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Reproduction in domestic animals = Zuchthygiene2010; 46(1); 141-148; doi: 10.1111/j.1439-0531.2010.01609.x

Membrane lipids of the stallion spermatozoon in relation to sperm quality and susceptibility to lipid peroxidation.

Abstract: Lipids were extracted from ejaculated spermatozoa from seven individual stallions to distinguish neutral lipids (NL) and polar lipids (PL) and determine their variation among stallions and their relationship with sperm quality and sperm susceptibility to lipid peroxidation. The isolated fatty acids were correlated with sperm quality (membrane integrity, mitochondrial membrane potential (ΔΨm) and expression of active caspases) and the sensitivity of the sperm plasma membrane to LPO. The miristic (C14: 0), palmitic (C16: 0), stearic (C18: 0) and oleic (C18: 1n9) acids were predominant among the NLs. Within the phospholipid fraction, the docosapentanoic acid (C22: 5n6) was dominant, albeit varying among stallions. Surprisingly, the percentage of polyunsaturated fatty acids was positively correlated with sperm quality and a low propensity for LPO, probably because these particular fatty acids provide a higher fluidity of the plasma membrane. The stallion showing the poorest sperm membrane integrity plus a high level of LPO in his ejaculate had a lower percentage (p<0.05) of this fatty acid in his sperm plasma membranes.
Publication Date: 2010-05-12 PubMed ID: 20456666DOI: 10.1111/j.1439-0531.2010.01609.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article examines the connection between the lipid composition of stallion sperm cells and their quality, as well as susceptibility to lipid peroxidation (LPO).

Research Methodology

  • The study worked with sperm samples extracted from seven individual stallions.
  • Researchers isolated neutral lipids (NL) and polar lipids (PL) from these samples, and analyzed their variations across different stallions.
  • This analysis was then examined in relation to key indicators of sperm quality, namely membrane integrity, mitochondrial membrane potential, and the expression of active caspases.
  • They also looked at how the lipid composition affected a sperm cell’s susceptibility to lipid peroxidation (LPO), a process that can damage cell structures by oxidizing the lipids in the cell membrane.

Key Findings

  • Within the sperm sample lipids, certain types of fatty acids were found to be dominant, namely miristic (C14: 0), palmitic (C16: 0), stearic (C18: 0) and oleic (C18: 1n9) acids in the neutral lipids, and docosapentanoic acid (C22: 5n6) in the phospholipid fraction.
  • The docosapentanoic acid, however, showed variation among different stallions.
  • Interestingly, the researchers found a positive correlation between a higher percentage of polyunsaturated fatty acids and better sperm quality, along with a lower tendency for LPO.
  • This is attributed to the higher fluidity provided to the plasma membrane by these specific fatty acids.
  • Conversely, the stallion with the worst sperm membrane integrity and high LPO levels in his ejaculate had a noticeably lower percentage of this fatty acid in his sperm plasma membranes.

Implications and Conclusions

  • This study suggests that the lipid constitution of stallion sperm plays a vital role in determining their quality and their vulnerability to lipid peroxidation.
  • The specific positive role of polyunsaturated fatty acids could encourage further research into dietary or supplement solutions to improve equine reproductive success.
  • However, the evident variation in lipid composition among different stallions might point towards the need for individualized approaches to managing stallion fertility.

Cite This Article

APA
García BM, Fernández LG, Ferrusola CO, Salazar-Sandoval C, Rodríguez AM, Martinez HR, Tapia JA, Morcuende D, Peña FJ. (2010). Membrane lipids of the stallion spermatozoon in relation to sperm quality and susceptibility to lipid peroxidation. Reprod Domest Anim, 46(1), 141-148. https://doi.org/10.1111/j.1439-0531.2010.01609.x

Publication

ISSN: 1439-0531
NlmUniqueID: 9015668
Country: Germany
Language: English
Volume: 46
Issue: 1
Pages: 141-148

Researcher Affiliations

García, B Macías
  • Veterinary Teaching Hospital, Laboratory of Spermatology, University of Extremadura, Cáceres, Spain.
Fernández, L González
    Ferrusola, C Ortega
      Salazar-Sandoval, C
        Rodríguez, A Morillo
          Martinez, H Rodríguez
            Tapia, J A
              Morcuende, D
                Peña, F J

