Bound NO in human red blood cells: fact or artifact?
Bound NO in human red blood cells: fact or artifact?
There has been considerable debate over the nature and chemistry of the interaction between nitric oxide (NO) and red blood cells (RBCs), in particular whether hemoglobin consumes or conserves NO bioactivity. Given the vast range of nitrosation levels reported for human RBCs in the literature, we sought to investigate whether there was a common denominator that could account for such discrepancies across different methodologies and reaction conditions and if such a pathway may exist in physiology. Here, we show that there are marked differences in reactivity toward NO between human and rat hemoglobin, which offers a mechanistic explanation for why basal levels of NO-adducts in primate RBCs are considerably lower than those in rodents. We further demonstrate that the inadvertent introduction of trace amounts of nitrite and incomplete thiol alkylation lead to rapid heme and thiol nitros(yl)ation, with generation of nitrosylhemoglobin (NOHb) and S-nitrosohemoglobin (SNOHb), while neither species is detectable in human RBCs at physiological nitrite concentrations. Thus, caution should be exercised in interpreting experimental results on SNOHb/NOHb levels that were obtained in the absence of knowledge about the degree of nitrite contamination, in particular when a physiological role for such species is implicated.
nitric oxide, nitrite, nitrosation, hemoglobin, erythrocytes
221-228
Bryan, Nathan S.
709ff51c-c864-4862-9e3f-c5cfd3961025
Rassaf, Tienush
a820a375-219a-4fa2-ae10-e77f4b1eb37c
Rodriguez, Juan
055ad15f-3cf3-4366-a11c-9a313cf2fa60
Feelisch, Martin
8c1b9965-8614-4e85-b2c6-458a2e17eafd
June 2004
Bryan, Nathan S.
709ff51c-c864-4862-9e3f-c5cfd3961025
Rassaf, Tienush
a820a375-219a-4fa2-ae10-e77f4b1eb37c
Rodriguez, Juan
055ad15f-3cf3-4366-a11c-9a313cf2fa60
Feelisch, Martin
8c1b9965-8614-4e85-b2c6-458a2e17eafd
Abstract
There has been considerable debate over the nature and chemistry of the interaction between nitric oxide (NO) and red blood cells (RBCs), in particular whether hemoglobin consumes or conserves NO bioactivity. Given the vast range of nitrosation levels reported for human RBCs in the literature, we sought to investigate whether there was a common denominator that could account for such discrepancies across different methodologies and reaction conditions and if such a pathway may exist in physiology. Here, we show that there are marked differences in reactivity toward NO between human and rat hemoglobin, which offers a mechanistic explanation for why basal levels of NO-adducts in primate RBCs are considerably lower than those in rodents. We further demonstrate that the inadvertent introduction of trace amounts of nitrite and incomplete thiol alkylation lead to rapid heme and thiol nitros(yl)ation, with generation of nitrosylhemoglobin (NOHb) and S-nitrosohemoglobin (SNOHb), while neither species is detectable in human RBCs at physiological nitrite concentrations. Thus, caution should be exercised in interpreting experimental results on SNOHb/NOHb levels that were obtained in the absence of knowledge about the degree of nitrite contamination, in particular when a physiological role for such species is implicated.
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Published date: June 2004
Keywords:
nitric oxide, nitrite, nitrosation, hemoglobin, erythrocytes
Organisations:
Clinical & Experimental Sciences
Identifiers
Local EPrints ID: 337845
URI: http://eprints.soton.ac.uk/id/eprint/337845
ISSN: 1089-8603
PURE UUID: ad4d57d9-3627-4bb6-88bf-e859a230b15e
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Date deposited: 22 Jun 2012 09:06
Last modified: 15 Mar 2024 03:41
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Author:
Nathan S. Bryan
Author:
Tienush Rassaf
Author:
Juan Rodriguez
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