E. Schilling, D. Smidt, B. Sacher, D. Petac, S. Kaschab
{"title":"荧光显微镜对早期牛胚胎活力的诊断","authors":"E. Schilling, D. Smidt, B. Sacher, D. Petac, S. Kaschab","doi":"10.1051/RND:19790924","DOIUrl":null,"url":null,"abstract":"Summary. A fluorescence microscopy technique using diacetylfluorescin (FDA) as a substrate has been tested for the evaluation of the viability of early bovine embryos. Five to 8-day old cattle embryos were incubated in PBS containing FDA concentrations of 1 : 400 000 or 1 : 800 000 for 3 to 5 min at room temperature. Embryos were then examined by reflected light fluorescence using a KP 490 and 520 barrier filter in a Zeiss Axiomat microscope. Their mitotic activity after 24 hrs culture in vitro was used to determine their viability. After 3 min of incubation in the FDA medium, 85 p. 100 of the brilliantly fluorescing embryos showed mitoses after culture. None of the non-fluorescing embryos developed in vitro. Some embryos (about 6 p. 100) contained both dead and living cells as determined using the FDA test ; a few of these differentially reactive embryos were viable, but most of them were not. Short-term incubation of embryos in FDA medium probably did not impair their development, and no teratogenic effects could be seen in 17 to 20-day old rabbit fetuses transferred after the FDA test.","PeriodicalId":7885,"journal":{"name":"Annales De Biologie Animale Biochimie Biophysique","volume":"25 1","pages":"1625-1629"},"PeriodicalIF":0.0000,"publicationDate":"1979-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"27","resultStr":"{\"title\":\"Diagnosis of the viability of early bovine embryos by fluorescence microscopy\",\"authors\":\"E. Schilling, D. Smidt, B. Sacher, D. Petac, S. Kaschab\",\"doi\":\"10.1051/RND:19790924\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Summary. A fluorescence microscopy technique using diacetylfluorescin (FDA) as a substrate has been tested for the evaluation of the viability of early bovine embryos. Five to 8-day old cattle embryos were incubated in PBS containing FDA concentrations of 1 : 400 000 or 1 : 800 000 for 3 to 5 min at room temperature. Embryos were then examined by reflected light fluorescence using a KP 490 and 520 barrier filter in a Zeiss Axiomat microscope. Their mitotic activity after 24 hrs culture in vitro was used to determine their viability. After 3 min of incubation in the FDA medium, 85 p. 100 of the brilliantly fluorescing embryos showed mitoses after culture. None of the non-fluorescing embryos developed in vitro. Some embryos (about 6 p. 100) contained both dead and living cells as determined using the FDA test ; a few of these differentially reactive embryos were viable, but most of them were not. Short-term incubation of embryos in FDA medium probably did not impair their development, and no teratogenic effects could be seen in 17 to 20-day old rabbit fetuses transferred after the FDA test.\",\"PeriodicalId\":7885,\"journal\":{\"name\":\"Annales De Biologie Animale Biochimie Biophysique\",\"volume\":\"25 1\",\"pages\":\"1625-1629\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1979-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"27\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annales De Biologie Animale Biochimie Biophysique\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1051/RND:19790924\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales De Biologie Animale Biochimie Biophysique","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/RND:19790924","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Diagnosis of the viability of early bovine embryos by fluorescence microscopy
Summary. A fluorescence microscopy technique using diacetylfluorescin (FDA) as a substrate has been tested for the evaluation of the viability of early bovine embryos. Five to 8-day old cattle embryos were incubated in PBS containing FDA concentrations of 1 : 400 000 or 1 : 800 000 for 3 to 5 min at room temperature. Embryos were then examined by reflected light fluorescence using a KP 490 and 520 barrier filter in a Zeiss Axiomat microscope. Their mitotic activity after 24 hrs culture in vitro was used to determine their viability. After 3 min of incubation in the FDA medium, 85 p. 100 of the brilliantly fluorescing embryos showed mitoses after culture. None of the non-fluorescing embryos developed in vitro. Some embryos (about 6 p. 100) contained both dead and living cells as determined using the FDA test ; a few of these differentially reactive embryos were viable, but most of them were not. Short-term incubation of embryos in FDA medium probably did not impair their development, and no teratogenic effects could be seen in 17 to 20-day old rabbit fetuses transferred after the FDA test.