Effects of Hot-Melt Extruded Nano-Copper as an Alternative for the Pharmacological Dose of Copper Sulfate in Weanling Pigs.
Bioavailability
Copper sulfate
Growth performance
Nano-copper
Weanling pigs
Journal
Biological trace element research
ISSN: 1559-0720
Titre abrégé: Biol Trace Elem Res
Pays: United States
ID NLM: 7911509
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
received:
02
07
2020
accepted:
05
10
2020
pubmed:
21
10
2020
medline:
29
6
2021
entrez:
20
10
2020
Statut:
ppublish
Résumé
This study was conducted to investigate the effects of hot-melt extrusion (HME)-processed copper (Cu) sulfate supplementation on the growth performance, gut microbiota, metabolic function of Cu, and bioavailability of Cu in weanling pigs fed a corn-soybean meal basal diets. A total of 180 piglets (Yorkshire × Landrace × Duroc) of mixed-sex randomly were allotted to six treatments on the basis of initial average body weight (6.36 ± 0.39 kg) to six dietary treatments. There were six replicates in each treatment with 5 pigs per replicates. The dietary treatments included levels of CuSO
Identifiants
pubmed: 33078307
doi: 10.1007/s12011-020-02426-y
pii: 10.1007/s12011-020-02426-y
doi:
Substances chimiques
Copper
789U1901C5
Copper Sulfate
LRX7AJ16DT
Types de publication
Journal Article
Randomized Controlled Trial, Veterinary
Langues
eng
Sous-ensembles de citation
IM
Pagination
2925-2935Subventions
Organisme : Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries
ID : 116073-3
Références
Song CJ, Gan SQ, He J, Shen XY (2020) Effects of nano-zinc on immune function in Qianbei-Pockmarked goats. Biol Trace Elem Res. https://doi.org/10.1007/s12011-020-02182-z
Wu T, Song ML, Song CJ, Shen XY (2020) Seasonal synamics of copper deficiency in Wumeng semi-fine wool sheep. Biol Trace Elem Res 197:487–494. https://doi.org/10.1007/s12011-019-02018-5
doi: 10.1007/s12011-019-02018-5
pubmed: 31953598
Armstrong TA, Cook DR, Ward MM, Williams CM, Spears JW (2004) Effect of dietary copper source (cupric citrate and cupric sulfate) and concentration on growth performance and fecal copper excretion in weanling pigs. J Anim Sci 82:1234–1240. https://doi.org/10.1093/ansci/82.4.1234
doi: 10.1093/ansci/82.4.1234
pubmed: 15080347
Fry RS, Ashwell MS, Lloyd KE, O'Nan AT, Flowers WL, Stewart KR, Spears JW (2012) Amount and source of dietary copper affects small intestine morphology, duodenal lipid peroxidation, hepatic oxidative stress, and mRNA expression of hepatic copper regulatory proteins in weanling pigs. J Anim Sci 90:3112–3119. https://doi.org/10.2527/jas.2011-4403
doi: 10.2527/jas.2011-4403
pubmed: 22585802
Huang YL, Ashwell MS, Fry RS, Lloyd KE, Flowers WL, Spears JW (2015) Effect of dietary copper amount and source on copper metabolism and oxidative stress of weanling pigs in short-term feeding. J Anim Sci 93:2948–2955. https://doi.org/10.2527/jas.2014-8082
doi: 10.2527/jas.2014-8082
pubmed: 26115281
McDowell LR (2003) Mineral in animal and human nutrition (No. Ed. 2). Elsevier Science BV
Van Kuijk SJA, Fleuren MA, Balemans AP, Han Y (2019) Weaned piglets prefer feed with hydroxychloride trace minerals to feed with sulfate minerals. Transl Anim Sci 3:709–716. https://doi.org/10.1093/tas/txz035
