Relationship between cholesterol and sperm quality in ChinoSantandereano (Bos taurus) bulls
DOI:
https://doi.org/10.17533/udea.rccp.e358073Keywords:
bovine reproduction, bull selection, cattle, membrane lipids, seminal quality, sperm, sperm functional competence, sperm membrane, sperm motility, sperm qualityAbstract
Background: The assessment of seminal quality parameters is often the initial step in bull selection for siring or conservation purposes. While these parameters provide insights into fertility, delving into the molecular dynamics occurring within sperm cells can complement this primary reproductive evaluation. Cholesterol, one of the most active molecules on the sperm membrane surface, has been linked to critical processes that confer functional features required for reaching the oocyte and achieving fertilization. The complexity of cholesterol dynamics in the sperm surface, including membrane lipid remodeling, is relevant to numerous processes that precede fertilization. Objective: To elucidate the correlation between sperm quality parameters and cholesterol levels in sperm cells from Chino-Santandereano bulls, a Colombian creole breed renowned for its high sperm quality, yet unfortunately facing imminent extinction. Methods: Semen samples were collected from ten Chino-Santandereano bulls to evaluate sperm motility, viability, and sperm functional competence (SFC) immediately after collection. Simultaneously, cholesterol was extracted from sperm membranes using a methanol-chloroform solution, and cholesterol levels were measured by spectrophotometry using a specific commercial kit. A Pearson's correlation test was used to determine the relationship between cholesterol concentration and seminal quality parameters. Results: Our results revealed a strong negative correlation between cholesterol quantity and the average SFC. Additionally, cholesterol levels were also negatively associated with sperm motility. This suggests that cholesterol dynamics, particularly cholesterol output, play a more significant role in sperm functionality than cholesterol content. Conclusions: Monitoring cholesterol output from the sperm membrane appears to be an interesting alternative to complement the initial reproductive evaluation in bulls. The intricate nature of these relationships deserves further experimental work to fully comprehend the implications of cholesterol for the reproductive potential of Chino-Santandereano bulls’ semen and offer insights for enhancing sperm quality in other breeds.
Downloads
References
Beer-Ljubić B, Aladrović J, Marenjak TS, Laskaj R, Majić-Balić I, Milinković-Tur S. Cholesterol concentration in seminal plasma as a predictive tool for quality semen evaluation. Theriogenology 2009; 72(8), 1132–1140. https://doi.org/10.1016/j.theriogenology.2009.07.009
Brito LFC, Silva AEDF, Rodrigues LH, Vieira FV, Deragon LAG, Kastelic JP. Effects of environmental factors, age and genotype on sperm production and semen quality in Bos indicus and Bos taurus AI bulls in Brazil. Anim Repro Sci 2002 ; 70(3–4), 181–190. https://doi.org/10.1016/S0378-4320(02)00009-X
Caballero J, Frenette G, Sullivan R. Post testicular sperm maturational changes in the bull: Important role of the epididymosomes and prostasomes. Vet Med Int 2011; 757194. https://doi.org/10.4061/2011/757194
Díaz HPV, Espinoza JEP, Malca EA. Addition of methyl-β-cyclodextrin loaded with cholesterol (CLC) on the cryopreservation of semen of Holstein Friesian bulls. Rev Inv Vet Perú 2019; 30(4), 1611–1618. http://dx.doi.org/10.15381/rivep.v30i4.17159
Ernst R, Ejsing CS, Antonny B. Homeoviscous Adaptation and the Regulation of Membrane Lipids. J Mol Biol 2016; 428(24 Pt A), 4776–4791. https://doi.org/10.1016/j.jmb.2016.08.013
Fernández JCN, Herrera NP, Vergara MA, Coronado LM, Rúgeles CP, Rueda FA, Cardozo JC. Seminal plasma proteins and sperm quality of Romosinuano and Costeño con Cuernos bulls. Rev Inv Vet Perú 2022; 33(2), 1–15. https://doi.org/10.15381/rivep.v33i2.21033
Girouard J, Frenette G, Sullivan R. Seminal plasma proteins regulate the association of lipids and proteins within detergent-resistant membrane domains of bovine spermatozoa. Biol Repro 2008; 78(5), 921–931. https://doi.org/10.1095/biolreprod.107.066514
Hung P, Suarez, SS. Alterations to the Bull Sperm Surface Proteins That Bind Sperm to Oviductal Epithelium1. Biol Repro 2012; 87(4). https://doi.org/10.1095/biolreprod.112.099721
Keber R, Rozman D, Horvat S. Sterols in spermatogenesis and sperm maturation. J Lipid Res 2013; 54(1), 20–33. https://doi.org/10.1194/jlr.R032326
