Cooling of porcine semen in an extender supplemented with isoespintanol

ABSTRACT: Spermatozoa experience oxidative, osmotic, chemical, and thermal stresses when cooled, which degrade the quality and fertilizing capacity of the cells. Adding antioxidants to the sperm extender mitigates these alterations. This study evaluated the effect of isoespintanol (ISO) on boar seme...

Full description

Bibliographic Details
Main Authors: Giovanni Restrepo Betancur, Kelly Vanessa Zapata, Paola Andrea Colorado Vidal, Yudith Sánchez, Benjamín Alberto Rojano
Format: Article
Language:English
Published: Universidade Federal de Santa Maria 2023-05-01
Series:Ciência Rural
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782023001100702&lng=en&tlng=en
_version_ 1797826195330433024
author Giovanni Restrepo Betancur
Kelly Vanessa Zapata
Paola Andrea Colorado Vidal
Yudith Sánchez
Benjamín Alberto Rojano
author_facet Giovanni Restrepo Betancur
Kelly Vanessa Zapata
Paola Andrea Colorado Vidal
Yudith Sánchez
Benjamín Alberto Rojano
author_sort Giovanni Restrepo Betancur
collection DOAJ
description ABSTRACT: Spermatozoa experience oxidative, osmotic, chemical, and thermal stresses when cooled, which degrade the quality and fertilizing capacity of the cells. Adding antioxidants to the sperm extender mitigates these alterations. This study evaluated the effect of isoespintanol (ISO) on boar semen subjected to cooling. Fifteen ejaculates from five boars (Susscrofadomestica) were extended in Beltsville thawing solution (BTS) supplemented with 0 µM (control), 5 µM (ISO5), 10 µM (ISO10), 15 µM (ISO15), 20 µM (ISO20), 25 µM (ISO25), and 30 µM (ISO30) of ISO, which were then cooled for five days at 16 °C. Sperm kinetics, total motility (TM), and progressive motility (PM) were evaluated every 24 h using an IVOS computer-assisted sperm analysis (CASA) system. On day 1 and day 5 of cooling, a hypoosmotic test, spectrofluorometry, and flow cytometry were performed to evaluate the following: membrane functionality, measured as a function of hypoosmotic swelling (HOS); total antioxidant capacity (TAC); reactive oxygen species (ROS); and mitochondrial membrane potential (Δ¥M). Regression analysis and comparison of means using the Duncan test were performed. The ISO added had a slight impact on sperm motility, as evidenced by a reduction in TM at 24 h of cooling (but not prior) with the addition of 20 µM of ISO. Similarly, no effect of the ISO on the kinetics and functional integrity of the sperm membrane was observed at 96 h of cooling; however, the regression coefficients indicated that the ISO lowered the rate of decrease in sperm motility and the proportion of rapid spermatozoa relative to the concentration of ISO used. The ISO did not affect the TAC of the cooled semen; however, different concentrations of ISO lowered ROS production in the semen after 96 h of cooling. ISO also impacted the Δ¥M of the spermatozoa at 0 h of cooling, increasing the proportion of low Δ¥M cells and decreasing the proportion of high Δ¥M cells. In conclusion, ISO can reduce the loss of quality and oxidative stress occurring in boar semen during cooling and can modulate the mitochondrial activity of sperm.
first_indexed 2024-03-13T11:05:08Z
format Article
id doaj.art-1ade886391de4631ad5cd7a096ad1f52
institution Directory Open Access Journal
issn 1678-4596
language English
last_indexed 2024-03-13T11:05:08Z
publishDate 2023-05-01
publisher Universidade Federal de Santa Maria
record_format Article
series Ciência Rural