                  MeSH Terms

                  • Animals
                  • Caspases / metabolism
                  • Cell Membrane / chemistry
                  • Cell Membrane / ultrastructure
                  • Fatty Acids / analysis
                  • Horses
                  • Lipid Peroxidation
                  • Male
                  • Membrane Fluidity
                  • Membrane Lipids / analysis
                  • Membrane Potential, Mitochondrial
                  • Spermatozoa / chemistry
                  • Spermatozoa / physiology
                  • Spermatozoa / ultrastructure

                  Citations

                  This article has been cited 22 times.
                  1. Qin C, Lu G, Lin X, Wang Z, Yang S, Teng L, Lin X, Li F, Huang S, Hu C. Supplementation of Trimethylamine N-Oxide or Betaine in Semen Improves Quality of Boar Spermatozoa Stored at 17 °C Following Hydrostatic Pressure Stress. Life (Basel) 2025 Oct 15;15(10).
                    doi: 10.3390/life15101606pubmed: 41157279google scholar: lookup
                  2. 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
                  3. Meng DD, Kang YD, Chang DH. Research progress on the adverse effects of high-altitude environment to the male reproductive system: a review study. Front Endocrinol (Lausanne) 2025;16:1573502.
                    doi: 10.3389/fendo.2025.1573502pubmed: 40438393google scholar: lookup
                  4. Martínez-Torres M, Sánchez-Rivera UÁ, Medrano A, Hernández-Gónzalez EO, Dávila-Govantes R, Castro-Camacho YJ, Cruz-Cano NB. Semen Evaluation from Dominant Males of the Viviparous Mexican Lizard Sceloporus torquatus, Wiegmann, 1828 (Sauria: Phrynosomatidae). Vet Sci 2025 Apr 13;12(4).
                    doi: 10.3390/vetsci12040363pubmed: 40284865google scholar: lookup
                  5. Song M, Jia B, Dai D, Xu X, Cao J, Guo J, Wang L, Zhong T, Zhan S, Li L, Zhang H. Effect of chitosan on buck semen quality and semen plasma metabolites during low-temperature storage. Front Vet Sci 2025;12:1544234.
                    doi: 10.3389/fvets.2025.1544234pubmed: 40151569google scholar: lookup
                  6. Anastas ZM, Silla AJ, Byrne PG, Hobbs RJ, McFadden MS, Daly J, O'Brien JK. Effect of Bovine Serum Albumin (BSA) Concentration on Cryopreservation of Booroolong Frog Sperm with Evaluation of Post-Thaw Motility in Caffeine. Vet Sci 2025 Jan 8;12(1).
                    doi: 10.3390/vetsci12010030pubmed: 39852905google scholar: lookup
                  7. Xu Z, Yang Z, Bao L, Lu B, Li X, Zhan X, Huang X, Liu Y. Coenzyme Q10 Improves the Post-Thaw Sperm Quality in Dwarf Surfclam Mulinia lateralis. Antioxidants (Basel) 2024 Sep 4;13(9).
                    doi: 10.3390/antiox13091085pubmed: 39334744google scholar: lookup
                  8. Berean DI, Bogdan LM, Cimpean R. Advancements in Understanding and Enhancing Antioxidant-Mediated Sperm Cryopreservation in Small Ruminants: Challenges and Perspectives. Antioxidants (Basel) 2024 May 21;13(6).
                    doi: 10.3390/antiox13060624pubmed: 38929062google scholar: lookup
                  9. Mogielnicka-Brzozowska M, Cichowska AW. Molecular Biomarkers of Canine Reproductive Functions. Curr Issues Mol Biol 2024 Jun 17;46(6):6139-6168.
                    doi: 10.3390/cimb46060367pubmed: 38921038google scholar: lookup
                  10. Prochowska S, Bonarska-Kujawa D, Bobak Ł, Eberhardt M, Niżański W. Fatty acid composition and biophysical characteristics of the cell membrane of feline spermatozoa. Sci Rep 2024 May 3;14(1):10214.
                    doi: 10.1038/s41598-024-61006-5pubmed: 38702489google scholar: lookup
