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1Academic Journal
المؤلفون: de Castro Meira, Felipe Rodrigo, Campos Damasceno dos Santos, Alice, Tassar Estorani Martins, Carolyna, Rosa Figueiredo Souza, Livia, Ávila Machado, Melissa
المصدر: RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218; Vol. 5 No. 10 (2024): CLICK HERE TO ACCESS THE ARTICLES; e5105845 ; RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218; Vol. 5 Núm. 10 (2024): HAGA CLIC AQUÍ PARA ACCEDER A LOS ARTÍCULOS; e5105845 ; RECIMA21 - Revista Científica Multidisciplinar - ISSN 2675-6218; v. 5 n. 10 (2024): CLIQUE AQUI PARA ACESSAR OS ARTIGOS; e5105845 ; RECIMA21 -Revista Científica Multidisciplinar - ISSN 2675-6218; Vol. 5 N.º 10 (2024): CLIQUE AQUI PARA ACESSAR OS ARTIGOS; e5105845 ; 2675-6218
مصطلحات موضوعية: Preservação da Fertilidade, Neoplasias, Oncologia Médica, Preservación de la fertilidad, Oncología Médica, Fertility Preservation, Neoplasms, Medical Oncology
وصف الملف: application/pdf
Relation: https://recima21.com.br/index.php/recima21/article/view/5845/3964; https://recima21.com.br/index.php/recima21/article/view/5845
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2Academic Journal
المؤلفون: Jheymmy Lorena Garces Gomez, Ana Bolena Bonilla Bustos, Miriam Elizabeth Argueta, Liliana María Mejía De Beldjenna
المصدر: Interdisciplinary Journal of Epidemiology and Public Health, Vol 5, Iss 1 (2022)
مصطلحات موضوعية: síndrome de mayer-rokitansky-kuster-hauser, mrkh, resección septum, preservación de la fertilidad, trastorno congénito, anomalia, sindrome, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
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3Report
المؤلفون: Paredes Contreras,Mariana Selene, O Pérez,Luis Oswaldo De la, Rivera Coyotzi,Eleazar, Castañeda Díaz,Marisela
المصدر: Ginecología y obstetricia de México v.91 n.8 2023
مصطلحات موضوعية: miometral aumentada, malformación arteriovenosa uterina, cirugía de mínima invasión, preservación de la fertilidad, hemorragia uterina, laparoscopia
وصف الملف: text/html
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4Academic Journal
المؤلفون: Ormart, Elizabeth, Curado, Constanza, Pasquali, Evelyn, Dlabach, Sofía, Geremías, Agustina
المصدر: ENCUENTROS LATINOAMERICANOS (Segunda Época) ENCLAT ISSN 1688-437X; Vol. 5 No. 2 (2021): Sección de Estudios de Género. Tecnología y reproducción en América Latina; 85-111 ; Encuentros Latinoamericanos (segunda época) ; Vol. 5 Núm. 2 (2021): Sección de Estudios de Género. Tecnología y reproducción en América Latina; 85-111 ; v. 5 n. 2 (2021): Seção de estudos de gênero. Tecnologia e reprodução na América Latina; 85-111 ; 1688-437X
مصطلحات موضوعية: Representaciones, Cuidado y preservación de la fertilidad, Jóvenes, Proyecto familiar, Representations, Care and Preservation of Fertility, Youth, Family Project, Representações, Cuidado e Preservação da Fertilidade, Juventude, Projeto Família
وصف الملف: application/pdf
Relation: https://ojs.fhce.edu.uy/index.php/enclat/article/view/1430/1668; https://ojs.fhce.edu.uy/index.php/enclat/article/view/1430
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5Academic Journal
المصدر: Ginecología y obstetricia de México v.90 n.3 2022
مصطلحات موضوعية: Tumor limítrofe del ovario, tumor de ovario, neoplasias del ovario, prese preservación de la fertilidad, escisión de ganglios linfáticos, linfadenectomía, recurrencia de neoplasias, local, estadificación de neoplasias, México, Seguridad Social
وصف الملف: text/html
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6Dissertation/ Thesis
المؤلفون: Blanes Martínez, Ángel Arturo
Thesis Advisors: Bonilla Musoles, Fernando, Sánchez Serrano, María, Bonilla Bartret, Francisco, Departament de Pediatria, Obstetrícia i Ginecologia
مصطلحات موضوعية: corteza ovárica, hd live, preservación de la función, preservación de la fertilidad, ecografía 3D/4D, trasplante ortotópico, tejido ovárico, modo silueta, cancer y embarazo
URL الوصول: http://hdl.handle.net/10550/61350
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7Dissertation/ Thesis
المؤلفون: Blanes Martínez, Ángel Arturo
Thesis Advisors: Bonilla Musoles, Fernando, Sánchez Serrano, María, Bonilla Bartret, Francisco, Departament de Pediatria, Obstetrícia i Ginecologia
مصطلحات موضوعية: corteza ovárica, hd live, preservación de la función, preservación de la fertilidad, ecografía 3D/4D, trasplante ortotópico, tejido ovárico, modo silueta, cancer y embarazo
URL الوصول: http://hdl.handle.net/10803/571844
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8Dissertation/ Thesis
المؤلفون: Blanes Martínez, Ángel Arturo
Thesis Advisors: Bonilla Musoles, Fernando, Sánchez Serrano, María, Bonilla Bartret, Francisco, Departament de Pediatria, Obstetrícia i Ginecologia
مصطلحات موضوعية: corteza ovárica, hd live, preservación de la función, preservación de la fertilidad, ecografía 3D/4D, trasplante ortotópico, tejido ovárico, modo silueta, cancer y embarazo
URL الوصول: http://hdl.handle.net/10803/580411
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9Academic Journal
المؤلفون: Estrella Durá-Ferrandis, Cristina Saéz-Mansilla, Sarah E. Murphy, Andrea C. Johnson, Kenneth P. Tercyak
المصدر: Psicooncologia, Vol 16, Iss 1, Pp 127-141 (2019)
مصطلحات موضوعية: cancer, preservación de la fertilidad, oncofertilidad, distrés emocional, actitudes, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Psychology, BF1-990
وصف الملف: electronic resource
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10Academic Journal
المؤلفون: Osorio Torres, Carmen Rosa
المصدر: Interciencia médica; Vol. 11 Núm. 2 (2021): abr - jun; 19-35 ; Interciencia médica; Vol. 11 No. 2 (2021): abr - jun; 19-35 ; 2810-837X ; 10.56838/icmed.v11i2
مصطلحات موضوعية: Endometriosis e infertilidad, adenopmiosis, endometrioma, preservación de la fertilidad
وصف الملف: application/pdf
Relation: https://intercienciamedica.com/intercienciamedica/article/view/23/22; https://intercienciamedica.com/intercienciamedica/article/view/23
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11Academic Journal
المؤلفون: Batiza Resendiz,Víctor Alfonso, Aguilar Melgar,Ashanti, Luna Rojas,Rosa Martha, Pérez-Peña,Efraín, Gutiérrez Gutiérrez,Antonio, Ruvalcaba Castrellón,Luis Arturo, Salazar López-Ortiz,Carlos, Michel Vergara,Jorge Alejandro, Shaw Dulin,Robin Jennifer, Barquet Muñoz,Salim Abraham, Hernández López,Luis Arturo, García Rodríguez,Francisco José, Cortés Esteban,Patricia, Sánchez Llamas,Benito, Rodríguez Calderóon,Ricardo, Maldonado Rosas,Israel
المصدر: Ginecología y obstetricia de México v.88 n.11 2020
مصطلحات موضوعية: Preservación de la fertilidad, prenatal, adolescentes, cáncer, supervivientes a largo plazo, reserva ovárica
وصف الملف: text/html
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12Book
المؤلفون: Asensio-Del-Barrio, Cristina, Palma Ruiz, Matilde
المساهمون: Ministerio de Sanidad, Servicios Sociales e Igualdad (España)
مصطلحات موضوعية: Criopreservación de ovocitos, Criopreservación de tejido ovárico, Preservación de la fertilidad, Pacientes oncológicas, Revisión sistemática, Evaluación de Tecnologías Sanitarias
Relation: Estudio de la efectividad y de la seguridad de la criopreservación de ovocitos y de tejido ovárico para la preservación de la fertilidad en pacientes oncológicas. Madrid: Agencia de Evaluación de Tecnologías Sanitarias (AETS) - Instituto de Salud Carlos III, Ministerio de Ciencia; 2018. Informes de Evaluación de Tecnologías Sanitarias.; http://hdl.handle.net/20.500.12105/7284; ISCIII NIPO pdf: 062-18-011-1 NIPO epub: 062-18-012-7 MSCBS NIPO pdf: 680-18-081-7 NIPO epub: 680-18-082-2
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13Academic Journal
المؤلفون: Durá-Ferrandis, Estrella, Saéz-Mansilla, Cristina, Murphy, Sarah E., Johnson, Andrea C., Tercyak, Kenneth P.
