Adeldust, H., Farzinpour, A., Farshad, A., Rostamzadeh, J., & Béjar, M. L. (2021). Effect of orally administrated letrozole on reproduction performance and gene expression of FOXJ1, LPR2 and PVRL3 in reproductive tract in aged roosters.
Theriogenology,
161, 131–139.
https://doi.org/10.1016/j.theriogenology.2020.11.020
Aitken, R. J., & Roman, S. D. (2009). Antioxidant systems and oxidative stress in the testes. In C. Y. Cheng (Ed.),
Molecular mechanisms in spermatogenesis (pp. 154–171).
https://doi.org/10.4161/oxim.1.1.6843
Alizadeh, M., Aghaei, A., Vakili, S. T., & Nazari, M. (2025). Effect of L-serine amino acid and choline supplementation on sperm quality of aged broiler breeder roosters.
Iranian Journal of Animal Science Research. Advance online publication.
https://doi.org/10.22067/ijasr.2025.94457.1260
Amin Altawash, A. S., Zareh Shahneh, A., Moravej, H., Ansari, M., & Deldar, H. (2019). Improvement of testis histological parameters and relative expression of StAR gene in Chrysin-fed roosters.
Iranian Journal of Animal Science,
50(3), 207–215.
https://doi.org/10.22059/ijas.2018.240313.653554
Asadi, N., Bahmani, M., Kheradmand, A., & Rafieian-Kopaei, M. (2017). The impact of oxidative stress on testicular function and the role of antioxidants in improving it: A review.
Journal of Clinical and Diagnostic Research,
11(5), IE01–IE05.
https://doi.org/10.7860/JCDR/2017/23927.9886
Asl, R. S., Shariatmadari, F., Sharafi, M., Torshizi, M. A. K., & Shahverdi, A. (2018). Improvements in semen quality, sperm fatty acids, and reproductive performance in aged Ross breeder roosters fed a diet supplemented with a moderate ratio of n-3: n-6 fatty acids.
Poultry Science,
97(11), 4113–4121.
https://doi.org/10.3382/ps/pey278
Attia, Y. A., El-Naggar, A. S., Abou-Shehema, B. M., & Abdella, A. A. (2019). Effect of supplementation with trimethylglycine (betaine) and/or vitamins on semen quality, fertility, antioxidant status, DNA repair and welfare of roosters exposed to chronic heat stress.
Animals,
9(8), Article 547.
https://doi.org/10.3390/ani9080547
Billah, M. M., Khatiwada, S., Lecomte, V., Morris, M. J., & Maloney, C. A. (2022). Ameliorating high-fat diet-induced sperm and testicular oxidative damage by micronutrient-based antioxidant intervention in rats.
European Journal of Nutrition,
61(7), 3741–3753.
https://doi.org/10.1007/s00394-022-02917-9
Bronson, R., Mikhailik, A., Schwedes, J., Gnatenko, D., & Hatchwell, E. (2017). Detection of candidate nectin gene mutations in infertile men with severe teratospermia.
Journal of Assisted Reproduction and Genetics,
34(10), 1295–1302.
https://doi.org/10.1007/s10815-017-0985-4
Cerolini, S., Kelso, K. A., Noble, R. C., Speake, B. K., Pizzi, F., & Cavalchini, L. G. (1997). Relationship between spermatozoan lipid composition and fertility during aging of chickens.
Biology of Reproduction,
57(5), 976–980.
https://doi.org/10.1095/biolreprod57.5.976
Chiari, N. (2017). Food security: The challenge of nutrition in the new century. Religions: Beyond Anthropocentrism, 5, 145. https://doi.org/10.7358/rela-2017-002-chia
Christenson, L. K., & Strauss III, J. F. (2000). Steroidogenic acute regulatory protein (StAR) and the intramitochondrial translocation of cholesterol.
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids,
1529(1–3), 175–187.
https://doi.org/10.1016/S1388-1981(00)00147-5
Crisóstomo, L., Videira, R. A., Jarak, I., Starčević, K., Mašek, T., Rato, L., & Alves, M. G. (2022). Inherited metabolic memory of high‐fat diet impairs testicular fatty acid content and sperm parameters.
