Oxidative status and lipid peroxidation benefits in Japanese quail breeder supplemented with selenium-enriched yeast and antioxidant blend

Authors

DOI:

https://doi.org/10.5433/1679-0359.2026v47n2p415

Keywords:

Ascorbic acid, Malonaldehyde, Organic minerals.

Abstract

The micronutrient selenium (Se) is essential in poultry nutrition and is primarily supplied through diet. Studies have shown that organic Se sources, such as selenomethionine, selenocysteine, and selenium-enriched yeast, have higher bioavailability than inorganic sources such as selenite. This study aimed to evaluate the productive performance and antioxidative status of quail breeders supplemented with selenium-enriched yeast (SeY) alone or as part of an antioxidant blend and their progeny. A total of 420 quails were assigned to five treatments: a basal diet (BD) with 0.25 mg/kg mg kg–¹ Se from sodium selenite (SS); BD + 0.3 mg kg–¹ SeY (0.3 SeY); BD + 0.6 mg kg–¹ SeY (0.6 SeY); BD + 0.3 mg kg–¹ SeY + 6.37 mg kg–¹ antioxidant blend (0.3 SeY+AB); and BD + 0.6 mg kg–¹ SeY + 13.08 mg kg–¹ antioxidant blend (0.6 SeY+AB), with 12 replicates of two males and five females per treatment. Breeder parameters evaluated included productive performance, egg quality, serum biochemistry, antioxidant activity, and lipid peroxidation. The performance of the progeny was assessed from days 1 to 35, with 4 replicates of 25 chicks hatched from eggs of each breeder treatment. Data were analyzed by ANOVA, and means were compared using Tukey’s test with SAS v.9.0. No differences in breeder productive performance or egg quality were observed among treatments. In the first 15 days of life progeny from SeY treatments had lower body weight (P < 0.05). With the addition of AB, body weights were like those observed in the BD group. From days 15 to 35, progeny from the 0.3 SeY treatment showed lower body weight compared to the BD and both AB-supplemented groups. Breeders fed diets containing SeY, either alone or as part of antioxidant blend, had lower serum cholesterol and triglyceride concentrations than those fed the basal diet. In quail breeders, antioxidant capacity (DPPH%) was higher and lipid peroxidation was lower in the serum, liver, and egg yolk in all groups supplemented with SeY, regardless of AB inclusion. It was concluded that SeY supplementation, with or without AB, is recommended to produce fertile eggs in Japanese quails due to its beneficial effects on antioxidant status and blood lipid profile.

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Author Biographies

Aires Santos Silva, Universidade Estadual de Maringá

Master student in the Graduate Program in Animal Science, Universidade Estadual de Maringá, UEM, Maringá, PR, Brazil.

Marina Ximenes da Silva, Universidade Estadual de Maringá

Master student in the Graduate Program in Animal Science, UEM, Maringá, PR, Brazil.

Marcos Adriano Pereira Barbosa, Universidade Estadual de Maringá

Master student in the Graduate Program in Animal Science, UEM, Maringá, PR, Brazil.

Weslley Rogerio Rodrigues, Universidade Estadual de Maringá

Undergraduate student in Animal Science, UEM, Maringá, PR, Brazil.

Paula Toshimi Matumoto Pintro, Universidade Estadual de Maringá

Profa. Dra., Department of Agronomy, UEM, Maringá, PR, Brazil.

Tatiana Carlesso dos Santos, Universidade Estadual de Maringá

Profa. Dra., Department of Animal Science, UEM, Maringá, PR, Brazil.

References

Abd El-Hack, M. E., Mahrose, K., Arif, M., Chaudhry, M. T., Saadeldin, I. M., Saeed, M., Soomro, R. N., Abbasi, I. H. R., & Rehman, Z. U. (2017). Alleviating the environmental heat burden on laying hens by feeding on diets enriched with certain antioxidants (vitamin E and selenium) individually or combined. Environmental Science and Pollution Research, 24(11), 10708–10717. doi: 10.1007/s11356-017-8690-5

Ames, B. N. (2001). DNA damage from micronutrient deficiencies is likely to be a major cause of cancer. Mutation Research, 475(1-2), 7-20. doi: 10.1016/S0027-5107(01)00070-5

Barbosa, K. B. F., Costa, N. M. B., Alfenas, R. C. G., Paula, S. O. de, Minim, V. P. R., & Bressan, J. (2010). Estresse oxidativo: conceito, implicações e fatores modulatórios. Revista de Nutrição, 23(4), 629-643. doi: 10.1590/S1415-52732010000400013

Brito, J. M. F., Silva, G. S., Boiago, M. M., Rodrigues, P. H. M., Lima, L. D., Nääs, I. A., & Garcia, R. G. (2023). Soybean oil and selenium yeast supplementation in quail diets: Productive performance, fatty acid profile, enzyme activity, and oxidative stability of meat. European Journal of Lipid Science and Technology, 125(4), 118-220. doi: 10.1002/ejlt.202200118

Chen, Y., Wang, J., Zhang, H., Liu, X., & Zhao, L. (2025). Comparative effects of organic and nano-selenium on egg quality and antioxidant capacity in layer hens. Foods, 14(9), 1454. doi: 10.3390/foods14091454

Chen, Y., Zhang, R., Liu, Y., Wang, X., & Li, J. (2023). Effects of various selenium-enriched yeasts on performance, egg quality, egg selenium deposition, and antioxidant capacity of laying hens. Poultry Science, 102(12), 103-168. doi: 10.1016/j.psj.2023.103168

Ding, X., Cai, C., Jia, R., Bai, S., Zeng, Q., Mao, X., Xu, S., Zhang, K., & Wang, J. (2022). Dietary resveratrol improved production performance, egg quality, and intestinal health of laying hens under oxidative stress. Poultry Science, 101(6), 101886. doi: 10.1016/j.psj.2022.101886.

