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Effect of extender supplementation with low-molecular-weight antioxidants on selected quality parameters of cryopreserved canine spermatozoa

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07 juil. 2018
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Fig. 1

The effect of semen extender supplementation with different concentrations and combinations of Trolox (water-soluble vitamin E) and L-ascorbic acid (vitamin C) on the total motility of frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 20 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05
The effect of semen extender supplementation with different concentrations and combinations of Trolox (water-soluble vitamin E) and L-ascorbic acid (vitamin C) on the total motility of frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 20 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05

Fig. 2

The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on the progressive motility of frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05
The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on the progressive motility of frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05

Fig. 3

The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on plasma membrane integrity in frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05
The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on plasma membrane integrity in frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05

Fig. 4

The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on mitochondrial activity in frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05
The effect of semen extender supplementation with different concentrations of low-molecular-weight antioxidants on mitochondrial activity in frozen-thawed canine spermatozoa during 2 h of incubation. The presented values are means ±SD for 16 ejaculates from four dogs. Values marked with different letters (a, b) differ significantly at P ≤ 0.05