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

Document Type : Research Paper

Authors

1 Department of Animal and Poultry Nutrition, Animal Science Faculty, Gorgan University of Agricultural Science and Natural Resources, Gorgan, Iran.

2 Department of Animal and Poultry nutrition, Animal Science Faculty, Gorgan University of Agricultural Science and Natural Resources, Gorgan, Iran.

Abstract

The present study aims to investigate the effect of different forms of chromium (inorganic chromium, chromium-methionine and chromium nanoparticles) on blood parameters, antioxidant status and immunoglobin of Afshar ewes during the transition period and lambs. They were done under the influence of heat stress. 40 pregnant Afshar ewes from 42 ± 2 days before the expected parturition in a completely randomized design. Four experimental treatments were assigned with ten replications. Experimental treatments include basic diet without chromium supplement (control), basic diet containing 3 mg of chromium in mineral form per kg of dry matter, basic diet containing 3 mg of chromium in the form of chromium-methionine per kg of dry matter and The basic diet contained 3 mg of chromium in the form of chromium nanoparticles per kilogram of dry matter. The results showed that the addition of different forms of chromium to the ewes' diet caused a significant increase in the concentration of red blood cells, hemoglobin and blood hematocrit compared to the control group (P<0.05). Adding chromium to the diet of ewes caused a significant decrease in white blood cells (P<0.05). In experimental treatments, no significant difference was observed in terms of platelets, average volume of red blood cells, average concentration of red blood cells, neutrophils, lymphocytes, monocytes, and eosinophils. The concentration of superoxide desmutase, glutathione peroxidase, catalase, triiodothyronine and tetraiodothyronine in the blood in the treatments receiving different forms of chromium also increased compared to the control group (P<0.05). The results showed that the concentration of malondialdehyde and total antioxidant capacity in ewes and lambs receiving chromium supplementation was lower than the control treatment (P<0.05). However, there was no significant difference between different experimental treatments in terms of ceruloplasmin concentration and the ratio of T4 to T3 (P<0.05). The concentration of IgG and IgM in lambs receiving different forms of chromium also increased compared to the control group (P<0.05). In general, the use of chromium, especially in the form of chromium-methionine and chromium nanoparticles, is recommended during the transition period of ewes under the influence of heat stress.

Keywords

Main Subjects


Extended Abstract

Introduction

It is very important to choose the appropriate form of chromium in the ration of ewes in the transition period and under the influence of heat stress in order to improve the performance of ewes and newborn lambs and reduce the negative effects of stress in these conditions. The present study is to investigate the effect of using different forms of chromium (inorganic chromium, chromium-methionine and chromium nanoparticles) on blood parameters, antioxidant status and immunoglobulin of Afshar ewes during the transition period and their lambs under the influence of heat stress. Done.

 

Materials and Methods

     In the summer of 1401, 40 pregnant Afshari ewes were assigned to four experimental treatments with ten replications in a completely random design from 42 ± 2 days before the expected birth. The experimental treatments include the basic diet without chromium supplementation (control), the basic diet containing 3 mg of chromium in mineral form per kg of dry matter, the basic diet containing 3 mg of chromium in the form of chromium-methionine per kg of dry matter, and the basic diet containing 3 milligrams of chromium in the form of chromium nanoparticles per kilogram of dry matter. The basic ration was adjusted according to the tables of the National Sheep Research Association and supplements were added to the basic ration daily. The ewes were all balanced for age, number of embryos, weight, expected calving date and color. The accuracy of pregnancy and the possible time of delivery were confirmed through pregnancy synchronization and ultrasound of the ewes before the experiment. The experiment started 42 days before calving and lasted for 84 days.

