Jankovicová Jana, Simon Michal, Antalíková Jana, Horovská L'ubica
Institute of Animal Biochemistry and Genetics, Slovak Academy of Sciences, Moyzesova 61, 900 28 Ivanka pri Dunaji, Slovak Republic.
Acta Vet Hung. 2008 Mar;56(1):133-8. doi: 10.1556/AVet.56.2008.1.14.
Artificial insemination with frozen-thawed spermatozoa is commonly used in cattle breeding. A simple and fast procedure is needed for routine evaluation of the acrosomal status of frozen-thawed bovine sperm. Therefore, the purpose of this study was to test two staining procedures used to determine the viability and integrity of acrosome of frozen-thawed bovine spermatozoa. Double staining and Hoechst/FITC-Pisum sativum agglutinin (FITC-PSA) labelling were tested for evaluating the viability and acrosome reaction induced by calcium ionophore of bull spermatozoa. In our experiments no significant differences were detected in the frequency of acrosome-reacted sperm either by double staining (37.98%) or by FITC-PSA labelling (39.33%). The viability of sperm stained by the double staining method was 67.17%, and a higher portion of viable sperm (82.67%) was observed by staining with the Hoechst procedure (P < 0.01). On the basis of the results obtained it is concluded that both methods can be used for detecting the acrosome reaction of frozen-thawed bovine spermatozoa.
冷冻解冻精子的人工授精常用于奶牛养殖。需要一种简单快速的程序来常规评估冷冻解冻牛精子的顶体状态。因此,本研究的目的是测试两种用于确定冷冻解冻牛精子顶体活力和完整性的染色程序。对双染法和Hoechst/异硫氰酸荧光素 - 豌豆凝集素(FITC - PSA)标记法进行了测试,以评估公牛精子经钙离子载体诱导后的活力和顶体反应。在我们的实验中,通过双染法(37.98%)或FITC - PSA标记法(39.33%)检测到的顶体反应精子频率没有显著差异。双染法染色的精子活力为67.17%,而通过Hoechst法染色观察到的活精子比例更高(82.67%)(P < 0.01)。根据获得的结果得出结论,两种方法均可用于检测冷冻解冻牛精子的顶体反应。