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Theriogenology2010; 75(5); 811-818; doi: 10.1016/j.theriogenology.2010.10.021

Fatty acids and plasmalogens of the phospholipids of the sperm membranes and their relation with the post-thaw quality of stallion spermatozoa.

Abstract: Fatty acids and plasmalogens were extracted from the phospholipids of the plasma membrane of stallion spermatozoa, to determine their relation with sperm quality after freezing and thawing. Sperm quality was rated using a quality index that combined the results of the analysis of sperm motility and velocity (CASA analysis), membrane status and mitochondrial membrane potential (flow cytometry) post thaw. Receiving operating system (ROC) curves were used to evaluate the value of specific lipid components of the sperm membrane herein studied as forecast of potential freezeability. From all parameters studied the ratio of percentage of C16 plasmalogens related to total phospholipids was the one with the better diagnostic value. For potentially bad freezers, the significant area under the ROC-curve was 0.74, with 75% sensitivity and 79.9% specificity for a cut off value of 26.9. Also the percentage of plasmalogens respect to total phospholipids gave good diagnostic value for bad freezers. On the other hand, the percentage of C18 fatty aldehydes related to total phospholipids of the sperm membrane properly forecasted freezeability with an area under the ROC curve of 0.70 with 70% sensitivity and 62.5% specificity for a cut off value of 0.32.
Publication Date: 2010-12-08 PubMed ID: 21144567DOI: 10.1016/j.theriogenology.2010.10.021Google Scholar: Lookup
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  • Journal Article

Summary

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The research investigates the relationship between certain fats and compounds in the cell membranes of stallion sperm and the sperm’s quality post-freezing and thawing process. The study identified that specific percentages of these substances could predict the sperm’s ability to endure freezing and thawing.

Overview of the Research

  • The researchers studied horse sperm, particularly focusing on the phospholipids of their plasma membranes – the outer boundary of the cell that controls what enters and exits.
  • There are two main substances they were interested in: fatty acids and plasmalogens, both of which are key components of these membranes.
  • Their goal was to understand whether there’s a connection between the ratios of these compounds and the sperm quality after freezing and thawing. This is vital since freezing sperm is a common method for preserving male fertility.

Methodology and Results

  • The researchers evaluated sperm quality using a combination of factors: the sperm’s movement and speed, the status of their membranes, and the potential of their mitochondrial membranes.
  • They used receiver operating characteristic (ROC) curves in their statistics to see how specific components (here, our target compounds in the membrane) could predict a positive outcome (here, the ability to survive freezing).
  • The most telling ratio found was the percentage of C16 plasmalogens relative to total phospholipids. In cases of potentially bad outcomes (e.g., low sperm viability after freezing), the significant region under the ROC curve was 0.74, indicating a fairly strong correlation.
  • Additionally, the percentage of C18 fatty aldehydes to total phospholipids could predict freezing viability, with a ROC curve area of 0.70.

Implications of the Study

  • The study lends a fresh perspective on the lipid composition of sperm membranes and its role in determining sperm quality after freezing and thawing.
  • Identifying the percentages of certain lipids that lead to higher or poorer quality sperm after freezing could help improve sperm freezing methods, which could ultimately have a significant impact on animal breeding and even human fertility treatments.

Cite This Article

APA
Macías García B, González Fernández L, Ortega Ferrusola C, Morillo Rodríguez A, Gallardo Bolaños JM, Rodríguez Martinez H, Tapia JA, Morcuende D, Peña FJ. (2010). Fatty acids and plasmalogens of the phospholipids of the sperm membranes and their relation with the post-thaw quality of stallion spermatozoa. Theriogenology, 75(5), 811-818. https://doi.org/10.1016/j.theriogenology.2010.10.021

Publication

ISSN: 1879-3231
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 75
Issue: 5
Pages: 811-818

Researcher Affiliations

Macías García, B
  • Veterinary Teaching Hospital, Laboratory of Equine Reproduction, University of Extremadura, Avd de Universidad s/n, Cáceres, Spain.
González Fernández, L
    Ortega Ferrusola, C
      Morillo Rodríguez, A
        Gallardo Bolaños, J M
          Rodríguez Martinez, H
            Tapia, J A
              Morcuende, D
                Peña, F J

