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    The effect of different dietary zinc sources on mineral deposition and antioxidant indices in rabbit tissues

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    [EN] The purpose of this study was to compare the effect of dietary zinc from inorganic and organic sources on the concentration of Zn, Cu, Mn and Fe in plasma, tissues and faeces of rabbits. Simultaneously, the activities of total superoxide dismutase (SOD), specific Cu/Zn SOD, glutathione peroxidase (GPx), lipid peroxidation and total antioxidant capacity (TAC) in liver and kidney were also determined. Ninety-six 49-day-old broiler rabbits were allocated to 4 dietary treatments, each replicated 6 times with 4 animals per replicate. For the subsequent 6 wk, the rabbits were fed an identical basal diet (BD) supplemented with an equivalent dose of Zn (100 mg/kg) from different sources. Group 1 (control) received the unsupplemented BD, while the BD for groups 2, 3 and 4 was supplemented with Zn from Zn sulphate, Zn chelate of glycine hydrate (Zn-Gly) and Zn chelate of protein hydrolysate (Zn-Pro), respectively. The intake of dietary Zn sulphate resulted in an increase in Zn plasma concentration (1.85 vs. 1.48 mg/L; P<0.05) compared to the control group. Feeding the diets enriched with Zn increased the deposition of Zn in the liver (P<0.05), irrespective of the Zn source. The addition of Zn-Pro resulted in significantly higher Cu uptake in liver (P<0.05) than in the control and Zn sulphate group (56.0 vs. 35.0 and 36.7 mg/kg dry matter (DM), respectively). Neither Mn nor Fe concentration in plasma and tissues were affected by dietary Zn supplementation, with the exception of Fe deposition in muscle, which was significantly decreased (P<0.05) in rabbits supplemented with inorganic Zn sulphate compared to control and Zn-Gly group (9.8 vs. 13.3 and 12.2 mg/kg DM, respectively). Intake of organic Zn-Gly significantly increased the activities of total SOD (43.9 vs. 35.9 U/mg protein; P<0.05) and Cu/Zn SOD (31.1 vs. 23.8 U/mg protein; P<0.01) as well as TAC (37.8 vs. 31.2 μmol/g protein; P<0.05) in the kidney when compared to that of the control group. The presented results did not indicate any differences between dietary Zn sources in Zn deposition and measured antioxidant indices in rabbit tissues. Higher dietary Zn intake did not cause any interactions with respect to Mn, Cu and Fe deposition in liver and kidney tissues, but did increase the faecal mineral concentrations. Dietary organic Zn-Gly improved the antioxidant status in rabbit kidney.This work was supported by the Slovak Research and Development Agency under contract nº. APVV-0667-12 and by the project ITMS 26220220204.Čobanová, K.; Chrastinová, Ľ.; Chrenková, M.; Polačiková, M.; Formelová, Z.; Ivanišinová, O.; Ryzner, M.... (2018). The effect of different dietary zinc sources on mineral deposition and antioxidant indices in rabbit tissues. World Rabbit Science. 26(3):241-248. https://doi.org/10.4995/wrs.2018.9206SWORD241248263Alscher D.M., Braun N., Biegger D., Stuelten C., Gawronski K., Mürdter T.E., Kuhlmann U., Fritz P. 2005. Induction of metallothionein in proximal tubular cells by zinc and its potential as an endogenous antioxidant. Kidney Blood Press Res., 28: 127-133. https://doi.org/10.1159/000084921Ao T., Pierce J.L., Power R., Pescatore A.J., Cantor A.H., Dawson K.A., Ford M.J. 2009. Effects of feeding different forms of zinc and copper on the performance and tissue mineral content of chicks. Poultry Sci., 88: 2171-2175. https://doi.org/10.3382/ps.2009-00117AOAC 2005. Official Methods of Analysis. 18th Edition. Association of Official Analytical Chemists, Gaithersburg, USA.Bao Y.M., Choct M., Iji P.A., Brueton K. 2007. Effect of organically complexed copper, iron, manganese and zinc on broiler performance, mineral excretion and accumulation in tissues. J. Appl. Poult, Res., 16: 448-455. https://doi.org/10.1093/japr/16.3.448Benzie I.F.F., Strain J.J. 1996. The ferric reducing ability of plasma (FRAP) as a measure of "Antioxidant Power": The FRAP Assay. Anal. Biochem., 239: 70-76. https://doi.org/10.1006/abio.1996.0292Bulbul A.T., Bulbul S., Kucukersan M., Sireli M., Eryavuz A. 2008. Effect of dietary supplementation of organic and inorganic Zn, Cu and Mn on oxidant/antioxidant balance in laying hens. Kafkas Univ. Vet. Fak., 14: 19-24.Bradford M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilising the principle of protein-dye binding. Anal. Biochem., 72: 248-254.https://doi.org/10.1016/0003-2697(76)90527-3Casado C., Moya V.J., Pascual J.J., Blas E., Cervera C. 2011. Effect of oxidation state of dietary sunflower oil and dietary zinc and α-tocopheryl acetate supplementation on performance of growing rabbits. World Rabbit Sci., 19: 191-202. https://doi.org/10.4995/wrs.2011.940Cortese M.M., Suschek C.V., Wetzel W., Kroncke K.D., Kolb-Bachofen V. 2008. Zinc protects endothelial cells from hydrogen peroxide via Nrf2-dependent stimulation of glutathione biosynthesis. Free Radic Biol Med., 44: 2002-2012. https://doi.org/10.1016/j.freeradbiomed.2008.02.013Farombi