
Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility andin vitrofertilization in bovine epididymal sperm
- Author
- M Nichi, Tom Rijsselaere (UGent) , JDA Losano, DSR Angrimani, GKV Kawai, IGF Goovaerts, Ann Van Soom (UGent) , VH Barnabe, JBP De Clercq and PEJ Bols
- Organization
- Abstract
- The maintaining of the epididymis at lower temperatures during storage and transport improves sperm quality. Our study aimed to test whether epididymis storage temperature (post-mortem) and sperm cryopreservation affect sperm kinetics, membrane integrity, mitochondrial potential and fertility capacity. Thirty-six epididymides were collected from 18 bulls after slaughter and divided into two groups: at 4 or 34 degrees C for 2-3hr. The sperm was collected from the epididymis cauda. The evaluation consisted of computer-assisted sperm analysis (CASA), SYBR14/PI/JC1 to evaluate membrane integrity, mitochondrial membrane potential (MMP) and measurement of lipid peroxidation (TBARS). The sperm was then frozen using an automatic device. After thawing, sperm samples were evaluated by the same variables and further in vitro fertilization rates. Cryopreservation negatively affected sperm motility in samples stored at 4 and 34 degrees C. Nevertheless, the 4 degrees C samples yielded higher rates of blastocyst formation. Pre-freeze sperm motility, progressive motility and velocity were higher in sperm from epididymis stored at 4 degrees C while post-thaw sperm motility, progressive motility and velocity remained the same among samples from epididymis stored at 4 or 34 degrees C. However, with regard to the kinetic patterns, samples collected from epididymis stored at 34 degrees C had lower values when compared to those stored at 4 degrees C prior the cryopreservation process. Our results indicate that epididymis handling conditions after cryopreservation may affect sperm quality after thawing, especially due to compromised MMP in sperm collected from epididymis stored at higher temperatures.
- Keywords
- bulls, epididymides sperm, JC-1, reactive oxygen species, thiobarbituric acid-reactive substances, RED DEER, OXIDATIVE STRESS, SEMINAL PLASMA, SEMEN QUALITY, SPERMATOZOA, POSTMORTEM, VIABILITY, RECOVERY, BULL, 4-DEGREES-C
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8526922
- MLA
- Nichi, M., et al. “Evaluation of Epididymis Storage Temperature and Cryopreservation Conditions for Improved Mitochondrial Membrane Potential, Membrane Integrity, Sperm Motility Andin Vitrofertilization in Bovine Epididymal Sperm.” REPRODUCTION IN DOMESTIC ANIMALS, vol. 52, no. 2, 2017, pp. 257–63, doi:10.1111/rda.12888.
- APA
- Nichi, M., Rijsselaere, T., Losano, J., Angrimani, D., Kawai, G., Goovaerts, I., … Bols, P. (2017). Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility andin vitrofertilization in bovine epididymal sperm. REPRODUCTION IN DOMESTIC ANIMALS, 52(2), 257–263. https://doi.org/10.1111/rda.12888
- Chicago author-date
- Nichi, M, Tom Rijsselaere, JDA Losano, DSR Angrimani, GKV Kawai, IGF Goovaerts, Ann Van Soom, VH Barnabe, JBP De Clercq, and PEJ Bols. 2017. “Evaluation of Epididymis Storage Temperature and Cryopreservation Conditions for Improved Mitochondrial Membrane Potential, Membrane Integrity, Sperm Motility Andin Vitrofertilization in Bovine Epididymal Sperm.” REPRODUCTION IN DOMESTIC ANIMALS 52 (2): 257–63. https://doi.org/10.1111/rda.12888.
- Chicago author-date (all authors)
- Nichi, M, Tom Rijsselaere, JDA Losano, DSR Angrimani, GKV Kawai, IGF Goovaerts, Ann Van Soom, VH Barnabe, JBP De Clercq, and PEJ Bols. 2017. “Evaluation of Epididymis Storage Temperature and Cryopreservation Conditions for Improved Mitochondrial Membrane Potential, Membrane Integrity, Sperm Motility Andin Vitrofertilization in Bovine Epididymal Sperm.” REPRODUCTION IN DOMESTIC ANIMALS 52 (2): 257–263. doi:10.1111/rda.12888.
- Vancouver
- 1.Nichi M, Rijsselaere T, Losano J, Angrimani D, Kawai G, Goovaerts I, et al. Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility andin vitrofertilization in bovine epididymal sperm. REPRODUCTION IN DOMESTIC ANIMALS. 2017;52(2):257–63.
- IEEE
- [1]M. Nichi et al., “Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility andin vitrofertilization in bovine epididymal sperm,” REPRODUCTION IN DOMESTIC ANIMALS, vol. 52, no. 2, pp. 257–263, 2017.
@article{8526922, abstract = {{The maintaining of the epididymis at lower temperatures during storage and transport improves sperm quality. Our study aimed to test whether epididymis storage temperature (post-mortem) and sperm cryopreservation affect sperm kinetics, membrane integrity, mitochondrial potential and fertility capacity. Thirty-six epididymides were collected from 18 bulls after slaughter and divided into two groups: at 4 or 34 degrees C for 2-3hr. The sperm was collected from the epididymis cauda. The evaluation consisted of computer-assisted sperm analysis (CASA), SYBR14/PI/JC1 to evaluate membrane integrity, mitochondrial membrane potential (MMP) and measurement of lipid peroxidation (TBARS). The sperm was then frozen using an automatic device. After thawing, sperm samples were evaluated by the same variables and further in vitro fertilization rates. Cryopreservation negatively affected sperm motility in samples stored at 4 and 34 degrees C. Nevertheless, the 4 degrees C samples yielded higher rates of blastocyst formation. Pre-freeze sperm motility, progressive motility and velocity were higher in sperm from epididymis stored at 4 degrees C while post-thaw sperm motility, progressive motility and velocity remained the same among samples from epididymis stored at 4 or 34 degrees C. However, with regard to the kinetic patterns, samples collected from epididymis stored at 34 degrees C had lower values when compared to those stored at 4 degrees C prior the cryopreservation process. Our results indicate that epididymis handling conditions after cryopreservation may affect sperm quality after thawing, especially due to compromised MMP in sperm collected from epididymis stored at higher temperatures.}}, author = {{Nichi, M and Rijsselaere, Tom and Losano, JDA and Angrimani, DSR and Kawai, GKV and Goovaerts, IGF and Van Soom, Ann and Barnabe, VH and De Clercq, JBP and Bols, PEJ}}, issn = {{0936-6768}}, journal = {{REPRODUCTION IN DOMESTIC ANIMALS}}, keywords = {{bulls,epididymides sperm,JC-1,reactive oxygen species,thiobarbituric acid-reactive substances,RED DEER,OXIDATIVE STRESS,SEMINAL PLASMA,SEMEN QUALITY,SPERMATOZOA,POSTMORTEM,VIABILITY,RECOVERY,BULL,4-DEGREES-C}}, language = {{eng}}, number = {{2}}, pages = {{257--263}}, title = {{Evaluation of epididymis storage temperature and cryopreservation conditions for improved mitochondrial membrane potential, membrane integrity, sperm motility andin vitrofertilization in bovine epididymal sperm}}, url = {{http://doi.org/10.1111/rda.12888}}, volume = {{52}}, year = {{2017}}, }
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