المصدر: Psicooncología; Vol. 16 No. 1 (2019); 127-141 ; Psicooncología; Vol. 16 Núm. 1 (2019); 127-141 ; 1988-8287 ; 1696-7240
مصطلحات موضوعية: cancer, fertility preservation, oncofertility, distress, attitudes, preservación de la fertilidad, oncofertilidad, distrés emocional, actitudes
وصف الملف: application/pdf
Relation: https://revistas.ucm.es/index.php/PSIC/article/view/63652/4564456549470; Adams E, Hill E, Watson E. Fertility preservation in cancer survivors: a national survey of oncologists´ current knowledge, practice and attitudes. Br J Cancer 2013; 108:1602- 15. doi:10.1038/bjc.2013.139; Armuand GM, Rodriguez-Wallberg KA, Wettergren L, Ahlgren J, Enblad G, Höglund M, et al. Sex differences in fertility-related information received by young adult cancer survivors. J Clin Oncol 2012; 30:2147-53. doi:10.1200/JCO.2011.40.6470; Avis NE, Crawford S, Manuel J. Psychosocial problems among younger women with breast cancer. Psychooncology 2004;13:295-308. doi:10.1002/pon.744; Bastings L, Baysal O, Beerendonk CC, IntHout J, Traas MA, Verhaak CM, et al. Deciding about fertility preservation after specialist counselling. Human Reprod 2014; 29:1721-9. doi:10.1093/humrep/deu136; Bender C, Paraska K, Sereika S, Ryan CM, Berga SL. Cognitive function and reproductive hormones in adjuvant therapy for breast cancer: A critical review. J Pain Symptom Manage 2001; 21:407-424. doi:10.1016/S0885-3924(01)00268-8; Bloom JR, Stewart SL, Oakley-Girvan I, Banks PJ, Shema S. Quality of life of younger breast cancer survivors: persistence of problems and sense of wellbeing. Psychooncology 2012;21:655-66. doi:10.1002/pon.1965; Canada AL, Schover LR. The psychosocial impact of interrupted childbearing in long-term female cancer survivors. Psychooncology 2012; 21:134-43. doi:10.1002/pon.1875; Carter J, Chi DS, Brown CL, Abu-Rustum NR, Sonoda Y, Aghajanian C, et al. Cancer- Related Infertility in Survivorship. Inter J Gynecol Cancer 2010; 20:2-8. doi:10.1111/ IGC.0b013e3181bf7d3f; Corney RH, Swinglehurst JF.Young childless women with breast cancer in the UK: a qualitative study of their fertility-related experiences, options, and the information given by health professionals. Psychooncology 2014; 23:20-6. doi:10.1002/pon.3365 Derogatis LR. Brief Symptom Inventory (BSI-18). Administration, Scoring and Procedures Manual. Minneapolis, NCs Pearson, Inc, 2001.; Deshpande N, Braun IM, Meyer FL Impact of infertility preservation counselling and treatment on psychological outcome among women with cancer: A systematic review. Cancer 2015; 15:3938-47. doi:10.1002/cncr.29637; Donnez J, Jadoul P, Squifflet J, Van Langendonckt A, Donnez O, van Eyck AS, et al. Ovarian tissue cryopreservation and transplantation in cancer patients. Best Pract Res Clin Obstet Gynaecol 2010; 24):87-100. doi:10.1016/j.bpobgyn.2009.09.003; Duffy CM, Allen SM, Clark MA. Discussions regarding reproductive health for young women with breast cancer undergoing chemotherapy. J Clin Oncol 2005; 23:766-773. doi:10.1200/JCO.2005.01.134.; Ethics Committee of the American Society for Reproductive Medicine. Fertility preservation and reproduction in cancer patients. Fertil Steril 2005; 83:1622-8. doi:10.1016/j.fertnstert.2005.03.013; Forman EJ, Anders CK, Behera MA. A nationwide survey of oncologists regarding treatment-related infertility and fertility preservation in female cancer patients. Ferti Steril 2010; 94:1652-6. doi:10.1016/j.fertnstert.2009.10.008; Geue K, Richter D, Schmidt R, Sender A, Siedentopf F, Brähler E, Stöbel-Richter Y. The desire for children and fertility issues among young German cancer survivors. J Adolesc 2014; 54:527-35. doi:10.1016/j.jadohealth.2013.10.005; Gibson DM, Myers JE. The effect of social coping resources and growth-fostering relationships on infertility stress in women. J Ment Health Couns 2002;24:68–80; Gonz PA, Greendale GA, Peterson L, Kahn B, Bower JL Breast cancer in younger women: reproductive and late health effects of treatment. J Clin Oncol 2003; 21:4184-93. doi:10.1200/JCO.2003.04.196 Hammond C, Abrams JR, Syrjala DL. Fertility and risk factors for elevated infertility concern in 10-year hematopoietic cell transplant rurvivors and case-matched controls. J Clin Oncol 2007; 25: 3511-7; Hershberger PE, Finnegan L, Pierce PF, Scoccia B. The decision-making process of young adult women with cancer who considered fertility cryopreservation. J Obst Gynecol Neonatal Nurs 2013; 42:59-69. doi:10.1111/j.1552-6909.2012.01426.x; Hill KA, Nadler T, Mandel R, Burlein-Hall S, Librach C, Glass K, Warner E . Experience of young women diagnosed with breast cancer who undergo fertility preservation consultation. Clin Breast Cancer 2012; 12: 127-32. doi:10.1016/j.clbc.2012.01.002; ISFP Practical Committee of the American Society for Reproductive Medicine. Testing and interpreting measures of ovarian reserve: A committee opinion. Ferti Steril 2012; 9: 1407-15. doi:10.1016/j.fertnstert.2012.09.036; ISFP Practice Committee, Kim SS, Donnez J, Barri P, Pellicer A, Patrizio P, Rosenwaks Z, et al. Recommendations for fertility preservation in patients with lymphoma, leukemia, and breast cancer. J Assist Reprod Genet 2012; 29:465-8. doi:10.1007/s10815-012- 9786-y; Kim J, Han JY, Shaw B, McTavish F, Gustafson D. The roles of social support and coping strategies in predicting breast cancer patients’ emotional well-being: testing mediation and moderation models. J Health Psychol 2010; 15:543-552. doi:10.1177/1359105309355338; Landeta O, Calvete E. Adaptación y validación de la Escala Multidimensional de Apoyo Social Percibido. Ansiedad y Estrés 2002; 8(2-3):173-82; Letorneau JM, Ebbel EE, Katz PP, Katz A, Ai WZ, Chien AJ, et al. Pretreatment fertility counseling and fertility preservation improve quality of life in reproductive age women with cancer. Cancer 2012; 15:1710-7. doi:10.1002/cncr.26459 Linkeviciute A, Boniolo G, Chiavari L, Peccatori FA. Fertility preservation in cancer patients: The global framework. Cancer Treat Rev 2014; 40:1019-27. doi:10.1016/j. ctrv.2014.06.001; Loren AW, Mangu PB, Beck LN, Brennan L, Magdalinski AJ, Patridge AH, et al. Fertility preservation for patients with cancer: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol 2013;31:2500-10. doi:10.1200/JCO.2013.49.2678; Partridge AH, Gelber S, Peppercorn J, Sampson E, Knudsen K, Laufer M, et al. Web- Based survey of fertility issues in young women with breast cancer. J Clin Oncol 2004;22:4174-83. doi:10.1200/JCO.2004.01.159; Penrose R, Beatty L, Mattiske J, Koczwara B. Fertility and cancer – a qualitative study of Australian cancer survivors. Support Care Cancer 2012;20:1259–65. doi:10.1007/ s00520-011-1212-y; Perz J, Ussher J, Gilbert E. Loss, uncertainty, or acceptance: subjective experience of changes to fertility after breast cancer. Eur J Cancer Care 2014; 23:514-22; Quinn GP, Vadaparampil ST, Lee JH, Jacobsen PB, Bepler G, Lancaster J, et al. Physician referral for fertility preservation in oncology patients: a national study of practice behaviors. J Clin Oncol 2009; 27:5952-7. doi:10.1200/JCO.2009.23.0250; Reh AE, Lu L, Weinerman R, Grifo J, Krey L, Noyes N.Treatment outcomes and quality-of-life assessment in a university-based fertility preservation program: results of a registry of female cancer patients at 2 years. J Assist; Schmidt L, Holstein BE, Christensen U, Boivin J. Communication and coping as predictors of fertility problem stress: cohort study of 816 participants who did not achieve a delivery after 12 months of fertility treatment. Hum Reprod 2005;20:3248–56. doi:10.1093/humrep/dei193; Schover L. Motivation for Parenthood After Cancer: A Review. JNCI Monographs 2005; 34: 2-5. doi:10.1093/jncimonographs/lgi010; Schover LR, Brey K, Lichtin A, Lipshultz LI, Jeha S. Knowledge and experience regarding cancer, infertility, and sperm banking in younger male survivors. J Clin Oncol 2002; 20:1880-90. PMID: 11919248; Siegel R, Ma J, Zou Z, Jemal A. (2014) Cancer Statistics, 2014. CA Cancer J Clin 2014: 64: 9-29. doi:10.3322/caac.21208; Thewes B, Meiser A, Taylor KA, Phillips S, Pendlebury A, Capp A, et al. Fertility- and menopause-related information needs of younger women with a diagnosis of early breast cancer. J Clin Oncol 23: 5155-65. doi:10.1200/JCO.2005.07.773; Trèves R, Grynberg M, le Parco S, Finet A, Poulain M, Fanchin R. Female fertility preservation in cancer patients: an instrumental tool for the envisioning a postdisease life. Future Oncol 2014; 10: 969-74; Wenzel L, Dogan-Ates A, Habbal R, Berlowitz R, Goldstein DP, Bernstein M, et al. Defining and measuring reproductive concerns of female cancer survivors. JNCI Monographs 2005;34:94-8. doi:10.1093/jncimonographs/lgi017; Woodruff TK, Clayman ML, Waimey KE, editors. Oncofertility communication: sharing information and building relationships across disciplines. New York, Springer, 2014.; Zanagnolo V, Sartori E, Trussardi E, Pasinetti B, Maggino T. Preservation of ovarian function, reproductive ability and emotional attitudes in patients with malignant ovarian tumors. Eur J Obstet Gynecol Reprod Biol 2005;23: 235-43. doi:10.1016/j. ejogrb.2005.04.010; https://revistas.ucm.es/index.php/PSIC/article/view/63652
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14Report
المؤلفون: Mateo-Sánez,Henry A., Mateo-Madrigal,Daniela, Dávalos-Álvarez,Adrián, Domínguez-Dorame,Fernanda, Ku-González,Jeanneth
المصدر: Cirugía y cirujanos v.88 suppl.2 2020
مصطلحات موضوعية: Preservación de la fertilidad, Teratoma bilateral, Teratoma maduro, Tumor de células germinales
وصف الملف: text/html
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15Report
المؤلفون: Noris-Martínez,Aziru, Pérez-López,José Del Carmen, García-Hernández,Gabriel Gerardo, Martínez-Hernández,Clara Magdalena, Mandujano-Álvarez,Gabriel Juan, Ramírez-López,Patricia
المصدر: Ginecología y obstetricia de México v.88 n.2 2020
مصطلحات موضوعية: Neoplasias del ovario, proliferación celular, lavado peritoneal, preservación de la fertilidad, laparoscopia, biopsia, quimioterapia
وصف الملف: text/html
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16Academic Journal
المصدر: Revista Colombiana de Obstetricia y Ginecología, Vol 66, Iss 3, Pp 202-209 (2015)
مصطلحات موضوعية: neoplasias del cuello uterino, preservación de la fertilidad, conización, procedimientos quirúrgicos ginecológicos, escisión del ganglio linfático, Gynecology and obstetrics, RG1-991