                  11. Di Nisio A, De Toni L, Sabovic I, Vignoli A, Tenori L, Dall'Acqua S, Sut S, La Vignera S, Condorelli RA, Giacone F, Ferlin A, Foresta C, Garolla A. Lipidomic Profile of Human Sperm Membrane Identifies a Clustering of Lipids Associated with Semen Quality and Function. Int J Mol Sci 2023 Dec 25;25(1).
                    doi: 10.3390/ijms25010297pubmed: 38203468google scholar: lookup
                  12. Pasciu V, Nieddu M, Sotgiu FD, Baralla E, Berlinguer F. An Overview on Assay Methods to Quantify ROS and Enzymatic Antioxidants in Erythrocytes and Spermatozoa of Small Domestic Ruminants. Animals (Basel) 2023 Jul 13;13(14).
                    doi: 10.3390/ani13142300pubmed: 37508077google scholar: lookup
                  13. Prasinou P, De Amicis I, Fusaro I, Bucci R, Cavallini D, Parrillo S, Caputo M, Gramenzi A, Carluccio A. The Lipidomics of Spermatozoa and Red Blood Cells Membrane Profile of Martina Franca Donkey: Preliminary Evaluation. Animals (Basel) 2022 Dec 20;13(1).
                    doi: 10.3390/ani13010008pubmed: 36611618google scholar: lookup
                  14. Sánchez-Rivera UÁ, Medrano A, Cruz-Cano NB, Alcántar-Rodríguez A, Dávila-Govantes R, Castro-Camacho YJ, Martínez-Torres M. Implementation of a method for sperm cryopreservation in sceloporine lizards. Conserv Physiol 2022;10(1):coac068.
                    doi: 10.1093/conphys/coac068pubmed: 36382339google scholar: lookup
                  15. Jakop U, Müller K, Müller P, Neuhauser S, Callealta Rodríguez I, Grunewald S, Schiller J, Engel KM. Seminal lipid profiling and antioxidant capacity: A species comparison. PLoS One 2022;17(3):e0264675.
                    doi: 10.1371/journal.pone.0264675pubmed: 35259184google scholar: lookup
                  16. Pintus E, Ros-Santaella JL. Impact of Oxidative Stress on Male Reproduction in Domestic and Wild Animals. Antioxidants (Basel) 2021 Jul 20;10(7).
                    doi: 10.3390/antiox10071154pubmed: 34356386google scholar: lookup
                  17. Evans HC, Dinh TTN, Ugur MR, Hitit M, Sajeev D, Kaya A, Topper E, Nicodemus MC, Smith GD, Memili E. Lipidomic markers of sperm cryotolerance in cattle. Sci Rep 2020 Nov 19;10(1):20192.
                    doi: 10.1038/s41598-020-77089-9pubmed: 33214639google scholar: lookup
                  18. Collodel G, Moretti E, Noto D, Iacoponi F, Signorini C. Fatty Acid Profile and Metabolism Are Related to Human Sperm Parameters and Are Relevant in Idiopathic Infertility and Varicocele. Mediators Inflamm 2020;2020:3640450.
                    doi: 10.1155/2020/3640450pubmed: 32934603google scholar: lookup
                  19. 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
                  20. Menezes EB, Velho ALC, Santos F, Dinh T, Kaya A, Topper E, Moura AA, Memili E. Uncovering sperm metabolome to discover biomarkers for bull fertility. BMC Genomics 2019 Sep 18;20(1):714.
                    doi: 10.1186/s12864-019-6074-6pubmed: 31533629google scholar: lookup
                  21. Plaza Davila M, Martin Muñoz P, Tapia JA, Ortega Ferrusola C, Balao da Silva C C, Peña FJ. Inhibition of Mitochondrial Complex I Leads to Decreased Motility and Membrane Integrity Related to Increased Hydrogen Peroxide and Reduced ATP Production, while the Inhibition of Glycolysis Has Less Impact on Sperm Motility. PLoS One 2015;10(9):e0138777.
                    doi: 10.1371/journal.pone.0138777pubmed: 26407142google scholar: lookup
                  22. Sakkas D, Ramalingam M, Garrido N, Barratt CL. Sperm selection in natural conception: what can we learn from Mother Nature to improve assisted reproduction outcomes?. Hum Reprod Update 2015 Nov-Dec;21(6):711-26.
                    doi: 10.1093/humupd/dmv042pubmed: 26386468google scholar: lookup