E.O., Hansen M., Raven-Haren G., Moller P., Dragsted L.O. 2004. Commonly consumed and naturally occuring dietary substances affect biomarkers of oxidative stress and DNA damage in the healthy rats. Food Chem. Toxicol., 2: 15-22.Gresakova L., Venglovska K., Cobanova K. 2016. Dietary manganese source does not affect Mn, Zn and Cu tissue deposition and the activity of manganese-containing enzymes in lambs. J. Trace Elem. Med. Biol. 38: 138-143. https://doi.org/10.1016/j.jtemb.2016.05.003Chrastinová Ľ., Čobanová K., Chrenková M., Poláčiková M., Formelová Z., Lauková A., Ondruška Ľ., Pogány Simonová M., Strompfová V., Mlyneková Z., Kalafová A., Grešáková Ľ. 2016. Effect of dietary zinc supplementation on nutrient digestibility and fermentation characteristics of caecal content in physiological experiment with young rabbits. Slovak J. Anim. Sci., 49: 23-31.Ivanišinová O., Grešáková Ľ., Ryzner M., Oceľová V., Čobanová K. 2016. Effects of feed supplementation with various zinc sources on mineral concentration and selected antioxidant indices in tissues and plasma of broiler chickens. Acta Vet. Brno, 85: 285-291. https://doi.org/10.2754/avb201685030285Jo C., Ahn D.U. 1998. Fluorometric analysis of 2-thiobarbituric acid reactive substances in turkey. Poultry Sci., 77: 475-480. https://doi.org/10.1093/ps/77.3.475King J.C., Brown K.H., Gibson R.S., Krebs N.F., Lowe N.M., Siekmann J.H., Raiten D.J. 2016. Biomarkers of nutrition for development (BOND) - Zinc review. J. Nutr., 146: 858S-885S. https://doi.org/10.3945/jn.115.220079King J.C., Shames D.M., Woodhouse L.R. 2000. Zinc homeostasis in humans. J. Nutr., 130: 1360S-1366S. https://doi.org/10.1093/jn/130.5.1360SKwiecien M., Winiarska-Mieczan A., Milczarek A., Klebaniuk R. 2017. Biological response of broiler chickens to decreasing dietary inclusion levels of zinc glycine chelate. Biol. Trace Elem. Res., 175: 204-213. https://doi.org/10.1007/s12011-016-0743-yMa W., Niu H., Feng J., Wang Y., Feng J. 2011. Effects of zinc glycine chelate on oxidative stress, contents of trace elements, and intestinal morphology in broilers. Biol. Trace Elem. Res., 142: 546-556. https://doi.org/10.1007/s12011-010-8824-9Marklund S., Marklund G. 1974. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem., 47: 469-474. https://doi.org/10.1111/j.1432-1033.1974.tb03714.xNessrin S., Abdel-Khalek A.M., Gad S.M. 2012. Effect of supplemental zinc, magnesium or iron on performance and some physiological traits of growing rabbits. Asian J. Poult. Sci., 6: 23-30. https://doi.org/10.3923/ajpsaj.2012.23.30Nutritional Research Council (NRC), 1977. Nutrient requirements of rabbits. National Academies of Science, Washington DC, USA.Oteiza P.I. 2012. Zinc and the modulation of redox homeostasis. Free Radic. Biol. Med., 53: 1748-1759. https://doi.org/10.1016/j.freeradbiomed.2012.08.568Paglia D.E., Valentine W.N. 1967. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J. Lab. Clin. Med., 70: 158-169.Powell S.R. 2000. The antioxidant properties of zinc. J. Nutr., 130: 1447S-1454S. https://doi.org/10.1093/jn/130.5.1447SSalomonsson A.C., Theander O., Westerlund O. 1984. Chemical characterization of some Swedish cereals whole meal and bran fractions. Swedish J. Agric. Res. 14: 11-117.Skřivan M., Skřivanová V., Marounek M. 2005. Effects of dietary zinc, iron, and copper in layer feed on distribution of these elements in eggs, liver, excreta, soil, and herbage. Poultry Sci. 84: 1570-1575. https://doi.org/10.1093/ps/84.10.1570Spears, J.W. 1996. Optimizing mineral levels and sources for farm animals. In Kornegay E.T. (ed). Nutrient Management of Food Animals to Enhance and Protect the Environment, CRC Press, Inc., Boca Raton, FL, 259-275.Sunder G.S., Kumar V.C., Panda A.K., Raju M.V.L.N., Rao S.V.R. 2013. Effect of supplemental organic Zn and Mn on broiler performance, bone measures, tissue mineral uptake and immune response at 35 d of age. Curr. Res. Poult. Sci., 3: 1-11. https://doi.org/10.3923/crpsaj.2013.1.11Suttle N.F. 2010. Mineral nutrition of livestock, 4th Edition. CABI Publishing, Wallingford, Oxfordshire, UK. https://doi.org/10.1079/9781845934729.0000Swiatkiewicz S., Arczewska-Wlosek A., Jozefiak D. 2014. The efficacy of organic minerals in poultry nutrition: review and implications of recent studies. World Poultry Sci. J., 70:475-485. https://doi.org/10.1017/S0043933914000531Van Soest P.J., Robertson J.B., Lewis B.A. 1991. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J. Diary Sci., 74: 3583-3597. https://doi.org/10.3168/jds.S0022-0302(91)78551-2Wiseman J., Villamide M.J., De Blas C., Carabaño M.J., Carabaño R.M. 1992. Prediction of the digestible energy and digestibility of gross energy of feed for rabbits. 1. Individual classes of feeds. Anim. Feed Sci. Technol., 39: 27-38. https://doi.org/10.1016/0377-8401(92)90029-6Yan J.Y., Zhang G.W., Zhang C., Tang L., Kuang S.Y. 2017. Effect of dietary organic zinc sources on growth performance, incidence of diarrhoea, serum and tissue zinc concentrations, and intestinal morphology in growing rabbits. World Rabbit Sci., 25: 43-49. https://doi.org/10.4995/wrs.2017.577

