Skip to main content
Log in

Zinc uptake by blood cells of rats in zinc deficiency and inflammation

  • Published:
Biological Trace Element Research Aims and scope Submit manuscript

Abstract

In zinc deficiency, the function of leukocytes is impaired. However, the results of studies on the zinc concentration of blood cells in zinc deficiency are conflicting, probably in part because of technical and analytical problems. The aim of this study was to investigate, under standard conditions, the uptake of65Zn-labeled zinc by blood cells, taken from zinc-deficient rats and from rats in which an inflammation is induced. In both conditions, the serum zinc concentration is reduced. In clinical practice, this makes it difficult to determine whether the decrease in serum zinc is the result of a real or an apparent zinc deficiency. In stress, like an inflammatory disease, the decrease of zinc reflects an apparent zinc deficiency because of redistribution of serum zinc into the liver and because of decrease in serum albumin concentration. Over 70% of the serum zinc is bound to albumin. Blood cells from zinc-deficient and control rats were isolated using a discontinuous Percoll gradient and incubated under nearly physiological conditions in a65Zn-containing medium. A significant increase in the in vitro uptake of65Zn-labeled zinc by the blood cells of zinc-deficient rats was seen: erythrocytes 1.3, mononuclear cells 2.0, and polymorphonuclear cells 2.6 times the control values. During inflammation, no change in65Zn-labeled zinc uptake by erythrocytes and mononuclear cells was demonstrated after 2 d, although the serum zinc and albumin concentrations were decreased, but a small but significant increase in zinc uptake by polymorphonuclear cells was observed. This study of65Zn uptake in vitro under standard conditions may prove of value for distinguishing in patients real zinc deficiency from apparent zinc deficiency owing to, e.g., stress, although additional experiments should be performed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. W. R. Todd, C. A. Elvehjem, and E. J. Hart,Am. J. Physiol. 107, 146–156 (1934).

    CAS  Google Scholar 

  2. E. J. Moynahan,Lancet ii, 399–400 (1974).

    Article  Google Scholar 

  3. W. J. Pories, J. H. Henzel, C. G. Rob, and W. H. Strain,Lancet i, 121–124 (1967).

    Article  Google Scholar 

  4. W. L. Weston, J. C. Huff, J. R. Humbert, K. M. Hambidge, K. H. Neldner, and P. A. Walravens,Arch. Dermatol. 113, 422–425 (1977).

    Article  PubMed  CAS  Google Scholar 

  5. J. D. Bogden, J. M. Oleske, E. M. Munves, M. A. Laverhar, K. S. Bruening, F. W. Kemp, J. Holding, T. N. Denny, and B. D. Louria,Am. J. Clin. Nutr. 46, 101–109 (1987).

    PubMed  CAS  Google Scholar 

  6. A. S. Prasad, A. Miale, Z. Farid, H. H. Sandstead, A. R. Schulert, and W. L. Darby,Arch. Int. Med. 111, 407 (1963).

    CAS  Google Scholar 

  7. L. S. Valberg, P. R. Flanigan, A. Kertesz, and D. C. Bondy,Dig. Dis. Sci. 31, 724–731 (1986).

    Article  PubMed  CAS  Google Scholar 

  8. C. C. Ainley, J. Cason, L. K. Carlson, B. M. Slavin, and R. P. H. Thompson,Clin. Sci. 75, 277–283 (1988).

    PubMed  CAS  Google Scholar 

  9. H. P. Field, A. J. Whiley, T. R. Srinivasan, B. E. Walker, and J. Kellerher,Internat. J. Vit. Nutr. Res. 57, 311–317 (1987).