doi: 10.1093/tas/txz035
pubmed: 32704838
pmcid: 7200832
Carpenter CB, Woodworth JC, DeRouchey JM, Tokach MD, Goodband RD, Dritz SS, Wu F, Usry JL (2019) Effects of increasing copper from tri-basic copper chloride or a copper-methionine chelate on growth performance of nursery pigs. Transl Anim Sci 3:369–376. https://doi.org/10.1093/tas/txy091
doi: 10.1093/tas/txy091
pubmed: 32704807
Pineda L, Sawosz E, Vadalasetty KP, Chwalibog A (2013) Effect of copper nanoparticles on metabolic rate and development of chicken embryos. Anim Feed Sci Technol 186:125–129. https://doi.org/10.1016/j.anifeedsci.2013.08.012
doi: 10.1016/j.anifeedsci.2013.08.012
Chi YK, Xiong KN, Chen H, Min XY, Xiao H, Liao JJ, Shen XY (2019) Effect of grazing to copper pollution meadow on copper metabolism in Wumeng semi-fine wool sheep. Pol J Environ Stud 28:1083–1091
doi: 10.15244/pjoes/87102
Raje K, Ojha S, Mishra A, Munde VK, Rawat C, Chaudhary SK (2018) Impact of supplementation of mineral nano particles on growth performance and health status of animals: a review. J Entomol Zool Stud 6:1690–1694
Koo JS, Lee SY, Nam SY, Azad MOK, Kim MJ, Kim KY, Chae BJ, Kang WS, Cho HJ (2018) Preparation of cupric sulfate-based self-emulsifiable nanocomposites and their application to the photothermal therapy of colon adenocarcinoma. Biochem Biophys Res Commun 503:2471–2477. https://doi.org/10.1016/j.bbrc.2018.07.002
doi: 10.1016/j.bbrc.2018.07.002
pubmed: 30208513
Lee SY, Nam SY, Choi YH, Kim MJ, Koo JS, Chae BJ, Kang WS, Cho HJ (2017) Fabrication and characterizations of hot-melt extruded nanocomposites based on zinc sulfate monohydrate and Soluplus. Appl Sci 7:902. https://doi.org/10.3390/app7090902
doi: 10.3390/app7090902
Lee JH, Hosseindoust A, Kim MJ, Kim KY, Choi YH, Moturi J, Song CH, Lee SY, Cho HJ, Chae BJ (2019) Effects of hot melt extrusion processed nano-iron on growth performance, blood composition, and iron bioavailability in weanling pigs. J Anim Sci Technol 61:216–224. https://doi.org/10.5187/jast.2019.61.4.216
doi: 10.5187/jast.2019.61.4.216
pubmed: 31452908
pmcid: 6686143
Lee JH, Hosseindoust A, Kim MJ, Kim KY, Choi YH, Lee SH, Lee SY, Cho HJ, Chae BJ (2020a) Supplemental hot melt extruded nano-selenium increases expression profiles of antioxidant enzymes in the livers and spleens of weanling pigs. Anim Feed Sci Technol 262:114381–114389. https://doi.org/10.1016/j.anifeedsci.2019.114381
doi: 10.1016/j.anifeedsci.2019.114381
Kumar A, Hosseindoust A, Kim MJ, Kim KY, Choi YH, Lee SH, Lee SY, Lee JH, Cho HJ, Kang WS, Chae BJ (2020) Nano-sized zinc in broiler chickens: effects on growth performance, zinc concentration in organs, and intestinal morphology. J Poult Sci:0190115. https://doi.org/10.2141/jpsa.0190115
Lee JH, Hosseindoust A, Kim MJ, Kim KY, Choi YH, Lee SH, Lee SY, Cho HJ, Kang WS, Chae BJ (2020b) Biological evaluation of hot-melt extruded nano-selenium and the role of selenium on the expression profiles of selenium-dependent antioxidant enzymes in chickens. Biol Trace Elem Res 194:536–544. https://doi.org/10.1007/s12011-019-01801-8
doi: 10.1007/s12011-019-01801-8
pubmed: 31270730
