The Effect of Vitamin and Mineral Supplement Injection during the Transition Period on Inflammatory and Antioxidant Indices of Dairy Cows

Document Type : Research Articles

Authors

1 Department of Animal Sciences Research, Agricultural and Natural Resources Research Center of Golestan Province, Gorgan, Iran

2 Animal Science Research Institute of IRAN, Agricultural Research Education and Extension Organization (AREEO), Iran

Abstract

Introduction: The physiological transition of dairy cows from late pregnancy to early lactation is accompanied by major changes in the utilization of carbohydrates, amino acids, and lipids by adipose tissue, liver, and skeletal muscle, which are in response to the energy deficit of early lactation, resulting from abundant milk production without adequate compensation in feed intake. On the other hand, increased inflammation, oxidative stress, adipose tissue mobilization, and metabolic disorders occur during the transition period. Inflammation is an evolutionarily conserved response that underlies many physiological and pathological processes; in response to stimuli associated with infection and tissue damage, immune components initiate a response and cause inflammation. Among the essential micronutrients, antioxidant supplements such as minerals and vitamins are of particular importance. Minerals and vitamins, which play an important role in the immune system, help fight infections and diseases, and are in a way a modulator of the inflammatory process, play a role in the antioxidant system through their presence in several significant proteins. Considering the importance of a successful transition from the transition period to the lactation period and its effects on animal performance and health, a study was conducted to investigate the effect of vitamin and mineral supplement injections during the transition period on inflammatory and antioxidant indices of dairy cows.
Materials and Methods: For this purpose, 32 cows with an average milk production of 19 ± 2.7 kg, multiple calving (second calving) and a body condition score of 3.5 ± 0.25 were divided into 4 treatments and 8 replications in a completely randomized design at the end of the gestation period. The experimental treatments included: 1) control group (no vitamin and mineral supplement injection), 2) treatment receiving injectable vitamin supplement, 3) treatment receiving injectable mineral supplement, and 4) treatment receiving both injectable vitamin and mineral supplements. Supplements were injected subcutaneously 28 days before calving. The vitamin supplement contained 50,000 IU of vitamin A (palmitate), 25,000 IU of vitamin D3, 21 mg of vitamin E (acetate), 6 mg of vitamin B1, 2 mg of vitamin B2, 5 mg of vitamin B6, 12.5 mg of vitamin B3 (nicotinamide), 3 μg of vitamin B12, 6 mg of di-panthenol, and 2 mg of vitamin C, and its injection dose was 20 ml per cow as recommended by the manufacturer, and the mineral supplement contained 400 mg of calcium bromide gluconate, 22 mg of magnesium hypophosphite, and 2 mg of copper per ml, and its injection dose was 100 ml per cow as recommended by the manufacturer. The cows were examined for health and multiple births before grouping; all animals were healthy and monogamous. To measure blood biochemical metabolites, inflammatory markers, and antioxidant status, blood samples were collected from 6 replicates of each treatment on days 21 before parturition, the day of parturition, and 21 days after parturition.
Results and Discussion: Albumin, globulin and albumin:globulin ratio were affected by the experimental treatments; so that the injection of minerals, vitamins and minerals and vitamins together caused a decrease in albumin and albumin:globulin ratio and an increase in globulin in the blood of cows. The injection of minerals and vitamins had no effect on the parameters of glucose, cholesterol, triglycerides, total protein and urea. On the other hand, time also affected the parameters of glucose, cholesterol, triglycerides, total protein, albumin, globulin and albumin:globulin ratio. Insulin, catalase, cortisol, glutathione peroxidase, malondialdehyde, superoxide dismutase and total antioxidant status were affected by the experimental treatments; So that by injecting minerals, vitamins and minerals and vitamins together, insulin increased and total antioxidant status, catalase, cortisol, glutathione peroxidase, malondialdehyde and superoxide dismutase decreased, and the lowest amount of glutathione peroxidase was for the group receiving minerals and vitamins simultaneously. All hormonal parameters and antioxidant indices were also affected by time. Haptoglobin, serum amyloid A, ceruloplasmin and vitamin D concentrations were affected by the experimental treatments, such that minerals and vitamins decreased the concentrations of haptoglobin, serum amyloid A and ceruloplasmin and increased vitamin D, and the lowest serum amyloid A and ceruloplasmin levels were for the group receiving minerals and vitamins simultaneously. All inflammatory indices were also affected by time. Alkaline phosphatase enzyme activity was affected by the experimental treatments, and minerals and vitamins decreased the activity of this enzyme. Aspartate transaminase and alanine aminotransferase enzymes were not affected by the experimental treatments. Time affected alkaline phosphatase enzyme activity, but other parameters were not affected by time.
Conclusion: Injection of minerals and vitamins in late pregnancy to dairy cows caused a significant effect on the parameters of albumin, globulin, albumin:globulin ratio, insulin, catalase, cortisol, glutathione peroxidase, malondialdehyde, superoxide dismutase, total antioxidant status, haptoglobin, ceruloplasmin, serum amyloid A, vitamin D and alkaline phosphatase in the blood of cows receiving minerals and vitamins compared to the control group. Considering the greater improvement of co-injection of minerals and vitamins on albumin, glutathione peroxidase, serum amyloid A and ceruloplasmin in the blood of the treated cows, simultaneous injection of minerals and vitamins is recommended for cows in late pregnancy.

