Int J Angiol 1999; 8(3): 154-156
DOI: 10.1007/BF01616444
Original Articles

© Georg Thieme Verlag KG Stuttgart · New York

Lowered total intracellular magnesium status in a subgroup of hypertensives

Klaus Kisters1 , Faruk Tokmak1 , Markus Kosch1 , Karl Heinz Dietl2 , Gerald Westermann1
  • 1Medizinische Universität-Poliklinik, Westfälische Wilhelms-Universität, Münster
  • 2Chirurgische Klinik und Poliklinik, Westfälische Wilhelms-Universität Münster, Germany
Presented in part at The 40th Annual World Congress, International College of Angiology, Lisbon, Portugal, June 1998.
Further Information

Publication History

Publication Date:
24 April 2011 (online)

Abstract

A new method to determine total Mg++ content in lymphocytes was developed, offering advantages for routine measurements as compared to fluorescence methods. Intracellular total Mg++ measurements were performed in lymphocytes of 18 healthy subjects and 19 untreated essential hypertensive patients. Mg++ content was referred to lymphocytic and membrane protein, which was determined according to Bradford's method. Mg++ measurements were performed by atomic absorption spectroscopy using a Video 12 apparatus of Thermo Electron Instrumentation Laboratory, Andover, USA. The results show that in patients with essential hypertension total intralymphocytic Mg++ content is significantly lower (0.07 ± 0.05 mmol/g lymphocytic protein, mean ± s.d.) as compared to controls (0.11 ± 0.04 mmol/g lymphocytic protein, mean ± s.d., p < 0.05).

Free intracellular Mg++ content was measured in lymphocytes by the fluorescent indicator mag-fura-II, showing no significant differences in normotensives and hypertensives (0.30 ± 0.16 versus 0.38 ± 0.17 mmol/l). Additionally, in platelets free intracellular Mg++ concentrations were not found of significant difference in normotensives and hypertensives (0.52 ± 0.23 versus 0.47 ± 0.27 mmol/l) using mag-fura-II. In plasma Mg++ concentrations there was no significant difference in the normotensive and hypertensive group (0.92 ± 0.07 versus 0.88 ± 0.07 mmol/l). There was no correlation between plasma or free or total cellular magnesium concentrations in both groups. Furthermore this method seems also suitable for routine measurements of total intracellular Mg++ concentrations in even larger measurements like mag-fur-II. Lowered total intracellular Mg++ concentrations in a subgroup of primary hypertensives may contribute to the development of this disorder, perhaps due to different buffering systems.

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