In vitro viability of canine spermatozoa frozen in tris-fructose-citric acid extender with ethylene glycol

Authors

  • Camila Infantosi Vannucchi Universidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Reprodução Animal, São Paulo, SP
  • Silvia Edelweiss Crusco dos Santos Universidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Reprodução Animal, São Paulo, SP
  • José Antonio Visintin Universidade de São Paulo, Faculdade de Medicina Veterinária e Zootecnia, Departamento de Reprodução Animal, São Paulo, SP

DOI:

https://doi.org/10.1590/S1413-95961999000400007

Keywords:

Ethylene glycol, Cryoprotectants, Freezing, Semen, Dog

Abstract

The use of frozen semen has become increasingly popular in canine artificial insemination, stimulating research to improve freezing methods and extenders. In this study, was compared the final concentration of 5% ethylene glycol used in 3 equilibration protocols. In Method I, one part of semen was added to two parts of tris-fructose-citric acid with 7.5% ethylene glycol (Extender 2) and frozen without cooling. In Method II, one part of semen was added to two parts of tris-fructose-citric acid with 7.5% ethylene glycol (Extender 2) and cooled at 5ºC for 1 hour before freezing. In Method III, one part of semen was added to one part of tris-fructose-citric without ethylene glycol (Extender 1) and cooled at 5ºC for 1 hour. Just after this period, one part of 5ºC cooled tris-fructose-citric acid containing 15% ethylene glycol (Extender 3) was added to the previous extended semen, maintained at 5ºC for one additional hour and frozen. For freezing in each procedure semen was packaged in 0.5 ml plastic straws and placed for 20 minutes in vapor 5 cm above liquid nitrogen and then lowered into the liquid nitrogen and stored. All samples were thawed by immersion for 30 sec in a 37ºC water bath and immediately evaluated. Progressive motility was best after Method III (63%), which was not different from fresh semen (94%) but was better (p< 0.05) than after Method II (25%) or Method I (6%). Forward velocity was again best after Method III (2.9) comparable to fresh semen (4.6) and Method II (2.5), but better (p< 0.05) than Method I (1.7). Morphological abnormalities were lowest after Method III, but were not significantly different from Methods II or I. Most common abnormalities were detached heads and bent, hairpin and coiled tails. It was concluded that slow, step-wise equilibration in tris-fructose-citrate extender followed by extender with ethylene glycol before freezing seems to produce the best progressive motility and forward velocity in frozen-thawed canine spermatozoa.

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Published

1999-01-01

How to Cite

Vannucchi, C. I., Santos, S. E. C. dos, & Visintin, J. A. (1999). In vitro viability of canine spermatozoa frozen in tris-fructose-citric acid extender with ethylene glycol. Brazilian Journal of Veterinary Research and Animal Science, 36(4), 205-211. https://doi.org/10.1590/S1413-95961999000400007

Issue

Section

VETERINARY MEDICINE

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