وصف الملف: electronic resource
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17Academic Journal
المؤلفون: Mónica Isabel Vásquez-Arenas, Lina Echeverri-Álvarez, Gabriel Rendón-Pereira, Rene Pareja-Franco
المصدر: Revista Colombiana de Obstetricia y Ginecología, Vol 66, Iss 2, Pp 124-130 (2015)
مصطلحات موضوعية: preservación de la fertilidad, neoplasias del cuello uterino, quimioterapia, terapia neoadyuvante, laparoscopia, Gynecology and obstetrics, RG1-991
وصف الملف: electronic resource
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18
المؤلفون: García Rodríguez, María
المساهمون: Gaytán Muñoz, María
مصطلحات موضوعية: Maduración in vitro (IVM), Preservación de la fertilidad, Maduración ovocitaria, Tecnología de la reproducción asistida (ART), Fecundación in vitro (IVF), Complejo cúmulo-ovocitario (COC)
Relation: García Rodríguez, M. (2023). Estado actual de la maduración in vitro de ovocitos [Trabajo Fin de Estudios, Universidad Europea de Madrid]. Repositorio de Trabajos Fin de Estudios TITULA; https://hdl.handle.net/20.500.12880/6437
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19
المؤلفون: Viana Pareja, Ainoa
المساهمون: Gónzalez Ravina, Cristina
مصطلحات موضوعية: Transgénero, Preservación de la fertilidad, Vitrificación de ovocitos, FtM, Hombres transgénero, Mujeres transgénero
Relation: Viana Pareja, A. (2023). Preservación de la fertilidad en personas transgénero: un enfoque multidisciplinario [Trabajo Fin de Estudios, Universidad Europea de Madrid]. Repositorio de Trabajos Fin de Estudios TITULA; https://hdl.handle.net/20.500.12880/6454
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20Dissertation/ Thesis
المؤلفون: Rueda Amador, Luis Andres
المساهمون: Restrepo Betancur, Giovanni, Grupo de investigación en biotecnología animal GIBA, Rueda Amador, Luis
مصطلحات موضوعية: 570 - Biología::573 - Sistemas fisiológicos específicos en animales, histología regional y fisiología en los animales, 590 - Animales::599 - Mamíferos, 630 - Agricultura y tecnologías relacionadas::637 - Procesamiento lechero y productos relacionados, 570 - Biología::572 - Bioquímica, Preservación de semen, Semen, Espermatozoides, Preservación de la fertilidad, Semen Preservation, Spermatozoa, Fertility Preservation, Reproducción dirigida, Reproduction control, Evaluación, Metabolismo, Criopreservación, Tiempo de almacenamiento, Bovino, Evaluation, Metabolism, Sperm, Cryopreservation, Storage time, Bovine
وصف الملف: xvii, 89 páginas; application/pdf
Relation: Abdelhafez, F., Bedaiwy, M., El-Nashar, S. A., Sabanegh, E., & Desai, N. (2009). Techniques for cryopreservation of individual or small numbers of human spermatozoa: A systematic review. Human Reproduction Update, 15(2), 153–164. https://doi.org/10.1093/humupd/dmn061; Adamkovicova, M., Toman, R., Martiniakova, M., Omelka, R., Babosova, R., Krajcovicova, V., Grosskopf, B., & Massanyi, P. (2016). Sperm motility and morphology changes in rats exposed to cadmium and diazinon. Reproductive Biology and Endocrinology, 14(1). https://doi.org/10.1186/s12958-016-0177-6; Agarwal, A., Nallella, K. P., Allamaneni, S. S. R., & Said, T. M. (2004). Role of antioxidants in treatment of male infertility: An overview of the literature. In Reproductive BioMedicine Online (Vol. 8, Issue 6, pp. 616–627). Elsevier. https://doi.org/10.1016/S1472-6483(10)61641-0; Agarwal, A., Makker, K., & Sharma, R. (2008). Clinical relevance of oxidative stress in male factor infertility: An update. In American Journal of Reproductive Immunology (Vol. 59, Issue 1, pp. 2–11). https://doi.org/10.1111/j.1600-0897.2007.00559.x; Agca, Y., Gilmore, J., Byers, M., Woods, E. J., Liu, J., & Critser, J. K. (2002). Osmotic characteristics of mouse spermatozoa in the presence of extenders and sugars. Biology of Reproduction, 67(5), 1493–1501. https://doi.org/10.1095/biolreprod.102.005579; Ahmed, H., Andrabi, S. M. H., Shah, S. A. H., & Jahan, S. (2019). Effect of Cryopreservation on Casa Characteristics, Mitochondrial Transmembrane Potential, Plasma and Acrosome Integrities, Morphology and in vivo Fertility of Buffalo Bull Spermatozoa. Cryo Letters, 40(3), 173–180.; Aitken, R., Baker, M., & Nixon, B. (2015). Are sperm capacitation and apoptosis the opposite ends of a continuum driven by oxidative stress? Asian Journal of Andrology, 17(4), 633. https://doi.org/10.4103/1008-682X.153850; Aitken, R. J., & Clarkson, J. S. (1987). Cellular basis of defective sperm function and its association with the genesis of reactive oxygen species by human spermatozoa. Reproduction, 81(2), 459–469. https://doi.org/10.1530/jrf.0.0810459; Aitken, R. John, Gibb, Z., Mitchell, L. A., Lambourne, S. R., Connaughton, H. S., & De Iuliis, G. N. (2012). Sperm motility is lost in vitro as a consequence of mitochondrial free radical production and the generation of electrophilic aldehydes but can be significantly rescued by the presence of nucleophilic thiols. Biology of Reproduction, 87(5), 1–11. https://doi.org/10.1095/biolreprod.112.102020; Akyol, N., Varisli, O., & Kızıl, S. (2018). Effects of long-term storage on some spermatological parameters in cryopreserved bull semen. Cryo-Letters, 39, 354–358.; Albrizio, M., Moramarco, A. M., Nicassio, M., Micera, E., Zarrilli, A., & Lacalandra, G. M. (2015). Localization and functional modification of L-type voltage-gated calcium channels in equine spermatozoa from fresh and frozen semen. Theriogenology, 83(3), 421–429. https://doi.org/10.1016/j.theriogenology.2014.10.005; Amirat, L., Tainturier, D., Jeanneau, L., Thorin, C., Gérard, O., Courtens, J. L., & Anton, M. (2004). Bull semen in vitro fertility after cryopreservation using egg yolk LDL: A comparison with Optidyl®, a commercial egg yolk extender. Theriogenology, 61(5), 895–907. https://doi.org/10.1016/S0093-691X(03)00259-0; Amaral, A., Castillo, J., Estanyol, J. M., Ballesca, J. L., Ramalho-Santos, J., & Oliva, R. (2013). Human sperm tail proteome suggests new endogenous metabolic pathways. Molecular and Cellular Proteomics, 12(2), 330–342. https://doi.org/10.1074/mcp.M112.020552; Anzar, M., Kroetsch, T., & Boswall, L. (2011). Cryopreservation of bull semen shipped overnight and its effect on post-thaw sperm motility, plasma membrane integrity, mitochondrial membrane potential and normal acrosomes. Animal Reproduction Science, 126(1–2), 23–31. https://doi.org/10.1016/j.anireprosci.2011.04.018; Arav, A. (1999). Device and methods for multigradient directional cooling and warming of biological samples.; Arbaiza-Barnechea, M. D., & Cabrera-Villanueva, P. C. (2021). Efecto de la criopreservación espermática en la fragmentación del ADN, viabilidad, y parámetros cinéticos en toros Brown Swiss. Revista Colombiana de Ciencia Animal - RECIA, 13(1), e787. https://doi.org/10.24188/recia.v13.n1.2021.787; Arenas Ríos, E., Rodríguez Tobón, A., López Trinidad, B. P., Retana Sandoval, F. M., Rodríguez Tobón, E., Jimenez Salazar, J. E., & León-Galván, M. A. (2014). Participación de las especies reactivas de oxígeno en la fisiología espermática. Revista Iberoamericana de Ciencias, 1(7), 73–81.; Ashwood-Smith, M. J., & Friedmann, G. B. (1979). Lethal and chromosomal effects of freezing, thawing, storage time, and x-irradiation on mammalian cells preserved at - 196 ° in dimethyl sulfoxide. Cryobiology, 16(2), 132–140. https://doi.org/10.1016/0011-2240(79)90023-3; Bailey, J. L., Bilodeau, J. F., & Cormier, N. (2000). Minireview: Semen cryopreservation in domestic animals: A damaging and capacitating phenomenon. In Journal of Andrology (Vol. 21, Issue 1, pp. 1–7). https://doi.org/10.1002/j.1939- 4640.2000.tb03268.x; Bailey, J., Morrier, A., & Cormier, N. (2003). Semen cryopreservation: Successes and persistent problems in farm species. In Canadian Journal of Animal Science (Vol. 83, Issue 3, pp. 393–401). https://doi.org/10.4141/A03-024; Baker, M. A., Nixon, B., Naumovski, N., & Aitken, R. J. (2012). Proteomic insights into the maturation and capacitation of mammalian spermatozoa. In Systems Biology in Reproductive Medicine (Vol. 58, Issue 4, pp. 211–217). Taylor & Francis. https://doi.org/10.3109/19396368.2011.639844; Bansal, A. K., & Bilaspuri, G. S. (2011). Impacts of oxidative stress and antioxidants on semen functions. In Veterinary Medicine International (Vol. 2011). https://doi.org/10.4061/2011/686137; Barkawi, A. H., Elsayed, E. H., Ashour, G., & Shehata, E. (2006). Seasonal changes in semen characteristics, hormonal profiles and testicular activity in Zaraibi goats. Small Ruminant Research, 66(1–3), 209–213. https://doi.org/10.1016/j.smallrumres.2005.09.007; Baumber, J., Ball, B. A., & Linfor, J. J. (2005). Assessment of the cryopreservation of equine spermatozoa in the presence of enzyme scavengers and antioxidants. American Journal of Veterinary Research, 66(5), 772–779. https://doi.org/10.2460/ajvr.2005.66.772; Bean, B. H., Pickett, B. W., & Martig, R. C. (1963). Influence of Freezing Methods, Extenders, and Storage Temperatures on Motility and pH of Frozen Bovine Semen. Journal of Dairy Science, 46(2), 145–149. https://doi.org/10.3168/jds.S0022- 0302(63)88990-0; Benchaib, M., Braun, V., Lornage, J., Hadj, S., Salle, B., Lejeune, H., & Guérin, J. F. (2003). Sperm DNA fragentation decreases the pregnancy rate in an assisted reproductive technique. Human Reproduction, 18(5), 1023–1028. https://doi.org/10.1093/humrep/deg228; Bergeron, A., & Manjunath, P. (2006). New insights towards understanding the mechanisms of sperm protection by egg yolk and milk. Molecular Reproduction and Development, 73(10), 1338–1344. https://doi.org/10.1002/mrd.20565; Bilodeau, J.-F., Chatterjee, S., Sirard, M.