    Does Herbal and/or Zinc Dietary Supplementation Improve the Antioxidant and Mineral Status of Lambs with Parasite Infection?

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    This study was conducted to evaluate the effect of feed supplementation with a medicinal herbs mixture (Hmix) and organic zinc (Zn), alone or in combination, on the antioxidant responses and mineral status of lambs infected with the gastrointestinal nematode parasite Haemonchus contortus. A total of 24 experimentally infected lambs were randomly allocated to 1 of 4 dietary treatments (n = 6). The diets included an unsupplemented control diet (CON) and the CON further supplemented with Hmix, Zn, or both Hmix + Zn. Antioxidant enzymes activities, lipid peroxidation, total antioxidant capacity (TAC) and microelement (Zn, Cu, Fe, Mn) concentrations were analyzed in serum, liver, kidney, and intestinal mucosa. Zinc treatment elevated the superoxide dismutase activities in the duodenal mucosa and ileal TAC. Intake of Hmix resulted in higher kidney and ileal catalase activity and also influenced the TAC of the liver and intestinal mucosa. The inclusion of Hmix or Zn alone into the diet increased glutathione peroxidase activity in the blood, liver and duodenal mucosa. Tissue mineral uptake was not affected by herbal supplementation. Organic Zn intake increased the serum and liver Zn levels and influenced the Cu concentration in duodenal mucosa. Dietary supplementation with Hmix and/or Zn might promote the antioxidant status of lambs infected with Haemonchus spp

    Effect of lignin on oxidative stress in chickens fed a diet contaminated with zearalenone

