Journals / Journal of advances in vetbio science and techniques / 2026 / Issue: 2

Effect of the balance between flaxseed and animal fat on FADS2 gene expression in the liver of Japanese quail (Coturnix japonica)

Seda Ekici(Veterinary Control Central Research Institute, Ankara, Türkiye)0000-0002-7982-5261
Aydın Daş(HARRAN ÜNİVERSİTESİ)0000-0003-0371-5434
Pages
—
Publication Date
2026-09-25
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Results demonstrated a significant effect of dietary treatment on hepatic FADS2 expression (P < 0.001).

📌 3 Key Takeaways

🎯
Objective & Hypothesis:This study investigated the effects of dietary lipid composition on hepatic FADS2 gene expression in Japanese quail (Coturnix japonica), focusing on graded combinations of animal fat and flaxseed inclusion.
📊
Key Findings & Data:A total of 80 quail were randomly allocated into four dietary groups (n = 20 per group), in which animal fat levels were progressively increased (0–5%) while flaxseed levels were decreased (5–0%).
💡
Conclusion & Impact:Results demonstrated a significant effect of dietary treatment on hepatic FADS2 expression (P < 0.001).
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Japanese quail · FADS2 · flaxseed

Abstract

This study investigated the effects of dietary lipid composition on hepatic FADS2 gene expression in Japanese quail (Coturnix japonica), focusing on graded combinations of animal fat and flaxseed inclusion. A total of 80 quail were randomly allocated into four dietary groups (n = 20 per group), in which animal fat levels were progressively increased (0–5%) while flaxseed levels were decreased (5–0%). All diets were formulated to contain approximately 24% crude protein and 3000 kcal/kg metabolizable energy. At the end of the experimental period, hepatic tissue samples were collected, and FADS2 gene expression was quantified using real-time PCR. Relative gene expression was calculated using the 2⁻ΔΔCt method with ACTB as the reference gene. Statistical analysis was performed using one-way ANOVA followed by Tukey’s post hoc test. Results demonstrated a significant effect of dietary treatment on hepatic FADS2 expression (P < 0.001). Relative expression analysis revealed a progressive increase in FADS2 expression across dietary groups, with fold changes of 1.18, 2.94, and 4.75 in Groups 2, 3, and 4, respectively, compared with the calibrator group. Post hoc analysis indicated significant differences particularly between low and high animal fat inclusion groups. The response pattern suggested a non-linear modulation of hepatic FADS2 expression in response to dietary lipid composition. In conclusion, increasing dietary animal fat levels combined with decreasing flaxseed supplementation significantly upregulated hepatic FADS2 gene expression in Japanese quail. These findings suggest that dietary fatty acid composition is an important regulator of hepatic lipid metabolism at the transcriptional level and may be relevant for nutritional strategies aimed at modulating lipid quality in poultry products.

🔖

Cite This Article

Ekici, S., Yığın, A., Daş, A. (2026). Effect of the balance between flaxseed and animal fat on FADS2 gene expression in the liver of Japanese quail (Coturnix japonica). Journal of advances in vetbio science and techniques, Issue: 2. https://doi.org/10.31797/vetbio.1869858

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (32)

