Zinc Oxide Nanoparticles-Enriched Extender Enhances Cryosurvival and Antioxidant Defense of Buffalo Spermatozoa

Authors

  • Richakumari M Patel Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.
  • Kirankumar H Parmar Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.
  • Meet T Chaudhari Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.
  • Dinesh V Chaudhari Department of Veterinary Gynaecology and Obstetrics, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.
  • Mohsin M Pathan Department of Physiology and Biochemistry, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.
  • Jignesh J Parmar Veterinary Clinical Complex, College of Veterinary Science & Animal Husbandry, Kamdhenu University, Anand, Gujarat-388001, India.

DOI:

https://doi.org/10.48165/ijvsbt.22.1.22

Keywords:

Antioxidant status, Buffalo bulls, Zinc oxide nanoparticles, Cryopreservation, TFYG extender

Abstract

The present study was conducted at the Central Sperm Station of the College of Veterinary Science in Anand, to evaluate the effect  of zinc oxide nanoparticles (ZnONPs) on the post-thaw quality of buffalo bull semen. A total 18 ejaculates from four mature healthy  breeding bulls were collected using an artificial vagina and evaluated for semen quality. Semen samples showing >70% initial motility  were diluted in Tris fructose egg yolk glycerol (TFYG) extender, divided into four aliquots supplemented with 0 (control), 10, 25, and 50  µg/mL ZnONPs, equilibrated at 4°C, frozen in liquid nitrogen vapour, and stored at -196 °C overnight. Post-thaw semen was evaluated  for sperm motility, viability, morphology, acrosome integrity, plasma membrane integrity (HOST), lipid peroxidation (MDA), and total  antioxidant capacity (TAC). Statistical analysis revealed that a significant (p<0.05) improvement was observed in post-thaw sperm  motility, viability, plasma membrane and acrosome integrity, and antioxidant activity in ZnONPs-supplemented groups compared to  the control. The 25 µg/mL ZnONPs concentration showed the most significant enhancement (p<0.05) in sperm quality parameters,  accompanied by a significant reduction (p<0.05) in lipid peroxidation levels and an increase in total antioxidant capacity, indicating  optimal protection against oxidative damage, followed by 10 µg/mL, while higher concentration (50 µg/mL) showed a detrimental effect.

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Published

2026-01-10

How to Cite

Patel, R. M., Parmar, K. H., Chaudhari, M. T., Chaudhari, D. V., Pathan, M. M., & Parmar, J. J. (2026). Zinc Oxide Nanoparticles-Enriched Extender Enhances Cryosurvival and Antioxidant Defense of Buffalo Spermatozoa. Indian Journal of Veterinary Sciences and Biotechnology, 22(1), 110-114. https://doi.org/10.48165/ijvsbt.22.1.22