Effect of ß-glucan from Euglena gracilis as an antioxidant on goat semen cryopreservation
This study aimed to determine the influence of different doses of β-glucan on post-thaw spermatological parameters, lipid peroxidation, and total antioxidant activity of buck semen. In the non-breeding season, semen was collected from bucks twice weekly. After then, ejaculates were pooled and divide...
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Veröffentlicht in: | Journal of the Hellenic Veterinary Medical Society 2024-07, Vol.75 (2), p.7361-7370 |
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container_title | Journal of the Hellenic Veterinary Medical Society |
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creator | Ustuner, B Soylu, MK Sengul, E Karakci, D Gokce, E Aktar, A Ak Sonat, F Cimen, T Huraydin, O Yılmaz, MM Nur, Z |
description | This study aimed to determine the influence of different doses of β-glucan on post-thaw spermatological parameters, lipid peroxidation, and total antioxidant activity of buck semen.
In the non-breeding season, semen was collected from bucks twice weekly. After then, ejaculates were pooled and divided into four equal aliquots: β-glucan concentrations of 1 mM (βG1), 2 mM (βG2), and 4 mM (βG4), and a control group without antioxidants. Each sample group was diluted for cryopreservation using a dilution method involving two steps. The experimental groups were then evaluated for several parameters including sperm motility, plasma membrane functional integrity [hypoosmotic swelling test (HOST)], damaged acrosome rate [FITC-Pisum sativum agglutinin (FITC-PSA)], DNA integrity [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)], mitochondrial membrane potential using JC-1, evaluation of lipid peroxidation, and determination of total antioxidant activity.
The post-thaw motility and plasma functional integrity of the control group were significantly lower than those values in the βG groups (P < 0.05). Although the numerically greatest acrosome damage was detected in the control group, it was only statistically different from βG1 and βG4 (P |
doi_str_mv | 10.12681/jhvms.34504 |
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In the non-breeding season, semen was collected from bucks twice weekly. After then, ejaculates were pooled and divided into four equal aliquots: β-glucan concentrations of 1 mM (βG1), 2 mM (βG2), and 4 mM (βG4), and a control group without antioxidants. Each sample group was diluted for cryopreservation using a dilution method involving two steps. The experimental groups were then evaluated for several parameters including sperm motility, plasma membrane functional integrity [hypoosmotic swelling test (HOST)], damaged acrosome rate [FITC-Pisum sativum agglutinin (FITC-PSA)], DNA integrity [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)], mitochondrial membrane potential using JC-1, evaluation of lipid peroxidation, and determination of total antioxidant activity.
The post-thaw motility and plasma functional integrity of the control group were significantly lower than those values in the βG groups (P < 0.05). Although the numerically greatest acrosome damage was detected in the control group, it was only statistically different from βG1 and βG4 (P<0.05). While the DNA fragmentation rate of the control group was higher than βG4 group (P<0.05), it was similar to βG1 and βG2 groups (P>0.05). There was no statistical difference among all the groups regarding low mitochondrial membrane potential, MDA, and TAC rates.
In line with our results, supplementation of 1mM, 2 mM and 4 mM β-glucan to freezing extender improves the post-thaw spermatological characteristics of goat semen.</description><identifier>ISSN: 1792-2720</identifier><identifier>EISSN: 2585-3724</identifier><identifier>DOI: 10.12681/jhvms.34504</identifier><language>eng</language><ispartof>Journal of the Hellenic Veterinary Medical Society, 2024-07, Vol.75 (2), p.7361-7370</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-2975-2594 ; 0000-0001-5999-4685 ; 0000-0003-4918-0607 ; 0000-0002-1884-1874 ; 0000-0002-4125-6841 ; 0000-0002-3308-0778 ; 0000-0001-6050-791X ; 0000-0002-4690-1029 ; 0000-0002-7678-3289 ; 0000-0001-5280-9360 ; 0000-0002-1438-221X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ustuner, B</creatorcontrib><creatorcontrib>Soylu, MK</creatorcontrib><creatorcontrib>Sengul, E</creatorcontrib><creatorcontrib>Karakci, D</creatorcontrib><creatorcontrib>Gokce, E</creatorcontrib><creatorcontrib>Aktar, A</creatorcontrib><creatorcontrib>Ak Sonat, F</creatorcontrib><creatorcontrib>Cimen, T</creatorcontrib><creatorcontrib>Huraydin, O</creatorcontrib><creatorcontrib>Yılmaz, MM</creatorcontrib><creatorcontrib>Nur, Z</creatorcontrib><title>Effect of ß-glucan from Euglena gracilis as an antioxidant on goat semen cryopreservation</title><title>Journal of the Hellenic Veterinary Medical Society</title><description>This study aimed to determine the influence of different doses of β-glucan on post-thaw spermatological parameters, lipid peroxidation, and total antioxidant activity of buck semen.
