Skip to main content
Log in

Selected zinc metabolism parameters in premenopausal and postmenopausal women with moderate and severe primary arterial hypertension

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

Abstract

The aim of this study was to compare zinc (Zn) metabolism parameters in groups of premenopausal and postmenopausal women with moderate and severe primary arterial hypertension. The study included 38 women, of which 15 were premenopausal and 23 were postmenopausal. Postmenopausal women had a positive correlation between total (ERCt-Zn) and oubain-dependent (ERCos-Zn) rate constants of Zn efflux from lymphocyte (k = 0.52). In premenopausal women’s ERCos-Zn was negatively but weakly correlated with serum Zn (Zn-s) (k = 0.35). The Zn ERCt-Zn and ERCos-Zn did not show any correlation with age, as did Zn-s. Lymphocyte Zn correlated negatively with age only in premenopausal women (k = -0.62).

The renin-angiotensin-aldosterone system correlated with Zn metabolism parameters. In premenopausal women, plasma renin activity and serum aldosterone showed positive correlations with lymphocyte Zn (Zn-l) (k = 0.63 andk = 0.41, respectively), and in postmenopausal women, it correlated negatively with Zn-s (k = -0.38) and whole aldosterone correlated negatively with ERCos-Zn (k = -0.41).

Positive correlations between Zn metabolism parameters and arterial blood pressure in premenopausal women were as follows: ERCt-Zn with diastolic blood pressure (dRR) (k = 0.40) and ERCos-Zn with dRR (k = 0.47). In postmenopausal women, the correlations between ERC-t-Zn and dRR and systolic blood pressure (sRR) were negative (k = -0.53 andk = -0.63, respectively). A similar situation was observed between dRR and sRR and Zn-s (k = -0.40 andk = -0.38, respectively). The body mass index (BMI) was positively correlated with ERCt-Zn in premenopausal women (k = 0.36), whereas in postmenopausal, it was negatively correlated with ERCos-Zn (k = -0.42). For the whole group, negative correlations were seen between ZnS and dRR and sRR (k = -0.36 andk = -0.39, respectively) and between ERCos-Zn and BMI (k = -0.39). The results presented show differences in Zn metabolism in arterial hypertension between premenopausal and post-menopausal women. The role of estrogens in these differences is disscused.

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. N. Kaplan,Clinical Hypertension, 6th ed., William & Wilkins, Baltimore, pp. 97-98 (1994).

    Google Scholar 

  2. S. Tubek, Gender differences in selected zinc metabolism parameters in patients with mild primary arterial hypertension,Biol. Trace Element Res. 114, 55–64 (2006).

    Article  CAS  Google Scholar 

  3. E. D. Thompson, P. E. Olsson, G. D. Mayer, P. J. Walsh, E. Burge, and C. Hogstrand, Effects of 17 beta-estradiol on levels and distribution of metallothionein and zinc in squirrelfish,Am. J. Physiol. Regul. Integr. Comp. Physiol. 280, R527-R535 (2001).

    PubMed  CAS  Google Scholar 

  4. M. E. Wastney, S. Ahmed, and R. I. Henkin, Changes in regulation of human zinc metabolism with age,Am. J. Physiol.,263(5 Pt. 2), R1162-R1168 (1992).

    Google Scholar 

  5. P. Darlu, J. M. Lalouel, J. G. Henrotte, and D. C. Rao, A genetic study of red blood zinc concentration in man,Hum. Heredity 33, 311–320 (1983).

    Article  PubMed  CAS  Google Scholar 

  6. R. D. Lindeman, M. L. Clark, and J. P. Colmore, Influence of age and sex on plasma and red-cell zinc concentration,J. Gerontol. 26, 358–363 (1971).

    PubMed  CAS  Google Scholar 

  7. S. Tubek, The zinc content in lymphocytes and the activity of zinc ions efflux from lymphocytes in primary arterial hypertension,Biol. Trace Element Res. 107, 89–99 (2005).

    Article  CAS  Google Scholar 

  8. M. G. Matera, D. De Santis, S. Maione, et al., Antihypertensive drugs and urinary excretion of zinc in genetically hypertensive rats,Curr. Ther. Res. 46, 667–680 (1989).

