Dergiler / Turkish Journal of Veterinary and Animal Sciences / 2018 / Cilt: 42 - Sayı: 4

Effects of different extenders and additives on liquid storage of Awassi ram semen

Sayfa
230–242
Yayın Tarihi
2018-08-09
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The role of oxidative stress and MMP are considerable in liquid storage.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The aim of this study was to evaluate the effects of different extenders and additives on ram semen during liquid storage and to demonstrate the role of oxidative stress parameters on this process.
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Temel Bulgular & Veri:In the present study, ejaculates taken by artificial vagina twice a week from 4 rams during the breeding season were used.
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Sonuç & Katkı:The role of oxidative stress and MMP are considerable in liquid storage.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Awassi ram · extenders · liquid storage

Abstract

The aim of this study was to evaluate the effects of different extenders and additives on ram semen during liquid storage and to demonstrate the role of oxidative stress parameters on this process. In the present study, ejaculates taken by artificial vagina twice a week from 4 rams during the breeding season were used. They were mixed and used if motility and viability were above 70% and there was a 95% intact acrosome. The semen specimens were diluted by Tris-citrate-glucose (TRIS), Tris-TES (TEST), HEPES-buffered Tyrode lactate (TL-HEPES), and Dulbecco?s phosphate-buffered saline (PBS) extenders supplemented with different additives [centrifuged egg yolk, Equex-STM, bovine serum albumin (BSA), and ethylenediaminetetraacetic acid (EDTA)]. The specimens were stored at 4 °C for up to 96 h and evaluated for motility, membrane integrity, acrosome integrity, mitochondrial membrane potential (MMP), and oxidative stress parameters. At the end of the 96-h storage, the highest sperm motility was 64.2 ± 3.7% (P < 0.05) and significant loss of sperm motility and membrane integrity were not detected in extender TEST-3, but the MMP rate significantly declined. Acrosome integrity was not affected by storage time or extender types. BSA and EDTA decreased lipid peroxidation (LPO) and total oxidant status (TOS), but did not positively affect motility or membrane integrity. As a result, TRIS, TEST, and TL-HEPES-3 were observed to provide better protection for ram semen during liquid storage at 4 °C than other extenders. The role of oxidative stress and MMP are considerable in liquid storage.

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Bu Makaleye Atıf Yap

VARIŞLI, Ö., TAŞKIN, A., AKYOL, N. (2018). Effects of different extenders and additives on liquid storage of Awassi ram semen. Turkish Journal of Veterinary and Animal Sciences, Cilt: 42 - Sayı: 4, 230–242. https://ajindex.com/articles/121449

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Kaynakça (14)

  1. Salamon S, Maxwell WM. Storage of ram semen. Anim Reprod Sci 2000; 62: 77-111.
  2. Windsor DP, Szell AZ, Buschbeck C, Edward AY, Milton JTB, Buckrell BC. Transcervical artificial insemination of Australian merino ewes with frozen–thawed semen. Theriogenology 1994; 42: 147-157.
  3. Paulenz H, Adnoy T, Fossen OH, Söderquist L. Effect on field fertility of addition of gelatine, different dilution rates and storage times of cooled ram semen after vaginal insemination. Reprod Domest Anim 2010; 45: 706-710.
  4. Salamon S, Maxwell WMC. Frozen storage of ram semen II. Causes of low fertility after cervical insemination and methods of improvement. Anim Reprod Sci 1995; 38: 1-36. Epstein H. The Awassi sheep with special references to the improved dairy type. FAO Animal Production Health Paper 1985; 57: 141-158.
  5. Semerci A, Çelik AD. General overview of ovine breeding in Turkey. Journal of Agricultural Faculty of Mustafa Kemal University 2016; 21: 182-196.
  6. Pollott GE, Gootwine E. A genetic analysis of complete lactation milk production in improved Awassi sheep. Livest Prod Sci 2001; 71: 37-47.
  7. Johnson LA, Weitze KF, Fiser P, Maxwell WM. Storage of boar semen. Anim Reprod Sci 2000; 62: 143-172.
  8. Barbas JP, Mascarenhas RD. Cryopreservation of domestic animal sperm cells. Cell Tissue Bank 2009; 10: 49-62
  9. Batellier F, Vidament M, Fauquant J, Duchamp G, Arnaud G, Yvon JM, Magistrini M. Advances in cooled semen technology. Anim Reprod Sci 2001; 68: 181-190.
  10. Lopez-Saez A, Ortiz L, Gallego L, Garde JJ. Liquid storage (5°C) of ram semen in different diluents. Arch Andrology 2000; 44: 155-164.
  11. Province CA, Squires EL, Pickett BW, Amann RP. Cooling rates, storage temperatures, and fertility of extended equine spermatozoa. Theriogenology 1985; 23: 925-934. Aurich C. Factors affecting the plasma membrane function of cooled–stored stallion spermatozoa. Anim Reprod Sci 2005; 89: 65-75.
  12. Jones RC, Foote RH. Effect of osmolality and phosphate, TRIS, TES, MES, and HEPES hydrogen ion buffers on the motility of bull spermatozoa stored at 37 or 5 °C. Aust J Biol Sci 1972; 25: 1047-1055. Holt WV. Fundamental aspects of sperm cryobiology: the importance of species and individual differences. Theriogenology 2000; 53: 47-58.
  13. Si W, Benson JD, Men H, Critser JK. Osmotic tolerance limits and effects of cryoprotectants on the motility, plasma membrane integrity and acrosomal integrity of rat sperm. Cryobiology 2006; 53: 336-348.
  14. Varisli O, Uguz C, Agca C, Agca Y. Effect of chilling on the motility and acrosom