 

Results

    The results showed that the addition of different forms of chromium to the diet of ewes caused a significant increase in the concentration of red blood cells, hemoglobin and blood hematocrit compared to the control group (P<0.05). Adding different forms of chromium to the diet of ewes caused a significant decrease in white blood cells (P<0.05). In experimental treatments, no significant difference was observed in platelet, mean corposcular volume, mean corpuscular hemoglobin concentration, neutrophil, lymphocyte, monocyte and eosinophil blood. The concentration of superoxide desmutase, glutathione peroxidase, catalase, triiodothyronine and tetraiodothyronine in the blood in the treatments receiving different forms of chromium also increased compared to the control group (P<0.05). The results showed that the concentration of malondialdehyde and total antioxidant capacity in ewes and lambs receiving chromium supplementation was lower than the control treatment (P<0.05). However, there was no significant difference between different experimental treatments in terms of ceruloplasmin concentration and the ratio of T4 to T3 (P<0.05). The concentration of IgG and IgM in lambs receiving different forms of chromium also increased compared to the control group (P<0.05).

 

CONCLUSIONS

    In general, it is recommended to receive chromium, especially in the form of chromium-methionine and chromium nanoparticles during the period of transfer of ewes under the influence of heat stress.

REFERNSES
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 biology79, 120-134.‏
Arthington, J. D., Corah, L. R., Minton, J. E., Elsasser, T. H., & Blecha, F. (1997). Supplemental dietary chromium does not influence ACTH, cortisol, or immune responses in young calves inoculated with bovine herpesvirus-1. Journal of Animal Science75(1), 217-223.‏
Bach, A., Huntington, G. B., Calsamiglia, S., & Stern, M. D. (2000). Nitrogen metabolism of early lactation cows fed diets with two different levels of protein and different amino acid profiles. Journal of Dairy Science83(11), 2585-2595.‏
Bagath, M., Krishnan, G., Devaraj, C., Rashamol, V. P., Pragna, P., Lees, A. M., & Sejian, V. (2019). The impact of heat stress on the immune system in dairy cattle: A review. Research in Veterinary Science126, 94-102.‏
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 Science85(9), 2173-2179.‏
Bernhard, B. C., Burdick, N. C., Rounds, W., Rathmann, R. J., Carroll, J. A., Finck, D. N., & Johnson, B. J. (2012). Chromium supplementation alters the performance and health of feedlot cattle during the receiving period and enhances their metabolic response to a lipopolysaccharide challenge–. Journal of Animal Science90(11), 3879-3888.‏
Besong, S., Jackson, J. A., Trammell, D. S., & Akay, V. (2001). Influence of supplemental chromium on concentrations of liver triglyceride, blood metabolites and rumen VFA profile in steers fed a moderately high fat diet. Journal of Dairy Science84(7), 1679-1685.‏
Broucek, J., Kisac, P., & Uhrincat, M. (2009). Effect of hot temperatures on the hematological parameters, health and performance of calves. International Journal of Biometeorology53, 201-208.‏
Burton, J. L., Mallard, B. A., & Mowat, D. N. (1993). Effects of supplemental chromium on immune responses of periparturient and early lactation dairy cows. Journal of Animal Science71(6), 1532-1539.‏
Cao, J., Guo, F., Zhang, L., Dong, B., & Gong, L. (2014). Effects of dietary Selenomethionine supplementation on growth performance, antioxidant status, plasma selenium concentration, and immune function in weaning pigs. Journal of Animal Science and Biotechnology5(1), 1-7.‏
