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ToolsJames, Philip E., Lang, Derek, Tufnell-Barret, Timothy, Milsom, Alex B. and Frenneaux, Michael P. (2004) Vasorelaxation by red blood cells and impairment in diabetes: Reduced nitric oxide and oxygen delivery by glycated hemoglobin. Circulation Research, 94 (7). pp. 976-983. ISSN 0009-7330
Full text not available from this repository.Abstract
Vascular dysfunction in diabetes is attributed to lack of bioavailable nitric oxide (NO) and is postulated as a primary cause of small vessel complications as a result of poor glycemic control. Although it has been proposed that NO is bound by red blood cells (RBCs) and can induce relaxation of blood vessels distal to its site of production in the normal circulation, the effect of RBC glycation on NO binding and relaxation of hypoxic vessels is unknown. We confirm RBC-induced vessel relaxation is inversely related to tissue oxygenation and is proportional to RBC S-nitrosohemoglobin (HbSNO) content (but not nitrosylhemoglobin content). We show more total NO bound inside highly glycated RBCs (0.0134 versus 0.0119 NO/Hb, respectively; P
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | animals,aorta, thoracic,cell hypoxia,diabetes mellitus,endothelium, vascular,erythrocytes,glycosylation,hemoglobin a, glycosylated,hemoglobins,male,microcirculation,nitric oxide,oxygen,phenylephrine,rabbits,triazenes,vasoconstrictor agents,vasodilation,omega-n-methylarginine,sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being |
| Faculty \ School: | Faculty of Medicine and Health Sciences > Norwich Medical School |
| UEA Research Groups: | Faculty of Medicine and Health Sciences > Research Groups > Cardiovascular and Metabolic Health |
| Depositing User: | Pure Connector |
| Date Deposited: | 13 Mar 2015 16:20 |
| Last Modified: | 07 Oct 2024 15:30 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/52625 |
| DOI: | 10.1161/01.RES.0000122044.21787.01 |
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