecke B, Meinecke-Tillmann S

机构信息

Ambulatorische und Geburtshilfliche Veterinaerklinik, Justus-Liebig-Universitaet Giessen, Germany.

出版信息

J Reprod Fertil. 1993 May;98(1):195-201. doi: 10.1530/jrf.0.0980195.

Abstract

The effects of alpha-amanitin on cumulus enclosed and denuded porcine oocytes exposed to this heterogeneous nuclear RNA (hnRNA) synthesis inhibitor at different times (0, 0.5, 1, 2, 4, 6, 8, 12 and 20 h) after the start of culture was investigated. A further objective was to determine the sequence of nuclear progression after removing the inhibitor. The addition of 10 micrograms alpha-amanitin ml-1 to a gonadotrophin containing medium (10 iu PMSG ml-1 in TCM 199) at 0, 0.5 or 1 h after the onset of culture prevented cumulus expansion, and only 4.4, 6.4 and 3.5% of oocytes underwent germinal vesicle breakdown. This inhibitory effect was considerably reduced by delaying the addition of the drug to the culture medium for 2-8 h (2 h: 34.9%, 4 h: 53.5%, 6 h: 46.9%, 8 h: 59.2% germinal vesicle breakdown), and no inhibition of nuclear maturation was observed when alpha-amanitin was added after 12 or 20 h following explantation of the oocytes. When cumulus-oocyte complexes were cultured for > or = 2 h in inhibitor-free medium and then transferred to medium supplemented with alpha-amanitin, full cumulus expansion was observed in all cases, at the end of the 44 h culture. Denudation of the oocytes before culture in either medium supplemented with alpha-amanitin or microinjection of alpha-amanitin into the ooplasm at concentrations of 1.0 and 10.0 mg ml-1 remained without any effect on nuclear progression.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了在培养开始后不同时间点(0、0.5、1、2、4、6、8、12和20小时),α-鹅膏蕈碱对暴露于这种异质性核RNA(hnRNA)合成抑制剂的卵丘包裹和裸化猪卵母细胞的影响。另一个目标是确定去除抑制剂后核进展的顺序。在培养开始后0、0.5或1小时,向含有促性腺激素的培养基(TCM 199中10 iu/ml孕马血清促性腺激素)中添加10微克/毫升α-鹅膏蕈碱可阻止卵丘扩展,只有4.4%、6.4%和3.5%的卵母细胞发生生发泡破裂。将药物添加到培养基中的时间推迟2至8小时(2小时:34.9%,4小时:53.5%,6小时:46.9%,8小时:59.2%生发泡破裂),这种抑制作用会显著降低,当在卵母细胞植入后12或20小时添加α-鹅膏蕈碱时,未观察到对核成熟的抑制作用。当卵丘-卵母细胞复合体在无抑制剂的培养基中培养≥2小时,然后转移到添加α-鹅膏蕈碱的培养基中时,在44小时培养结束时,所有情况下均观察到完全的卵丘扩展。在添加α-鹅膏蕈碱的培养基中培养前对卵母细胞进行去卵丘处理,或以1.0和10.0毫克/毫升的浓度将α-鹅膏蕈碱显微注射到卵细胞质中,对核进展均无任何影响。(摘要截于250字)

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