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Difference between revisions of "Rocha 2010 Nitric Oxide"

From Bioblast
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{{Publication
{{Publication
|title=Rocha BS, Gago B, Barbosa RM, Laranjinha J (2010) Diffusion of nitric oxide through the gastric wall upon reduction of nitrite by red wine: physiological impact.Β  Nitric Oxide 22: 235-241.
|title=Rocha BS, Gago B, Barbosa RM, Laranjinha J (2010) Diffusion of nitric oxide through the gastric wall upon reduction of nitrite by red wine: physiological impact.Β  Nitric Oxide 22:235-41.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20083218 PMID:20083218]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20083218 PMID:20083218]
|authors=Rocha BS, Gago B, Barbosa RM, Laranjinha J
|authors=Rocha BS, Gago B, Barbosa RM, Laranjinha J
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{{Labeling
{{Labeling
|organism=Rat
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|organism=Rat
|additional=stomach
|additional=stomach
}}
}}

Revision as of 14:45, 4 March 2015

Publications in the MiPMap
Rocha BS, Gago B, Barbosa RM, Laranjinha J (2010) Diffusion of nitric oxide through the gastric wall upon reduction of nitrite by red wine: physiological impact. Nitric Oxide 22:235-41.

Β» PMID:20083218

Rocha BS, Gago B, Barbosa RM, Laranjinha J (2010) Nitric Oxide

Abstract: In this work we showed that nitric oxide produced via red wine- and ascorbate-dependent reduction of nitrite diffuses through the rat stomach, inducing smooth muscle relaxation. The studies encompassed ex vivo and in vivo models of diffusion. Regarding the former, luminal *NO generated from a mixture of physiologic nitrite and ascorbate or wine diffuses across the stomach wall, being 8-20% of that produced in the mucosal side detected at high microM range (>100 microM) in the serosal side. In order to evaluate whether cellular dysfunction was associated with *NO diffusion at the microM range, the gastric tissue exposed to *NO was evaluated in terms of carbachol-induced muscle contraction in fundal strips and mitochondrial respiration and showed to remain functional and metabolically active. Moreover, pre-contracted gastric strips were shown to relax 86.5+/-5.5% (control) and 75.0+/-4.0% (nitrite/ascorbate-exposed tissue) when challenged with acidified nitrite. The studies in the living animal support the diffusion of luminal *NO to the gastric vasculature as, following addition of nitrite/ascorbate to rat stomach in vivo, *NO was not detected in the serosal environment but concentrations as high as 31 microM of *NO were detected outside the stomach after cardiac arrest. Collectively, the results establish a link between the consumption of nitrite and dietary reductants (e.g., wine polyphenols) and stomach muscle relaxation via the local chemical generation of *NO. β€’ Keywords: nitric oxide, nitrite, stomach, diffusion, polyphenols, relaxation


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Organism: Rat 




HRR: Oxygraph-2k 

stomach