ArticleOriginal scientific text
Title
Determination of sperm acrosin activity in the arctic fox (Alopex lagopus L.) – using method developed for human spermatozoa
Authors 1, 1, 2
Affiliations
- University of Technology and Life Sciences in Bydgoszcz, Faculty of Animal Breeding and Biology, Department of Biology of Small Ruminants and Environmental Biochemistry, Mazowiecka 28, 85-084 Bydgoszcz, Poland
- Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, University of Warmia and Mazury in Olsztyn, Faculty of Environmental Sciences and Fisheries, Department of Ichthyology, M. Oczapowskiego 5, 10-719 Olsztyn, Poland
Abstract
The aim of the study was to adapt a method to determine acrosin activity of human spermatozoa to arctic fox (Alopex lagopus L.) spermatozoa. We modified this method by reducing sperm count per sample from 1÷10 × 106 to 25÷200 × 103, incubation time from 180 minutes to 60 minutes, and Triton X-100 concentration in the reaction mixture from 0.01% to 0.005% per 100 cm3. It has also confirmed that arctic fox seminal plasma is rich in proteinases and their inhibitors. To completely abolish the inhibitory effect of seminal plasma on acrosin activity it is recommended to wash the spermatozoa four times. Benzamidine served an inhibitor of acrosin activity.
Bibliography
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