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26 Baobab oil supplemented extender preserves post-thaw bull sperm quality parameters
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The processes of semen cryopreservation and thawing affect sperm membrane integrity and motility and increases morphological defects as well as DNA damage. The most influential cause of this is oxidative stress. When endogenous antioxidant capacity of seminal plasma is reduced during the freeze-thawing process, plant extracts exhibiting strong antioxidant activity can be used as supplements for compensation. Baobab oil has gained interest because it is rich in powerful antioxidants, which could protect sperm cells from oxidative damage during cryopreservation. Our study aimed to assess the effects of baobab oil on post-thaw sperm quality parameters in an egg-yolk-based extender. Thirty semen ejaculates were collected from 15 Nguni bulls using an electro ejaculator. Semen samples were randomly allocated to control (no baobab oil), 20 μL (1%), 50 μL (2.5%), and 100 μL (5%) baobab oil per millilitre extender. Following dilution, semen samples were loaded into 0.25-mL semen straws, equilibrated for 4 h at 5°C, and transferred into a controlled rate programmable freezer. The frozen semen straws were stored in a liquid nitrogen tank (−196°C) until thawing. Semen straws were thawed (37°C/60 minutes) after 1 week of cryopreservation and analysed for (1) sperm motility using a computer-aided sperm analyser, (2) morphological defects and viability using eosin-nigrosin stain, (3) membrane integrity by hypo-osmotic swelling test, and (4) DNA integrity by terminal deoxynucleotidyl transferase dUTP nick end labelling assay. Data was analysed using analysis of variance. Treatment means were compared in relation to the control group by Dunnett's test. We found that supplementing semen extender with baobab oil at 1% significantly (P < 0.05) preserved sperm DNA integrity (88.3 ± 3.7) and membrane integrity (74.0 ± 4.2) when compared with the control group (71.7 ± 3.7 and 55.8 ± 4.4, respectively). Baobab oil supplementation either at 1% (5.9 ± 0.5), 2.5% (7.2 ± 0.5), or 5% (6.0 ± 0.5) significantly reduced sperm morphological defects compared with control (9.5 ± 0.5). Total motility (1% (72.7%), 2.5% (72.7%), 5% (71.9%), control (59.3%)) and viability (1% (79.1%), 2.5% (79.8%), 5% (77.8%), control (67.6%)) were also improved by supplementation; however, the difference was not significant. In conclusion, it was demonstrated that supplementing bull semen extender with 1% baobab oil protects sperm from morphological defects, maintains membrane integrity, as well as preserves sperm DNA. All the baobab oil supplementation levels preserved post-thaw bull-sperm quality parameters.
Title: 26 Baobab oil supplemented extender preserves post-thaw bull sperm quality parameters
Description:
The processes of semen cryopreservation and thawing affect sperm membrane integrity and motility and increases morphological defects as well as DNA damage.
The most influential cause of this is oxidative stress.
When endogenous antioxidant capacity of seminal plasma is reduced during the freeze-thawing process, plant extracts exhibiting strong antioxidant activity can be used as supplements for compensation.
Baobab oil has gained interest because it is rich in powerful antioxidants, which could protect sperm cells from oxidative damage during cryopreservation.
Our study aimed to assess the effects of baobab oil on post-thaw sperm quality parameters in an egg-yolk-based extender.
Thirty semen ejaculates were collected from 15 Nguni bulls using an electro ejaculator.
Semen samples were randomly allocated to control (no baobab oil), 20 μL (1%), 50 μL (2.
5%), and 100 μL (5%) baobab oil per millilitre extender.
Following dilution, semen samples were loaded into 0.
25-mL semen straws, equilibrated for 4 h at 5°C, and transferred into a controlled rate programmable freezer.
The frozen semen straws were stored in a liquid nitrogen tank (−196°C) until thawing.
Semen straws were thawed (37°C/60 minutes) after 1 week of cryopreservation and analysed for (1) sperm motility using a computer-aided sperm analyser, (2) morphological defects and viability using eosin-nigrosin stain, (3) membrane integrity by hypo-osmotic swelling test, and (4) DNA integrity by terminal deoxynucleotidyl transferase dUTP nick end labelling assay.
Data was analysed using analysis of variance.
Treatment means were compared in relation to the control group by Dunnett's test.
We found that supplementing semen extender with baobab oil at 1% significantly (P < 0.
05) preserved sperm DNA integrity (88.
3 ± 3.
7) and membrane integrity (74.
0 ± 4.
2) when compared with the control group (71.
7 ± 3.
7 and 55.
8 ± 4.
4, respectively).
Baobab oil supplementation either at 1% (5.
9 ± 0.
5), 2.
5% (7.
2 ± 0.
5), or 5% (6.
0 ± 0.
5) significantly reduced sperm morphological defects compared with control (9.
5 ± 0.
5).
Total motility (1% (72.
7%), 2.
5% (72.
7%), 5% (71.
9%), control (59.
3%)) and viability (1% (79.
1%), 2.
5% (79.
8%), 5% (77.
8%), control (67.
6%)) were also improved by supplementation; however, the difference was not significant.
In conclusion, it was demonstrated that supplementing bull semen extender with 1% baobab oil protects sperm from morphological defects, maintains membrane integrity, as well as preserves sperm DNA.
All the baobab oil supplementation levels preserved post-thaw bull-sperm quality parameters.
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