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Protective role of antifreeze proteins on sterlet (Acipenser ruthenus) sperm during cryopreservation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12310%2F18%3A43897599" target="_blank" >RIV/60076658:12310/18:43897599 - isvavai.cz</a>

  • Alternative codes found

    RIV/60077344:_____/18:00499985 RIV/60076658:12520/18:43897599

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s10695-018-0538-5" target="_blank" >https://link.springer.com/article/10.1007/s10695-018-0538-5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10695-018-0538-5" target="_blank" >10.1007/s10695-018-0538-5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Protective role of antifreeze proteins on sterlet (Acipenser ruthenus) sperm during cryopreservation

  • Original language description

    The loss of sperm quality in sterlet (Acipenser ruthenus) due to freeze-thaw process in cryopreservation was investigated in the present study. Two antifreeze proteins (AFPI or AFPIII) were used at different concentrations of 0.1, 1, 10, and 100g/mL. We compared motility, curvilinear velocity, and plasma membrane integrity of fresh, cryopreserved sperm, and sperm cryopreserved in the presence of antifreeze proteins. Fresh sperm (control) had 85 +/- 4% motility and 160 +/- 2m/s curvilinear velocity, respectively. After cryopreservation, the motility of frozen-thawed sperm without addition of antifreeze proteins significantly decreased (44 +/- 9%), compared to the control. The highest motility of frozen-thawed sperm was obtained in cryopreserved sperm with addition of 1g/mL of AFPIII (58 +/- 14%). No significant differences were observed in curvilinear velocity between fresh sperm and cryopreserved sperm with/without addition of AFPI or AFPIII. The flow cytometry analysis revealed that fresh sperm contained 94.5 +/- 6% live cells, while the cryopreserved sperm only contained 26.6 +/- 14% live cells. Supplementation of antifreeze proteins has significantly improved the percentage of live cells in frozen-thawed sperm, except 0.1g/ml of AFPI group. No significant difference in percentage of live cells was detected in the sperm cryopreserved with 10g/mL of AFPI or AFPIII, compared to fresh sperm. Thus, addition of antifreeze proteins to cryopreservation medium could be considered to improve the post-thawed sperm quality of sterlet.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    40103 - Fishery

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Fish Physiology and Biochemistry

  • ISSN

    0920-1742

  • e-ISSN

  • Volume of the periodical

    44

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    7

  • Pages from-to

    1527-1533

  • UT code for WoS article

    000453883600009

  • EID of the result in the Scopus database

    2-s2.0-85050196634