In the non-breeding season, semen was collected from bucks twice weekly. After then, ejaculates were pooled and divided into four equal aliquots: β-glucan concentrations of 1 mM (βG1), 2 mM (βG2), and 4 mM (βG4), and a control group without antioxidants. Each sample group was diluted for cryopreservation using a dilution method involving two steps. The experimental groups were then evaluated for several parameters including sperm motility, plasma membrane functional integrity [hypoosmotic swelling test (HOST)], damaged acrosome rate [FITC-Pisum sativum agglutinin (FITC-PSA)], DNA integrity [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)], mitochondrial membrane potential using JC-1, evaluation of lipid peroxidation, and determination of total antioxidant activity.
The post-thaw motility and plasma functional integrity of the control group were significantly lower than those values in the βG groups (P < 0.05). Although the numerically greatest acrosome damage was detected in the control group, it was only statistically different from βG1 and βG4 (P<0.05). While the DNA fragmentation rate of the control group was higher than βG4 group (P<0.05), it was similar to βG1 and βG2 groups (P>0.05). There was no statistical difference among all the groups regarding low mitochondrial membrane potential, MDA, and TAC rates.
In line with our results, supplementation of 1mM, 2 mM and 4 mM β-glucan to freezing extender improves the post-thaw spermatological characteristics of goat semen.</description><issn>1792-2720</issn><issn>2585-3724</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNotkM1Kw0AURgdRsNTufIB5AKfObzJZSolaKLjRjZswuZ0bI0mmzKTFPo0P44sZonDgbD6-xSHkVvC1kJkV958fpz6tlTZcX5CFNNYwlUt9SRYiLySTueTXZJVSW3Nu8sJwKRbkvUT0MNKA9OebNd0R3EAxhp6Wx6bzg6NNdNB2baJuYpgY2_DV7ifTMNAmuJEm3_uBQjyHQ_TJx5ObNsMNuULXJb_695K8PZavm2e2e3nabh52DISUI1PcIfAMzN5ntQYjFGYZaglWqtopjchBFSiVRQu8QKwBa62RO4XWa1RLcvf3CzGkFD1Wh9j2Lp4rwas5TTWnqeY06hdCI1qi</recordid><startdate>20240710</startdate><enddate>20240710</enddate><creator>Ustuner, B</creator><creator>Soylu, MK</creator><creator>Sengul, E</creator><creator>Karakci, D</creator><creator>Gokce, E</creator><creator>Aktar, A</creator><creator>Ak Sonat, F</creator><creator>Cimen, T</creator><creator>Huraydin, O</creator><creator>Yılmaz, MM</creator><creator>Nur, Z</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2975-2594</orcidid><orcidid>https://orcid.org/0000-0001-5999-4685</orcidid><orcidid>https://orcid.org/0000-0003-4918-0607</orcidid><orcidid>https://orcid.org/0000-0002-1884-1874</orcidid><orcidid>https://orcid.org/0000-0002-4125-6841</orcidid><orcidid>https://orcid.org/0000-0002-3308-0778</orcidid><orcidid>https://orcid.org/0000-0001-6050-791X</orcidid><orcidid>https://orcid.org/0000-0002-4690-1029</orcidid><orcidid>https://orcid.org/0000-0002-7678-3289</orcidid><orcidid>https://orcid.org/0000-0001-5280-9360</orcidid><orcidid>https://orcid.org/0000-0002-1438-221X</orcidid></search><sort><creationdate>20240710</creationdate><title>Effect of ß-glucan from Euglena gracilis as an antioxidant on goat semen cryopreservation</title><author>Ustuner, B ; Soylu, MK ; Sengul, E ; Karakci, D ; Gokce, E ; Aktar, A ; Ak Sonat, F ; Cimen, T ; Huraydin, O ; Yılmaz, MM ; Nur, Z</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c122t-30afc06c5de6b4c513f66f42c823ba34ff0c39f238f8c09ffbcfb44f0a3f8e4f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Ustuner, B</creatorcontrib><creatorcontrib>Soylu, MK</creatorcontrib><creatorcontrib>Sengul, E</creatorcontrib><creatorcontrib>Karakci, D</creatorcontrib><creatorcontrib>Gokce, E</creatorcontrib><creatorcontrib>Aktar, A</creatorcontrib><creatorcontrib>Ak