National Research Council (NRC) (2012) Nutrient requirements of swine. National Academy Press, Washington, DC
AOAC (2007) Official methods of analysis of the Association of Official Analytical Chemists International. 18th. Gaithersburg
Fenton TW, Fenton M (1979) An improved procedure for the determination of chromic oxide in feed and feces. Can J Anim Sci 59:631–634. https://doi.org/10.4141/cjas79-081
doi: 10.4141/cjas79-081
Bryant MP, Robinson IM (1961) An improved nonselective culture medium for ruminal bacteria and its use in determining diurnal variation in numbers of bacteria in the rumen. J Dairy Sci 44:1446–1453. https://doi.org/10.3168/jds.S0022-0302(61)89906-2
doi: 10.3168/jds.S0022-0302(61)89906-2
Bryant MP (1972) Commentary on the Hungate technique for culture for anaerobic bacteria. Am J Clin Nutr 25:1324–1330. https://doi.org/10.1093/ajcn/25.12.1324
doi: 10.1093/ajcn/25.12.1324
pubmed: 4565349
Uni Z, Noy Y, Sklan D (1998) Posthatch development of mucosal function in the broiler small intestine. Poult Sci 77:75–82. https://doi.org/10.1093/ps/77.1.75
doi: 10.1093/ps/77.1.75
pubmed: 9469755
Gonzales-Eguia A, Fu CM, Lu FY, Lien TF (2009) Effects of nanocopper on copper availability and nutrients digestibility, growth performance and serum traits of piglets. Livest Sci 126:122–129. https://doi.org/10.1016/j.livsci.2009.06.009
doi: 10.1016/j.livsci.2009.06.009
Wang MQ, Du YJ, Wang C, Tao WJ, He YD, Li H (2012) Effects of copper-loaded chitosan nanoparticles on intestinal microflora and morphology in weaned piglets. Biol Trace Elem Res 149:184–189. https://doi.org/10.1007/s12011-012-9410-0
doi: 10.1007/s12011-012-9410-0
pubmed: 22544767
Han XY, Du WL, Huang QC, Xu ZR, Wang YZ (2012) Changes in small intestinal morphology and digestive enzyme activity with oral administration of copper-loaded chitosan nanoparticles in rats. Biol Trace Elem Res 145:355–360. https://doi.org/10.1007/s12011-011-9191-x
doi: 10.1007/s12011-011-9191-x
pubmed: 21882065
Luo XG, Dove CR (1996) Effect of dietary copper and fat on nutrient utilization, digestive enzyme activities, and tissue mineral levels in weanling pigs. J Anim Sci 74:1888–1896. https://doi.org/10.2527/1996.7481888x
doi: 10.2527/1996.7481888x
pubmed: 8856443
Dove CR (1995) The effect of copper level on nutrient utilization of weanling pigs. J Anim Sci 73:166–171. https://doi.org/10.2527/1995.731166x
doi: 10.2527/1995.731166x
pubmed: 7601730
Scott A, Vadalasetty KP, Łukasiewicz V, Jaworski S, Wierzbicki M, Chwalibog A, Sawosz E (2018) Effect of different levels of copper nanoparticles and copper sulphate on performance, metabolism and blood biochemical profiles in broiler chicken. J Anim Physiol Anim Nutr 102:364–373. https://doi.org/10.1111/jpn.12754
doi: 10.1111/jpn.12754
Chung YC, Su YP, Chen CC, Jia G, Wang HL, Wu JCG, Lin JG (2004) Relationship between antibacterial activity of chitosan and surface characteristics of cell wall. Acta Pharmacol Sin 25:932–936
pubmed: 15210068
Kim BE, Turski ML, Nose Y, Casad M, Rockman HA, Thiele DJ (2010) Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs. Cell Metab 11:353–363. https://doi.org/10.1016/j.cmet.2010.04.003
doi: 10.1016/j.cmet.2010.04.003
pubmed: 20444417
pmcid: 2901851
