Stock A E, Hansel W
Department of Physiology, New York State College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Theriogenology. 1992 Oct;38(4):757-68. doi: 10.1016/0093-691x(92)90038-s.
This study was designed to establish a sensitive bioassay for bovine platelet-activating factor (PAF), to determine if the bovine embryo secretes PAF in vitro and if PAF release is correlated with the embryo's potential to establish a pregnancy. Using an equine platelet aggregation assay, lipid extracted culture media from 33 Day-7 embryos (individually cultured for 18 hours in 1 ml of Ham's F10 containing 0.4% BSA at 37 degrees C in an air: CO2 mixture of 95:5 prior to their transfer to recipient heifers) and from control media (n=15, Ham's F10+0.4% BSA incubated simultaneously without embryos) were investigated. In addition, culture media from Day-6 (n=6) and Day-1 (2-cell, n=12) bovine embryos that were cultured for 4 hours but not transferred were examined. The aggregation assay proved to be sensitive to 5 pg of PAF. The assay proved to be specific, since the PAF receptor antagonist SRI 63-441 inhibited platelet aggregation induced by culture media in dosages comparable to aggregation induced by synthetic PAF18. From the 15 Day-7 embryos that established a pregnancy 2 contained measurable amounts of PAF in their culture media. No PAF was detected in the culture media from 13 embryos that succeeded, in the 18 embryos that failed to establish a pregnancy, or in the control media. One of 6 Day-6 embryos and 3 of 12 Day-1 (2-cell) embryos secreted detectable amounts of PAF into the culture media. Although the results indicate that some bovine embryos release PAF or a PAF-like substance in vitro, PAF measurements in the culture medium seem not to be a suitable method for the evaluation of bovine embryos prior to transfer.
本研究旨在建立一种灵敏的牛血小板活化因子(PAF)生物测定法,以确定牛胚胎在体外是否分泌PAF,以及PAF的释放是否与胚胎建立妊娠的潜力相关。使用马血小板聚集试验,对来自33个第7天胚胎(在转移至受体母牛前,于37℃、95:5的空气:二氧化碳混合气体环境下,在含0.4%牛血清白蛋白的1ml哈姆氏F10培养基中单独培养18小时)的脂质提取培养基以及对照培养基(n = 15,哈姆氏F10 + 0.4%牛血清白蛋白,无胚胎同时培养)进行了研究。此外,还检测了未转移的培养4小时的第6天(n = 6)和第1天(2细胞期,n = 12)牛胚胎的培养基。该聚集试验被证明对5 pg的PAF敏感。该试验具有特异性,因为PAF受体拮抗剂SRI 63 - 441能以与合成PAF诱导聚集相当的剂量抑制培养基诱导的血小板聚集。在15个成功妊娠的第7天胚胎中,有2个胚胎的培养基中含有可测量的PAF量。在13个成功妊娠的胚胎、18个未成功妊娠的胚胎的培养基以及对照培养基中均未检测到PAF。6个第6天胚胎中有1个、12个第1天(2细胞期)胚胎中有3个向培养基中分泌了可检测量的PAF。尽管结果表明一些牛胚胎在体外释放PAF或类似PAF的物质,但在培养基中测量PAF似乎不是评估移植前牛胚胎的合适方法。