Sonat, F</creatorcontrib><creatorcontrib>Cimen, T</creatorcontrib><creatorcontrib>Huraydin, O</creatorcontrib><creatorcontrib>Yılmaz, MM</creatorcontrib><creatorcontrib>Nur, Z</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the Hellenic Veterinary Medical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ustuner, B</au><au>Soylu, MK</au><au>Sengul, E</au><au>Karakci, D</au><au>Gokce, E</au><au>Aktar, A</au><au>Ak Sonat, F</au><au>Cimen, T</au><au>Huraydin, O</au><au>Yılmaz, MM</au><au>Nur, Z</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of ß-glucan from Euglena gracilis as an antioxidant on goat semen cryopreservation</atitle><jtitle>Journal of the Hellenic Veterinary Medical Society</jtitle><date>2024-07-10</date><risdate>2024</risdate><volume>75</volume><issue>2</issue><spage>7361</spage><epage>7370</epage><pages>7361-7370</pages><issn>1792-2720</issn><eissn>2585-3724</eissn><abstract>This study aimed to determine the influence of different doses of β-glucan on post-thaw spermatological parameters, lipid peroxidation, and total antioxidant activity of buck semen.
In the non-breeding season, semen was collected from bucks twice weekly. After then, ejaculates were pooled and divided into four equal aliquots: β-glucan concentrations of 1 mM (βG1), 2 mM (βG2), and 4 mM (βG4), and a control group without antioxidants. Each sample group was diluted for cryopreservation using a dilution method involving two steps. The experimental groups were then evaluated for several parameters including sperm motility, plasma membrane functional integrity [hypoosmotic swelling test (HOST)], damaged acrosome rate [FITC-Pisum sativum agglutinin (FITC-PSA)], DNA integrity [terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL)], mitochondrial membrane potential using JC-1, evaluation of lipid peroxidation, and determination of total antioxidant activity.
The post-thaw motility and plasma functional integrity of the control group were significantly lower than those values in the βG groups (P < 0.05). Although the numerically greatest acrosome damage was detected in the control group, it was only statistically different from βG1 and βG4 (P<0.05). While the DNA fragmentation rate of the control group was higher than βG4 group (P<0.05), it was similar to βG1 and βG2 groups (P>0.05). There was no statistical difference among all the groups regarding low mitochondrial membrane potential, MDA, and TAC rates.
In line with our results, supplementation of 1mM, 2 mM and 4 mM β-glucan to freezing extender improves the post-thaw spermatological characteristics of goat semen.</abstract><doi>10.12681/jhvms.34504</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2975-2594</orcidid><orcidid>https://orcid.org/0000-0001-5999-4685</orcidid><orcidid>https://orcid.org/0000-0003-4918-0607</orcidid><orcidid>https://orcid.org/0000-0002-1884-1874</orcidid><orcidid>https://orcid.org/0000-0002-4125-6841</orcidid><orcidid>https://orcid.org/0000-0002-3308-0778</orcidid><orcidid>https://orcid.org/0000-0001-6050-791X</orcidid><orcidid>https://orcid.org/0000-0002-4690-1029</orcidid><orcidid>https://orcid.org/0000-0002-7678-3289</orcidid><orcidid>https://orcid.org/0000-0001-5280-9360</orcidid><orcidid>https://orcid.org/0000-0002-1438-221X</orcidid></addata></record> |
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title | Effect of ß-glucan from Euglena gracilis as an antioxidant on goat semen cryopreservation |
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