Caroprese, M., Marzano, A., Entrican, G., Wattegedera, S., Albenzio, M., & Sevi, A. (2009). Immune response of cows fed polyunsaturated fatty acids under high ambient temperatures. Journal of Dairy Science92(6), 2796-2803.‏
Chang, X., Mallard, B. A., & Mowat, D. N. (1996). Effects of chromium on health status, blood neutrophil phagocytosis and in vitro lymphocyte blastogenesis of dairy cows. Veterinary Immunology and Immunopathology52(1-2), 37-52.‏
Chang, X., & Mowat, D. N. (1992). Supplemental chromium for stressed and growing feeder calves. Journal of Animal Science70(2), 559-565.‏
Choi, S. J., Oh, J. M., & Choy, J. H. (2010). Biocompatible nanoparticles intercalated with anticancer drug for target delivery: pharmacokinetic and biodistribution study. Journal of Nanoscience and Nanotechnology10(4), 2913-2916.‏
Das, R., Sailo, L., Verma, N., Bharti, P., Saikia, J., & Kumar, R. (2016). Impact of heat stress on health and performance of dairy animals: a review. Vet World 9: 260–268.‏
Depew, C. L., Bunting, L. D., Fernandez, J. M., Thompson Jr, D. L., & Adkinson, R. W. (1998). Performance and metabolic responses of young dairy calves fed diets supplemented with chromium tripicolinate. Journal of Dairy Science81(11), 2916-2923.‏
Domínguez-Vara, I. A., González-Muñoz, S. S., Pinos-Rodríguez, J. M., Bórquez-Gastelum, J. L., Bárcena-Gama, R., Mendoza-Martínez, G. & Landois-Palencia, L. L. (2009). Effects of feeding selenium-yeast and chromium-yeast to finishing lambs on growth, carcass characteristics, and blood hormones and metabolites. Animal Feed Science and Technology152(1-2), 42-49.‏
Duffield, T. F., Merrill, J. K., & Bagg, R. N. (2012). Meta-analysis of the effects of monensin in beef cattle on feed efficiency, body weight gain, and dry matter intake. Journal of Animal Science90(12), 4583-4592.‏
Faldyna, M., Pechova, A., & Krejci, J. (2003). Chromium supplementation enhances antibody response to vaccination with tetanus toxoid in cattle. Journal of Veterinary Medicine, Series B50(7), 326-331.‏
Gehrig, S. M., van der Poel, C., Sayer, T. A., Schertzer, J. D., Henstridge, D. C., Church, J. E., ... & Lynch, G. S. (2012). Hsp72 preserves muscle function and slows progression of severe muscular dystrophy. Nature484(7394), 394-398.‏
Gentry, L. R., Fernandez, J. M., Ward, T. L., White, T. W., Southern, L. L., Bidner, T. D. & Sahlu, T. (1999). Dietary protein and chromium tripicolinate in Suffolk wether lambs: effects on production characteristics, metabolic and hormonal responses, and immune status. Journal of Animal Science77(5), 1284-1294.‏
Ghasemi Kasmaei, F., & Safari Manjegh Tappeh, S. (2022). Comparison of the effect of organic, inorganic and nano-chromium supplements on growth performance and blood parameters of Mehraban fattening lambs. International Journal of Plant, Animal and Environmental Science, 14(3), 95-102.
Ghorbani, A., Sadri, H., Alizadeh, A. R., & Bruckmaier, R. M. (2012). Performance and metabolic responses of Holstein calves to supplemental chromium in colostrum and milk. Journal of Dairy Science95(10), 5760-5769.‏
Gong, J., & Xiao, M. (2016). Selenium and antioxidant status in dairy cows at different stages of lactation. Biological Trace Element Research171, 89-93.‏
Haldar, S., Mondal, S., Samanta, S., & Ghosh, T. K. (2009). Effects of dietary chromium supplementation on glucose tolerance and primary antibody response against pestedespetitsruminants in dwarf Bengal goats (Capra hircus). Animal3(2), 209-217.‏
Harvey, K. M., Cooke, R. F., & Marques, R. D. S. (2021). Supplementing trace minerals to beef cows during gestation to enhance productive and health responses of the offspring. Animals11(4), 1159.‏
