Viability of guinea pig (Cavia porcellus) spermatozoa diluted in Tris-buffer extenders stored at 5.00 ˚C

Document Type : Original Article

Authors

1 DVM Graduate, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

2 Department of Clinical Pathology and Internal Medicine, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

3 Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

4 Department of Theriogenology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

Abstract
The cooling procedure markedly diminishes the quality of guinea pig (Cavia porcellus) sperms, primarily because their membranes are highly susceptible to this process. This susceptibility triggers the generation of reactive oxygen species and free radicals, ultimately leading to lipid peroxidation in the sperm membrane. Surprisingly, there has been a lack of research on the use of Tris-based extenders to safeguard guinea pig sperm under refrigeration conditions. This study aimed to assess the viability of guinea pig spermatozoa diluted in Tris buffer-based extenders during storage at 5.00 ˚C. Sperm collection was carried out through castration of the animals. For this study, 10 adult male guinea pigs were utilized, being divided into four groups including phosphate-buffered saline (PBS), human tubal fluid (HTF), Tris-citric-glucose (TCG), and Tris-fructose-yolk (TFY) cultures. Evaluations including sperm motility, morphology, plasma membrane integrity, viability, and total count were conducted at 0, 24, and 48 hr after sampling. The results obtained indicated that at the 24-hr and 48-hr marks of the experiment, both overall and progressive motility percentages, viability, plasma membrane integrity, and morphology of sperms in the PBS and HTF cultures exhibited a significant increase in comparison with the TCG and TFY cultures. Consequently, it can be inferred that PBS and HTF cultures are highly effective in preserving the quality of guinea pig spermatozoa.

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  1. Stan F. Anatomical particularities of male reproductive system of Guinea pigs (Cavia porcellus). Bull UASVM Vet Med 2015; 72(2): 288-295.
  2. Chawla S, Jena S, Nayak S. The laboratory Guinea pig. In: Nagarajan P, Gudde R, Srinivasan R (Eds). Essentials of laboratory animal science: principles and practices. Gateway, Singapore: Springer 2021; 239-251.
  3. Shek WR, Smith AL, Pritchett-Corning KR. Micro-biological quality control for laboratory rodents and lagomorphs. In: Fox JG, Anderson LC, Otto GM, et al (Eds). Laboratory animal medicine. 3rd Boston, USA: Academic Press 2015; 463-510.
  4. Cepeda R, Adaro L, Peñailillo Morphometric variations of chinchilla laniger prostate and plasmatic testosterone concentration during its annual reproductive cycle [Spanish]. Int J Morphol 2006; 24(1): 89-97.
  5. Di Iorio M, Manchisi A, Rocco M, et al. Comparison of different extenders on the preservability of rabbit semen stored at 5 ˚C for 72 hours. Ital J Anim Sci 2014; 13(4): 710-714.
  6. Rodriguez-Martinez H. Cryopreservation of porcine gametes, embryos and genital tissues: state of the art. In: Katko I (Ed). Current frontiers in cryobiology. Rijeka, Croatia: InTech 2012: 231-258.
  7. Rijsselaere T, Van Soom A, Tanghe S, et al. New techniques for the assessment of canine semen quality: a review. Theriogenology 2005; 64(3): 706-719.
  8. Guinea pigs. In: Mitchell M, Tully TN (Eds). Manual of exotic pet practice. Amsterdam, The Netherlands: Elsevier Health Sciences 2009; 456-473.
  9. Quesenberry KE, Carpenter JW. Ferrets, rabbits and rodents: Clinical medicine and surgery. Amsterdam, The Netherlands: Elsevier Health Sciences 2012; 467-482.
  10. Wyrobek AJ, Gordon LA, Burkhart JG, et al. An evaluation of the mouse sperm morphology test and other sperm tests in nonhuman mammals: a report of the U.S. Environmental Protection Agency Gene-Tox Program. Mutat Res 1983; 115(1): 1-72.
  11. El-Keraby FE, Osman KT, Ganah HB, et al. Soymilk-based extender for cryopreservation of bovine semen. J Anim Poult Prod 2010; 1(2): 61-69.
  12. López-Gatius F, Sances G, Sancho M, et al. Effect of solid storage at 15 degrees C on the subsequent motility and fertility of rabbit semen. Theriogenology 2005; 64(2): 252-260.
  13. Nagy S, Sinkovics G, Kovács A. Viability and acrosome integrity of rabbit spermatozoa processed in a gelatin-supplemented extender. Anim Reprod Sci 2002; 70(3-4): 283-286.
  14. Roca J, Martínez S, Vázquez JM, et al. Viability and fertility of rabbit spermatozoa diluted in Tris-buffer extenders and stored at 15 degrees C. Anim Reprod Sci 2000; 64(1-2): 103-112.
  15. Kemal Duru N, Morshedi M, Oehninger S. Effects of hydrogen peroxide on DNA and plasma membrane integrity of human spermatozoa. Fertil Steril 2000; 74(6): 1200-1207.
  16. Noorafshan A, Karbalay-Doust S, Valizadeh A, et al. Ameliorative effects of curcumin on the structural parameters of seminiferous tubules and Leydig cells in metronidazole-treated mice: a stereological approach. Exp Toxicol Pathol 2011; 63(7-8): 627-633.
  17. El-Kelawy H, Tawfeek M, El-Gaafary M, et al. Viability and fertilizing ability of extended rabbit semen stored at 5 degrees C. In Proceedings: 10th World rabbit congress. Sharm EL-Sheikh, Egypt 2012; 3-6.
  18. Martins-Bessa A, Rocha A, Mayenco-Aguirre A. Comparing ethylene glycol with glycerol for cryopreservation of canine semen in egg-yolk TRIS extenders. Theriogenology 2006; 66(9): 2047-2055.
  19. Bustani GS, Baiee FH. Semen extenders: an evaluative overview of preservative mechanisms of semen and semen extenders. Vet World 2021; 14(5): 1220-1233.
Volume 15, Issue 12
December 2024
Pages 691-696

  • Receive Date 24 February 2024
  • Revise Date 11 June 2024
  • Accept Date 29 June 2024