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Title: | Dietary polyunsaturated fatty acid supplementation improves the quality of stallion cryopreserved semen |
Keywords: | Cryopreservation Fertility Membrane integrity Spermatozoa motility Omega-3 |
Issue Date: | 2017 |
Publisher: | Elsevier |
Citation: | RODRIGUES, P. G. et al. Dietary polyunsaturated fatty acid supplementation improves the quality of stallion cryopreserved semen. Journal of Equine Veterinary Science, [S.l.], v. 54, p. 18-23, 2017. |
Abstract: | The objective was to assess the influence of polyunsaturated fatty acid supplementation on the quality of fresh, cooled, and frozen-thawed stallion semen. Ten stallions received their normal diet (control group) or normal diet plus 150 mL of polyunsaturated fatty acid (PUFA) linseed-based oil (PUFA group). Semen was collected every 15 days during 60 days. Stallions were reversed across the treatments after a sixty-day interval. Semen was evaluated at 2, 6, 12, and 24 hours after cooling and 24 hours after freezing. Motility (MOT), vigor, membrane viability, morphology, acrosome integrity, and osmotic tolerance test (OTT) were evaluated. In the frozen-thawed semen, sperm dynamic characteristics were analyzed by computer-assisted sperm analysis and thiobarbituric acid reactive substances (TBARs) determined. The effects of treatment, time, semen type, and their interactions were submitted to PROCMIX (SAS) and means compared by the Tukey test. There was no treatment effect on the quality of fresh and cooled semen. However, frozen-thawed semen MOT, vigor, and OTT were superior (P < .05) in control compared to PUFA group. An interactive effect of sample day by treatment was observed, such that, TBARs increased over time (P = .002) in the PUFA group after 15, 30, 45, and 60 days from the beginning of supplementation. Thus, sperm may become more susceptible to the reactive oxygen species, probably due to the incorporation of polyunsaturated fat in the cell membrane. The addition of PUFA-enriched oil may be an alternative for improving frozen-thawed semen quality by increasing its MOT and resistance to osmotic changes to which sperm cells are submitted during the freezing process. |
URI: | https://www.j-evs.com/article/S0737-0806(15)30101-5/abstract http://repositorio.ufla.br/jspui/handle/1/30303 |
Appears in Collections: | DZO - Artigos publicados em periódicos |
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