Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol

The study aimed to evaluate cryo-injury during the cryopreservation in <i>Sorubim cuspicaudus</i> sperm with ethylene glycol (EG) at different rates (6, 8, 10%). Fresh, prefrozen, and post-thawed sperm quality as motility total, velocities, mitochondria damage (Mit-d), membrane damage (M...

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Main Authors: Víctor Atencio-García, Denia Padilla-Izquierdo, Juana Robles-González, Martha Prieto-Guevara, Sandra Pardo-Carrasco, José Espinosa-Araujo
Format: Article
Language:English
Published: MDPI AG 2023-01-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/13/2/235
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author Víctor Atencio-García
Denia Padilla-Izquierdo
Juana Robles-González
Martha Prieto-Guevara
Sandra Pardo-Carrasco
José Espinosa-Araujo
author_facet Víctor Atencio-García
Denia Padilla-Izquierdo
Juana Robles-González
Martha Prieto-Guevara
Sandra Pardo-Carrasco
José Espinosa-Araujo
author_sort Víctor Atencio-García
collection DOAJ
description The study aimed to evaluate cryo-injury during the cryopreservation in <i>Sorubim cuspicaudus</i> sperm with ethylene glycol (EG) at different rates (6, 8, 10%). Fresh, prefrozen, and post-thawed sperm quality as motility total, velocities, mitochondria damage (Mit-d), membrane damage (Mem-d), and DNA fragmentation (DNA-f), were examined. The Mit-d, Mem-d, and DNA-f were evaluated through flow cytometry. High motility (>95%) and a low percentage of Mem-d (1.0 ± 0.5%), Mit-d (1.4 ± 0.9%), and DNA-f (2.4 ± 0.8%) were recorded for fresh semen. Prefrozen semen increases in Mit-d and DNA-f were observed compared to fresh semen (<i>p</i> < 0.05). In thawed semen, increased Mit-d (2.6 to 3-fold), Mem-d (6 to 1-fold), and DNA-f (3.3 to 6.6-fold) compared to prefrozen was observed. Thawed semen showed Mit-d (34 to 37-fold), Mem-d (24.5 to 26.6-fold) and DNA-f (13 to 18.5-fold) increased high. In conclusion, the present study demonstrated that mitochondria, membrane, and DNA integrity undergo significant damage during both pre-freezing and freezing/thawing with EG inclusion percentages from 6 to 10% that affect its fertilizing capacity, which is reduced to half of that obtained with fresh semen. It is suggested that a cryoprotective solution composed of 6% EG, 6% glucose, and 5% skimmed milk powder is a useful protocol for the cryopreservation of <i>S. cuspicaudus</i> semen.
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spelling doaj.art-b134eb9cdea44558bf716021a4dc56b22023-11-30T20:53:06ZengMDPI AGAnimals2076-26152023-01-0113223510.3390/ani13020235Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene GlycolVíctor Atencio-García0Denia Padilla-Izquierdo1Juana Robles-González2Martha Prieto-Guevara3Sandra Pardo-Carrasco4José Espinosa-Araujo5CINPIC, Fishculture Research Institute, School of Veterinary Medicine and Zootechnics, Department of Aquaculture Sciences, University of Córdoba, Montería 230002, ColombiaSchool of Basic Sciences, Department of Biology, University of Córdoba, Montería 230002, ColombiaSchool of Basic Sciences, Department of Mathematics and Statistics, Universidad de Córdoba, Montería 230002, ColombiaCINPIC, Fishculture Research Institute, School of Veterinary Medicine and Zootechnics, Department of Aquaculture Sciences, University of Córdoba, Montería 230002, ColombiaSchool of Agricultural Sciences, Department of Animal Husbandry, National University of Colombia, Medellín 050034, ColombiaCINPIC, Fishculture Research Institute, School of Veterinary Medicine and Zootechnics, Department of Aquaculture Sciences, University of Córdoba, Montería 230002, ColombiaThe study aimed to evaluate cryo-injury during the cryopreservation in <i>Sorubim cuspicaudus</i> sperm with ethylene glycol (EG) at different rates (6, 8, 10%). Fresh, prefrozen, and post-thawed sperm quality as motility total, velocities, mitochondria damage (Mit-d), membrane damage (Mem-d), and DNA fragmentation (DNA-f), were examined. The Mit-d, Mem-d, and DNA-f were evaluated through flow cytometry. High motility (>95%) and a low percentage of Mem-d (1.0 ± 0.5%), Mit-d (1.4 ± 0.9%), and DNA-f (2.4 ± 0.8%) were recorded for fresh semen. Prefrozen semen increases in Mit-d and DNA-f were observed compared to fresh semen (<i>p</i> < 0.05). In thawed semen, increased Mit-d (2.6 to 3-fold), Mem-d (6 to 1-fold), and DNA-f (3.3 to 6.6-fold) compared to prefrozen was observed. Thawed semen showed Mit-d (34 to 37-fold), Mem-d (24.5 to 26.6-fold) and DNA-f (13 to 18.5-fold) increased high. In conclusion, the present study demonstrated that mitochondria, membrane, and DNA integrity undergo significant damage during both pre-freezing and freezing/thawing with EG inclusion percentages from 6 to 10% that affect its fertilizing capacity, which is reduced to half of that obtained with fresh semen. It is suggested that a cryoprotective solution composed of 6% EG, 6% glucose, and 5% skimmed milk powder is a useful protocol for the cryopreservation of <i>S. cuspicaudus</i> semen.https://www.mdpi.com/2076-2615/13/2/235cryodamageplasma membranemitochondriaDNA fragmentationreproduction
spellingShingle Víctor Atencio-García
Denia Padilla-Izquierdo
Juana Robles-González
Martha Prieto-Guevara
Sandra Pardo-Carrasco
José Espinosa-Araujo
Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
Animals
cryodamage
plasma membrane
mitochondria
DNA fragmentation
reproduction
title Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
title_full Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
title_fullStr Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
title_full_unstemmed Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
title_short Damage to <i>Sorubim cuspicaudus</i> Sperm Cryopreserved with Ethylene Glycol
title_sort damage to i sorubim cuspicaudus i sperm cryopreserved with ethylene glycol
topic cryodamage
plasma membrane
mitochondria
DNA fragmentation
reproduction
url https://www.mdpi.com/2076-2615/13/2/235
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