Role of nitrite, urate and pepsin in the gastroprotective effects of saliva

Dietary nitrate is now recognized as an alternative substrate for nitric oxide (•NO) production in the gut. This novel pathway implies the sequential reduction of nitrate to nitrite, •NO and other bioactive nitrogen oxides but the physiological relevance of these oxidants has remained elusive. We ha...

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Main Authors: Bárbara S. Rocha, Jon O Lundberg, Rafael Radi, João Laranjinha
Format: Article
Language:English
Published: Elsevier 2016-08-01
Series:Redox Biology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231716300271
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author Bárbara S. Rocha
Jon O Lundberg
Rafael Radi
João Laranjinha
author_facet Bárbara S. Rocha
Jon O Lundberg
Rafael Radi
João Laranjinha
author_sort Bárbara S. Rocha
collection DOAJ
description Dietary nitrate is now recognized as an alternative substrate for nitric oxide (•NO) production in the gut. This novel pathway implies the sequential reduction of nitrate to nitrite, •NO and other bioactive nitrogen oxides but the physiological relevance of these oxidants has remained elusive. We have previously shown that dietary nitrite fuels an hitherto unrecognized nitrating pathway at acidic gastric pH, through which pepsinogen is nitrated in the gastric mucosa, yielding a less active form of pepsin in vitro. Here, we demonstrate that pepsin is nitrated in vivo and explore the functional impact of protein nitration by means of peptic ulcer development. Upon administration of pentagastrin and human nitrite-rich saliva or sodium nitrite to rats, nitrated pepsin was detected in the animal's stomach by immunoprecipitation. •NO was measured in the gastric headspace before and after nitrite instillation by chemiluminescence. At the end of each procedure, the stomach's lesions, ranging from gastric erosions to haemorrhagic ulcers, were scored. Nitrite increased gastric •NO by 200-fold (p<0.05) and nitrated pepsin was detected both in the gastric juice and the mucosa (p<0.05). Exogenous urate, a scavenger of nitrogen dioxide radical, blunted •NO detection and inhibited pepsin nitration, suggesting an underlining free radical-dependent mechanism for nitration. Functionally, pepsin nitration prevented the development of gastric ulcers, as the lesions were only apparent when pepsin nitration was inhibited by urate. In sum, this work unravels a novel dietary-dependent nitrating pathway in which pepsin is nitrated and inactivated in the stomach, preventing the progression of gastric ulcers.
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spelling doaj.art-e7199628143e43e7a02ab1fc74fd465c2022-12-22T03:02:45ZengElsevierRedox Biology2213-23172016-08-018C40741410.1016/j.redox.2016.04.002Role of nitrite, urate and pepsin in the gastroprotective effects of salivaBárbara S. Rocha0Jon O Lundberg1Rafael Radi2João Laranjinha3Faculty of Pharmacy and Center for Neurosciences and Cell Biology, University of Coimbra, Health Sciences Campus, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalDepartment of Physiology and Pharmacology, Karolinska Institute, Stockholm, SwedenDepartamento de Bioquímica, Facultad de Medicina, Universidad de La República, Montevideo, UruguayFaculty of Pharmacy and Center for Neurosciences and Cell Biology, University of Coimbra, Health Sciences Campus, Azinhaga de Santa Comba, 3000-548 Coimbra, PortugalDietary nitrate is now recognized as an alternative substrate for nitric oxide (•NO) production in the gut. This novel pathway implies the sequential reduction of nitrate to nitrite, •NO and other bioactive nitrogen oxides but the physiological relevance of these oxidants has remained elusive. We have previously shown that dietary nitrite fuels an hitherto unrecognized nitrating pathway at acidic gastric pH, through which pepsinogen is nitrated in the gastric mucosa, yielding a less active form of pepsin in vitro. Here, we demonstrate that pepsin is nitrated in vivo and explore the functional impact of protein nitration by means of peptic ulcer development. Upon administration of pentagastrin and human nitrite-rich saliva or sodium nitrite to rats, nitrated pepsin was detected in the animal's stomach by immunoprecipitation. •NO was measured in the gastric headspace before and after nitrite instillation by chemiluminescence. At the end of each procedure, the stomach's lesions, ranging from gastric erosions to haemorrhagic ulcers, were scored. Nitrite increased gastric •NO by 200-fold (p<0.05) and nitrated pepsin was detected both in the gastric juice and the mucosa (p<0.05). Exogenous urate, a scavenger of nitrogen dioxide radical, blunted •NO detection and inhibited pepsin nitration, suggesting an underlining free radical-dependent mechanism for nitration. Functionally, pepsin nitration prevented the development of gastric ulcers, as the lesions were only apparent when pepsin nitration was inhibited by urate. In sum, this work unravels a novel dietary-dependent nitrating pathway in which pepsin is nitrated and inactivated in the stomach, preventing the progression of gastric ulcers.http://www.sciencedirect.com/science/article/pii/S2213231716300271NitrateNitriteTyrosine nitrationStomach
spellingShingle Bárbara S. Rocha
Jon O Lundberg
Rafael Radi
João Laranjinha
Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
Redox Biology
Nitrate
Nitrite
Tyrosine nitration
Stomach
title Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
title_full Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
title_fullStr Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
title_full_unstemmed Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
title_short Role of nitrite, urate and pepsin in the gastroprotective effects of saliva
title_sort role of nitrite urate and pepsin in the gastroprotective effects of saliva
topic Nitrate
Nitrite
Tyrosine nitration
Stomach
url http://www.sciencedirect.com/science/article/pii/S2213231716300271
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AT joaolaranjinha roleofnitriteurateandpepsininthegastroprotectiveeffectsofsaliva