Abstract

In this study, the effect of conjugated linoleic acid (10trans, 12cis) (CLA) on refrigerated boar sperm quality parameters up to 14days at 17°C was assessed. Semen was extended in Androhep and divided into four treatments supplemented with CLA (25, 50, 100 and 200μm) and control group, then kept for 2h at 22°C. Afterwards an aliquot of each treatment was removed, and mitochondrial activity, viability, lipid membrane peroxidation (LPO) and stability of the sperm plasma membrane were assessed by flow cytometry. The remaining extended semen was maintained at 17°C until 336h, repeating the same analysis every 48h. Regarding percentage of live spermatozoa, no statistical differences were observed among treatments up to 96h. After this time, viability decreased significantly (p<0.05) for CLA concentrations of 100 and 200μm. Despite these results, there was an individual response to CLA. Although in the control group, the boar A presented better results when compared with the other boars, especially at concentrations of 50 and 100μm boar B showed significantly higher results (p<0.05). Supplementation with CLA improved (p<0.05) LPO, but not the mitochondrial membrane potential of sperm. The highest two CLA concentrations showed to be toxic for sperm as all results were lower than the observed for the control. In conclusion, CLA at 50μm seems to be an efficient concentration for reducing the oxidative stress, decreasing LPO, maintaining viability, membrane stability and mitochondrial potential on refrigerated boar spermatozoa.

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