DOI QR코드

DOI QR Code

Effects of vitamin K supplementation on reproductive performance and bone metabolism-related biochemical markers in lactation sows

  • Huakai Wang (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) ;
  • Yu Zhang (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) ;
  • Yongxi Ma (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University)
  • Received : 2023.03.15
  • Accepted : 2023.05.01
  • Published : 2023.10.01

Abstract

Objective: This study was conducted to evaluate the effects of vitamin K (VK) supplementation on reproductive performance and bone metabolism-related biochemical markers in sows. Methods: Twenty-four Large White×Landrace sows (mean parity 4.04) were randomly assigned to two dietary treatments (NC diet, a basal diet with 0.5 mg/kg of VK3; VK diet, a basal diet with 5 mg/kg of VK3) with twelve replicates per treatment and one sow per replicate according to parity. The experiment started on day 107 of gestation and lasted until day 21 of lactation (weaning). Results: We observed that there were no differences (p>0.05) in average daily feed intake, backfat loss of sows, live piglet number at birth and weaning, average birth weight, average weaning weight, and average daily gain of piglets between two treatments. The apparent total tract digestibility of phosphorus was increased (p<0.05) in VK sows compared with NC sows. The serum bone alkaline phosphatase, osteocalcin, type I procollagen amino-terminal peptide, and type I procollagen carboxyl-terminal peptide on day of farrowing were higher (p<0.05) in VK sows than in NC sows. The serum phosphorus, parathyroid hormone, tartrate-resistant acid phosphatase, and tumor necrosis factor-alpha on day of weaning were lower (p<0.05) in VK sows compared with NC sows. Conclusion: Therefore, the overall results suggested that increasing dietary VK3 (0.5 to 5 mg/kg) during lactation improved the apparent total tract digestibility of phosphorus and serum bone metabolism biochemical markers in sows.

Keywords

Acknowledgement

This work was supported by the National Natural Science Foundation of China (32072740).

References

  1. Engblom L, Stalder K, Lundeheim N. Premature removal and mortality of commercial sows. In: Book of abstracts of the 62nd annual meeting of the European Federation of Animal Science. Wageningen, Netherlands: Wageningen Academic Publishers, 2011.
  2. Anil SS, Anil L, Deen J. Effect of lameness on sow longevity. J Am Vet Med Assoc 2009;235:734-8. https://doi.org/10.2460/javma.235.6.734
  3. McNeil B, Calderon Diaz J, Bruns C, et al. Determining the time required to detect induced sow lameness using an embedded microcomputer-based force plate system. Am J Anim Vet Sci 2018;13:59-65. https://doi.org/10.3844/ajavsp.2018.59.6
  4. Pluym LM, Van Nuffel A, Van Weyenberg S, Maes D. Prevalence of lameness and claw lesions during different stages in the reproductive cycle of sows and the impact on reproduction results. Animal 2013;7:1174-81. https://doi.org/10.1017/S1751731113000232
  5. Aasmundstad T, Kongsro J, Wetten M, Dolvik NI, Vangen O. Osteochondrosis in pigs diagnosed with computed tomography: heritabilities and genetic correlations to weight gain in specific age intervals. Animal 2013;7:1576-82. https://doi.org/10.1017/S1751731113001158
  6. Faba L, Gasa J, Tokach MD, Varella E, Sola-Oriol D. Effects of supplementing organic microminerals and methionine during the rearing phase of replacement gilts on lameness, growth, and body composition. J Anim Sci 2018;96:327487. https://doi.org/10.1093/jas/sky195
  7. de Koning DB, van Grevenhof EM, Laurenssen BF, van Weeren PR, Hazeleger W, Kemp B. The influence of dietary restriction before and after 10 weeks of age on osteochondrosis in growing gilts. J Anim Sci 2013;91:5167-76. https://doi.org/10.2527/jas.2013-6591
  8. Morris JG. Vitamins in animal and human nutrition. Ames, IA, USA: John Wiley & Sons; 2008.
  9. Tsugawa N, Shiraki M. Vitamin K nutrition and bone health. Nutrients 2020;12:1909. https://doi.org/10.3390/nu12071909
  10. Tabb MM, Sun A, Zhou C, et al. Vitamin K2 regulation of bone homeostasis is mediated by the steroid and xenobiotic receptor SXR. J Biol Chem 2003;278:43919-27. https://doi.org/10.1074/jbc.M303136200
  11. Ichikawa T, Horie-Inoue K, Ikeda K, Blumberg B, Inoue S. Vitamin K2 induces phosphorylation of protein kinase A and expression of novel target genes in osteoblastic cells. J Mol Endocrinol 2007;39:239-47. https://doi.org/10.1677/JME-07-0048
  12. Katsuyama H, Saijoh K, Otsuki T, Tomita M, Fukunaga M, Sunami S. Menaquinone-7 regulates gene expression in osteoblastic MC3T3E1 cells. Int J Mol Med 2007;19:279-84. https://doi.org/10.3892/ijmm.19.2.279
  13. NRC. Nutrient requirements of swine (11th revised ed.). Washington DC, USA: National Academy Press; 2012.
  14. AOAC. Official methods of analysis, 19th ed.; Association of Official Agricultural Chemists: Arlington, VA, USA: AOAC; 2012.
  15. Karl JP, Fu X, Wang X, et al. Fecal menaquinone profiles of overweight adults are associated with gut microbiota composition during a gut microbiota-targeted dietary intervention. Am J Clin Nutr 2015;102:84-93. https://doi.org/10.3945/ajcn.115.109496
  16. Litta G. Optimum vitamin nutrition. Sheffield, UK: 5M Publishing Benchmark House 8 Smithy Wood Drive; 2012.
  17. Yang P, Wang HK, Li LX, Ma YX. The strategies for the supplementation of vitamins and trace minerals in pig production: surveying major producers in China. Anim Biosci 2021;34:1350-64. https://doi.org/10.5713/ajas.20.0521
  18. Tsugawa N, Uenishi K, Ishida H, et al. A novel method based on curvature analysis for estimating the dietary vitamin K requirement in adolescents. Clin Nutr 2012;31:255-60. https://doi.org/10.1016/j.clnu.2011.10.006
  19. Watanabe O, Hara H, Kasai T. Effect of a phosphorylated guar gum hydrolysate on increased calcium solubilization and the promotion of calcium absorption in rats. Biosci Biotechnol Biochem 2000;64:160-6. https://doi.org/10.1271/bbb.64.160
  20. Ben-awadh AN, Delgado-Calle J, Tu X, et al. Parathyroid hormone receptor signaling induces bone resorption in the adult skeleton by directly regulating the RANKL gene in osteocytes. Endocrinology 2014;155:2797-809. https://doi.org/10.1210/en.2014-1046
  21. Qu Z, Yang F, Hong J, et al. Parathyroid Hormone and Bone Mineral Density: A Mendelian Randomization Study. J Clin Endocrinol Metab 2000;105:e4038-45. https://doi.org/10.1210/clinem/dgaa579
  22. Zaidi M. Skeletal remodeling in health and disease. Nat Med 2007;13:791-801. https://doi.org/10.1038/nm1593
  23. Voorzanger-Rousselot N, Garnero P. Biochemical markers in oncology. Part I: molecular basis. Part II: clinical uses. Cancer Treat Rev 2007;33:230-83. https://doi.org/10.1016/j.ctrv.2007.01.008
  24. Wang T, He C. TNF-α and IL-6: the link between immune and bone system. Curr Drug Targets 2020;21:213-27. https://doi.org/10.2174/1389450120666190821161259