Molecular Nutrition & Food Research,
66(5), Article 2100680.
https://doi.org/10.1002/mnfr.202100680
Díaz Ruiz, E., Navas González, F. J., León Jurado, J. M., Arando Arbulu, A., Delgado Bermejo, J. V., & González Ariza, A. (2024). Effects of supplementation of different antioxidants to cryopreservation extender on the post-thaw quality of rooster semen-A meta-analysis.
Animals,
14(20), Article 2936.
https://doi.org/10.3390/ani14202936
Fagone, P., & Jackowski, S. (2013). Phosphatidylcholine and the CDP–choline cycle.
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids,
1831(3), 523–532.
https://doi.org/10.1016/j.bbalip.2012.09.009
Feng, Y., Ding, Y., Liu, J., Tian, Y., Yang, Y., Guan, S., & Zhang, C. (2015). Effects of dietary omega-3/omega-6 fatty acid ratios on reproduction in the young breeder rooster.
BMC Veterinary Research,
11, Article 73.
https://doi.org/10.1186/s12917-015-0394-9
Gallo, A., Esposito, M. C., Tosti, E., & Boni, R. (2021). Sperm motility, oxidative status, and mitochondrial activity: Exploring correlation in different species.
Antioxidants,
10(7), Article 1131.
https://doi.org/10.3390/antiox10071131
Hanley, P. J. (2023). Elusive physiological role of prostatic acid phosphatase (PAP): Generation of choline for sperm motility via auto-and paracrine cholinergic signaling.
Frontiers in Physiology,
14, Article 1327769.
https://doi.org/10.3389/fphys.2023.1327769
Harbs, J., Rinaldi, S., Keski-Rahkonen, P., Liu, X., Palmqvist, R., Van Guelpen, B., & Harlid, S. (2023). An epigenome-wide analysis of sex hormone levels and DNA methylation in male blood samples.
Epigenetics,
18(1), Article 2196759.
https://doi.org/10.1080/15592294.2023.2196759
Holeček, M. (2022). Serine metabolism in health and disease and as a conditionally essential amino acid.
Nutrients,
14(9), Article 1987.
https://doi.org/10.3390/nu14091987
Jiang, X., Li, X., Feng, W., Qin, Y., Li, Z., Nie, H., & Bai, W. (2021). Baking of methionine-choline deficient diet aggravates testis injury in mice.
Food and Chemical Toxicology,
154, Article 112245.
https://doi.org/10.1016/j.fct.2021.112245
Kansakar, U., Trimarco, V., Mone, P., Varzideh, F., Lombardi, A., & Santulli, G. (2023). Choline supplements: An update.
Frontiers in Endocrinology,
14, Article 1148166.
https://doi.org/10.3389/fendo.2023.1148166
Kotwicka, M., Jendraszak, M., & Jedrzejczak, P. (2011). Phosphatidylserine membrane translocation in human spermatozoa: Topography in membrane domains and relation to cell vitality.
The Journal of Membrane Biology,
240(3), 165–170.
https://doi.org/10.1007/s00232-011-9357-7
Krzysztof Blusztajn, J., & J Mellott, T. (2012). Choline nutrition programs brain development via DNA and histone methylation.
Central Nervous System Agents in Medicinal Chemistry,
12(2), 82–94.
https://doi.org/10.2174/187152412800792706
Kumagai, A., Kodama, H., Kumagai, J., Fukuda, J., Kawamura, K., Tanikawa, H., & Tanaka, T. (2002). Xanthine oxidase inhibitors suppress testicular germ cell apoptosis induced by experimental cryptorchidism.
Molecular Human Reproduction,
8(2), 118–123.
https://doi.org/10.1093/molehr/8.2.118
Li, J., Xin, Y., Li, J., Chen, H., & Li, H. (2023). Phosphatidylethanolamine N-methyltransferase: From functions to diseases.
Aging and Disease,
14(3), 879.
https://doi.org/10.14336/AD.2022.1025
Pan, S., Fan, M., Liu, Z., Li, X., & Wang, H. (2020). Serine, glycine and one-carbon metabolism in cancer.
International Journal of Oncology,
58(2), 158–170.
https://doi.org/10.3892/ijo.2020.5158
Partyka, A., Babapour, A., Mikita, M., Adeniran, S., & Niżański, W. (2023). Lipid peroxidation in avian semen.