-A., & Gagnon, C. (2000). Levels of antioxidant defenses are decreased in bovine spermatozoa after a cycle of freezing and thawing. Molecular Reproduction and Development, 55(3), 282–288. https://doi.org/10.1002/(SICI)1098-2795(200003)55:33.0.CO;2-7; Bollwein, H, Fuchs, I., & Koess, C. (2008). Interrelationship between plasma membrane integrity, mitochondrial membrane potential and DNA fragmentation in cryopreserved bovine spermatozoa. Reproduction in Domestic Animals, 43(2), 189–195. https://doi.org/10.1111/j.1439-0531.2007.00876.x; Bollwein, Heinrich, & Bittner, L. (2018). Impacts of oxidative stress on bovine sperm function and subsequent in vitro embryo development. Animal Reproduction, 15(Irrs), 703–710. https://doi.org/10.21451/1984-3143-AR2018-0041; Boveris, A., & Chance, B. (1973). The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen. Biochemical Journal, 134(3), 707–716. https://doi.org/10.1042/bj1340707; Bratton, R. W., Foote, R. H., & Cruthers, J. C. (1955). Preliminary Fertility Results with Frozen Bovine Spermatozoa. Journal of Dairy Science, 38(1), 40–46. https://doi.org/10.3168/jds.S0022-0302(55)94935-3; Braun, J., Schams, D., & Brem, G. (1990). Zur Fortpflanzungsfunktion bei experimentell erzeugten monozygoten Zwillingsbullen. Berliner Und Munchener Tierarztliche Wochenschrift, 103(6), 213–217. https://europepmc.org/article/med/2383230; Breitbart, H. (2002). Intracellular calcium regulation in sperm capacitation and acrosomal reaction. Molecular and Cellular Endocrinology, 187(1–2), 139–144. https://doi.org/10.1016/S0303-7207(01)00704-3; Brinsko, S. P., Crockett, E. C., & Squires, E. I. (2000). Effect of centrifugation and partial removal of seminal plasma on equine spermatozoal motility after cooling and storage. Theriogenology, 54, 129–138.; Brown, K. H. (2008). Fish mitochondrial genomics: Sequence, inheritance and functional variation. In Journal of Fish Biology (Vol. 72, Issue 2, pp. 355–374). John Wiley & Sons, Ltd. https://doi.org/10.1111/j.1095-8649.2007.01690.x; Bucak, M. N., Ateşşahin, A., & Yüce, A. (2008). Effect of anti-oxidants and oxidative stress parameters on ram semen after the freeze-thawing process. Small Ruminant Research, 75(2–3), 128–134. https://doi.org/10.1016/j.smallrumres.2007.09.002; Buch, N. C., Smith, V. R., & Tyler, W. J. (1956). Bull and Line Differences in the Survival of Spermatozoa after Freezing and Thawing. Journal of Dairy Science, 39(12), 1712–1716. https://doi.org/10.3168/jds.S0022-0302(56)94913-X; Cabrera V., P., & Pantoja A., C. (2012). Viabilidad Espermatica e Integridad del Aceosoma en Semen Congelado de Toros Nacionales. Revista de Investigaciones Veterinarias Del Perú, 23(2), 192–200. https://doi.org/10.15381/rivep.v23i2.899; Carmody, R. J., & Cotter, T. G. (2001). Signalling apoptosis: A radical approach. In Redox Report (Vol. 6, Issue 2, pp. 77–90). https://doi.org/10.1179/135100001101536085; Catena, M. Y. J. C. (1999). Evaluación de semen bovino congelado. Engormix.Com, 1(1), 1–9.; Chabory, E., Damon, C., Lenoir, A., Henry-Berger, J., Vernet, P., Cadet, R., Saez, F., & Drevet, J. R. (2010). Mammalian glutathione peroxidases control acquisition and maintenance of spermatozoa integrity. Journal of Animal Science, 88(4), 1321–1331. https://doi.org/10.2527/jas.2009-2583; Chabory, Eléonore, Damon, C., Lenoir, A., Kauselmann, G., Kern, H., Zevnik, B., Garrel, C., Saez, F., Cadet, R., Henry-Berger, J., Schoor, M., Gottwald, U., Habenicht, U., Drevet, J. R., & Vernet, P. (2009). Epididymis seleno-independent glutathione peroxidase 5 maintains sperm DNA integrity in mice. Journal of Clinical Investigation, 119(7), 2074–2085. https://doi.org/10.1172/jci38940; Chang, H.-Y., Huang, H.-C., Huang, T.-C., Yang, P.-C., Wang, Y.-C., & Juan, H.-F. (2013). Flow Cytometric Detection of Mitochondrial Membrane Potential. BIO- PROTOCOL, 3(8). https://doi.org/10.21769/BioProtoc.430; Chatterjee, S., & Gagnon, C. (2001). Production of reactive oxygen species by spermatozoa undergoing cooling, freezing, and thawing. Molecular Reproduction and Development, 59(4), 451–458. https://doi.org/10.1002/mrd.1052; Chen, X., Zhu, H., Hu, C., Hao, H., Zhang, J., Li, K., Zhao, X., Qin, T., Zhao, K., Zhu, H., & Wang, D. (2014). Identification of differentially expressed proteins in fresh and frozen-thawed boar spermatozoa by iTRAQ-coupled 2D LC-MS/MS. Reproduction, 147(3), 321–330. https://doi.org/10.1530/REP-13-0313; Chrenek, P., Spaleková, E., Olexikova, L., Makarevich, A., & Kubovicova, E. (2017). Quality of Pinzgau bull spermatozoa following different periods of cryostorage. Zygote, 25(2), 215–221. https://doi.org/10.1017/S0967199417000077; Cohen, J. (1973). Cross-overs, sperm redundancy and their close association. Heredity, 31(3), 408–413. https://doi.org/10.1038/hdy.1973.96; Collin, F. (2019). Chemical basis of reactive oxygen species reactivity and involvement in neurodegenerative diseases. In International Journal of Molecular Sciences (Vol. 20, Issue 10, p. 2407). Multidisciplinary Digital Publishing Institute. https://doi.org/10.3390/ijms20102407; Córdova, A., Strobel, P., Vallejo, A., Valenzuela, P., Ulloa, O., Burgos, R. A., Menarim, B., Rodríguez-Gil, J. E., Ratto, M., & Ramírez-Reveco, A. (2014). Use of hypometabolic TRIS extenders and high cooling rate refrigeration for cryopreservation of stallion sperm: Presence and sensitivity of 5’ AMP-activated protein kinase (AMPK). Cryobiology, 69(3), 473–481. https://doi.org/10.1016/j.cryobiol.2014.10.008; Coulter, G. H., & Foote, R. H. (1973). Sperm changes during processing in straws. J. Anim. Sci., 37(306).; Crespilho, A. M., Papa, F. O., Zahn, F. S., Guasti, P. N., & Dell’Aqua, J. A. (2009). Influence of Different Preservation Methods on Fertility of Bovine Semen. Biology of Reproduction, 81(1), 459–459. https://doi.org/10.1093/biolreprod/81.s1.459; Critser, J. K., Arneson, B. W., Aaker, D. V., Huse-Benda, A. R., & Ball, G. D. (1987). Cryopreservation of human spermatozoa. II. Postthaw chronology of motility and of zona-free hamster ova penetration. Fertility and Sterility, 47(6), 980–984. https://doi.org/10.1016/S0015-0282(16)59233-4; Curry, M. R. (2000). Cryopreservation of semen from domestic livestock. Reviews of Reproduction, 5, 46–52. https://doi.org/10.1007/978-1-4939-2193-5_10; Darin-Bennett, A., & White, I. G. (1977). Influence of the cholesterol content of mammalian spermatozoa on susceptibility to cold-shock. Cryobiology, 14(4), 466-470. https://doi.org/10.1016/0011-2240(77)90008-6; Darr, C. R., Varner, D. D., Teague, S., Cortopassi, G. A., Datta, S., & Meyers, S. A. (2016). Lactate and pyruvate are major sources of energy for stallion sperm with dose effects on mitochondrial function, motility, and ROS production. Biology of Reproduction, 95(2), 1–11. https://doi.org/10.1095/biolreprod.116.140707; Davis, R. O., & Gravance, C. G. (1994). Consistency of Sperm Morphology Classification Methods. Journal of Andrology, 15(1), 83–91. https://doi.org/10.1002/j.1939- 4640.1994.tb01690.x; de Lamirande, E., Jiang, H., Zini, A., Kodama, H., & Gagnon, C. (1997). Reactive oxygen species and sperm physiology. Reviews of Reproduction, 2(1), 48–54.; de Lamirande, E., & Gagnon, C. (1995). Impact of reactive oxygen species on spermatozoa: A balancing act between beneficial and detrimental effects. Human Reproduction, 10(SUPPL. 1), 15–21. https://doi.org/10.1093/humrep/10.suppl_1.15; De Leeuw, F. E., De Leeuw, A. M., Den Daas, J. H. G., Colenbrander, B., & Verkleij, A. J. (1993). Effects of various cryoprotective agents and membrane-stabilizing compounds on bull sperm membrane integrity after cooling and freezing. Cryobiology, 30(1), 32–44. https://doi.org/10.1006/cryo.1993.1005; Devenish, R. J., Prescott, M., & Rodgers, A. J. W. (2008). The Structure and Function of Mitochondrial F1F0-ATP Synthases. In International Review of Cell and Molecular Biology (Vol. 267, pp. 1–58). https://doi.org/10.1016/S1937-6448(08)00601-1; Di Santo, M., Tarozzi, N., Nadalini, M., & Borini, A. (2012). Human sperm cryopreservation: Update on techniques, effect on DNA integrity, and implications for ART. In Advances in Urology (pp. 1–12). https://doi.org/10.1155/2012/854837; Díaz, R., Lee-Estevez, M., Quiñones, J., Dumorné, K., Short, S., Ulloa-Rodríguez, P., Valdebenito, I., Sepúlveda, N., & Farías, J. G. (2019). Changes in Atlantic salmon (Salmo salar) sperm morphology and membrane lipid composition related to cold storage and cryopreservation. Animal Reproduction Science, 204, 50–59. https://doi.org/10.1016/j.anireprosci.2019.03.004; Dode, M. A. N., & Rumpf, R. (2002). Produção in vitro de embriões naespécie bovina. Biotecnologia Ciência & Desenvolvimento, 26, 32–37.; Du Plessis, S. S., Makker, K., Desai, N. R., & Agarwal, A. (2008). Impact of oxidative stress on IVF. In Expert Review of Obstetrics and Gynecology (Vol. 3, Issue 4, pp. 539–554). https://doi.org/10.1586/17474108.3.4.539; Dunn, H. O., & Hafs, H. D. (1953). Extenders and techniques for freezing bovine spermatozoa. Journal of Dairy Science, 36(6), 577–577.; Duru, N. K., Morshedi, M. S., Schuffner, A., & Oehninger, S. (2001). Cryopreservation- thawing of fractionated human spermatozoa is associated with membrane phosphatidylserine externalization and not DNA fragmentation. Journal of Andrology, 22(4), 646–651. https://doi.org/10.1002/j.1939-4640.2001.tb02225.x; Ensslin, M., Vogel, T., Calvete, J. J., Thole, H. H., Schmidtke, J., Matsuda, T., & Töpfer-Petersen, E. (1998). Molecular cloning and characterization of P47, a novel boar sperm- associated zona pellucida-binding protein homologous to a family of mammalian secretory proteins. Biology of Reproduction, 58(4), 1057–1064. https://doi.org/10.1095/biolreprod58.4.1057; Evans, J. P., Kopf, G. S., & Schultz, R. M. (1997). Characterization of the binding of recombinant mouse sperm fertilin β subunit to mouse eggs: Evidence for adhesive activity via an egg β1 integrin-mediated interaction. Developmental Biology, 187(1), 79–93. https://doi.org/10.1006/dbio.1997.8611; Ezzati, M., Shanehbandi, D., Hamdi, K., Rahbar, S., & Pashaiasl, M. (2020). Influence of cryopreservation on structure and function of mammalian spermatozoa: an overview. Cell and Tissue Banking, 21(1), 1–15. https://doi.org/10.1007/s10561-019-09797-0; Feldschuh, J., Brassel, J., Durso, N., & Levine, A. (2005). Successful sperm storage for 28 years. Fertility and Sterility, 84(4), 1017.e3-1017.e4. https://doi.org/10.1016/j.fertnstert.2005.05.015; Ferrusola, C. O., Fernández, L. G., Sandoval, C. S., García, B. M., Martínez, H. R., Tapia, J. A., & Peña, F. J. (2010). Inhibition of the mitochondrial permeability transition pore reduces “apoptosis like” changes during cryopreservation of stallion spermatozoa. Theriogenology, 74(3), 458–465. https://doi.org/10.1016/j.theriogenology.2010.02.029; Figueroa, E., Valdebenito, I., Zepeda, A. B., Figueroa, C. A., Dumorné, K., Castillo, R. L., & Farias, J. G. (2017). Effects