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Am J Physiol Heart Circ Physiol 284: H1577-H1584, 2003. First published January 9, 2003; doi:10.1152/ajpheart.00665.2002
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Vol. 284, Issue 5, H1577-H1584, May 2003

Effects of nitric oxide on red blood cell deformability

Melek Bor-Kucukatay1, Rosalinda B. Wenby2, Herbert J. Meiselman2, and Oguz K. Baskurt1

1 Department of Physiology, Faculty of Medicine, Akdeniz University, Antalya, 07070 Turkey; and 2 Department of Physiology and Biophysics, Keck School of Medicine, Los Angeles, California 90033

In addition to its known action on vascular smooth muscle, nitric oxide (NO) has been suggested to have cardiovascular effects via regulation of red blood cell (RBC) deformability. The present study was designed to further explore this possibility. Human RBCs in autologous plasma were incubated for 1 h with NO synthase (NOS) inhibitors [Nomega -nitro-L-arginine methyl ester (L-NAME) and S-methylisothiourea], NO donors [sodium nitroprusside (SNP) and diethylenetriamine (DETA)-NONOate], an NO precursor (L-arginine), soluble guanylate cyclase inhibitors (1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one and methylene blue), and a potassium channel blocker [triethylammonium (TEA)]. After incubation, RBC deformability at various shear stresses was determined by ektacytometry. Both NOS inhibitors significantly reduced RBC deformability above a threshold concentration, whereas the NO donors increased deformability at optimal concentrations. NO donors, as well as the NO precursor L-arginine and the potassium blocker TEA, were able to reverse the effects of NOS inhibitors. Guanylate cyclase inhibition reduced RBC deformation, with both SNP and DETA-NONOate able to reverse this effect. These results thus indicate the importance of NO as a determinant of RBC mechanical behavior and suggest its regulatory role for normal RBC deformability.

hemorheology; hemodynamics; regulation; cGMP


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