Keywords

Main Subjects


©2023 The author(s). This is an open access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source.

  1. Abdelnour, S. A., Abd El-Hack, M. E., Khafaga, A. F., Arif, M., Taha, A. E., & Noreldin, A. E. (2019). Stress biomarkers and proteomics alteration to thermal stress in ruminants: A review. Journal of Thermal Biology, 79, 120-134. https://doi.org/10.1016/j.jtherbio.2018.12.013
  2. Abdolmaleki, Z., Souri, M., Moeni, M., Tohidi, A., & Chashnidel, Y. (2018). Effect of dietary conjugated linoleic acid (CLA) Supplementation with injectable Se and VE supplement on productive performance and blood parameters of holstein dairy cows. Journal of Ruminant Research, 5(4), 101-118. https://doi.org/10.22069/ejrr.2017.13635.1568
  3. Abolghasemi, S., Bahrampour, J., Badakhshan, Y., Mirmahmoodi, R., & Barazandeh, A. (2023). The effect of intraperitoneal injection of vitamin C on feed intake and blood metabolites of Kermani sheep in severe heat stress. Veterinary Research and Biological Products, 36(3), 2-11. https://doi.org/10.22092/vj.2022.360234.2017
  4. Abuelo, A., Hernandez, J., Benedito, J. L., & Castillo, C. (2016). Association of oxidative status and insulin sensitivity in periparturient dairy cattle: An observational study. Journal of Animal Physiology and Animal Nutrition, 100, 279-286. https://doi.org/10.1111/jpn.12365
  5. Alhussien, M. N., Tiwari, S., Panda, B. S. K., Pandey, Y., Lathwal, S. S., & Dang, A. K. (2021). Supplementation of antioxidant micronutrients reduces stress and improves immune function/response in periparturient dairy cows and their calves. Journal of Trace Element and Medicine Biology, 65, 126718. https://doi.org/10.1016/j.jtemb.2021.126718
  6. Allen, M. S., & Bradford, B. J. (2009). Control of eating by hepatic oxidation of fatty acids. A Note of Caution. Appetite, 53(2), 272-273. https://doi.org/10.1016/j.appet.2009.06.005
  7. Asadi, M., Hatami, M., & Mohammadi Fard, H. (2025). The impacts of maternal b complex vitamin injection on goats and their offspring during the transition period. Iranian Journal of Applied Animal Science, 15(1), 87-95. https://doi.org/10.71798/ijas.2025.1202963
  8. Asadi, M., Fard, H. M., Araee, K. A., & Hatami, M. (2024a). Studying the impacts of maternal B complex vitamin injection on performance, metabolic diseases, hematological parameters, and antioxidant status in pregnant Sannen goats and their newborn kids during the transition period. Science of the Total Environment, 907, 167860. https://doi.org/10.1016/j.scitotenv.2023.167860
  9. Asadi, M., Ghoorchi, T., & Toghdory, A. (2024b). The effect of injection of different levels of selenium and vitamin e in late pregnancy of cows on performance, thyroid hormones, some blood metabolites and skeletal growth indices of their Calves. Iranian Journal of Applied Animal Science, 3(14), 371-379. https://doi.org/10.71798/ijas.2024.1184799
  10. Asadi, M., Ghoorchi, T., & Toghdory, A. (2024c). The effect of using different forms of chromium on hematological parameters and antioxidant status of Afshar ewes in the transition period and their lambs under the influence of heat stress. Iranian Journal of animal Science, 55(3), 547-563. https://doi.org/10.22059/ijas.2024.364592.653965
  11. Asadi, M., Toghdory, A., Ghoorchi, T., & Hatami, M. (2024d). The effect of maternal organic manganese supplementation on performance, immunological status, blood biochemical and antioxidant status of Afshari ewes and their newborn lambs in transition period. Journal of Animal Physiology and Animal Nutrition, 108, 493–499. https://doi.org/10.1111/jpn.13909
  12. Asadi, M., Ghoorchi, T., Toghdory, A., & Hoseini Sabeghi, H. (2021). Effect of different levels of selenium and vitamin E injection on thyroid hormones ‎metabolism and biochemical parameters in late pregnancy of Holstein cows and their ‎calf performance. Iranian Journal of animal Science, 52(3), 189-201. https://doi.org/10.22059/ijas.2021.325212.653832
