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Quality assessment of cryopreserved black-lip pearl oyster Pinctada margaritifera spermatozoa

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12520%2F18%3A43898754" target="_blank" >RIV/60076658:12520/18:43898754 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0044848617325620" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0044848617325620</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.aquaculture.2018.07.067" target="_blank" >10.1016/j.aquaculture.2018.07.067</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Quality assessment of cryopreserved black-lip pearl oyster Pinctada margaritifera spermatozoa

  • Original language description

    High quality of sperm is essential to a high fertilization rate, especially post- cryopreservation. Assessment of sperm integrity, motility and energy reserves before cryopreservation is necessary for selection of milt with optimal fertilizing potential. We describe the effect of cryopreservation on the quality of black-lip pearl oyster, Pinctada margaritifera var. cumingii sperm. Evaluated quality indices of fresh and frozen/thawed P. margaritifera spermatozoa, included morphology, ultrastructure and motility characteristics relative to the energy content (ATP) and its capacity to be sustained by mitochondrial respiration. Morphology and ultrastructure were quantitatively evaluated using images obtained by optical microscopy assisted by the Image J software and TEM, respectively. Sperm motility was assessed using Image J software combined with a computer assisted sperm analysis plugin adapted for assessing P. margaritifera spermatozoa. Other sperm quality parameters evaluated included O-2 consumption, ATP content, and creatine kinase activity. Frozen/thawed spermatozoa exhibited damage to the head but retained a compact spherical shape. Sperm motility indicators showed a significant decrease in quality resulting from the freeze/thaw process. The percent of motile cells was 54% compared to 84% in fresh sperm, O-2 consumption was 4.8 compared to 44 nanomol min(-1), ATP content was 0.72 nmol/10(9) spermatozoa in the activating medium compared to 4.54 nmol/10(9) spermatozoa, and creatine kinase activity was 9.06 x 10(-5) IU mg(-1) protein compared to 12.5 x 10(-5) IU mg(-1) protein. The cryopreservation protocol allowed obtaining an acceptable motility rate after thawing, confirming the predictive value of sperm motility measurements before cryopreservation in terms of their ability to withstand freezing process.

  • 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

    10604 - Reproductive biology (medical aspects to be 3)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Aquaculture

  • ISSN

    0044-8486

  • e-ISSN

  • Volume of the periodical

    497

  • Issue of the periodical within the volume

    DEC 2018

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    278-286

  • UT code for WoS article

    000442900300035

  • EID of the result in the Scopus database

    2-s2.0-85051024839