Hassan, F. A., Mahmoud, R., & El-Araby, I. E. (2017). Growth performance, serum biochemical, economic evaluation and IL6 gene expression in growing rabbits fed diets supplemented with zinc nanoparticles. Zagazig Veterinary Journal45(3), 238-249.‏
Hill, E. K., & Li, J. (2017). Current and future prospects for nanotechnology in animal production. Journal of Animal Science and Biotechnology8(1), 1-13.‏
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 Research149, 42-49.‏
Kargar, S., Mousavi, F., & Karimi-Dehkordi, S. (2018). Effects of chromium supplementation on weight gain, feeding behaviour, health and metabolic criteria of environmentally heat-loaded Holstein dairy calves from birth to weaning. Archives of Animal Nutrition72(6), 443-457.‏
Kargar, S., Mousavi, F., Karimi-Dehkordi, S., & Ghaffari, M. H. (2018). Growth performance, feeding behavior, health status, and blood metabolites of environmentally heat-loaded Holstein dairy calves fed diets supplemented with chromium. Journal of Dairy Science101(11), 9876-9887.‏
Kegley, E. B., Spears, J. W., & Brown Jr, T. T. (1996). Immune response and disease resistance of calves fed chromium nicotinic acid complex or chromium chloride. Journal of Dairy Science79(7), 1278-1283.‏
Kegley, E. B., Spears, J. W., & Brown Jr, T. T. (1997). Effect of shipping and chromium supplementation on performance, immune response, and disease resistance of steers. Journal of Animal Science75(7), 1956-1964.‏
Kegley, E. B., & Spears, J. W. (1995). Immune response, glucose metabolism, and performance of stressed feeder calves fed inorganic or organic chromium. Journal of Animal Science73(9), 2721-2726.‏
Keshri, A., Roy, D., Kumar, V., Kumar, M., Kushwaha, R., Vaswani, S. & Choudhury, S. (2021). Effect of chromium supplementation on rhythmic alterations in growth performance and nutrient utilization of growing cattle during heat stress. Biological Rhythm Research52(7), 1064-1072.‏
Khansari, D. N., Murgo, A. J., & Faith, R. E. (1990). Effects of stress on the immune system. Immunology Today11, 170-175.‏
Kumar, M., Kaur, H., Deka, R. S., Mani, V., Tyagi, A. K., & Chandra, G. (2015). Dietary inorganic chromium in summer-exposed buffalo calves (Bubalus bubalis): effects on biomarkers of heat stress, immune status, and endocrine variables. Biological Trace Element Research167, 18-27.‏
Kumar, N., Garg, A. K., Dass, R. S., Chaturvedi, V. K., Mudgal, V., & Varshney, V. P. (2009). Selenium supplementation influences growth performance, antioxidant status and immune response in lambs. Animal Feed Science and Technology153(1-2), 77-87.‏
Lashkari, S., Habibian, M., & Jensen, S. K. (2018). A review on the role of chromium supplementation in ruminant nutrition—effects on productive performance, blood metabolites, antioxidant status, and immunocompetence. Biological Trace Element Research186, 305-321.‏
Marcén, M., Ruiz, V., Serrano, M. J., Condón, S., & Mañas, P. (2017). Oxidative stress in E. coli cells upon exposure to heat treatments. International Journal of Food Microbiology241, 198-205.‏
Meyer, A. M., Reed, J. J., Neville, T. L., Thorson, J. F., Maddock-Carlin, K. R., Taylor, J. B., ... & Caton, J. S. (2011). Nutritional plane and selenium supply during gestation affect yield and nutrient composition of colostrum and milk in primiparous ewes. Journal of animal science89(5), 1627-1639.‏
Moeini, M. M., Kaki Soumar, S., Hozhabri, F., & Nikousefat, Z. (2018). The effect of black seed with chromium-methionine or zinc-methionine on the blood parameters, antioxidant capacity and performance of Sanjabi lambs under transport stress. Journal Ruminat Research,  6(1), 85-100. (In Persian).