                  MeSH Terms

                  • Animals
                  • Cell Membrane / chemistry
                  • Cell Membrane / physiology
                  • Cryopreservation / veterinary
                  • Fatty Acids / analysis
                  • Horses
                  • Hot Temperature
                  • Lipid Peroxidation
                  • Male
                  • Membrane Potential, Mitochondrial
                  • Phospholipids / chemistry
                  • Plasmalogens / analysis
                  • ROC Curve
                  • Semen Preservation / veterinary
                  • Sperm Motility
                  • Spermatozoa / physiology
                  • Spermatozoa / ultrastructure

                  Citations

                  This article has been cited 9 times.
                  1. Yuan C, Wang J, Lu W. Regulation of semen quality by fatty acids in diets, extender, and semen. Front Vet Sci 2023;10:1119153.
                    doi: 10.3389/fvets.2023.1119153pubmed: 37180054google scholar: lookup
                  2. Aguiar CS, Barros CHSC, Machado WM, Allaman IB, Leite AO, Barbosa LP, Snoeck PPDN. Effect of different concentrations of Trolox(®) in association with docosahexaenoic acid on equine semen freezing. Anim Reprod 2022;19(4):e20220010.
                    doi: 10.1590/1984-3143-AR2022-0010pubmed: 36504917google scholar: lookup
                  3. Gobato MLM, Segabinazzi LGTM, Scheeren VFC, Bandeira RS, Freitas-Dell'Aqua CP, Dell'Aqua JA Jr, Papa FO. Ability of donkey sperm to tolerate cooling: Effect of extender base and removal of seminal plasma on sperm parameters and fertility rates in mares. Front Vet Sci 2022;9:1011899.
                    doi: 10.3389/fvets.2022.1011899pubmed: 36225802google scholar: lookup
                  4. Catalán J, Yánez-Ortiz I, Tvarijonaviciute A, González-Aróstegui LG, Rubio CP, Barranco I, Yeste M, Miró J. Seminal Plasma Antioxidants Are Related to Sperm Cryotolerance in the Horse. Antioxidants (Basel) 2022 Jun 28;11(7).
                    doi: 10.3390/antiox11071279pubmed: 35883774google scholar: lookup
                  5. Shan S, Xu F, Hirschfeld M, Brenig B. Sperm Lipid Markers of Male Fertility in Mammals. Int J Mol Sci 2021 Aug 16;22(16).
                    doi: 10.3390/ijms22168767pubmed: 34445473google scholar: lookup
                  6. Peña FJ, O'Flaherty C, Ortiz Rodríguez JM, Martín Cano FE, Gaitskell-Phillips GL, Gil MC, Ortega Ferrusola C. Redox Regulation and Oxidative Stress: The Particular Case of the Stallion Spermatozoa. Antioxidants (Basel) 2019 Nov 19;8(11).
                    doi: 10.3390/antiox8110567pubmed: 31752408google scholar: lookup
                  7. Bodu M, Hitit M, Woldesenbet S, Uğur MR, Erdoğan Z, Greenwood OC, Murray RD, Cervantes AP, Memili E. Lipidomic Landscapes of Cryopreserved Sperm from Alpine and Spanish-Creole Bucks. Animals (Basel) 2025 Jun 27;15(13).
                    doi: 10.3390/ani15131897pubmed: 40646797google scholar: lookup
                  8. Catalán J, Yánez-Ortiz I, Torres-Garrido M, Ribas-Maynou J, Llavanera M, Barranco I, Yeste M, Miró J. Impact of Seminal Plasma Antioxidants on DNA Fragmentation and Lipid Peroxidation of Frozen-Thawed Horse Sperm. Antioxidants (Basel) 2024 Mar 6;13(3).
                    doi: 10.3390/antiox13030322pubmed: 38539855google scholar: lookup
                  9. Palazzese L, Turri F, Anzalone DA, Saragusty J, Bonnet J, Colotte M, Tuffet S, Pizzi F, Luciani A, Matsukawa K, Czernik M, Loi P. Reviving vacuum-dried encapsulated ram spermatozoa via ICSI after 2 years of storage. Front Vet Sci 2023;10:1270266.
                    doi: 10.3389/fvets.2023.1270266pubmed: 38098985google scholar: lookup