  13. Bates, A. J., Wells, M., Fitzpatrick, C., & Laven, R. A. (2025) Effect of a pre-calving injectable trace mineral supplement on white blood cell function in seasonally calving pastoral dairy cows. New Zealand Veterinary Journal, 73(2), 87-99. https://doi.org/10.1080/00480169.2024.2417925
  14. Bernabucci, U., Ronchi, B., Lacetera, N., & Nardone, A. (2002). Markers of oxidative status in plasma and erythrocytes of transition dairy cows during hot season. Journal of Dairy Science, 85, 2173-2179. https://doi.org/10.3168/jds.s0022-0302(02)74296-3
  15. Bernabucci, U., Ronchi, B., Lacetera, N., & Nardone, A. (2005). Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows. Journal of Dairy Science, 88, 2017–2026. https://doi.org/10.3168/jds.S0022-0302(05)72878-2
  16. Bertoni, G., Minuti, A., & Trevisi, E. (2015). Immune system, inflammation and nutrition in dairy cattle. Animal Production Science, 55, 943–948. http://dx.doi.org/10.1071/AN14863
  17. Bradford, B. J., Yuan, K., Farney, J. K., Mamedova, L. K., & Carpenter, A. J. (2015). Invited review: Inflammation during the transition to lactation: New adventures with an old flame. Journal of Dairy Science, 98, 6631–6650. https://doi.org/10.3168/jds.2015-9683
  18. Ceciliani, F., Ceron, J. J., Eckersall, P. D., & Sauerwein, H. (2012). Acute phase proteins in ruminants. Journal of Proteomics, 75, 4207–4231. https://doi.org/10.1016/j.jprot.2012.04.004
  19. Chandra, G., Aggarwal, A., Singh, A., & Kumar, M. (2014). Effect of vitamin E and zinc supplementation on liver enzymatic profile of pre-and post-partum Sahiwal cows. The Indian Journal of Animal Sciences, 84(5), 507-510. https://doi.org/10.56093/ijans.v84i5.40650
  20. Coleman, D. N., Alharthi, A. S., Liang, Y., Lopes, M. G., Lopreiato, V.,Vailati-Riboni, M., & Loor, J. J. (2021). Multifaceted role of one-carbon metabolism on immunometabolic control and growth during pregnancy, lactation and the neonatal period in dairy cattle. Journal of Animal Science and Biotechnology, 12(1), 1–28. https://doi.org/10.1186/s40104-021-00547-5
  21. Erb, C., Staudt, N., Flammer, J., & Nau, W. (2004). Ascorbic acid as a free radical scavenger in porcine and bovine aqueous humour. Ophtalmic. Research, 36, 38-42. https://doi.org/10.1159/000076108
  22. Ghasemi, E., Safari Foroshani, M. H., Alikhani, M., & Shirani-Shamsabadi, J. (2019). Metabolic profile and antioxidative status, body weight, and performance of dairy cows in the periparturient period. Iranian Journal of Animal Science, 50(3), 171-184. https://doi.org/10.22059/ijas.2019.282022.653709
  23. Giuliodori, M., Magnasco, R. P., Becu-Villalobos, D., Lacau-Mengido, I. M., Risco, C. A., & de la Sota, R. L. (2013). Clinical endometritis in an Argentinean herd of dairy cows: Risk factors and reproductive efficiency. Journal of Dairy Science, 96, 210-218. https://doi.org/10.3168/jds.2012-5682
  24. Gropper, S. S., Smith, J., & Groff, J. (2005). Advanced Nutrition and Human Metabolism: Copper transport and uptake. 4th Ed. Wadsworth. Belmont, CA. 449-451.
  25. Han, M. S., White, A., Perry, R. J., Camporez, J. P., Hidalgo, J., Shulman, G. I., & Davis, R. J. (2020). Regulation of adipose tissue inflammation by interleukin 6. Proceedings of the National Academy of Sciences, 117, 2751–2760. https://doi.org/10.1073/pnas.1920004117
  26. Hassanabadi, M., Mohri, M., & Seifi H. A. (2021). Effects of single injection of vitamin D3 on some immune and oxidative stress characteristics in transition dairy cows. Iranian Journal of Veterinary Science and Technology, 12(2), 25-35. https://doi.org/M10.22067/ijvst.2020.39239
  27. Holcombe, S. J., Wisnieski, L., Gandy, J., Norby, B., & Sordillo, L. M. (2018). Reduced serum vitamin D concentrations in healthy early-lactation dairy cattle. International Journal of Dairy Science, 3, 1–7. https://doi.org/10.3168/jds.2017-13547
