DOI QR코드

DOI QR Code

Effects of dietary copper on organ indexes, tissular Cu, Zn and Fe deposition and fur quality of growing-furring male mink (Mustela vison)

  • Wu, Xuezhuang (Feed Research Institute, Chinese Academy of Agricultural Sciences) ;
  • Gao, Xiuhua (Feed Research Institute, Chinese Academy of Agricultural Sciences) ;
  • Yang, Fuhe (State Key Laboratory for Molecular Biology of Special Economic Animals, Institute of Economic Animal and Plant Science, Chinese Academy of Agricultural Sciences)
  • Received : 2014.09.26
  • Accepted : 2015.01.09
  • Published : 2015.02.28

Abstract

The objectives of this study were to study the effects of different levels of dietary copper on organ indexes, tissular Cu, Zn and Fe deposition and fur quality of mink in the growing-furring periods. One hundred and five standard dark male mink were randomly assigned to seven groups with the following dietary treatments: basal diet with no supplemental Cu (Control); basal diet supplemented with either 6, 12, 24, 48, 96 and 192 mg/kg Cu from copper sulphate, respectively. The colour intensity scores displayed a linear trend (P = 0.057). The spleen Cu concentrations responded in a linear (P < 0.05) fashion with increasing level of Cu, but copper supplementation did not affect speen concentrations of Fe or Zn. Supplemental dose of Cu linearly increased (P < 0.05) liver Cu and Fe concentrations but did not alter (P > 0.10) liver Zn. Our results indicate that Cu plays an important role in the pigmentation in growing-furring mink, and supplemental dietary Cu in growing-furring mink improve hair colour, and copper has limited effects on liver mineral deposition.

