Journals / Turkish Journal of Veterinary and Animal Sciences / 2011 / Cilt: 35 - Sayı: 5

Intrauterine insemination with cat semen frozen with various extenders

Pages
311–318
Publication Date
2011-05-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In conclusion, cat semen extended and frozen with EY-TFC and EY-SMGT extenders was found to be successful in post-thaw motility and morphological defect rates.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The aim of this study was to investigate the post-thaw motility and morphological defect rates of cat semen frozen with various extenders, and pregnancy rates after intrauterine insemination (IUI).
📊
Key Findings & Data:Cats, 2 males and 14 queens, 2 to 3 years of age, and under the same managemental conditions were used.
💡
Conclusion & Impact:In conclusion, cat semen extended and frozen with EY-TFC and EY-SMGT extenders was found to be successful in post-thaw motility and morphological defect rates.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Cat semen · extender · frozen semen

Abstract

The aim of this study was to investigate the post-thaw motility and morphological defect rates of cat semen frozen with various extenders, and pregnancy rates after intrauterine insemination (IUI). Cats, 2 males and 14 queens, 2 to 3 years of age, and under the same managemental conditions were used. Semen was collected by means of an electro-ejaculator under general anesthesia. Based on spermatological traits, semen samples presumed suitable for freezing were extended with either tris-fructose-citric acid (EY-TFC) containing 20% egg yolk, or skimmed milk-glucose-taurine (EY-SMGT) containing 10% egg yolk extender, and frozen in 0.25 mL straws. For the extenders, post-thaw motility and morphological abnormality values were found to be efficient for IUI and no statistical significance was observed between the values of the extender groups. To achieve ovulation, queens showing behavioral estrus received 250 IU of hCG via IM route, 30 h prior to IUI. Under general anesthesia, queens were laparatomised on the medial line and the left and right uterine horn were taken out. Into both uterine horns, 2 straws containing 25 × 106 sperm each were thawed at 37 °C for 30 s and equally injected. Pregnancy was diagnosed using an ultrasonography device on the 19th day after IUI by detecting the embryonic vesicles. Of the 3 EY-TFC group queens found to be pregnant, 1 aborted and other 2 had early embryonic death (EED); the pregnancy rate was 42.90%. In a queen in the EY-SMGT group, no ovulation took place after the hCG injection. In 2 of the queens found to be pregnant in this group, EED occurred and the pregnancy rate was 33.30%. In conclusion, cat semen extended and frozen with EY-TFC and EY-SMGT extenders was found to be successful in post-thaw motility and morphological defect rates. Therefore, surgical IUI may be more effective for feline AI using frozen semen rather than intravaginal insemination.

Özet

The aim of this study was to investigate the post-thaw motility and morphological defect rates of cat semen frozen with various extenders, and pregnancy rates after intrauterine insemination (IUI). Cats, 2 males and 14 queens, 2 to 3 years of age, and under the same managemental conditions were used. Semen was collected by means of an electro-ejaculator under general anesthesia. Based on spermatological traits, semen samples presumed suitable for freezing were extended with either tris-fructose-citric acid (EY-TFC) containing 20% egg yolk, or skimmed milk-glucose-taurine (EY-SMGT) containing 10% egg yolk extender, and frozen in 0.25 mL straws. For the extenders, post-thaw motility and morphological abnormality values were found to be efficient for IUI and no statistical significance was observed between the values of the extender groups. To achieve ovulation, queens showing behavioral estrus received 250 IU of hCG via IM route, 30 h prior to IUI. Under general anesthesia, queens were laparatomised on the medial line and the left and right uterine horn were taken out. Into both uterine horns, 2 straws containing 25 × 106 sperm each were thawed at 37 °C for 30 s and equally injected. Pregnancy was diagnosed using an ultrasonography device on the 19th day after IUI by detecting the embryonic vesicles. Of the 3 EY-TFC group queens found to be pregnant, 1 aborted and other 2 had early embryonic death (EED); the pregnancy rate was 42.90%. In a queen in the EY-SMGT group, no ovulation took place after the hCG injection. In 2 of the queens found to be pregnant in this group, EED occurred and the pregnancy rate was 33.30%. In conclusion, cat semen extended and frozen with EY-TFC and EY-SMGT extenders was found to be successful in post-thaw motility and morphological defect rates. Therefore, surgical IUI may be more effective for feline AI using frozen semen rather than intravaginal insemination.