Jing M, Liu Y, Song W, Yan Y, Yan W, Liu R (2016) Oxidative damage induced by copper in mouse primary hepatocytes by single-cell analysis. Environ Sci Pollut Res 23:1335–1343. https://doi.org/10.1007/s11356-015-5360-3
doi: 10.1007/s11356-015-5360-3
Zhang H, Wu X, Mehmood K, Chang Z, Li K, Jiang X, Nabi F, Ijaz M, Rehman MU, Javed MT, Zhou D (2017) Intestinal epithelial cell injury induced by copper containing nanoparticles in piglets. Environ Toxicol Pharmacol 56:151–156. https://doi.org/10.1016/j.etap.2017.09.010
doi: 10.1016/j.etap.2017.09.010
pubmed: 28938148
Strauch BM, Niemand RK, Winkelbeiner NL, Hartwig A (2017) Comparison between micro-and nanosized copper oxide and water soluble copper chloride: interrelationship between intracellular copper concentrations, oxidative stress and DNA damage response in human lung cells. Part Fibre Toxicol 14:1–17. https://doi.org/10.1186/s12989-017-0209-1
doi: 10.1186/s12989-017-0209-1
Rhee JS, Won EJ, Kim RO, Lee J, Shin KH, Lee JS (2011) Expression of superoxide dismutase (SOD) genes from the copper-exposed polychaete, Neanthes succinea. Mar Pollut Bull 63:277–286. https://doi.org/10.1016/j.marpolbul.2011.04.023
doi: 10.1016/j.marpolbul.2011.04.023
pubmed: 21565362
Yang W, Wang J, Liu L, Zhu X, Wang X, Liu Z, Wang Z, Yang L, Liu G (2011) Effect of high dietary copper on somatostatin and growth hormone-releasing hormone levels in the hypothalami of growing pigs. Biol Trace Elem Res 143:893–900. https://doi.org/10.1007/s12011-010-8904-x
doi: 10.1007/s12011-010-8904-x
pubmed: 21110139
Wang J, Zhu X, Li X, Wang W, Wang X, Liu L, Deng Q, Bai G, Wang J, Feng H, Wang Z, Liu G (2011) Effects of copper on proliferation and autocrine secretion of insulin-like growth factor-1 (IGF-1) and IGF-binding protein-3 (IGFBP-3) in chondrocytes from newborn pigs in vitro. Biol Trace Elem Res 144:588–596. https://doi.org/10.1007/s12011-011-9033-x
doi: 10.1007/s12011-011-9033-x
pubmed: 22180012
Wang J, Zhu X, Guo Y, Wang Z, Zhao B, Yin Y, Liu G (2016) Influence of dietary copper on serum growth-related hormone levels and growth performance of weanling pigs. Biol Trace Elem Res 172:134–139. https://doi.org/10.1007/s12011-015-0574-2
doi: 10.1007/s12011-015-0574-2
pubmed: 26631054
Yang W, Wang J, Zhu X, Gao Y, Liu Z, Zhang L, Chen H, Shi X, Yang L, Liu G (2012) High lever dietary copper promote ghrelin gene expression in the fundic gland of growing pigs. Biol Trace Elem Res 150:154–157. https://doi.org/10.1007/s12011-012-9477-7
doi: 10.1007/s12011-012-9477-7
pubmed: 22911428
Scott A, Vadalasetty KP, Sawosz E, Łukasiewicz M, Vadalasetty RKP, Jaworski S, Chwalibog A (2016) Effect of copper nanoparticles and copper sulphate on metabolic rate and development of broiler embryos. Anim Feed Sci Technol 220:151–158. https://doi.org/10.1016/j.anifeedsci.2016.08.009
doi: 10.1016/j.anifeedsci.2016.08.009
Zhao J, Allee G, Gerlemann G, Ma L, Gracia MI, Parker D, Vazquez-Anon M, Harrell RJ (2014) Effects of a chelated copper as growth promoter on performance and carcass traits in pigs. Asian-Australas J Anim Sci 27:965–973. https://doi.org/10.5713/ajas.2013.13416
doi: 10.5713/ajas.2013.13416
pubmed: 25050038
pmcid: 4093573