  28. Horst, E. A., Kvidera, S. K., & Baumgard, H. (2021). Invited review: The influence of immune activation on transition cowhealth and performance—A critical evaluation of traditional dogmas. Journal of Dairy Science, 104, 8380–8410. https://doi.org/10.3168/jds.2021-20330
  29. Kafilzadeh, F., Shabankareh, H. K., & Targhibi, M. R. (2012). Effect of chromium supplementation on productive and reproductive performances and some metabolic parameters in late gestation and early lactation of dairy cows. Biological Trace Element Research, 149, 42-49. https://doi.org/10.1007/s12011-012-9390-0
  30. Kegley, E. B., Ball, J. J., & Beck, P. (2016). Impact of mineral and vitamin status on beef cattle immune function and health. Journal of Animal Science, 94, 59–69. https://doi.org/10.2527/jas.2016-0720
  31. Khan, M. Z., Huang, B., Kou, X., Chen, Y., Liang, H., Ullah, Q., Khan, I. M., Khan, A., Chai, W., & Wang, C. (2024). Enhancing bovine immune, antioxidant and anti-inflammatory responses with vitamins, rumen-protected amino acids, and trace minerals to prevent periparturient mastitis. Front Immunology, 14, 1290044. https://doi.org/10.3389/fimmu.2023.1290044
  32. Khansari, D. N., Murgo, A. J., & Faith, R. E. (1990). Effects of stress on the immune system. Immunology Today, 11, 170-175. https://doi.org/10.1016/0167-5699(90)90069-l
  33. McGuckin, M. M., Giesy, S. L., Overton, T. R., & Boisclair, Y. R. (2023). Inflammatory tone in liver and adipose tissue in dairy cows experiencing a healthy transition from late pregnancy to early lactation. Journal of Dairy Science, 106(11), 8122–8132. https://doi.org/10.3168/jds.2023-23373
  34. Medzhitov, R. (2008). Origin and physiological roles of inflammation. Nature, 454, 428–435. https://doi.org/10.1038/nature07201
  35. Moradian, M., Rahchmani, R., Banihasan, E., Gharebash, A. M., & Zeighamy, A., (2016). The effect of injection of vitamins A and E on passive transfer of immunoglobulin G and some blood parameters in calf. Journal of Ruminant Research, 4(2). (In Persian)
  36. Mousavi, S. R., Fatahnia, F., Taasoli, G., & Mohammadi. Y. (2022). Peripartum injection of vitamins (E and B12) and trace minerals (Selenium and Iron) in Holstein dairy cows: Effect on milk production and composition, body condition score and serum metabolites. Iranian Journal of Applied Animal Science, 12(2), 255-269. https://dorl.net/dor/20.1001.1.2251628.2022.12.2.5.6
  37. Movahednasab, M., Tahmasebi, A., Vakili, S. A., & Naserian, A. A. (2023). The effect of fat-soluble vitamins (A, D, E) and flaxseed oil on blood parameters and immune system of suckling calves. Iranian Journal of Animal Science Research, 15(2), 137-150. https://doi.org/10.22067/ijasr.2022.75288.1067
  38. Nanev, V., Vladov, I., & Kirazov, L. (2020). Serum trace elements and enzymes in lambs with introduced haemonchosis. Acta Morphologica et Anthropologica, 27(3-4), 43-48.
  39. Nasr Chaleshtori, P., Fadayifar, A., Azizi, A., & Azarfar, A. (2021). The effect of slow-release bolus of copper on performance and some blood metabolites of Lori-Bakhtiari pregnant ewes and their lambs. Iranian Journal of Animal Science Research, 13(2), 193-205. https://doi.org/10.22067/ijasr.v13i2.86149
  40. Nelson, T. M., Kerwin, A. L., Ferro, L. N., Ryan, C. M., Graef, G. M., Westhoff, T. A., Sipka, A. S., Barbano, D. M., Stone, B., Yoon, I., & Overton, T. R. (2022). Relationships of blood-based indices of liver health during the transition period with performance and health. Journal of Dairy Science, 105(Suppl. 1), 266. (Abstr.)
  41. Newton, K., & Dixit, V. M. (2012). Signaling in innate immunity and inflammation. Cold Spring Harbor Perspectives in Biology, 4, a006049. https://doi.org/10.1101/cshperspect.a006049