  1. Abdulla, N. R., Loh, T. C., Foo, H. L., Alshelmani, M. I., & Akit, H. (2019). Influence of dietary ratios of n-6: n-3 fatty acid on gene expression, fatty acid profile in liver and breast muscle tissues, serum lipid profile, and immunoglobulin in broiler chickens. Journal of Applied Poultry Research, 28(2), 454–469. https://doi.org/10.3382/japr/pfz008
  2. Alagawany, M., Elnesr, S. S., Farag, M. R., Abd El-Hack, M. E., Khafaga, A. F., Taha, A. E.,Tiwari, R., Yatoo, M. I., Bhatt, P., Khurana, S. K., & Dhama, K. (2019). Omega-3 and Omega-6 fatty acids in poultry nutrition: Effect on production performance and health. Animals, 9(8), 573. https://doi.org/10.3390/ani9080573
  3. Behnke, K. C. (1996). Feed manufacturing technology: current issues and challenges. Animal Feed Science and Technology, 62(1), 49–57. https://doi.org/10.1016/S0377-8401(96)01005-X
  4. Cao, Z., Wang, L., Zhang, Y., Chang, G., & Chen, G. (2025). Hepatic fatty acid profile and gut microbiome responses of ducks induced by dietary n-6/n-3 polyunsaturated fatty acid ratio. Poultry Science, 104, 105873. https://doi.org/10.1016/j.psj.2025.105873
  5. Cartoni Mancinelli, A., Di Veroli, A., Mattioli, S., Cruciani, G., Dal Bosco, A., & Castellini, C. (2022). Lipid metabolism analysis in liver of different chicken genotypes and impact on nutritionally relevant polyunsaturated fatty acids of meat. Scientific Reports, 12(1), 1888. https://doi.org/10.1038/s41598-022-05986-2
  6. Cherian, G. (2015). Nutrition and metabolism in poultry: role of lipids in early diet. Journal of Animal Science and Biotechnology, 6(1), 28. https://doi.org/10.1186/s40104-015-0029-9
  7. Cherian, G., Fraz, A., & Bionaz, M. (2023). Evaluating the impact of organic chromium on hepatic phospholipid fatty acid molecular species, transcription of genes associated with lipid metabolism and oxidative status in broiler chickens fed flaxseed. Poultry Science, 102(10), 102976. https://doi.org/10.1016/j.psj.2023.102976
  8. Ekmekçi, K. (2022). Döteryum oksitin sıcaklık, gama ve ultraviyole maruziyetlerine karşı yağ asitleri profiline etkilerinin incelenmesi (Publication No. 31969634) [Master’s thesis, Istanbul Sabahattin Zaim University]. ProQuest Dissertations & Theses Global.
  9. Erhan, F. (2020). Tavuk ve rat karaciğerinde yağ ve karbonhidrat metabolizmalarının karşılaştırılması (Publication No. 31152093) [Doctoral dissertation, Ankara University]. ProQuest Dissertations & Theses Global
  10. Ghobashy, M., Gaafar, K., Fathalla, S., Abu-Alya, I., & Abou-Elkhair, R. (2023). Beneficial effects of n-3 fatty acids as feed additive on broiler chicken. Matrouh Journal of Veterinary Medicine, 3(1), 58–69. https://doi.org/10.21608/mjvm.2023.294173
  11. Gonzalez-Soto, M., & Mutch, D. M. (2021). Diet regulation of long-chain PUFA synthesis: role of macronutrients, micronutrients, and polyphenols on Δ-5/Δ-6 desaturases and elongases 2/5. Advances in Nutrition, 12(3), 980–994. https://doi.org/10.1093/advances/nmaa142
  12. Hermier, D. (1997). Lipoprotein metabolism and fattening in poultry. Journal of Nutrition, 127(5 Suppl), 805S–808S. https://doi.org/10.1093/jn/127.5.805S
  13. Ji, T., Fang, B., Wu, F., Liu, Y., Cheng, L., Li, Y., & Zhu, L. (2023). Diet change improves obesity and lipid deposition in high-fat diet-induced mice. Nutrients, 15(23), 4978. https://doi.org/10.3390/nu15234978
  14. Jump, D. B., Tripathy, S., & Depner, C. M. (2013). Fatty acid–regulated transcription factors in the liver. Annual Review of Nutrition, 33(1), 249–269. https://doi.org/10.1146/annurev-nutr-071812-161139
  15. Kim, M., & Voy, B. H. (2021). Fighting fat with fat: n-3 polyunsaturated fatty acids and adipose deposition in broiler chickens. Frontiers in Physiology, 12, 755317. https://doi.org/10.3389/fphys.2021.755317