of cryopreservation on mitochondria of fish spermatozoa. In Reviews in Aquaculture (Vol. 9, Issue 1, pp. 76–87). John Wiley & Sons, Ltd. https://doi.org/10.1111/raq.12105; Flores C, V. L. (2015). Metabolismo espermático Sperm Metabolism. Gaceta de Ciencias Veterinarias, 20(1), 23–32.; Florman, H. M., Arnoult, C., Kazam, I. G., Li, C., & O’Toole, C. M. B. (1998). A perspective on the control of mammalian fertilization by egg- activated ion channels in sperm: A tale of two channels. Biology of Reproduction, 59(1), 12–16. https://doi.org/10.1095/biolreprod59.1.12; Ford, W. C. L. (2004). Regulation of sperm function by reactive oxygen species. Human Reproduction Update, 10(5), 387–399. https://doi.org/10.1093/HUMUPD/DMH034; Forero-Gonzalez, R. A., Celeghini, E. C. C., Raphael, C. F., Andrade, A. F. C., Bressan, F. F., & Arruda, R. P. (2012). Effects of bovine sperm cryopreservation using different freezing techniques and cryoprotective agents on plasma, acrosomal and mitochondrial membranes. Andrologia, 44(SUPPL.1), 154–159. https://doi.org/10.1111/j.1439-0272.2010.01154.x; Fraser, L., Strzezek, J., & Kordan, W. (2014). Post-thaw sperm characteristics following long-term storage of boar semen in liquid nitrogen. Animal Reproduction Science, 147(3–4), 119–127. https://doi.org/10.1016/j.anireprosci.2014.04.010; Gadella, B. M., & Harrison, R. A. P. (2002). Capacitation induces cyclic adenosine 3′,5′- monophosphate-dependent, but apoptosis-unrelated, exposure of aminophospholipids at the apical head plasma membrane of boar sperm cell. Biology of Reproduction, 67(1), 340–350. https://doi.org/10.1095/biolreprod67.1.340; Gadella, Bart M., Tsai, P. S., Boerke, A., & Brewis, I. A. (2008). Sperm head membrane reorganisation during capacitation. International Journal of Developmental Biology, 52(5–6), 473–480. https://doi.org/10.1387/ijdb.082583bg; Galloway, D. (1992). Abnormal Morphology of Bovine Spermatozoa,. Australian Veterinary Journal, 69(1), 22–22. https://doi.org/10.1111/j.1751-0813.1992.tb09864.x; Garrett, L. J. A., Revell, S. G., & Leese, H. J. (2008). Adenosine triphosphate production by bovine spermatozoa and its relationship to semen fertilizing ability. Journal of Andrology, 29(4), 449–458. https://doi.org/10.2164/jandrol.107.003533; Ghareeb, S., Haron, W., Yusoff, R., Yimer, N., Baiee, F., Ahmedeltayeb, T., & Ebrahimi, M. (2017). Post-Thaw Evaluation of Cryopreserved Bull Semen Extended In FourDifferent Semen Extenders. Australian Journal of Basic and Applied Sciences, 11(5), 80–87. https://www.researchgate.net/publication/322741133_Post- Thaw_Evaluation_of_Cryopreserved_Bull_Semen_Extended_In_Four_Different_Se men_Extenders; Gibb, Z., & Aitken, R. J. (2016). The Impact of Sperm Metabolism during in Vitro Storage: The Stallion as a Model. BioMed Research International, 1–8. https://doi.org/10.1155/2016/9380609; Gille, L., & Nohl, H. (2001). The ubiquinol/bc1 redox couple regulates mitochondrial oxygen radical formation. Archives of Biochemistry and Biophysics, 388(1), 34–38. https://doi.org/10.1006/abbi.2000.2257; Gomez, E., Irvine, D. S., & Aitken, R. J. (1998). Evaluation of a spectrophotometric assay for the measurement of malondialdehyde and 4-hydroxyalkenals in human spermatozoa: Relationships with semen quality and sperm function. International Journal of Andrology, 21(2), 81–94. https://doi.org/10.1046/j.1365- 2605.1998.00106.x; Gonçalves, F. S., Barretto, L. S. S., Arruda, R. P., Perri, S. H. V., & Mingoti, G. Z. (2010). Effect of antioxidants during bovine in vitro fertilization procedures on spermatozoa and embryo development. Reproduction in Domestic Animals, 45(1), 129–135. https://doi.org/10.1111/j.1439-0531.2008.01272.x; Goodson, S. G., Qiu, Y., Sutton, K. A., Xie, G., Jia, W., & O’Brien, D. A. (2012). Metabolic substrates exhibit differential effects on functional parameters of mouse sperm capacitation. Biology of Reproduction, 87(3). https://doi.org/10.1095/biolreprod.112.102673; Goshme, S., Asfaw, T., Demiss, C., & Besufekad, S. (2021). Evaluation of motility and morphology of frozen bull semen under different thawing methods used for artificial insemination in North Shewa zone, Ethiopia. Heliyon, 7(10), e08183. https://doi.org/10.1016/j.heliyon.2021.e08183; Graham, J. K. (2001). Assessment of sperm quality: A flow cytometric approach. Animal Reproduction Science, 68(3–4), 239–247. https://doi.org/10.1016/S0378- 4320(01)00160-9; Graham, J. K., Kunze, E., & Hammerstedt, R. H. (1990). Analysis of sperm cell viability, acrosomal integrity, and mitochondrial function using flow cytometry. Biology of Reproduction, 43(1), 55–64. https://doi.org/10.1095/biolreprod43.1.55; Gravance, C. G., Garner, D. L., Baumber, J., & Ball, B. A. (2000). Assessment of equine sperm mitochondrial function using JC-1. Theriogenology, 53(9), 1691–1703. https://doi.org/10.1016/S0093-691X(00)00308-3; Grötter, L. G., Cattaneo, L., Marini, P. E., Kjelland, M. E., & Ferré, L. B. (2019). Recent advances in bovine sperm cryopreservation techniques with a focus on sperm post‐ thaw quality optimization. Reproduction in Domestic Animals, 54(4), 655–665. https://doi.org/10.1111/rda.13409; Grynkiewicz, G., Poenie, M., & Tsien, R. Y. (1985a). A new generation of Ca2+ indicators with greatly improved fluorescence properties. In Journal of Biological Chemistry (Vol. 260, Issue 6, pp. 3440–3450). https://doi.org/10.1016/s0021-9258(19)83641-4; Grynkiewicz, G., Poenie, M., & Tsien, R. Y. (1985b). A new generation of Ca2+ indicators with greatly improved fluorescence properties. Journal of Biological Chemistry, 260(6), 3440–3450. https://doi.org/10.1016/s0021-9258(19)83641-4; Gualtieri, R., Kalthur, G., Barbato, V., Di Nardo, M., Adiga, S. K., & Talevi, R. (2021). Mitochondrial dysfunction and oxidative stress caused by cryopreservation in reproductive cells. In Antioxidants (Vol. 10, Issue 3, pp. 1–23). Multidisciplinary Digital Publishing Institute (MDPI). https://doi.org/10.3390/antiox10030337; Gürler, H., Malama, E., Heppelmann, M., Calisici, O., Leiding, C., Kastelic, J. P., & Bollwein, H. (2015). Effects of cryopreservation on sperm viability, synthesis of reactive oxygen species, and DNA damage of bovine sperm. Theriogenology, 86(2), 562–571. https://doi.org/10.1016/j.theriogenology.2016.02.007; Guthrie, H. D., & Welch, G. R. (2012). Effects of reactive oxygen species on sperm function. In Theriogenology (Vol. 78, Issue 8, pp. 1700–1708). Elsevier. https://doi.org/10.1016/j.theriogenology.2012.05.002; Hafez, E. S., & Hafez, B. (2000). Reproducción e inseminación artificial en animales.; Halliwell, B., Edition), J. G.-L. (British, & 1984, U. (n.d.). Lipid peroxidation, oxygen radicals, cell damage, and antioxidant therapy. Pascal-Francis.Inist.Fr. Retrieved December 22, 2022, from https://pascal- francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8895792; Hammerstedt, R. H., Graham, J. K., & Nolan, J. P. (1990). Cryopreservation of Mammalian Sperm: What We Ask Them to Survive. Journal of Andrology, 11(1), 73– 88. https://doi.org/10.1002/j.1939-4640.1990.tb01583.x; Haugan, T., Gröhn, Y. T., Kommisrud, E., Ropstad, E., & Reksen, O. (2007). Effects of sperm concentration at semen collection and storage period of frozen semen on dairy cow conception. Animal Reproduction Science, 97, 1–11. https://doi.org/10.1016/j.anireprosci.2005.12.010; Hayashi, Y., & Isobe, N. (2005). Characteristics of Cryopreserved Spermatozoa from a Holstein-Friesian Bull Thawed at Different Temperature. Journal of International Development and Cooperation, 12(1), 107–110. https://www.researchgate.net/publication/44843962_Characteristics_of_Cryopreserv ed_Spermatozoa_from_a_Holstein-; Henry, M. A., Noiles, E. E., Gao, D., Mazur, P., & Critser, J. K. (1993). Cryopreservation of human spermatozoa. IV. The effects of cooling rate and warming rate on the maintenance of motility, plasma membrane integrity, and mitochondrial function. Fertility and Sterility, 60(5), 911–918. https://doi.org/10.1016/s0015-0282(16)56296-7; Hernández Corredor, L., Camargo Rodríguez, O., Silva Torres, A., Montoya Páez, J. D., & Quintero Moreno, A. (2018). Efectos de la criopreservación sobre las subpoblaciones espermáticas en caprinos. Revista de Investigaciones Veterinarias Del Perú, 29(3), 882–893. https://doi.org/10.15381/rivep.v29i3.14169; Hernandez, D., & Carrillo, D. (2015). Aplicación del test hipoosmótico (HOST) en la evaluaci ́n de calidad seminal en ovinos criollos de pelo colombiano. Actas Iberoamericanas de Conservación Animal, 6, 165–171.; Hernandez, L., Quintero-Moreno, A., Rubio Parada, A., & Silva Torres, A. (2017). Evaluación de la calidad espermática mediante citometría de flujo en semen caprino criopreservado con dos diluyentes. Revista Científica Universidad Del Zulia, 27(1), 35–43.; Hezavehei, M., Sharafi, M., Kouchesfahani, H. M., Henkel, R., Agarwal, A., Esmaeili, V., & Shahverdi, A. (2018). Sperm cryopreservation: A review on current molecular cryobiology and advanced approaches. Reproductive BioMedicine Online, 37(3), 327–339. https://doi.org/https://doi.org/10.1016/j.rbmo.2018.05.012; Ho, H. C., & Suarez, S. S. (2001). Hyperactivation of mammalian spermatozoa: Function and regulation. In Reproduction (Vol. 122, Issue 4, pp. 519–526). Society for Reproduction and Fertility. https://doi.org/10.1530/rep.0.1220519; Holt, W. V. (2000). Basic aspects of frozen storage of semen. Animal Reproduction Science, 62(1–3), 3–22. https://doi.org/10.1016/S0378-4320(00)00152-4; Holt, W. V., & North, R. D. (1991). Cryopreservation, actin localization and thermotropic phase transitions in ram spermatozoa. Journal of Reproduction and Fertility, 91(2), 451–461. https://doi.org/10.1530/jrf.0.0910451; Holt, W. V., & North, R. D. (1994). Effects of temperature and restoration of osmotic equilibrium during thawing on the induction of plasma membrane damage in cryopreserved ram spermatozoa. Biology of Reproduction, 51(3), 414–424. https://doi.org/10.1095/biolreprod51.3.414; Holt, W. V., Penfold, L, M., Chenoweth, P., & Lorton, S. (2014). Fundamental and practical aspects of semen cryopreservation. Theories and Applications. https://books.google.hn/books?hl=en&lr=&id=hv6dAwAAQBAJ&oi=fnd&pg=PA76&ot