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使用特定放射免疫分析法检测植入前小鼠胚胎产生血小板活化因子的情况。

Examination for platelet-activating factor production by preimplantation mouse embryos using a specific radioimmunoassay.

作者信息

Smal M A, Dziadek M, Cooney S J, Attard M, Baldo B A

机构信息

Kolling Institute of Medical Research, Royal North Shore Hospital, St. Leonards, NSW, Australia.

出版信息

J Reprod Fertil. 1990 Nov;90(2):419-25. doi: 10.1530/jrf.0.0900419.

Abstract

A specific and highly sensitive radioimmunoassay was used to measure platelet-activating factor (PAF) production by preimplantation mouse embryos in vitro. Levels of PAF greater than 1 pg per embryo were not observed in 24-h culture medium from 2-cell embryos, compacted morulae or blastocysts, or in extracts from these embryos. Synthetic PAF added to embryos at the start of culture could be almost totally recovered after the incubation period, indicating negligible degradation of PAF during culture. PAF was also not detected in embryo samples using a washed rabbit-platelet aggregation assay. It can be concluded that mouse embryos do not produce substantial levels of PAF, or any of the biologically active analogues of PAF detected by the assay.

摘要

采用一种特异性强且灵敏度高的放射免疫分析法,来测定体外培养的植入前小鼠胚胎产生血小板活化因子(PAF)的情况。在来自二细胞胚胎、致密桑椹胚或囊胚的24小时培养基中,以及这些胚胎的提取物中,均未观察到PAF水平高于每胚胎1皮克。培养开始时添加到胚胎中的合成PAF在孵育期后几乎可以完全回收,这表明培养过程中PAF的降解可忽略不计。使用洗涤过的兔血小板聚集试验在胚胎样本中也未检测到PAF。可以得出结论,小鼠胚胎不会产生大量的PAF,或该分析方法检测到的任何PAF生物活性类似物。

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