On the dynamics of nitrite, nitrate and other biomarkers of nitric oxide production in inflammatory bowel disease
On the dynamics of nitrite, nitrate and other biomarkers of nitric oxide production in inflammatory bowel disease
Nitrite and nitrate are frequently used surrogate markers of nitric oxide (NO) production. Using rat models of acute and chronic DSS-induced colitis we examined the applicability of these and other NO-related metabolites, in tissues and blood, for the characterization of inflammatory bowel disease. Global NO dynamics were assessed by simultaneous quantification of nitrite, nitrate, nitroso and nitrosyl species over time in multiple compartments. NO metabolite levels were compared to a composite disease activity index (DAI) and contrasted with measurements of platelet aggregability, ascorbate redox status and the effects of 5-aminosalicylic acid (5-ASA). Nitroso products in the colon and in other organs responded in a manner consistent with the DAI. In contrast, nitrite and nitrate, in both intra- and extravascular compartments, exhibited variations that were not always in step with the DAI. Extravascular nitrite, in particular, demonstrated significant temporal instabilities, ranging from systemic drops to marked increases. The latter was particularly evident after cessation of the inflammatory stimulus and accompanied by profound ascorbate oxidation. Treatment with 5-ASA effectively reversed these fluctuations and the associated oxidative and nitrosative stress. Platelet activation was enhanced in both the acute and chronic model. Our results offer a first glimpse into the systemic nature of DSS-induced inflammation and reveal a greater complexity of NO metabolism than previously envisioned, with a clear dissociation of nitrite from other markers of NO production. The remarkable effectiveness of 5-ASA to abrogate the observed pattern of nitrite instability suggests a hitherto unrecognized role of this molecule in either development or resolution of inflammation. Its possible link to tissue oxygen consumption and the hypoxia that tends to accompany the inflammatory process warrants further investigation.
155-167
Saijo, Fumito
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Milsom, Alexandra B.
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Bryan, Nathan S.
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Bauer, Selena M.
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Vowinkel, Thorsten
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Ivanovic, Marina
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Andry, Chris
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Granger, D. Neil
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Rodriguez, Juan
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Feelisch, Martin
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15 February 2010
Saijo, Fumito
c66d3d87-1cdf-4f51-af1c-fdd1c7e772ea
Milsom, Alexandra B.
7a3c8b7d-d65a-46b4-9686-1208c539253b
Bryan, Nathan S.
709ff51c-c864-4862-9e3f-c5cfd3961025
Bauer, Selena M.
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Vowinkel, Thorsten
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Ivanovic, Marina
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Andry, Chris
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Granger, D. Neil
b660a156-ab9f-41da-978f-b69da71dfc51
Rodriguez, Juan
055ad15f-3cf3-4366-a11c-9a313cf2fa60
Feelisch, Martin
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Saijo, Fumito, Milsom, Alexandra B., Bryan, Nathan S., Bauer, Selena M., Vowinkel, Thorsten, Ivanovic, Marina, Andry, Chris, Granger, D. Neil, Rodriguez, Juan and Feelisch, Martin
(2010)
On the dynamics of nitrite, nitrate and other biomarkers of nitric oxide production in inflammatory bowel disease.
Nitric Oxide, 22 (2), .
(doi:10.1016/j.niox.2009.11.009).
(PMID:20005300)
Abstract
Nitrite and nitrate are frequently used surrogate markers of nitric oxide (NO) production. Using rat models of acute and chronic DSS-induced colitis we examined the applicability of these and other NO-related metabolites, in tissues and blood, for the characterization of inflammatory bowel disease. Global NO dynamics were assessed by simultaneous quantification of nitrite, nitrate, nitroso and nitrosyl species over time in multiple compartments. NO metabolite levels were compared to a composite disease activity index (DAI) and contrasted with measurements of platelet aggregability, ascorbate redox status and the effects of 5-aminosalicylic acid (5-ASA). Nitroso products in the colon and in other organs responded in a manner consistent with the DAI. In contrast, nitrite and nitrate, in both intra- and extravascular compartments, exhibited variations that were not always in step with the DAI. Extravascular nitrite, in particular, demonstrated significant temporal instabilities, ranging from systemic drops to marked increases. The latter was particularly evident after cessation of the inflammatory stimulus and accompanied by profound ascorbate oxidation. Treatment with 5-ASA effectively reversed these fluctuations and the associated oxidative and nitrosative stress. Platelet activation was enhanced in both the acute and chronic model. Our results offer a first glimpse into the systemic nature of DSS-induced inflammation and reveal a greater complexity of NO metabolism than previously envisioned, with a clear dissociation of nitrite from other markers of NO production. The remarkable effectiveness of 5-ASA to abrogate the observed pattern of nitrite instability suggests a hitherto unrecognized role of this molecule in either development or resolution of inflammation. Its possible link to tissue oxygen consumption and the hypoxia that tends to accompany the inflammatory process warrants further investigation.
Text
2009 Saijo et al - NO Biol Chem - Advance Online.pdf
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Published date: 15 February 2010
Organisations:
Clinical & Experimental Sciences
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Local EPrints ID: 337698
URI: http://eprints.soton.ac.uk/id/eprint/337698
ISSN: 1089-8603
PURE UUID: 1f9cc436-44d7-4a7e-93c8-6616f3008c4e
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Date deposited: 01 May 2012 16:43
Last modified: 15 Mar 2024 03:41
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Author:
Fumito Saijo
Author:
Alexandra B. Milsom
Author:
Nathan S. Bryan
Author:
Selena M. Bauer
Author:
Thorsten Vowinkel
Author:
Marina Ivanovic
Author:
Chris Andry
Author:
D. Neil Granger
Author:
Juan Rodriguez
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