AI Article Synopsis

  • Defective sperm can lead to fertilization issues, making optimal semen storage crucial for maintaining viability, and this study assesses the impact of zinc (Zn) nanoparticles as antioxidants during semen processing and cryopreservation in bulls.
  • The research involved 32 ejaculates from Holstein bulls, which were treated with varying concentrations of Zn nanoparticles during semen dilution, leading to improved plasma membrane integrity and mitochondrial activity in treated sperms, although no significant changes were noted in overall sperm motility or DNA fragmentation.
  • While the addition of Zn nanoparticles enhanced certain sperm quality markers, it didn't negatively impact embryo development rates during in vitro fertilization, suggesting a potential benefit for using Zn nanoparticles to improve semen quality without compromising reproductive outcomes.

Article Abstract

Defective sperms cause fertilization failure under both in vivo and in vitro conditions. Therefore, providing optimal conditions during semen storage is a prerequisite for maintaining viability. The current study investigated bull semen quality in vitro and in vivo when zinc (Zn) nanoparticles were used as antioxidant during semen processing and cryopreservation. In total, 32 ejaculates were collected from four Holstein bulls. All ejaculates were pooled and diluted with Bioxcell-extender containing 0 (control group), 10, 10, 10, 10, and 10 M of Zn nanoparticles. Several physical and biochemical sperm parameters were determined after freeze-thawing process. In vitro embryo development rate and pregnancy rate were monitored after in vitro fertilization or artificial insemination using semen treated with Zn nanoparticles. Plasma membrane integrity was improved (P < 0.05) in bull semen treated with 10 M (69.3%), and 10 (62.4%) of Zn nanoparticles compared to untreated group (51.3%). In addition, proportions of live spermatozoa with active mitochondria were increased (P < 0.05) in semen supplemented with Zn nanoparticles at concentration of 10 M (67.3%), and 10 (85.3%) compared to control group (49.8%). Moreover, the level of MDA was lower (P < 0.05) in semen with Zn nanoparticles at 10 M (2.97 mol/mL) and 10 (2.7 mol/mL) concentrations than control semen samples (3.77 mol/mL). However, sperm total and progressive motility, sperm viability, DNA fragmentation, and pregnancy rate were not affected by treatment of semen with Zn nanoparticles. On the other hand, supplementation of in vitro maturation media with 10 M Zn nanoparticles has increased blastocyst rate (P < 0.05) compared to other experimental groups, while addition of Zn nanoparticles-treated sperm during in vitro fertilization did not affect embryo development rate. In conclusion, supplementation of Zn nanoparticles to semen has improved its quality without affecting embryo development rate in vitro. However, in vitro embryo development rate was increased when Zn nanoparticles were supplemented to IVM media. This support the notion of Zn nanoparticles beneficial action on improving bovine gametes quality without affecting pregnancy rate.

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Source
http://dx.doi.org/10.1007/s12011-020-02153-4DOI Listing

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