  42. Omur, A., Kirbas, A., Aksu, E., Kandemir, F., Dorman, E., Kaynar, O., & Ucar, O. (2016). Effects of antioxidant vitamins (A, D, E) and trace elements (Cu, Mn, Se, Zn) on some metabolic and reproductive profiles in dairy cows during transition period. Polish Journal of Veterinary Sciences, 19(4), 697-706. https://doi.org/10.1515/pjvs-2016-0088
  43. Ongan, D., & Yuksel, A. (2017). What to eat for a better sleep in haemodialysis patients: Potential role of B vitamins intake and appetite. Pakistan Journal of Medical Sciences, 33(2), 417-424. https://doi.org/10.12669/pjms.332.11838
  44. Panahi Dorcheh, Z., Aliarabi, H., Farahavar, A., Maleki, M., & Yazdani, H. (2018). The effect of selenium and vitamin E injection times in late pregnant ewes on thyroid hormones metabolism, ewe's blood biochemical parameters and their lambs performance after birth. Iranian Journal of Animal Science Research, 9(4), 400-412. https://doi.org/10.22067/ijasr.v9i4.59749
  45. Senthilkumar, P., Nagalakshmi, D., Reddy, Y. R., & Sudhakar, K. (2009). Effect of different level and source of copper supplementation on immune response and copper dependent enzyme activity in lambs. Tropical Animal Health and Production, 41, 645-653. https://doi.org/10.1007/s11250-008-9236-0
  46. Shahbazi, F., Fatahnia, F., Shamsollahi, M., Jafari, H., & Mohammadi, Y. (2024). Effect of time and amount of vitamin AD3E injection in late pregnancy on colostrum quality, concentration of plasma parameters, and antioxidant status of Afshari ewes and their lambs. Animal Production Research, 13(1), 49-67. https://doi.org/10.22124/ar.2024.26232.1807
  47. Sharokhian Rezaee, M., Riasi, A., Ansari Mahyari, S., Khorvash, M., & Khorsandi, S. (2015). Effect gnrh, hcg and ad3e injection on reproductive performance and blood metabolites and progesterone of high producing dairy cows in summer season. Animal Science Research, 25(2), 97-107.
  48. Shen, X., Song, C., & Wu, T. (2021). Effects of nano-copper on antioxidant function in copper deprived Guizhou black goats. Biological Trace Element Research, 199(6), 2201-2207. https://doi.org/10.1007/s12011-020-02342
  49. Silva, T. H., Guimaraes, I., Menta, P. R., Fernandes, L., Paiva, D., Ribeiro, T. L., Celestino, M. L., Netto, A. S., Ballou, M. A., & Machado, V. S. (2022). Effect of injectable trace mineral supplementation on peripheral polymorphonuclear leukocyte function, antioxidant enzymes, health, and performance in dairy cows in semi-arid conditions. Journal of Dairy Science, 05(2), 1649-1660. https://doi.org/10.3168/jds.2021-20624
  50. Somagond, Y. M., Alhussien, M. N., & Dang, A. K. (2023). Repeated injection of multivitamins and multiminerals during the transition period enhances immune response by suppressing inflammation and oxidative stress in cows and oxidative stress in cows and their calves. Frontiers in Immunology, 14, 1059956. https://doi.org/10.3389/fimmu.2023.1059956
  51. Sordillo, L. M., & Aitken, S. L. (2009). Impact of oxidative stress on the health and immune function of dairy cattle. Veterinary Immunology and Immunopathology, 128(1-3), 104–109. https://doi.org/10.1016/j.vetimm.2008.10.305
  52. Suttle, N. (2010). Mineral Nutrition of Livestock, fourthed., CABInternational, Wallingford, UK, p. 579
  53. Toghdory, A., Asadi, M., Ghoorchi, T., & Hatami, M. (2023). Impacts of organic manganese supplementation on blood mineral, biochemical, and hematology in Afshari Ewes and their newborn lambs in the transition period. Journal of Trace Elements in Medicine and Biology, 79, 127215. https://doi.org/10.1016/j.jtemb.2023.127215
  54. Weiss, W. P. (2010). Antioxidant nutrients and milk quality. Extension Americas Research based learning network. July, 19.
  55. Wysocka , Snarska A., & Sobiech P. (2019). Copper – An essential micronutrient for calves and adult cattle. Journal of Elementology, 24(1), 101-110. https://doi.org/10.5601/jelem.2018.23.2.1645.
CAPTCHA Image