s=DC3JC7vqep&sig=fv5qM7bLU9aMWzgfLqZQjiIdw84&redir_esc=y#v=onepage&q &f=false; Hossain, M. S., Johannisson, A., Wallgren, M., Nagy, S., Siqueira, A. P., & Rodriguez- Martinez, H. (2011). Flow cytometry for the assessment of animal sperm integrity and functionality: State of the art. In Asian Journal of Andrology (Vol. 13, Issue 3, pp. 406–419). https://doi.org/10.1038/aja.2011.15; Isachenko, E., Isachenko, V., Katkov, I. I., Dessole, S., & Nawroth, F. (2003). Vitrification of mammalian spermatozoa in the absence of cryoprotectants: From past practical difficulties to present success. Reproductive BioMedicine Online, 6(2), 191–200. https://doi.org/10.1016/S1472-6483(10)61710-5; James, A. N., Green, H., Hoffman, S., Landry, A. M., Paccamonti, D., & Godke, R. A. (2002). Preservation of equine sperm stored in the epididymis at 4°C for 24, 48, 72 and 96 hours. Theriogenology, 58(2–4), 401–404. https://doi.org/10.1016/S0093- 691X(02)00883-X; Januskauskas, A., Johannisson, A., & Rodriguez-Martinez, H. (2003). Subtle membrane changes in cryopreserved bull semen in relation with sperm viability, chromatin structure, and field fertility. Theriogenology, 60(4), 743–758. https://doi.org/10.1016/S0093-691X(03)00050-5; Jeyendran, R. S., Ven, H. H. Van der, Perez-Pelaez, M., Crabo, B. G., & Zaneveld, L. J. D. (1984). Development of an assay to assess the functional integrity of the human sperm membrane and its relationship to other semen characteristics. Journal of Reproduction and Fertility, 70(1), 219–228. https://doi.org/10.1530/jrf.0.0700219; Jones, R., Mann, T., & Sherins, R. (1979). Peroxidative breakdown of phospholipids in human spermatozoa, spermicidal properties of fatty acid peroxides, and protective action of seminal plasma. Fertility and Sterility, 31(5), 531–537. https://doi.org/10.1016/S0015-0282(16)43999-3; Kamp, G., Büsselmann, G., & Lauterwein, J. (1996). Spermatozoa: Models for studying regulatory aspects of energy metabolism. In Experientia (Vol. 52, Issue 5, pp. 487– 494). Springer. https://doi.org/10.1007/BF01919321; Karu, T. I. (2010). Multiple roles of cytochrome c oxidase in mammalian cells under action of red and IR-A radiation. In IUBMB Life (Vol. 62, Issue 8, pp. 607–610). John Wiley & Sons, Ltd. https://doi.org/10.1002/iub.359; Karunakaran, M., & Devanathan, T. G. (2017). Evaluation of bull semen for fertility- associated protein, in vitro characters and fertility. Journal of Applied Animal Research, 45(1), 136–144. https://doi.org/10.1080/09712119.2015.1129343; Khalil, W. A., El-Harairy, M. A., Zeidan, A. E. B., Hassan, M. A. E., & Mohey-Elsaeed, O. (2018). Evaluation of bull spermatozoa during and after cryopreservation: Structural and ultrastructural insights. International Journal of Veterinary Science and Medicine, 6(1), 49–56. https://doi.org/10.1016/j.ijvsm.2017.11.001; Khan, I. M., Cao, Z., Liu, H., Khan, A., Rahman, S. U., Khan, M. Z., Sathanawongs, A., & Zhang, Y. (2021). Impact of Cryopreservation on Spermatozoa Freeze-Thawed Traits and Relevance OMICS to Assess Sperm Cryo-Tolerance in Farm Animals. In Frontiers in Veterinary Science (Vol. 8, p. 139). Frontiers Media S.A.; Kiani Esfahani, A., Tavalaee, M., Deemeh, M. R., Hamiditabar, M., & Nasr Esfahani, M. H. (2012). DHR123: An alternative probe for assessment of ROS in human spermatozoa. Systems Biology in Reproductive Medicine, 58(3), 168–174. https://doi.org/10.3109/19396368.2012.681420; Kim, S.-H., Yu, D.-H., & Kim, Y.-J. (2010). Effects of cryopreservation on phosphatidylserine translocation, intracellular hydrogen peroxide, and DNA integrity in canine sperm. Theriogenology, 73(3), 282–292. https://doi.org/10.1016/j.theriogenology.2009.09.011; Koppers, A. J., De Iuliis, G. N., Finnie, J. M., McLaughlin, E. A., & Aitken, R. J. (2008). Significance of mitochondrial reactive oxygen species in the generation of oxidative stress in spermatozoa. Journal of Clinical Endocrinology and Metabolism, 93(8), 3199–3207. https://doi.org/10.1210/jc.2007-2616; Kumar, A., Prasad, J. K., Srivastava, N., & Ghosh, S. K. (2019). Strategies to Minimize Various Stress-Related Freeze-Thaw Damages during Conventional Cryopreservation of Mammalian Spermatozoa. In Biopreservation and Biobanking (Vol. 17, Issue 6, pp. 603–612). https://doi.org/10.1089/bio.2019.0037; Larsen, L., Scheike, T., Jensen, T. K., Bonde, J. P., Ernst, E., Hjollund, N. H. I., Zhou, Y., Skakkebæk, N. E., Giwercman, A., Bonde, J. P. E., Henriksen, T. B., Kolstad, H. A., Anderson, A. M., Giwercman, A., & Olsen, J. (2000). Computer-assisted semen analysis parameters as predictors for fertility of men from the general population. Human Reproduction, 15(7), 1562–1567. https://doi.org/10.1093/humrep/15.7.1562; Lee, A. J., Salisbury, G. W., Boyd, L. J., & Ingalls, W. (1977). In Vitro Aging of Frozen Bull Semen. Journal of Dairy Science, 60(1), 89–95. https://doi.org/10.3168/jds.S0022- 0302(77)83833-2; Leite, T. G., do Vale Filho, V. R., de Arruda, R. P., de Andrade, A. F. C., Emerick, L. L., Zaffalon, F. G., Martins, J. A. M., & Andrade, V. J. de. (2010). Effects of extender and equilibration time on post-thaw motility and membrane integrity of cryopreserved Gyr bull semen evaluated by CASA and flow cytometry. Animal Reproduction Science, 120, 31–38. https://doi.org/10.1016/j.anireprosci.2010.04.005; Lemma, A. (2011). Effect of Cryopreservation on Sperm Quality and Fertility. In Artificial Insemination in Farm Animals. https://doi.org/10.5772/16563; Lenzi, A., Picardo, M., Gandini, L., & Dondero, F. (1996). Lipids of the sperm plasma membrane: From polyunsaturated fatty acids considered as markers of sperm function to possible scavenger therapy. In Human Reproduction Update (Vol. 2, Issue 3, pp. 246–256). Oxford Academic. https://doi.org/10.1093/humupd/2.3.246; Lessard, C., Parent, S., Leclerc, P., Baileys, J. A. N. I. C. E. L., & Sullivan, R. (2000). Cryopreservation alters the levels of the bull sperm surface protein P25b. Journal of Andrology, 21(5), 700–707. https://doi.org/10.1002/j.1939-4640.2000.tb02138.x; Li, C. jin, Wang, D., & Zhou, X. (2016). Sperm proteome and reproductive technologies in mammals. In Animal Reproduction Science (Vol. 173, pp. 1–7). Elsevier. https://doi.org/10.1016/j.anireprosci.2016.08.008; Lin, Y., & Kan, F. W. K. (1996). Regionalization and redistribution of membrane phospholipids and cholesterol in mouse spermatozoa during in vitro capacitation. Biology of Reproduction, 55(5), 1133–1146. https://doi.org/10.1095/biolreprod55.5.1133; Lone, S. A., Shah, N., Yadav, H. P., Wagay, M. A., Singh, A., & Sinha, R. (2017). Sperm DNA damage causes, assessment and relationship with fertility: A review. Theriogenology Insight - An International Journal of Reproduction in All Animals, 7(1), 13. https://doi.org/10.5958/2277-3371.2017.00010.9; López-Fernández, C., Pérez-Llano, B., García-Casado, P., Sala, R., Gosálbez, A., Arroyo, F., Fernández, J. L., & Gosálvez, J. (2008). Sperm DNA fragmentation in a random sample of the Spanish boar livestock. Animal Reproduction Science, 103(1– 2), 87–98. https://doi.org/10.1016/j.anireprosci.2006.11.015; Losano, J., Angrimani, D., Dalmazzo, A., Rui, B., Brito, M., Mendes, C., Kawai, G., Vannucchi, C., Assumpção, M., Barnabe, V., & Nichi, M. (2017). Effect of mitochondrial uncoupling and glycolysis inhibition on ram sperm functionality. Reproduction in Domestic Animals, 52(2), 289–297. https://doi.org/10.1111/rda.12901; Macpherson, J. W. (1960). Semen Storage in Liquid Nitrogen. The Canadian Veterinary Journal, 1(7), 292–294. https://www.ncbi.nlm.nih.gov/pmc/articles/pmc1585590/; Malik, A., Laily, M., & Zakir, M. I. (2015). Effects of long term storage of semen in liquid nitrogen on the viability, motility and abnormality of frozen thawed Frisian Holstein bull spermatozoa. Asian Pacific Journal of Reproduction, 4(1), 22–25. https://doi.org/10.1016/S2305-0500(14)60052-X; Manjunath, P., Bergeron, A., Lefebvre, J., & Fan, J. (2007). Seminal plasma proteins: functions and interaction with protective agents during semen preservation. In Society of Reproduction and Fertility supplement (Vol. 65, pp. 217–228).; Mansour, N., Lahnsteiner, F., McNiven, M. A., Richardson, G. F., & Pelletier, C. S. (2011). Relationship between fertility and fatty acid profile of sperm and eggs in Arctic char, Salvelinus alpinus. Aquaculture, 318(3–4), 371–378. https://doi.org/10.1016/j.aquaculture.2011.05.023; Martín Cano, F. E., Gaitskell Phillips, G., Ortiz Rodríguez, J. M., Silva Rodríguez, A., Román, Á., Rojo-Domínguez, P., Alonso-Rodríguez, E., Tapia, J. A., Gil, M. C., Ortega-Ferrusola, C., & Peña, F. J. (2020). Proteomic profiling of stallion spermatozoa suggests changes in sperm metabolism and compromised redox regulation after cryopreservation. Journal of Proteomics, 221, 1–14. https://doi.org/10.1016/j.jprot.2020.103765; Martin, G., Cagnon, N., Sabido, O., Sion, B., Grizard, G., Durand, P., & Levy, R. (2007). Kinetics of occurrence of some features of apoptosis during the cryopreservation process of bovine spermatozoa. Human Reproduction, 22(2), 380–388. https://doi.org/10.1093/humrep/del399; Mazur, P, & Cole, K. (1989). Roles of unfrozen fraction, salt concentration, and changes in cell volume in the survival of frozen human erythrocytes. Cryobiology, 26(1), 1–29.; Mazur, Peter, Katkov, I. I., Katkova, N., & Critser, J. K. (2000). The enhancement of the ability of mouse sperm to survive freezing and thawing by the use of high concentrations of glycerol and the presence of an Escherichia coli membrane preparation (Oxyrase) to lower the oxygen concentration. Cryobiology, 40(3), 187– 209. https://doi.org/10.1006/cryo.2000.2238; Medeiros, C. M. O., Forell, F., Oliveira, A. T. D., & Rodrigues, J. L. (2002). Current status of sperm cryopreservation: Why isn’t it better? Theriogenology, 57(1), 327–344. https://doi.org/10.1016/S0093-691X(01)00674-4; Meryman, H. T. (1971). Osmotic stress as a mechanism of freezing injury. Cryobiology, 8(5), 489–500. https://doi.org/10.1016/0011-2240(71)90040-X; Mishra, C., Palai, T. K., Sarangi, L. N., Prusty, B. R., & Maharana, B. R. (2013). Candidate gene markers for sperm quality and fertility in bulls. Veterinary World, 6(11), 905–910. https://doi.org/10.14202/vetworld.2013.905-910; Moreno, J., & Galarza, D. (2019). Criopreservación de espermatozoides en