Khan, A. Z., Kumbhar, S., Hamid, M., Afzal, S., Parveen, F., Liu, Y., Shu, H., Mengistu, B. M., & Huang, K. (2016). Effects of selenium-enriched probiotics on heart lesions by influencing the mRNA expressions of selenoproteins and heat shock proteins in heat stressed broiler chickens. Veterinary Journal, 36(4), 460–464. doi: 10.1016/j.psj.2016,104587.

Li, W., Hydamaka, A. W., Lowry, L., & Beta, T. (2009). Comparison of antioxidant capacity and phenolic compounds of berries, chokecherry and seabuckthorn. Central European Journal of Biology, 4(4), 499–506. https://doi.org/10.2478/s11535-009-0041-1

Liu, H., Yu, Q., Fang, C., Chen, S., Tang, X., Ajuwon, K. M., & Fang, R. (2023). Effect of selenium on performance, egg quality, egg selenium content, and antioxidant capacity in laying hens: a meta-analysis. Poultry Science, 102(6), 102-181. doi: 10.1016/j.psj.2023.102681

Lu, J., Zhang, L., Ma, Q., & Dong, X. (2020). Efficacy evaluation of selenium-enriched yeast in laying hens: effects on performance, egg quality, organ development, and selenium deposition. Poultry Science, 99(12), 6267-6277. doi: 10.1016/j.psj.2020.07.012

Pym, R. A. E. (1969). A suspension weighing technique for the rapid determination of specific gravity of eggs. Australian Journal of Experimental Agriculture. 9(37), 131–134. doi: 10.1071/EA9690131.

Rostagno, H. S. (Ed.). (2017). Brazilian tables for poultry and swine: composition of feedstuffs and nutritional requirements (4nd ed.). Universidade Federal de Viçosa.

Sarmiento-García, A., Sevim, B., Olgun, O., & Ahmet-Gökmen, S. (2022). Effects of different inorganic selenium levels in laying quails (Coturnix coturnix japonica) diets on performance, egg quality, and serum biochemical parameters. Veterinaria México OA, 9 (14), 1046. doi: 10.22201/fmvz.24486760e.2022.1046

Schrauzer, G. N. (2000). Selenomethionine: a review of its nutritional significance, metabolism and toxicity. The Journal of Nutrition, 130(7), 1653-1656. doi: 10.1093/jn/130.7.1653

Skrivan, M., Marounek, M., Englmaierová, M., & Skrivanová, E. (2012). Influence of dietary vitamin C and selenium, alone and in combination, on the composition and oxidative stability of meat of broilers. Food Chemistry, 130(3), 660-664. doi: 10.1016/j.foodchem.2011.07.103.

Statistical Analysis System Institute (1989). SAS/STAT user's guide: statistics (version 6, 4nd ed.). SAS Institute.

Sunde, R. A., Li, J. L., & Taylor, R. M. (2016). Insights for defining nutritional requirements obtained from comparing biomarkers of selenium status in turkeys and chickens versus rats, mice, and lambs. Advances in Nutrition, 7(6), 1129-1138. doi: 10.3945/an.116.012872

Surai, P. F., & Fisinin, V. I. (2015). Vitagenes in poultry production: Part 1. Technological and environmental stresses. World's Poultry Science Journal, 71(4), 721-733. doi: 10.1017/S0043933915002500

Surai, P. F., & Kochish, I. I. (2019). Nutritional modulation of the antioxidant capacities in poultry: the case of selenium. Poultry Science, 98(10), 4231-4239. doi: 10.3382/ps/pez072

Teixeira, M. P. F., Abreu, M. L. T., Almendra, S. N. O., Sousa, T. O., Rodrigues, R. C., Lima, R. N., Holanda, M. C. R., Cardoso, J. F. S., Moraes, J. E., Leandro, N. S. M., Lopes, J. B., & Gonzaga, S., Neto. (2023). Vitamina C na ração de frangos de corte em estresse por calor cíclico. Research, Society and Development, 12(2), e1222484. doi: 10.33448/rsd-v12i2.2484

Torga, A. P., Teixeira, A. O., Reis, R. S., Moreira, L. M., Sousa, J. C. M., Melo, L. P., Rocha, M. H. M., Del Vesco, A. P., & Murakami, A. E. (2024). Egg quality and performance of Japanese quail supplemented with organic and inorganic selenium. Revista Brasileira de Saúde e Produção Animal, 25(15), 27- 45. doi: 10.1590/S1519-994020240070

Vital, A. C. P., Guerrero, A., Monteschio, J. de O., Valero, M. V., Carvalho, C. B., de Abreu Filho, B. A., Madrona, G. S., & do Prado, I. N. (2016). Effect of edible and active coating (with rosemary and oregano essential oils) on beef characteristics and consumer acceptability. PLOS ONE, 11(8), e0160535. https://doi.org/10.1371/journal.pone.0160535

Wang, T., Liu, Y., Zhang, X., Li, J., Chen, H., & Zhao, X. (2025). Effects of dietary selenium yeast supplementation on the production performance, egg quality, antioxidant and plasma biochemical parameters of laying hens. Scientific Reports, 15(4), 11644. doi: 10.1038/s41598-025-31644-4

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Published

2026-08-25

How to Cite

Silva, A. S., Silva, M. X. da, Barbosa, M. A. P., Rodrigues, W. R., Pintro, P. T. M., & Santos, T. C. dos. (2026). Oxidative status and lipid peroxidation benefits in Japanese quail breeder supplemented with selenium-enriched yeast and antioxidant blend. Semina: Ciências Agrárias, 47(2), 415–430. https://doi.org/10.5433/1679-0359.2026v47n2p415

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