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Heart and Vessels

, Volume 31, Issue 10, pp 1724–1730 | Cite as

Association of resistin with impaired membrane fluidity of red blood cells in hypertensive and normotensive men: an electron paramagnetic resonance study

  • Kazushi Tsuda
Short Communication

Abstract

Abnormalities in physical properties of the cell membranes may strongly be linked to hypertension. Recent evidence indicates that resistin may actively participate in the pathophysiology of insulin resistance, diabetes mellitus, hypertension and other circulatory disorders. The present study was undertaken to investigate the possible relationships among plasma resistin, oxidative stress and membrane fluidity (a reciprocal value of membrane microviscosity) in hypertension. We measured the membrane fluidity of red blood cells (RBCs) in hypertensive and normotensive men using an electron paramagnetic resonance (EPR) and spin-labeling method. The order parameter (S) for the spin-label agents (5-nitroxide stearate) in EPR spectra of red blood cell (RBC) membranes was significantly higher in hypertensive men than in normotensive men, indicating that membrane fluidity was decreased in hypertension. Plasma resistin levels were correlated with systolic blood pressure and 8-iso-prostaglandin F2α levels (an index of oxidative stress). Furthermore, the order parameter (S) of RBCs significantly correlated with plasma resistin and plasma 8-isoPG F2α, suggesting that reduced membrane fluidity of RBCs might be associated with hyperresistinemia and increased oxidative stress. Multivariate regression analysis showed that, after adjustment for confounding factors, plasma resistin might be an independent determinant of membrane fluidity of RBCs. The EPR study suggests that resistin might have a close correlation with impaired rheologic behavior of RBCs and microcirculatory dysfunction in hypertension, at least in part, via an oxidative stress-dependent mechanism.

Keywords

Resistin Oxidative stress Membrane fluidity Red blood cells Electron spin resonance Hypertension 

Notes

Acknowledgments

This study was supported in part by grants-in-aid for scientific research from the Ministry of Education, Science, Sports, Culture and Technology of Japan (20590710, 23590901, 26460926). A part of this study was presented at the 77th Annual Scientific Meeting of the Japanese Society of Circulation at Yokohama, Japan in 2013, and an abstract has been published in Circulation Journal (2013;77(suppl I):I-589).

Compliance with ethical standards

Conflict of interest

The author declared no conflicts of interest.

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Copyright information

© Springer Japan 2015

Authors and Affiliations

  1. 1.Cardiovascular Medicine, Cardiovascular and Metabolic Research CenterKansai University of Health SciencesOsakaJapan
  2. 2.Division of Cardiology, School of MedicineWakayama Medical UniversityWakayamaJapan

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