  16. Koppenol, A., et al. (2014). Effect of the ratio of dietary n-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid on broiler breeder performance, egg quality, and yolk fatty acid composition at different breeder ages. Poultry Science, 93(3), 564–573. https://doi.org/10.3382/ps.2013-03320
  17. Kumar, F., Tyagi, P. K., Mir, N. A., Tyagi, P. K., Dev, K., Bera, I., & Deo, C. (2019). Role of flaxseed meal feeding for different durations in the lipid deposition and meat quality in broiler chickens. Journal of the American Oil Chemists’ Society, 96(3), 261–271. https://doi.org/10.1002/aocs.12190
  18. Li, Y., Zhang, H., Wang, Y., & Zhang, L. (2020). Dietary fatty acids regulate hepatic lipid metabolism and fatty acid desaturase gene expression. Journal of Animal Science and Biotechnology, 11, 45. https://doi.org/10.1186/s40104-020-00443-7
  19. Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods, 25(4), 402–408. https://doi.org/10.1006/meth.2001.1262
  20. Liu, Y., Sun, D., Li, X., Ge, M., & Hou, Z. (2023). Research Note: Identification of core promoter region of the polyunsaturated fatty acid synthesis-related gene family in chicken. Poultry Science, 102(9), 102857. https://doi.org/10.1016/j.psj.2023.102857
  21. Mariamenatu, A. H., & Abdu, E. M. (2021). Overconsumption of Omega-6 polyunsaturated fatty acids versus deficiency of Omega-3 polyunsaturated fatty acids in modern-day diets. Journal of Lipids, 2021, 8848161. https://doi.org/10.1155/2021/8848161
  22. Nakamura, M. T., & Nara, T. Y. (2004). Structure, function, and dietary regulation of Δ6, Δ5, and Δ9 desaturases. Annual Review of Nutrition, 24, 345–376. https://doi.org/10.1146/annurev.nutr.24.121803.063211
  23. Nobakht, A., Tabatbaei, S., & Khodaei, S. (2011). Effects of different sources and levels of vegetable oils on performance, carcass traits and accumulation of vitamin E in breast meat of broilers. Current Research Journal of Biological Sciences, 3 (6), 601–605.
  24. NRC. (1994). Nutrient requirements of poultry (9th rev. ed.). National Academy Press.
  25. Qin, N., Shan, X., Sun, X., Liswaniso, S., Chimbaka, I. M., & Xu, R. (2020). Evaluation and validation of the six housekeeping genes for normalizing mRNA expression in the ovarian follicles and several tissues in chicken. Brazilian Journal of Poultry Science, 22, eRBCA-2019.
  26. Shimano, H., & Sato, R. (2017). SREBP-regulated lipid metabolism: convergent physiology—divergent pathophysiology. Nature Reviews Endocrinology, 13(12), 710–730. https://doi.org/10.1038/nrendo.2017.91
  27. Sierżant, K., Piksa, E., Konkol, D., Lewandowska, K., & Asghar, M. U. (2023). Performance and antioxidant traits of broiler chickens fed with diets containing rapeseed or flaxseed oil and optimized quercetin. Scientific Reports, 13(1), 14011. https://doi.org/10.1038/s41598-023-41282-3
  28. Su, F., & Koeberle, A. (2024). Regulation and targeting of SREBP-1 in hepatocellular carcinoma. Cancer and Metastasis Reviews, 43(2), 673–708. https://doi.org/10.1007/s10555-023-10156-5
  29. Sun, J., Li, J., Li, Y., Du, J., Zhao, N., Mai, K., & Ai, Q. (2022). Regulation of Δ6Fads2 gene involved in LC-PUFA biosynthesis subjected to fatty acid in large yellow croaker and rainbow trout. Biomolecules, 12(5), 659. https:// doi.org/10.3390/biom12050659
  30. Talpur, M. (2023). Effect of chicken breeds on the meat quality and association with candidate gene expression. Pak. J. Agric. Sci., 60, 1-8.
  31. Wang, F., Feng, J., Yao, M., Dou, L., Nan, S., Pang, X., & Nie, C. (2024). Dietary succinate reduces fat deposition through gut microbiota and lipid metabolism in broilers. Poultry Science, 103(8), 103954. https://doi.org/10.1016/j.psj.2024.103954
  32. Zhang, Y., Cao, Z., Wang, L., Dong, B., Qi, S., Xu, X., & Chen, G. (2023). Effects of linseed oil supplementation duration on fatty acid profile and fatty acid metabolism-related genes in the muscles of Chinese crested white ducks. Poultry Science, 102(10), 102896. https://doi.org/10.1016/j.psj.2023.102896