Moezzi, A., McDonagh, A. M., & Cortie, M. B. (2012). Zinc oxide particles: Synthesis, properties and applications. Chemical Engineering Journal185, 1-22.‏
Moonsie-Shageer, S., & Mowat, D. N. (1993). Effect of level of supplemental chromium on performance, serum constituents, and immune status of stressed feeder calves. Journal of Animal Science71(1), 232-238.‏
Moreira, P. S. A., Palhari, C., & Berber, R. C. A. (2020). Dietary chromium and growth performance animals: a review. Scientific Electronic Archives13(7), 59-66.‏
Mousaie, A., Valizadeh, R., Naserian, A. A., Heidarpour, M., & Mehrjerdi, H. K. (2014). Impacts of feeding selenium-methionine and chromium-methionine on performance, serum components, antioxidant status, and physiological responses to transportation stress of Baluchi ewe lambs. Biological Trace Element Research162, 113-123.‏
Mousavi, F., Karimi-Dehkordi, S., Kargar, S., & Ghaffari, M. H. (2019). Effect of chromium supplementation on growth performance, meal pattern, metabolic and antioxidant status and insulin sensitivity of summer-exposed weaned dairy calves. Animal13(5), 968-974.‏
Mousavi, F., Karimi-Dehkordi, S., Kargar, S., & Khosravi-Bakhtiari, M. (2019). Effects of dietary chromium supplementation on calf performance, metabolic hormones, oxidative status, and susceptibility to diarrhea and pneumonia. Animal Feed Science and Technology248, 95-105.‏
Arruda, A. G., Godden, S., Rapnicki, P., Gorden, P., Timms, L., Aly, S. S & Champagne, J. (2013). Randomized noninferiority clinical trial evaluating 3 commercial dry cow mastitis preparations: I. Quarter-level outcomes. Journal of Dairy Science96(7), 4419-4435.‏
Munck, A., Guyre, P. M., & Holbrook, N. J. (1984). Physiological functions of glucocorticoids in stress and their relation to pharmacological actions. Endocrine Reviews5(1), 25-44.‏
National Research Council. (2007). Nutrient Requirements of Small Ruminants. Sheep, goats, cervide and new world camelids. Washington, DC: National Academy Press.
Ohh, S. J., & Lee, J. Y. (2005). Dietary chromium-methionine chelate supplementation and animal performance. Asian-Australasian Journal of Animal Sciences18(6), 898-907.‏
Pantelić, M., Jovanović, L. J., Prodanović, R., Vujanac, I., Đurić, M., Ćulafić, T. & Kirovski, D. (2018). The impact of the chromium supplementation on insulin signalling pathway in different tissues and milk yield in dairy cows. Journal of Animal Physiology and Animal Nutrition102(1), 41-55.‏
Phan, T. T. V., Huynh, T. C., Manivasagan, P., Mondal, S., & Oh, J. (2019). An up-to-date review on biomedical applications of palladium nanoparticles. Nanomaterials10(1), 66.‏
Qi, Z., Gao, J., Zhao, C., Zhang, Y., Liu, Y., Wang, X., & Li, H. (2018). PSXVII-30 Effects of dietary supplementation of yeast chromium and dihydropyridine on serum biochemical indices and HSP70 mRNA expression of lactating dairy cows in summer. Journal of Animal Science96(suppl_3), 448-449.‏
Regoli, F., & Principato, G. (1995). Glutathione, glutathione-dependent and antioxidant enzymes in mussel, Mytilus galloprovincialis, exposed to metals under field and laboratory conditions: implications for the use of biochemical biomarkers. Aquatic Toxicology, 31(2), 143-164.‏
Robinson, J. J., McDonald, I., Fraser, C., & Crofts, R. M. J. (1977). Studies on reproduction in prolific ewes: I. Growth of the products of conception. The Journal of Agricultural Science88(3), 539-552.‏
Sahin, K., Sahin, N., & Kucuk, O. (2003). Effects of chromium, and ascorbic acid supplementation on growth, carcass traits, serum metabolites, and antioxidant status of broiler chickens reared at a high ambient temperature (32 C). Nutrition Research23(2), 225-238.‏