🔖

Cite This Article

BARAN, A., TEK, Ç., DEMİR, K., SABUNCU, A., ÖZDAŞ, Ö. B. (2011). Intrauterine insemination with cat semen frozen with various extenders. Turkish Journal of Veterinary and Animal Sciences, Cilt: 35 - Sayı: 5, 311–318. https://ajindex.com/articles/121837

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Farstad, W.: Current state in biotechnology in canine and feline reproduction. Anim. Reprod. Sci., 2000; 60: 375-387. Axnér, E., Linde-Forsberg, C.: Semen collection and assessment, and artifi cial insemination in the cat. In: Concannon, P.W., England, G., Verstegen, J., Linde-Forsberg, C., (eds.), Recent Advances in Small Animal Reproduction. International Veterinary Information Service, Ithaca, New York, USA. 2002.
  2. Platz, C.C., Wildt, D.E., Seager, S.W.J.: Pregnancy in the domestic cat aft er artificial insemination with previously frozen spermatozoa. J. Reprod. Fertil., 1978; 52: 279-282.
  3. Tsutsui, T., Tanaka, A., Takagi, Y., Nakagawa, K., Fujimoto, Y., Murai, M., Anzai, M., Hori, T.: Unilateral intrauterine horn insemination of fresh semen in cats. J. Vet. Med. Sci., 2000; 62: 1241-1245.
  4. Zambelli, D., Castagnetti, C.: Transcervical insemination with fresh or frozen semen in the domestic cat: new technique and preliminary results. ESDAR Newsletter, 2001; 6: 34. Zambelli, D., Buccioli, M., Castagnetti, C., Belluzzi, S.: Vaginal and cervical anatomic modifi cations during the oestrus cycle in relation to transcervical catheterization in the domestic cat. In: Proceedings of the 3rd EVSSAR Congress, 2002; 185. Tanaka, A., Tagaki, Y., Nagakawa, K., Fujimoto, Y., Hori, T., Tsutsui, T.: Artifi cial intravaginal insemination using fresh semen in cats. J. Vet. Med. Sci., 2000; 62: 1163-1167.
  5. Tsutsui, T., Tanaka, A., Takagi, Y., Nakagawa, K., Fujimoto, Y., Murai, M., Anzai, M., Hori, T.: Unilateral intrauterine horn insemination of frozen semen in cats. J. Vet. Med. Sci., 2000; 62: 1247-1251.
  6. Chatdarong, K., Axnér, E., Manee-In, S., Th uwanut, P., Linde- Forsberg, C.: Pregnancy in the domestic cat aft er vaginal or transcervical insemination with fresh and frozen semen. Th eriogenology, 2007; 68: 1326-1333.
  7. Villaverde, A.I.S.B., Melo, C.M., Martin, I., Ferreira, T.H., Papa, F.O., Taconeli, C.A., Lopes, M.D.: Comparison of effi ciency between two artifi cial insemination methods using frozen-thawed semen in domestic cat (Felis catus) Artifi cial insemination in domestic cats. Anim. Reprod. Sci., 2009; 114: 434-442.
  8. Sojka, N.J., Jennings, L.L., Hamner, C.E.: Artifi cial insemination in the cat (Felis catus). Lab. Anim. Care, 1970; 20: 198-204.
  9. Baran, A., Bacınoğlu, S., Evecen, M., Evrim Şahin, B., Alkan, S., Demir, K., Ak, K., İleri, I.K.: Freezing of cat semen in straws with diff erent glycerol levels containing tris extender. Turk. J. Vet. Anim. Sci., 2004; 28: 54