    CAS  Google Scholar 

  10. D. B. Milne, N. V. C. Ralston, and J. C. Wallwork,Clin. Chem. 31, 65–69 (1985).

    PubMed  CAS  Google Scholar 

  11. R. K. Berry, M. C. Bell, and P. L. Wright,J. Nutr. 88, 284–290 (1966).

    PubMed  CAS  Google Scholar 

  12. L. B. Sasser, M. C. Bell, and G. E. Jarboe,J. Anim. Sci. 41, 1679–1685 (1975).

    PubMed  CAS  Google Scholar 

  13. P. Rabbani, A. S. Prasad, and D. Koniuch,Fed. Proc. 37, 254 (1978).

    Google Scholar 

  14. J. P. Van Wouwe, M. Veldhuizen, J. J. M. De Goeij, and C. J. A. Van den Hamer,Biol. Trace Elem. Res. 25, 57–69 (1990).

    Article  PubMed  Google Scholar 

  15. A. A. Van Barneveld, and H. Morse,Z. Versuchstierk 24, 24 (1982).

    Google Scholar 

  16. P. E. Johnson, J. R. Hunt, and N. V. C. Ralston,J. Nutr. 118, 1205–1209 (1988).

    PubMed  CAS  Google Scholar 

  17. D. B. Milne, N. V. C. Ralston, and J. C. Wallwork,J. Nutr. 115, 1073–1080 (1985).

    PubMed  CAS  Google Scholar 

  18. K. H. Falchuk,N. Engl. J. Med. 296, 1129–1134 (1977).

    Article  PubMed  CAS  Google Scholar 

  19. N. W. Solomons, C. O. Elson, R. S. Pekarek, R. A. Jacob, H. H. Sandstead, and I. H. Rosenberg,Infect. Immun. 22, 637–639 (1978).

    PubMed  CAS  Google Scholar 

  20. E. L. Giroux and R. I. Henkin,Biochim. Biophys. Acta 273, 64–72 (1972).

    PubMed  CAS  Google Scholar 

  21. J. K. Chester and M. Will,Br. J. Nutr. 38, 297 (1978).

    Article  Google Scholar 

  22. J. C. Smith, L. Babuska, and R. Ferretti,Am. J. Clin. Nutr. 35, 2991 (1982).

    Google Scholar 

  23. J. O. A. Torrubia and R. Garay,J. Cell Physiol. 138, 316–322 (1989).

    Article  PubMed  CAS  Google Scholar 

  24. M. M. Bayer-Berger, C. Cavadini, R. Mansourian, H. Dirren, A. Bart, and J. Freeman,Clin. Nutr. suppl 8, 64 (1989).

    Article  Google Scholar 

  25. J. Bates and G. J. McClain,Am. J. Clin. Nutr. 34, 1655–1660 (1981).

    PubMed  CAS  Google Scholar 

  26. E. J. Kararskis and A. Schuna,Am. J. Clin. Nutr. 33, 2609–2612 (1980).

    Google Scholar 

  27. S. L. Wolman, G. H. Anderson, E. B. Marliss, and K. N. Jeejeebhoy,Gastroenterology 76, 458–467 (1979).

    PubMed  CAS  Google Scholar 

  28. L. C. Bate,Int. J. Appl. Radiat. Isot. 17, 417 (1966).

    Article  PubMed  CAS  Google Scholar 

  29. R. C. Fleming, K. A. Huizenga, J. T. McCall, J. Gildea, and R. Dennis,Dig. Dis. Sci. 26, 865–870 (1981).

    Article  PubMed  CAS  Google Scholar 

  30. J. Patrick and C. Dervish,CRC Crit. Rev. Clin. Lab. Sci. 20, 95–114 (1984).

    CAS  Google Scholar 

  31. C. Cornelisse, C. J. A. Van den Hamer, and J. Van der Sluys Veer,Int. J. Nucl. Med. Biol. 11, 143–147 (1984).

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

A part of this study has been presented at the Meeting of The American Gastroenterological Association on May 12–18, 1990, San Antonio, TX, and has been published in abstract inGastroenterology 98 suppl., A423.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Naber, T.H.J., van den Hamer, C.J.A., van den Broek, W.J.M. et al. Zinc uptake by blood cells of rats in zinc deficiency and inflammation. Biol Trace Elem Res 35, 137–152 (1992). https://doi.org/10.1007/BF02783726

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02783726

Index Entries

Navigation