Polish Journal of Veterinary Sciences,
26(4), 497–509.
https://doi.org/10.24425/pjvs.2023.145050
Prasetiyono, B. W. H. E., Ondho, Y. S., Subrata, A., Pratiwi, P. K., Zahra, M. B., Itmamulwafa, T., & Widiyanto, W. (2020). The effect of choline chloride supplementation on the reproductive performance of Simmental bulls fed protected protein in the ration.
Buletin Peternakan,
44(2), 83–89.
https://doi.org/10.21059/buletinpeternak.v44i2.55338
Rodríguez-Paredes, M., & Esteller, M. (2011). Cancer epigenetics reaches mainstream oncology.
Nature Medicine,
17(3), 330–339.
https://doi.org/10.1038/nm.2305
Sabah, S., & Dikmen, B. Y. (2023). Relationships between morphological characteristics of roosters in broiler breeders at different age periods.
Journal of Poultry Research,
20(1), 25–31.
https://doi.org/10.34233/jpr.1314476
Salari, H. R., Jafari Ahangari, Y., & Ansari Pirsaraie, Z. (2021). Changes of testis histology parameters and relative expression of TGF‑β4 & StAR genes in roosters fed CoQ10 and omega‑3 fatty acids.
Journal of Animal Production,
23(2), 293–302.
https://doi.org/10.22059/jap.2021.314795.623578
Santiago-Moreno, J., Bernal, B., Perez-Cerezales, S., Castano, C., Toledano-Díaz, A., Esteso, M. C., & Blesbois, E. (2019). Seminal plasma amino acid profile in different breeds of chicken: Role of seminal plasma on sperm cryoresistance.
PLOS ONE,
14(1), Article e0209910.
https://doi.org/10.1371/journal.pone.0209910
Shan, S., Xu, F., Hirschfeld, M., & Brenig, B. (2021). Sperm lipid markers of male fertility in mammals.
International Journal of Molecular Sciences,
22(16), Article 8767.
https://doi.org/10.3390/ijms22168767
Sharma, A. K., & Bansal, P. (Eds.). (2023). Serine proteases: Role in human health and disease. Walter de Gruyter.
Singh Rawat, B., Venkataraman, R., Budhwar, R., & Tailor, P. (2022). Methionine-and choline-deficient diet identifies an essential role for DNA methylation in plasmacytoid dendritic cell biology.
The Journal of Immunology,
208(4), 881–897.
https://doi.org/10.4049/jimmunol.2100763
Stocco, D. M., Clark, B. J., Reinhart, A. J., Williams, S. C., Dyson, M., Dassi, B., & Orly, J. (2001). Elements involved in the regulation of the StAR gene.
Molecular and Cellular Endocrinology,
177(1–2), 55–59.
https://doi.org/10.1016/S0303-7207(01)00423-3
Xiong, N., Liu, S., Hu, W., Liu, Y., Ding, X., Wu, B., & Zheng, W. (2025). Selenium yeast alleviates diquat-induced oxidative stress and testicular damage in roosters.
Animal Reproduction Science,
273, Article 107760.
https://doi.org/10.1016/j.anireprosci.2024.107760
Zangar, R. C., Davydov, D. R., & Verma, S. (2004). Mechanisms that regulate production of reactive oxygen species by cytochrome P450.
Toxicology and Applied Pharmacology,
199(3), 316–331.
https://doi.org/10.1016/j.taap.2004.01.018
Zhang, X., Peng, J., Wu, M., Sun, A., Wu, X., Zheng, J., & Gao, G. (2023). Broad phosphorylation mediated by testis-specific serine/threonine kinases contributes to spermiogenesis and male fertility.
Nature Communications,
14(1), Article 2629.
https://doi.org/10.1038/s41467-023-38357-0
Zhou, X., He, L., Wu, C., Zhang, Y., Wu, X., & Yin, Y. (2017). Serine alleviates oxidative stress via supporting glutathione synthesis and methionine cycle in mice.
Molecular Nutrition & Food Research,
61(11), Article 1700262.
https://doi.org/10.1002/mnfr.201700262
Zhou, X., He, L., Zuo, S., Zhang, Y., Wan, D., Long, C., & Yin, Y. (2018). Serine prevented high-fat diet-induced oxidative stress by activating AMPK and epigenetically modulating the expression of glutathione synthesis-related genes.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease,
1864(2), 488–498.
https://doi.org/10.1016/j.bbadis.2017.11.009