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    The effect of lignin supplementation to a diet contaminated with zearalenone (ZEA) on antioxidant status was studied in female chickens of the ISA BROWN laying strain. From the day of hatching to 2 weeks of age, four groups of chickens were fed the same uncontaminated control diet. After 14 days, Group 1 (control) continued to receive the uncontaminated diet, while Group 2 was fed an identical diet enriched with 0.5% chemically modified lignin. Simultaneously, chickens of Group 3 were switched to a diet contaminated with 7.9 mg/kg ZEA and those of Group 4 to an identical contaminated diet supplemented with 0.5% lignin. At 6 weeks of age blood and tissue samples were collected. Feeding of a diet contaminated with a high level of ZEA resulted in elevated glutathione peroxidase (GPx) activity in the duodenal mucosa and kidney tissues, and an increased γ-glutamyltransferase (GGT) activity in the plasma, indicative of oxidative stress. In the liver tissue, no mycotoxin-induced response in GPx and thioredoxin reductase (TrxR) activities occurred, and the malondialdehyde (MDA) level was even reduced. Neither the plasma levels of retinol and α-tocopherol nor the activities of superoxide dismutase in erythrocytes and GPx in blood were affected in birds fed the contaminated diet. The only effect of lignin supplemented to the contaminated feed was that it prevented the increase of GPx activity in the duodenal mucosa as an indicator of oxidative stress

    Production of Intestinal Mucins, sIgA, and Metallothionein after Administration of Zinc and Infection of <i>Ascaridia galli</i> in Chickens: Preliminary Data

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    The effect of inorganic zinc and Ascaridia galli infection was studied on MUC1, MUC2 (mucin), sIgA (secretory immunoglobulin A), and metallothionein in the intestines of broilers. Thirty-five-day-old chickens (n = 24), COBB 500 breed, were included in a 14-day experiment. Chickens were divided into 4 groups of 6 chickens each: control ©, Ascaridia galli (AG), Zinc group (Zn), and combined group (AG + Zn). Samples from the intestine for determination of MUC1, MUC2, sIgA, and metallothionein were taken at 7 and 14 days during necropsy. Samples from the jejunum for determination of MUC1, MUC2, sIgA, and metallothionein were taken at 7 and 14 days during necropsy. The results demonstrated that 12 days’ administration of inorganic zinc increased production of MUC1 (p p Ascaridia galli-infected group (Ag + Zn) in comparison to control (C). The beneficial effect of zinc was also revealed in the production of sIgA (p p Ascaridia galli-infected chickens

    Effects of herbal nutraceuticals and/or zinc against Haemonchus contortus in lambs experimentally infected

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    Abstract Background The gastrointestinal parasitic nematode Haemonchus contortus is a pathogenic organism resistant to several anthelmintics. This study assessed the efficacy of a medicinal herbal mixture (Herbmix) and organic zinc, as an essential trace element for the proper functioning of both unspecific and specific immune defensive mechanisms, against experimental infections with H. contortus in lambs. All lambs were infected orally with approximately 5000 third-stage larvae of a strain of H. contortus susceptible to anthelmintics (MHco1). Twenty-four female lambs 3–4 months of age were divided into four groups: unsupplemented animals (control), animals supplemented with Herbmix (Hmix), animals supplemented with organic zinc (Zn) and animals supplemented with Herbmix and organic zinc (Hmix+Zn). Eggs per gram (EPG) of faeces were quantified 20, 28, 35, 42, 49, 56, 62 and 70 d post-infection and mean abomasal worm counts were assessed 70 d post-infection. Samples of blood were collected from each animal 7, 35, 49 and 70 d post-infection. Results Quantitative analyses of the bioactive compounds in Herbmix identified three main groups: flavonoids (9964.7 μg/g), diterpenes (4886.1 μg/g) and phenolic acids (3549.2 μg/g). Egg counts in the lambs treated with Hmix, Zn and Hmix+Zn decreased after 49 d. The EPGs in the Zn and Hmix+Zn groups were significantly lower on day 56 (P < 0.05 and P < 0.01, respectively), and the EPGs and mean worm counts were significantly lower on day 70 in all supplemented groups (P < 0.05 and P < 0.01). Hemograms of complete red blood cells of each animal identified clinical signs of haemonchosis after day 35. Serum calprotectin concentrations and IgA levels were significantly affected by treatment. The treatment influenced serum malondialdehyde concentrations (P < 0.05) and sulfhydryl groups (P < 0.01) of antioxidant status. The mineral status was unaltered in all lambs. Conclusion A direct anthelmintic impact on the viability of nematodes was not fully demonstrated, but the treatments with herbal nutraceuticals and zinc likely indirectly contributed to the increase in the resistance of the lambs to nematode infection

    The effects of high dose of two manganese supplements (organic and inorganic) on the rumen microbial ecosystem

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    The effects of high dose of two manganese supplements (organic and inorganic) on the rumen microbial ecosystem after four months of treatment of 18 lambs divided into three treatment groups were studied. We examined the enzyme activities (α-amylase, xylanase, and carboxymethyl cellulase), total and differential microscopic counts of rumen ciliates, total microscopic counts of bacteria, and fingerprinting pattern of the eubacterial and ciliates population analyzed by PCR-DGGE
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