    CAS  Google Scholar 

  9. G. Vivoli, M. Bergomi, S. Rovesti, M. Pinotti, and E. Caselgrandi, Zinc, copper and zinc- or copper-dependent enzymes in human hypertension,Biol. Trace. Element Res. 49, 97–106 (1995).

    CAS  Google Scholar 

  10. G. J. L. Zozaya, M. P. Viluria, and A. Castro, Urinary excretion of zinc in patients with essential arterial hypertension,Res. Commun. Chem. Pathol. Pharmacol. 48, 445–453 (1985).

    Google Scholar 

  11. M. D. Chen, P. Y. Lin, C. T. Tsou, J. J. Wang, and W. H. Lin, Selected metals status in patients with nonisulin-dependent diabetes mellitus,Biol. Trace Element Res. 50, 119–124 (1995).

    Google Scholar 

  12. W. B. Kinlaw, A. S. Levine, and J. E. Morley, Abnormal zinc metabolism in type II diabetes mellitus,Am. J. Med. 75, 273–280 (1983).

    Article  PubMed  CAS  Google Scholar 

  13. N. Ddo Marreiro, M. Fisberg, and S. M. Cozzolino, Zinc nuritional status in obese children and adolescents,Biol. Trace Element Res. 86, 107–122 (2002).

    Google Scholar 

  14. N. Ddo Marreiro, M. Fisberg, and S. M. Cozzolino, Zinc nuritional status and its relationship with hyperinsulinemia in obese children and adolescents,Biol. Trace Element Res. 100, 137–149 (2004).

    Article  Google Scholar 

  15. A. Boyum, Isolation of mononuclear cells and granulocytes from blood. II. Isolation of mononuclear cells by centrifugation and of granulocytes by combining centrifugation and sendimentation of 1 g,Scand. J. Clin. Lab. Invest. 21(Suppl. 97), 77–85 (1968).

    CAS  Google Scholar 

  16. A. Noworolska, Antygeny onkopłodowe w komórkach szeregu mielocytarnego, Praca doktorska. AM Wrocław (1984).

  17. A. M. Heagerty, R. F. Bing, M. Miluer, H. Thuston, and J. W. Shales, Leucocyte membrane sodium transport in normotensive populations; dissociation of abnormalities of sodium efflux from raised blood pressure,Lancet 2, 894–905, (1982).

    Article  PubMed  CAS  Google Scholar 

  18. Perkin-Elmer,Analytical Methods for Atomic Absorption Spectrometry, Perkin-Elmer, Norwalk, CT (1971).

    Google Scholar 

  19. A. J. Turner, C. D. Brown, J. A. Carson, and K. Barens, The neprilysin family in health and disease,Adv. Exp. Med. Biol. 477, 229–240 (2000).

    Article  PubMed  CAS  Google Scholar 

  20. W. R. Harlan, J. R. Landis, R. L. Schmouder, N. G. Goldstein, and L. C. Harlan, Blood lead and blood pressure. Relationship in the adolescent and adult US population,JAMA 253, 530–534 (1985).

    Article  PubMed  CAS  Google Scholar 

  21. B. Hennig, Y. Wang, S. Ramasamy, and C. J. McClain, Zinc deficiency alters barrier function of cultured porcine endothelial cells,J. Nutr. 122, 1242–1247 (1992).

    Google Scholar 

  22. B. Hennig, Y. Wang, S. Ramasamy, and C. J. McClain, Zinc protects against tumor necrosis factor-induced disruption of porcine endothelial cell monolayer inegrity,J. Nutr. 123, 1003–1009 (1993).

    PubMed  CAS  Google Scholar 

  23. S. Tubek, The zinc content in lymphocytes and the activity of zinc ions efflux from lymphocytes in primary arterial hypertension,Biol. Trace Element Res. 107, 89–99 (2005).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tubek, S. Selected zinc metabolism parameters in premenopausal and postmenopausal women with moderate and severe primary arterial hypertension. Biol Trace Elem Res 116, 249–255 (2007). https://doi.org/10.1007/BF02698009

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02698009

Index entries

Navigation