especies domésticas y silvestres: estado actual de los avances tecnológicos (Sperm cryopreservation in domestic and wild species: a review of recent advances). Revista Ecuatoriana de Ciencia Animal, 3, 18–38. http://revistaecuatorianadecienciaanimal.com/index.php/RECA/article/view/116; Morris, G. J. (2006). Rapidly cooled human sperm: no evidence of intracellular ice formation. Human Reproduction, 21(8), 2075–2083. https://doi.org/10.1093/humrep/del116; Moustafa, M., Sharma, R. K., Thornton, J., Mascha, E., Abdel-Hafez, M. A., Thomas, A. J., & Agarwal, A. (2004). Relationship between ROS production, apoptosis and DNA denaturation in spermatozoa from patients examined for infertility. Human Reproduction, 19(1), 129–138. https://doi.org/10.1093/humrep/deh024; Muiño-Blanco, T., Pérez-Pé, R., & Cebrián-Pérez, J. A. (2008). Seminal plasma proteins and sperm resistance to stress. In Reproduction in Domestic Animals (Vol. 43, Issue SUPPL.4, pp. 18–31). John Wiley & Sons, Ltd. https://doi.org/10.1111/j.1439- 0531.2008.01228.x; Nallella, K. P., Sharma, R. K., Said, T. M., & Agarwal, A. (2004). Inter-sample variability in post-thaw human spermatozoa. Cryobiology, 49(2), 195–199. https://doi.org/10.1016/j.cryobiol.2004.07.003; Naresh, S., & Atreja, S. K. (2015). The protein tyrosine phosphorylation during in vitro capacitation and cryopreservation of mammalian spermatozoa. In Cryobiology (Vol. 70, Issue 3, pp. 211–216). Academic Press. https://doi.org/10.1016/j.cryobiol.2015.03.008; Nazari, H., Ahmadi, E., Hosseini Fahraji, H., Afzali, A., & Davoodian, N. (2021). Cryopreservation and its effects on motility and gene expression patterns and fertilizing potential of bovine epididymal sperm. Veterinary Medicine and Science, 7(1), 127–135. https://doi.org/10.1002/vms3.355; Neild, D. M., Gadella, B. M., Chaves, M. G., Miragaya, M. H., Colenbrander, B., & Agüero, A. (2003). Membrane changes during different stages of a freeze-thaw protocol for equine semen cryopreservation. Theriogenology, 59(8), 1693–1705. https://doi.org/10.1016/S0093-691X(02)01231-1; Nicolas, M., Alvarez, M., Borragán, S., Martinez-Pastor, F., Chamorro, C. A., Alvarez- Rodriguez, M., de Paz, P., & Anel, L. (2012). Evaluation of the qualitative and quantitative effectiveness of three media of centrifugation (Maxifreeze, Cushion Fluid Equine, and PureSperm 100) in preparation of fresh or frozen-thawed brown bear spermatozoa. Theriogenology, 77(6), 1119–1128. https://doi.org/10.1016/j.theriogenology.2011.10.016; Noiles, E. E., Bailey, J. L., & Storey, B. T. (1995). The temperature dependence in the hydraulic conductivity, lp, of the mouse sperm plasma membrane shows a discontinuity between 4 and 0°C. Cryobiology, 32(3), 220–238. https://doi.org/10.1006/cryo.1995.1022; O’Brien, E., Esteso, M. C., Castaño, C., Toledano-Díaz, A., Bóveda, P., Martínez- Fresneda, L., López-Sebastián, A., Martínez-Nevado, E., Guerra, R., López Fernández, M., Vega, R. S., Guillamón, F. G., & Santiago-Moreno, J. (2019). Effectiveness of ultra-rapid cryopreservation of sperm from endangered species, examined by morphometric means. Theriogenology, 129, 160–167. https://doi.org/10.1016/j.theriogenology.2019.02.024; O’Connell, M., McClure, N., & Lewis, S. E. M. (2002). The effects of cryopreservation on sperm morphology, motility and mitochondrial function. Human Reproduction, 17(3), 704–709. https://doi.org/10.1093/humrep/17.3.704; O’Flaherty, C., Breininger, E., Beorlegui, N., & Beconi, M. T. (2005). Acrosome reaction in bovine spermatozoa: Role of reactive oxygen species and lactate dehydrogenase C4. Biochimica et Biophysica Acta - General Subjects, 1726(1), 96–101. https://doi.org/10.1016/j.bbagen.2005.07.012; Ozkavukcu, S., Erdemli, E., Isik, A., Oztuna, D., & Karahuseyinoglu, S. (2008). Effects of cryopreservation on sperm parameters and ultrastructural morphology of human spermatozoa. Journal of Assisted Reproduction and Genetics, 25(8), 403–411. https://doi.org/10.1007/s10815-008-9232-3; Pagl, R., Aurich, J. E., Müller-Schlösser, F., Kankofer, M., & Aurich, C. (2006). Comparison of an extender containing defined milk protein fractions with a skim milk- based extender for storage of equine semen at 5 °C. Theriogenology, 66(5), 1115– 1122. https://doi.org/10.1016/j.theriogenology.2006.03.006; Parks, J. E., & Graham, J. K. (1992). Effects of cryopreservation procedures on sperm membranes. Theriogenology, 38(2), 209–222. https://doi.org/10.1016/0093- 691X(92)90231-F; Parrish, J. J., Susko-Parrish, J. L., & Graham, J. K. (1999). In vitro capacitation of bovine spermatozoa: Role of intracellular calcium. Theriogenology, 51(2), 461–472. https://doi.org/10.1016/S0093-691X(98)00240-4; Pegg, D., & Diaper, M. (1989). The ‘unfrozen fraction’ hypothesis of freezing injury to human erythrocytes: a critical examination of the evidence. Cryobiology, 26(1), 30– 43.; Peña, F. J., Macías García, B., Samper, J. C., Aparicio, I. M., Tapia, J. A., & Ortega Ferrusola, C. (2011). Dissecting the molecular damage to stallion spermatozoa: The way to improve current cryopreservation protocols? In Theriogenology (Vol. 76, Issue 7, pp. 1177–1186). https://doi.org/10.1016/j.theriogenology.2011.06.023; Pereira, R., Sá, R., Barros, A., & Sousa, M. (2017). Major regulatory mechanisms involved in sperm motility. In Asian Journal of Andrology (Vol. 19, Issue 1, pp. 5–14). Wolters Kluwer -- Medknow Publications. https://doi.org/10.4103/1008-682X.167716; Peris-Frau, P., Soler, A. J., Iniesta-Cuerda, M., Martín-Maestro, A., Sánchez-Ajofrín, I., Medina-Chávez, D. A., Fernández-Santos, M. R., García-álvarez, O., Maroto- Morales, A., Montoro, V., & Garde, J. J. (2020). Sperm cryodamage in ruminants: Understanding the molecular changes induced by the cryopreservation process to optimize sperm quality. International Journal of Molecular Sciences, 21(8). https://doi.org/10.3390/ijms21082781; Peris, S. I., Bilodeau, J.-F., Dufour, M., & Bailey, J. L. (2007). Impact of cryopreservation and reactive oxygen species on DNA integrity, lipid peroxidation, and functional parameters in ram sperm. Molecular Reproduction and Development, 74(7), 878– 892. https://doi.org/10.1002/mrd.20686; Pickett, B. W., Martig, R. C., & Cowan, W. A. (1961). Preservation of Bovine Spermatozoa at −79 and −196° C. Journal of Dairy Science, 44(11), 2089–2096. https://doi.org/10.3168/jds.S0022-0302(61)90023-6; Pommer, A. C., Rutllant, J., & Meyers, S. A. (2002). The role of osmotic resistance on equine spermatozoal function. Theriogenology, 58(7), 1373–1384. https://doi.org/10.1016/S0093-691X(02)01039-7; Pommer, A. C., Rutllant, J., & Meyers, S. A. (2003). Phosphorylation of protein tyrosine residues in fresh and cryopreserved stallion spermatozoa under capacitating conditions. Biology of Reproduction, 68(4), 1208–1214. https://doi.org/10.1095/biolreprod.102.011106; Prihantoko, K. D., Kusumawati, A., Widayati, D. T., & Pangestu, M. (2020). Effects of storage duration on mitochondrial activity and dna fragmentation of post-thawed spermatozoa from several ongole grade bull in Indonesia. Veterinary Practitioner, 21(2), 264–268.; Pryor, W. (1976). Free radicals in biology. In Antioxidants and the Skin (pp. 21–29). Academic Press. https://doi.org/10.1201/9781315207254-2; Raad, G., Bakos, H. W., Bazzi, M., Mourad, Y., Fakih, F., Shayya, S., Mchantaf, L., & Fakih, C. (2021). Differential impact of four sperm preparation techniques on sperm motility, morphology, DNA fragmentation, acrosome status, oxidative stress, and mitochondrial activity: A prospective study. Andrology, 9(5), 1549–1559. https://doi.org/10.1111/andr.13038; Ramírez-Reveco, A., Hernández, J. L., & Aros, P. (2016). Long‐Term Storing of Frozen Semen at −196°C does not Affect the Post-Thaw Sperm Quality of Bull Semen. In Cryopreservation in Eukaryotes. InTech. https://doi.org/10.5772/64948; Reers, M., Smith, T. W., & Chen, L. B. (1991). J-Aggregate Formation of a Carbocyanine as a Quantitative Fluorescent Indicator of Membrane Potential. Biochemistry, 30(18), 4480–4486. https://doi.org/10.1021/bi00232a015; Ribeiro-Peres, A., Munita-Barbosa, L., Yumi-Kanazawa, M., Mello-Martins, M. I., & Ferreira De Souza, F. (2014). Criopreservación de espermatozoides bovinos extraídos de la cola del epidídimo utilizando los métodos convencional y automatizado. Archivos de Medicina Veterinaria, 46(1), 31–38. https://doi.org/10.4067/S0301-732X2014000100005; Rodriguez-Martinez, H., Tienthai, P., Suzuki, K., Funahashi, H., Ekwall, H., & Johannisson, A. (2001). Involvement of oviduct in sperm capacitation and oocyte development in pigs. In Reproduction (Cambridge, England) Supplement (Vol. 58, pp. 129–145). https://doi.org/10.1530/biosciprocs.16.0010; Rodriguez, O. L., Berndtson, W. E., Ennen, B. D., & Pickett, B. W. (1975). Effect of rates of freezing, thawing and level of glycerol on the survival of bovine spermatozoa in straws. Journal of Animal Science, 41(1), 129–136. https://doi.org/10.2527/jas1975.411129x; Roldan, E. R. S. (1998). Signal transduction during mammalian sperm acrosomal exocytosis. In Gametes: Development and function (pp. 219–228). https://www.researchgate.net/profile/Eduardo- Roldan/publication/349771261_Signal_transduction_during_mammalian_sperm_acr osomal_exocytosis/links/60410c5792851c077f187c70/Signal-transduction-during- mammalian-sperm-acrosomal-exocytosis.pdf; Rubio, J. L., Quintero, A. A., & González, D. M. (2009). Efecto de la criopreservación sobre la integridad de la membrana plasmática y acrosomal de espermatozoides de toros. Revista Cientifica de La Facultad de Ciencias Veterinarias de La Universidad Del Zulia, 19(4), 382–389. http://ve.scielo.org/scielo.php?pid=S0798- 22592009000400010&script=sci_arttext&tlng=pt; Ruiz, E., Diez, C., López, M., & Enriquez, J. (2007). The Role of the Mitochondrion in Sperm Function: Is There a Place for Oxidative Phosphorylation or Is This a Purely Glycolytic Process? In The Mitochondrion in Germline and Early Development (pp. 3–14).; Sa-Ardrit, M., Saikhun, J., Thongtip, N., Damyang, M., Mahasawangkul, S., Angkawanish, T., Jansittiwate, S., Faisaikarm, T., Kitiyanant, Y., Pavasuthipaisit, K., & Pinyopummin, A. (2006). Ultrastructural alterations of frozen-thawed Asian elephant (Elephas maximus) spermatozoa. International Journal of Andrology, 29(2), 