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Nitric oxide scavenging by red blood cells as a function of hematocrit and oxygenation. J Biol Chem 2005 Nov 25;280(47):39024-32

Date

09/28/2005

Pubmed ID

16186121

DOI

10.1074/jbc.M509045200

Scopus ID

2-s2.0-28244459618 (requires institutional sign-in at Scopus site)   160 Citations

Abstract

The reaction rate between nitric oxide and intraerythrocytic hemoglobin plays a major role in nitric oxide bioavailability and modulates homeostatic vascular function. It has previously been demonstrated that the encapsulation of hemoglobin in red blood cells restricts its ability to scavenge nitric oxide. This effect has been attributed to either factors intrinsic to the red blood cell such as a physical membrane barrier or factors external to the red blood cell such as the formation of an unstirred layer around the cell. We have performed measurements of the uptake rate of nitric oxide by red blood cells under oxygenated and deoxygenated conditions at different hematocrit percentages. Our studies include stopped-flow measurements where both the unstirred layer and physical barrier potentially participate, as well as competition experiments where the potential contribution of the unstirred layer is limited. We find that deoxygenated erythrocytes scavenge nitric oxide faster than oxygenated cells and that the rate of nitric oxide scavenging for oxygenated red blood cells increases as the hematocrit is raised from 15% to 50%. Our results 1) confirm the critical biological phenomenon that hemoglobin compartmentalization within the erythrocyte reduces reaction rates with nitric oxide, 2) show that extra-erythocytic diffusional barriers mediate most of this effect, and 3) provide novel evidence that an oxygen-dependent intrinsic property of the red blood cell contributes to this barrier activity, albeit to a lesser extent. These observations may have important physiological implications within the microvasculature and for pathophysiological disruption of nitric oxide homeostasis in diseases.

Author List

Azarov I, Huang KT, Basu S, Gladwin MT, Hogg N, Kim-Shapiro DB

Author

Neil Hogg PhD Associate Dean, Professor in the Biophysics department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Cell-Free System
Erythrocytes
Free Radical Scavengers
Hematocrit
Hemoglobins
Homeostasis
Humans
In Vitro Techniques
Kinetics
Methemoglobin
Nitric Oxide
Oxygen
Spectrophotometry