Leahy T, Gadella BM. New insights into the regulation of cholesterol efflux from the sperm membrane. Asian J Andro 2015; 561–567. https://doi.org/10.4103/1008-682X.153309
Lee DE, Lew MG, Woodbury DJ.Vesicle fusion to planar membranes is enhanced by cholesterol and low temperature. Chem Phys Lipids 2013; 166, 45–54. https://doi.org/10.1016/j.chemphyslip.2012.11.004
Leite RF, de Agostini Losano JD, de Souza Ramos Angrimani D, Sousa RGB, de Miranda Alves Á, Cavallin MD, Kawai GKV, Cortada CNM, Zuge RM, Nichi M. Reproductive parameters of Bos taurus and Bos indicus bulls during different seasons in tropical conditions: focus on an alternative approach to testicular assessments using ultrasonography. Anim Repro Sci 2021; 225, 1–11. https://doi.org/10.1016/j.anireprosci.2020.106668
Maldjian A, Pizzi F, Gliozzi T, Cerolini S, Penny P, Noble R. Changes in sperm quality and lipid composition during cryopreservation of boar semen. Theriogenology 2005; 15;63(2):411-21. https://doi.org/10.1016/j.theriogenology.2004.09.021
Parsons JB, Rock CO. Bacterial lipids: metabolism and membrane homeostasis. Pro Lipid Res 2013; 52(3), 249–276. https://doi.org/10.1016/j.plipres.2013.02.002
Pérez-Llano B, Sala R, Reguera G, García-Casado P. Changes in subpopulations of boar sperm defined according to viability and plasma and acrosome,membrane status observed during storage at 15°C. Theriogenology 2009; 71:311-317. https://doi.org/10.1016/j.theriogenology.2008.07.023
Petrunkina AM, Harrison RAP, Tsolova M, Jebe E, Töpfer-Petersen E. Signalling pathways involved in the control of sperm cell volume. Reproduction 2007; 133(1), 61–73. https://doi.org/10.1530/rep.1.01137
Purdy PH, Graham JK. Effect of Adding Cholesterol to Bull Sperm Membranes on Sperm Capacitation, the Acrosome Reaction, and Fertility1. Biol Repro 2004; 71(2), 522–527. https://doi.org/10.1095/biolreprod.103.025577
Rueda F, Garcés PT, Herrera LR, Arbeláez RL, Peña JM, Velásquez PH, Hernández VA, Cardozo CJ. Seminal plasma proteins increase the post-thaw sperm viability of Sanmartinero bull’s semen. Revista MVZ Cordoba 2013; 18(1), 3327–3335. http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0122-02682013000100011
Saez F, Drevet JR. Dietary Cholesterol and Lipid Overload: Impact on Male Fertility. Oxi Med Cell Longev, 2019; 4521786. https://doi.org/10.1155/2019/4521786
Shan S, Xu F, Hirschfeld M, Brenig B. Sperm lipid markers of male fertility in mammals. Int J Mol Sci 2021; 22(16). https://doi.org/10.3390/ijms22168767
Sheriff DS, Ali EF. Perspective on plasma membrane cholesterol efflux and spermatozoal function. J Hum Repro Sci 2010; 3(2), 68–75. https://doi.org/10.4103/0974-1208.69337
Travis AJ, Kopf GS. The role of cholesterol efflux in regulating the fertilization potential of mammalian spermatozoa. J Clinical Inv 2002; 110(6), 731–736. https://doi.org/10.1172/JCI16392
Valencia J, Yeste M, Quintero-Moreno A, Henao FJ. A new test based on the hypotonic resistance and functional competence to evaluate the sperm quality, cryotolerance and in vitro fertilizing ability in pigs. Theriogenology 2019; 140, 84–92. https://doi.org/10.1016/j.theriogenology.2019.08.022
White IG. Lipids and calcium uptake of sperm in relation to cold shock and preservation: a review. Repro Ferti Dev 1993; 5(6), 639–658. https://doi.org/10.1071/rd9930639
Witte TS, Sch S. Involvement of cholesterol , calcium and progesterone in the induction of capacitation and acrosome reaction of mammalian spermatozoa. Anim Repro Sci 2008; 102, 181–193. https://doi.org/10.1016/j.anireprosci.2007.07.007
Yang ST, Kreutzberger AJB, Lee J, Kiessling V, Tamm LK. The role of cholesterol in membrane fusion. Chem Phys Lipids 2016; 199, 136–143. https://doi.org/10.1016/j.chemphyslip.2016.05.003
Yeung CH, Barfield JP, Anapolski M, Cooper TG. Volume regulation of mature and immature spermatozoa in a primate model, and possible ion channels involved. Hum Repro 2004; 19(11), 2587–2593. https://doi.org/10.1093/humrep/deh466
Yeung CH, Barfield JP, Cooper TG. Physiological volume regulation by spermatozoa. Mol Cell Endo 2006; 250(1), 98–105. https://doi.org/https://doi.org/10.1016/j.mce.2005.12.030
Published
How to Cite
Issue
Section
License
Copyright (c) 2021 Revista Colombiana de Ciencias Pecuarias

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
The authors enable RCCP to reprint the material published in it.
The journal allows the author(s) to hold the copyright without restrictions, and will allow the author(s) to retain publishing rights without restrictions.