346– 352. https://doi.org/10.1111/j.1365-2605.2005.00578.x; Said, T. M., Gaglani, A., & Agarwal, A. (2010). Implication of apoptosis in sperm cryoinjury. In Reproductive BioMedicine Online (Vol. 21, Issue 4, pp. 456–462). Elsevier. https://doi.org/10.1016/j.rbmo.2010.05.011; Salazar, J. L., Teague, S. R., Love, C. C., Brinsko, S. P., Blanchard, T. L., & Varner, D. D. (2011). Effect of cryopreservation protocol on postthaw characteristics of stallion sperm. Theriogenology, 76(3), 409–418. https://doi.org/10.1016/j.theriogenology.2011.02.016; Salisbury, G. W. (1967). Aging Phenomena in Spermatozoa. III. Effect of Season and Storage at −79 to −88 C on Fertility and Prenatal Losses. Journal of Dairy Science, 50(10), 1683–1689. https://doi.org/10.3168/jds.S0022-0302(67)87694-X; Salisbury, G. W., & Hart, R. G. (1970). Gamete aging and its consequences. Biology of Reproduction. Supplement, 2, 1–13. https://doi.org/10.1095/biolreprod2.Supplement_2.1; Salvioli, S., Ardizzoni, A., Franceschi, C., & Cossarizza, A. (1997). JC-1, but not DiOC6(3) or rhodamine 123, is a reliable fluorescent probe to assess ΔΨ changes in intact cells: Implications for studies on mitochondrial functionality during apoptosis. FEBS Letters, 411(1), 77–82. https://doi.org/10.1016/S0014-5793(97)00669-8; Satorre, M., & Córdoba, M. (2010). Involvement of intracellular calcium and src tyrosine- kinase in capacitation of cryopreserved bovine spermatozoa. InVet, 12(1), 75–83.; Schober, D., Aurich, C., Nohl, H., & Gille, L. (2007). Influence of cryopreservation on mitochondrial functions in equine spermatozoa. Theriogenology, 68(5), 745–754. https://doi.org/10.1016/j.theriogenology.2007.06.004; Shimizu, T., & Johnson, K. A. (1983). Kinetic evidence for multiple dynein ATPase sites. Journal of Biological Chemistry, 258(22), 13841–13846. https://doi.org/10.1016/s0021-9258(17)43994-9; Shoshan-Barmatz, V., Krelin, Y., & Shteinfer-Kuzmine, A. (2018). VDAC1 functions in Ca2+ homeostasis and cell life and death in health and disease. In Cell Calcium (Vol. 69, pp. 81–100). Churchill Livingstone. https://doi.org/10.1016/j.ceca.2017.06.007; Sieme, H., Harrison, R. A. P., & Petrunkina, A. M. (2008). Cryobiological determinants of frozen semen quality, with special reference to stallion. Animal Reproduction Science, 107(3–4), 276–292. https://doi.org/10.1016/j.anireprosci.2008.05.001; Stohs, S. J. (1995). The role of free radicals in toxicity and disease. Journal of Basic and Clinical Physiology and Pharmacology, 6(3–4), 205–228. https://doi.org/10.1515/JBCPP .1995.6.3-4.205; Storey, B. T. (2008). Mammalian sperm metabolism: Oxygen and sugar, friend and foe. International Journal of Developmental Biology, 52(5–6), 427–437. https://doi.org/10.1387/ijdb.072522bs; Stornelli, M. C., Tittarelli, C. M., Savignone, C. A., & Stornelli, M. A. (2005). Efecto de los procesos de criopreservación sobre la fertilidad seminal. Analecta Veterinaria, 25(2), 28–35. http://sedici.unlp.edu.ar/handle/10915/11180; Stradaioli, G., Noro, T., Sylla, L., & Monaci, M. (2007). Decrease in glutathione (GSH) content in bovine sperm after cryopreservation: Comparison between two extenders. Theriogenology, 67(7), 1249–1255. https://doi.org/10.1016/j.theriogenology.2007.01.009; Sullivan, J. J., & Mixner, J. P. (1963). Effects of Storage Temperature and Length of Storage Time upon the Post-thawing Motility and Metabolic Activity of Frozen Bull Semen. Journal of Dairy Science, 46(8), 850–853. https://doi.org/10.3168/jds.S0022- 0302(63)89160-2; Sun, W., Jiang, S., Su, J., Zhang, J., Bao, X., Ding, R., Shi, P., Li, S., Wu, C., Zhao, G., Cao, G., Sun, Q. Y., Yu, H., & Li, X. (2020). The effects of cryopreservation on the acrosome structure, enzyme activity, motility, and fertility of bovine, ovine, and goat sperm. Animal Reproduction, 17(4), 1–10. https://doi.org/10.1590/1984-3143- AR2020-0219; Tanga, B. M., Qamar, A. Y., Raza, S., Bang, S., Fang, X., Yoon, K., & Cho, J. (2021). Semen evaluation: Methodological advancements in sperm quality-specific fertility assessment - A review. Animal Bioscience, 34(8), 1253–1270. https://doi.org/10.5713/ab.21.0072; Thomas, A. D., Meyers, S. A., & Ball, B. A. (2006). Capacitation Like Changes in Equine Spermatozoa following Cryopreservation. Theriogenology, 65(8), 1531–1550.; Thomas, C. A., Garner, D. L., Dejarnette, J. M., & Marshall, C. E. (1998). Effect of cryopreservation on bovine sperm organelle function and viability as determined by flow cytometry. Biology of Reproduction, 58(3), 786–793. https://doi.org/10.1095/biolreprod58.3.786; Thurston, L. M., Watson, P. F., & Holt, W. V. (1999). Sources of variation in the morphological characteristics of sperm subpopulations assessed objectively by a novel automated sperm morphology analysis system. Journal of Reproduction and Fertility, 117(2), 271–280. https://doi.org/10.1530/jrf.0.1170271; Thurston, Lisa M., Watson, P. F., & Holt, W. V. (2002). Semen cryopreservation: A genetic explanation for species and individual variation? Cryo-Letters, 23(4), 255– 262. https://www.researchgate.net/publication/5329483_Semen_cryopreservation_A_gen etic_explanation_for_species_and_individual_variation; Treulen, F., Arias, M. E., Aguila, L., Uribe, P., & Felmer, R. (2018). Cryopreservation induces mitochondrial permeability transition in a bovine sperm model. Cryobiology, 83(June), 65–74. https://doi.org/10.1016/j.cryobiol.2018.06.001; Triphan, J., Aumüller, G., Brandenburger, T., & Wilhelm, B. (2007). Localization and regulation of plasma membrane Ca2+-ATPase in bovine spermatozoa. European Journal of Cell Biology, 86(5), 265–273. https://doi.org/10.1016/j.ejcb.2007.02.003; Tulsiani, D. R. P., Zeng, H.-T., & Abou-Haila, A. (2007). Multiple signaling pathways leading to capacitation Biology of sperm capacitation: evidence for multiple signaling pathways. Reprod Fertil Suppl., 63(257–72).; Ugur, M. R., Saber Abdelrahman, A., Evans, H. C., Gilmore, A. A., Hitit, M., Arifiantini, R. I., Purwantara, B., Kaya, A., & Memili, E. (2019). Advances in Cryopreservation of Bull Sperm. In Frontiers in Veterinary Science (Vol. 6, p. 268). Frontiers Media S.A. https://doi.org/10.3389/fvets.2019.00268; Upadhyay, V. R., Ramesh, V., Dewry, R. K., Kumar, G., Raval, K., & Patoliya, P. (2021). Implications of cryopreservation on structural and functional attributes of bovine spermatozoa: An overview. In Andrologia (Vol. 53, Issue 8, p. e14154). John Wiley & Sons, Ltd. https://doi.org/10.1111/and.14154; Van Dop, C., Hutson, S. M., & Lardy, H. A. (1977). Pyruvate metabolism in bovine epididymal spermatozoa. Journal of Biological Chemistry, 252(4), 1303–1308. https://doi.org/10.1016/s0021-9258(17)40655-7; Van Overveld, F. W. P. C., Haenen, G. R. M. M., Rhemrev, J., Vermeiden, J. P. W., & Bast, A. (2000). Tyrosine as important contributor to the antioxidant capacity of seminal plasma. Chemico-Biological Interactions, 127(2), 151–161. https://doi.org/10.1016/S0009-2797(00)00179-4; Villa Duque, N., Amaya Torres, C. M., García Rojas, D., Nieto Omeara, N., & Terán Acuña, N. (2016). Efecto de la manipulación del semen criopreservado de bovinos Bos Taurus sobre la integridad espermática. CIENCIA Y AGRICULTURA, 13(1), 9. https://doi.org/10.19053/01228420.4802; Wang, A. W., Zhang, H., Ikemoto, I., Anderson, D. J., & Loughlin, K. R. (1997). Reactive oxygen species generation by seminal cells during cryopreservation. Urology, 49(6), 921–925. https://doi.org/10.1016/S0090-4295(97)00070-8; Watson, P. F. (1981). The effects of cold shock on sperm cell membranes. Trends in Biochemical Sciences, Effects of low temperatures on biological membranes, 189-21 8. https://ci.nii.ac.jp/naid/10027566484/; Watson, P. F. (1995). Recent developments and concepts in the cryopreservation of spermatozoa and the assessment of their post-thawing function. Reproduction, Fertility and Development, 7(4), 871–891. https://doi.org/10.1071/RD9950871; Watson, P. F. (2000). The causes of reduced fertility with cryopreserved semen. Animal Reproduction Science, 60–61, 481–492. https://doi.org/10.1016/S0378- 4320(00)00099-3; Wood, P. L., Scoggin, K., Ball, B. A., Troedsson, M. H., & Squires, E. L. (2016). Lipidomics of equine sperm and seminal plasma: Identification of amphiphilic (O- acyl)-ω-hydroxy-fatty acids. Theriogenology, 86(5), 1212–1221. https://doi.org/10.1016/j.theriogenology.2016.04.012; Woolley, D. M., & Richardson, D. W. (1978). Ultrastructural injury to human spermatozoa after freezing and thawing. Journal of Reproduction and Fertility, 53(2), 389–394. https://doi.org/10.1530/jrf.0.0530389; Yanagimachi, R. (1994). The physiology of Reproduction. Raven Press, 189–317.; Yildiz, C., Yavas, I., Bozkurt, Y., & Aksoy, M. (2015). Effect of cholesterol-loaded cyclodextrin on cryosurvival and fertility of cryopreserved carp (Cyprinus carpio) sperm. Cryobiology, 70(2), 190–194. https://doi.org/10.1016/j.cryobiol.2015.01.009; Yoon, S.-J., Kwon, W.-S., Rahman, M. S., Lee, J.-S., & Pang, M.-G. (2015). A Novel Approach to Identifying Physical Markers of Cryo-Damage in Bull Spermatozoa. PLOS ONE, 10(5), e0126232. https://doi.org/10.1371/journal.pone.0126232; Yoon, S. J., Rahman, M. S., Kwon, W. S., Ryu, D. Y., Park, Y. J., & Pang, M. G. (2016). Proteomic identification of cryostress in epididymal spermatozoa. Journal of Animal Science and Biotechnology, 7(1), 67. https://doi.org/10.1186/s40104-016-0128-2; Zamboni, L. (1987). The ultrastructural pathology of the spermatozoon as a cause of infertility: The role of electron microscopy in the evaluation of semen quality. In Fertility and Sterility (Vol. 48, Issue 5, pp. 711–734). Elsevier. https://doi.org/10.1016/s0015-0282(16)59520-x; Zhang, X. G., Hu, S., Han, C., Zhu, Q. C., Yan, G. J., & Hu, J. H. (2015). Association of heat shock protein 90 with motility of post-thawed sperm in bulls. Cryobiology, 70(2), 164–169. https://doi.org/10.1016/j.cryobiol.2014.12.010; Zhu, W. J., & Liu, X. G. (2000). Cryodamage to plasma membrane integrity in head and tail regions of human sperm. Asian Journal of Andrology, 2(2), 135–138. http://www.asiaandro.com/archive/1008-682X/2/135.htm; https://repositorio.unal.edu.co/handle/unal/84599; Universidad Nacional de Colombia; Repositorio Institucional Universidad Nacional de Colombia; https://repositorio.unal.edu.co/