spelling doaj.art-1ade886391de4631ad5cd7a096ad1f522023-05-16T07:34:28ZengUniversidade Federal de Santa MariaCiência Rural1678-45962023-05-01531110.1590/0103-8478cr20220508Cooling of porcine semen in an extender supplemented with isoespintanolGiovanni Restrepo Betancurhttps://orcid.org/0000-0002-8427-4433Kelly Vanessa Zapatahttps://orcid.org/0000-0002-3559-5783Paola Andrea Colorado Vidalhttps://orcid.org/0000-0002-9752-1800Yudith Sánchezhttps://orcid.org/0000-0001-8385-448XBenjamín Alberto Rojanohttps://orcid.org/0000-0003-3590-8046ABSTRACT: Spermatozoa experience oxidative, osmotic, chemical, and thermal stresses when cooled, which degrade the quality and fertilizing capacity of the cells. Adding antioxidants to the sperm extender mitigates these alterations. This study evaluated the effect of isoespintanol (ISO) on boar semen subjected to cooling. Fifteen ejaculates from five boars (Susscrofadomestica) were extended in Beltsville thawing solution (BTS) supplemented with 0 µM (control), 5 µM (ISO5), 10 µM (ISO10), 15 µM (ISO15), 20 µM (ISO20), 25 µM (ISO25), and 30 µM (ISO30) of ISO, which were then cooled for five days at 16 °C. Sperm kinetics, total motility (TM), and progressive motility (PM) were evaluated every 24 h using an IVOS computer-assisted sperm analysis (CASA) system. On day 1 and day 5 of cooling, a hypoosmotic test, spectrofluorometry, and flow cytometry were performed to evaluate the following: membrane functionality, measured as a function of hypoosmotic swelling (HOS); total antioxidant capacity (TAC); reactive oxygen species (ROS); and mitochondrial membrane potential (Δ¥M). Regression analysis and comparison of means using the Duncan test were performed. The ISO added had a slight impact on sperm motility, as evidenced by a reduction in TM at 24 h of cooling (but not prior) with the addition of 20 µM of ISO. Similarly, no effect of the ISO on the kinetics and functional integrity of the sperm membrane was observed at 96 h of cooling; however, the regression coefficients indicated that the ISO lowered the rate of decrease in sperm motility and the proportion of rapid spermatozoa relative to the concentration of ISO used. The ISO did not affect the TAC of the cooled semen; however, different concentrations of ISO lowered ROS production in the semen after 96 h of cooling. ISO also impacted the Δ¥M of the spermatozoa at 0 h of cooling, increasing the proportion of low Δ¥M cells and decreasing the proportion of high Δ¥M cells. In conclusion, ISO can reduce the loss of quality and oxidative stress occurring in boar semen during cooling and can modulate the mitochondrial activity of sperm.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782023001100702&lng=en&tlng=enantioxidantboarpreservationsemen qualityspermatozoa
spellingShingle Giovanni Restrepo Betancur
Kelly Vanessa Zapata
Paola Andrea Colorado Vidal
Yudith Sánchez
Benjamín Alberto Rojano
Cooling of porcine semen in an extender supplemented with isoespintanol
Ciência Rural
antioxidant
boar
preservation
semen quality
spermatozoa
title Cooling of porcine semen in an extender supplemented with isoespintanol
title_full Cooling of porcine semen in an extender supplemented with isoespintanol
title_fullStr Cooling of porcine semen in an extender supplemented with isoespintanol
title_full_unstemmed Cooling of porcine semen in an extender supplemented with isoespintanol
title_short Cooling of porcine semen in an extender supplemented with isoespintanol
title_sort cooling of porcine semen in an extender supplemented with isoespintanol
topic antioxidant
boar
preservation
semen quality
spermatozoa
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-84782023001100702&lng=en&tlng=en
work_keys_str_mv AT giovannirestrepobetancur coolingofporcinesemeninanextendersupplementedwithisoespintanol
AT kellyvanessazapata coolingofporcinesemeninanextendersupplementedwithisoespintanol
AT paolaandreacoloradovidal coolingofporcinesemeninanextendersupplementedwithisoespintanol
AT yudithsanchez coolingofporcinesemeninanextendersupplementedwithisoespintanol
AT benjaminalbertorojano coolingofporcinesemeninanextendersupplementedwithisoespintanol