Keywords

References

  1. Delhaize E, Loneragan JF, Webb J. Development of three copper metalloenzymes in clover leaves. Plant Physiol. 1985;78:4-7. https://doi.org/10.1104/pp.78.1.4
  2. Cobine PA, Pierrel F, Winge DR. Copper trafficking to the mitochondrion and assembly of copper metalloenzymes. Biochim Biophys Acta. 2006;1763:759-72. https://doi.org/10.1016/j.bbamcr.2006.03.002
  3. Rolff M, Schottenheim J, Decker H, Tuczek F. Copper-O2 reactivity of tyrosinase models towards external monophenolic substrates: molecular mechanism and comparison with the enzyme. Chem Soc Rev. 2011;40:4077-98. https://doi.org/10.1039/c0cs00202j
  4. Sendovski M, Kanteev M, Ben-Yosef VS, Adir N, Fishman A. First structures of an active bacterial tyrosinase reveal copper plasticity. J Mol Biol. 2011;405:227-37. https://doi.org/10.1016/j.jmb.2010.10.048
  5. Lopez-Serrano D, Solano F, Sanchez-Amat A. Involvement of a novel copper chaperone in tyrosinase activity and melanin synthesis in Marinomonas mediterranea. Microbiology. 2007;153:2241-9. https://doi.org/10.1099/mic.0.2007/006833-0
  6. NRC. Nutrient requirements of mink and foxes. 2nd rev. Washington, DC: Natl. Acad. Press; 1982.
  7. Aulerich R, Ringer R. Feeding copper sulfate: could it have benefits in nutrition of mink. Fur Rancher. 1976;56:4.
  8. Aulerich RJ, Ringer RK, Bleavins MR, Napolitano A. Effects of supplemental dietary copper on growth, reproductive performance and kit survival of Standard dark mink and the acute toxicity of copper to mink. J Anim Sci. 1982;55:337-43. https://doi.org/10.2527/jas1982.552337x
  9. Bush CR, Restum JC, Bursian SJ, Aulerich RJ. Responses of growing mink to supplemental dietary copper and biotin. Scientifur. 1995;19:141-7.
  10. McCarthy B, Travis H, Krook L, Warner R. Pantothenic acid deficiency in the mink. J Nutr. 1966;89:392-8. https://doi.org/10.1093/jn/89.4.392
  11. Hansen N, Finne L, Skrede A, Tauson A. Energy supply for the mink and the fox. In: NJF Report. Copenhagen, Denmark: Nordic Association of Agricultural Scientists; 1991. p. 59.
  12. Jariwala M, Suvarna S, Kumar GK, Amin A, Udas A. Study of the concentration of trace elements Fe, Zn, Cu, Se and their correlation in maternal serum, cord serum and colostrums. Indian J Clin Biochem. 2013;29:181-8.
  13. Lu CD, Schoknecht PA, Ellis KJ, Shypailo R, Su DR, Pond WG. Differential compensatory organ growth in young pigs after short-term rehabilitation from protein deficiency. Nutr Res. 1996;16:627-37. https://doi.org/10.1016/0271-5317(96)00040-1
  14. Rasmussen PV, Borsting CF. Effects of variations in dietary protein levels on hair growth and pelt quality in mink (Mustela vison). Can J Anim Sci. 2000;80:633-42. https://doi.org/10.4141/A99-063
  15. Statistical Analysis System (SAS). SAS/STAT user's guide: version 9.0. Cary, North Caroline: SAS Institute Inc; 2002. p. OpenURL.
  16. Fatemi Naieni F, Ebrahimi B, Vakilian HR, Shahmoradi Z. Serum iron, zinc, and copper concentration in premature graying of hair. Biol Trace Elem Res. 2012;146:30-4. https://doi.org/10.1007/s12011-011-9223-6
  17. Guclu BK, Kara K, Beyaz L, Uyanik F, Eren M, Atasever A. Influence of dietary copper proteinate on performance, selected biochemical parameters, lipid peroxidation, liver, and egg copper content in laying hens. Biol Trace Elem Res. 2008;125:160-9. https://doi.org/10.1007/s12011-008-8164-1
  18. Prohaska JR, Gybina AA. Intracellular copper transport in mammals. J Nutr. 2004;134:1003-6. https://doi.org/10.1093/jn/134.5.1003
  19. Wu X, Liu Z, Zhang T, Yang Y, Yang F, Gao X. Effects of dietary copper on nutrient digestibility, tissular copper deposition and Fur quality of growingfurring mink (mustela vison). Biol Trace Elem Res. 2014;158:166-75. https://doi.org/10.1007/s12011-014-9933-7
  20. Bleavins MR, Aulerich RJ, Ringer RK. Hexachlorobenzene‐induced effects on the lymphocyte blastogenic response to concanavalin a in the mink and European ferret. Environ Toxicol Chem. 1983;2:411-8. https://doi.org/10.1002/etc.5620020405
  21. Fisher GL. Function and homeostasis of copper and zinc in mammals. Sci Total Environ. 1975;4:373-412. https://doi.org/10.1016/0048-9697(75)90029-7
  22. Suttle N, Mills C. Studies of the toxicity of copper to pigs. Br J Nutr. 1966;20:149-61. https://doi.org/10.1079/BJN19660019
  23. Stejskal SM, Aulerich RJ, Slanker MR, Braselton WE, Lehning EJ, Napolitano AC. Element concentrations in livers and kidneys of ranch mink. J Vet Diagn Invest. 1989;1:343-8. https://doi.org/10.1177/104063878900100412
  24. Arredondo M, Nunez MT. Iron and copper metabolism. Mol Aspects Med. 2005;26:313-27. https://doi.org/10.1016/j.mam.2005.07.010
  25. Miyajima H. Aceruloplasminemia, an iron metabolic disorder. Neuropathology. 2003;23:345-50. https://doi.org/10.1046/j.1440-1789.2003.00521.x
  26. Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray R, Gitlin JD. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc Natl Acad Sci U S A. 1995;92:2539-43. https://doi.org/10.1073/pnas.92.7.2539

Cited by

  1. Effects of sources and concentrations of zinc on growth performance, nutrient digestibility, and fur quality of growing-furring female mink (Mustela vison)1 vol.95, pp.12, 2015, https://doi.org/10.2527/jas2017.1810
  2. Mineral Composition of Dry Dog Foods: Impact on Nutrition and Potential Toxicity vol.66, pp.29, 2015, https://doi.org/10.1021/acs.jafc.8b02552
  3. Effects of Copper Sources and Levels on Lipid Profiles, Immune Parameters, Antioxidant Defenses, and Trace Element Residues in Broilers vol.194, pp.1, 2020, https://doi.org/10.1007/s12011-019-01753-z