Lipid peroxidation, assessed with BODIPY-C11, increases after cryopreservation of stallion spermatozoa, is stallion-dependent and is related to apoptotic-like changes.
Abstract: Lipid peroxidation (LPO) of stallion spermatozoa was assessed in fresh semen and in samples of the same ejaculates after freezing and thawing. Particular attention was paid to individual differences in the susceptibility to LPO and its possible relationship with freezability. Innate levels of LPO were very low in fresh spermatozoa but increased after thawing, a change that was largely stallion-dependent. The level of LPO in fresh spermatozoa was not correlated with that of the thawed spermatozoa. Negative correlations existed between LPO and intact membranes post-thaw (r=-0.789, P<0.001), and also between LPO and spermatozoa with high mitochondrial membrane potential (Deltapsim) post-thaw (r=-0.689, P<0.001). LPO was also highly and significantly correlated with caspase activity. The correlation between caspase activity in ethidium positive cells and LPO was r=0.772, P<0.001. This LPO is unlikely to represent, per se, a sign of cryopreservation-induced injury, but it is apparently capable of triggering 'apoptotic-like changes' that could result in the sub-lethal cryodamage often seen among surviving spermatozoa.
Publication Date: 2009-04-20 PubMed ID: 19380427DOI: 10.1530/REP-08-0484Google Scholar: Lookup
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- Journal Article
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- Non-U.S. Gov't
Summary
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The research investigates how lipid peroxidation (LPO), which damages sperm cells, increases after the freezing and thawing process (cryopreservation) of stallion sperm. It shows that this increase varies depending on the individual stallion and may cause changes similar to apoptosis, a type of cell death, which could impact the survival rate of sperm cells after cryopreservation.
Understanding Lipid Peroxidation in Spermatozoa
- The researchers focused on lipid peroxidation (LPO) in stallion sperm cells. LPO is a process that damages cell membranes, leading to cell dysfunction or death.
- LPO was assessed both in freshly ejaculated sperm and again after the sperm had undergone freezing and thawing—a common practice in animal breeding called cryopreservation.
- The initial levels of LPO in fresh sperm were very low but significantly increased after thawing. This indicates that the freezing and thawing process may contribute to sperm damage.
Individual Differences and Correlations
- This increase in LPO after thawing was largely dependent on the individual stallion, indicating that some stallions’ sperm may be more susceptible to damage from the cryopreservation process than others.
- No correlation was found between the levels of LPO in fresh sperm and that of thawed sperm. This suggests that the susceptibility of sperm cells to LPO during cryopreservation may not be predicted by the level of LPO in fresh sperm.
- Negative correlations were observed between LPO and traits indicating healthy and functional sperm cells—such as intact membranes and high mitochondrial membrane potential—after thawing.
LPO, Caspase Activity, and ‘Apoptotic-like’ Changes
- The researchers discovered a significant correlation between LPO and caspase activity, an indicator of cell death. Specifically, they noted that LPO may be capable of triggering ‘apoptotic-like changes’ in sperm cells.
- Apoptosis is a programmed cell death process that occurs naturally in the body to eliminate damaged or unnecessary cells. However, in the case of spermatozoa, these ‘apoptotic-like changes’ could explain the sub-lethal cryodamage often seen among surviving sperm after cryopreservation.
- Though the research confirms the increase of LPO post-thaw, it suggests that LPO itself may not be a sign of cryopreservation-induced injury. Instead, it could be a potential triggering mechanism for these ‘apoptotic-like changes’ that result in sperm cell damage post-thaw.
Cite This Article
APA
Ortega Ferrusola C, González Fernández L, Morrell JM, Salazar Sandoval C, Macías García B, Rodríguez-Martinez H, Tapia JA, Peña FJ.
(2009).
Lipid peroxidation, assessed with BODIPY-C11, increases after cryopreservation of stallion spermatozoa, is stallion-dependent and is related to apoptotic-like changes.
Reproduction, 138(1), 55-63.
https://doi.org/10.1530/REP-08-0484 Publication
Researcher Affiliations
- Section of Reproduction and Obstetrics, Laboratory of Spermatology, Department of Herd Health and Medicine, Veterinary Teaching Hospital, University of Extremadura, Avda de la Universidad s/n, Cáceres 10071, Spain.
MeSH Terms
- Animals
- Apoptosis
- Boron Compounds
- Carbon Radioisotopes
- Caspases / metabolism
- Cell Survival
- Cryopreservation / veterinary
- Flow Cytometry
- Fluorescent Dyes
- Glutathione Peroxidase / metabolism
- Horses
- Lipid Peroxidation
- Male
- Membrane Potential, Mitochondrial
- Microscopy, Fluorescence
- Semen Preservation / adverse effects
- Semen Preservation / veterinary
- Spermatozoa / metabolism
- Spermatozoa / pathology
- Superoxide Dismutase / metabolism
Citations
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