SAS. (2004). Institute. User’s Guide. Version 9.1: Statistics. SAS Institute, Cary, NC.
Sordillo, L. M., & Aitken, S. L. (2009). Impact of oxidative stress on the health and immune function of dairy cattle. Veterinary Immunology and Immunopathology128(1-3), 104-109.‏
Spears, J. W. (2019). Boron, chromium, manganese, and nickel in agricultural animal production. Biological Trace Element Research188(1), 35-44.‏
Spears, J. W. (2000). Micronutrients and immune function in cattle. Proceedings of the nutrition society59(4), 587-594.‏
Stahlhut, H. S., Whisnant, C. S., Lloyd, K. E., Baird, E. J., Legleiter, L. R., Hansen, S. L., & Spears, J. W. (2006). Effect of chromium supplementation and copper status on glucose and lipid metabolism in Angus and Simmental beef cows. Animal Feed Science and Technology128(3-4), 253-265.‏
Subiyatno, A., Mowat, D. N., & Yang, W. Z. (1996). Metabolite and hormonal responses to glucose or propionate infusions in periparturient dairy cows supplemented with chromium. Journal of Dairy Science79(8), 1436-1445.‏
Sun, L. L., Gao, S. T., Wang, K., Xu, J. C., Sanz-Fernandez, M. V., Baumgard, L. H., & Bu, D. P. (2019). Effects of source on bioavailability of selenium, antioxidant status, and performance in lactating dairy cows during oxidative stress-inducing conditions. Journal of Dairy Science102(1), 311-319.‏
Sun, P., Wang, J., Liu, W., Bu, D. P., Liu, S. J., & Zhang, K. Z. (2017). Hydroxy-selenomethionine: A novel organic selenium source that improves antioxidant status and selenium concentrations in milk and plasma of mid-lactation dairy cows. Journal of Dairy Science100(12), 9602-9610.‏
Travan, A., Pelillo, C., Donati, I., Marsich, E., Benincasa, M., Scarpa, T. & Paoletti, S. (2009). Non-cytotoxic silver nanoparticle-polysaccharide nanocomposites with antimicrobial activity. Biomacromolecules10(6), 1429-1435.‏
Uyanik, F. (2001). The effects of dietary chromium supplementation on some blood parameters in sheep. Biological Trace Element Research84, 93-101.‏
WANG, H. F., YANG, W. R., WANG, Y. X., YANG, Z. B., & CUI, Y. H. (2011). The study on the effects of Chinese herbal mixtures on growth, activity of post-ruminal digestive enzymes and serum antioxidant status of beef cattle. Agricultural Sciences in China10(3), 448-455.‏
Wang, M. Q., Xu, Z. R., Zha, L. Y., & Lindemann, M. D. (2007). Effects of chromium nanocomposite supplementation on blood metabolites, endocrine parameters and immune traits in finishing pigs. Animal Feed Science and Technology139(1-2), 69-80.‏
Yan, L. J., Christians, E. S., Liu, L., Xiao, X., Sohal, R. S., & Benjamin, I. J. (2002). Mouse heat shock transcription factor 1 deficiency alters cardiac redox homeostasis and increases mitochondrial oxidative damage. The EMBO Journal21(19), 5164-5172.‏
Yari, M., Nikkhah, A., Alikhani, M., Khorvash, M., Rahmani, H., & Ghorbani, G. R. (2010). Physiological calf responses to increased chromium supply in summer. Journal of Dairy Science93(9), 4111-4120.‏
Yuan, K., Vargas-Rodriguez, C. F., Mamedova, L. K., Muckey, M. B., Vaughn, M. A., Burnett, D. D., ... & Bradford, B. J. (2014). Effects of supplemental chromium propionate and rumen-protected amino acids on nutrient metabolism, neutrophil activation, and adipocyte size in dairy cows during peak lactation. Journal of Dairy Science97(6), 3822-3831.‏
Zhang, F. J., Weng, X. G., Wang, J. F., Zhou, D., Zhang, W., Zhai, C. C., ... & Zhu, Y. H. (2014). Effects of temperature–humidity index and chromium supplementation on antioxidant capacity, heat shock protein 72, and cytokine responses of lactating cows. Journal of Animal Science92(7), 3026-3034.‏