Dias 2022 Free Radic Biol Med: Difference between revisions

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|title=Dias C, Lourenço CF, Laranjinha J, Ledo A (2022) Modulation of oxidative neurometabolism in ischemia/reperfusion by nitrite. https://doi.org/10.1016/j.freeradbiomed.2022.11.021
|title=Dias C, Lourenço CF, Laranjinha J, Ledo A (2022) Modulation of oxidative neurometabolism in ischemia/reperfusion by nitrite. https://doi.org/10.1016/j.freeradbiomed.2022.11.021
|info=Free Radic Biol Med [Epub ahead of print]. [https://www.ncbi.nlm.nih.gov/pubmed/36403737 PMID: 36403737 Open Access]
|info=Free Radic Biol Med [Epub ahead of print]. [https://www.ncbi.nlm.nih.gov/pubmed/36403737 PMID: 36403737 Open Access]
|authors=Dias C, Lourenço CF, Laranjinha J, Ledo A
|authors=Dias C, Lourenco CF, Laranjinha J, Ledo A
|year=2022
|year=2022
|journal=Free Radic Biol Med
|journal=Free Radic Biol Med
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|keywords=Hippocampus, Ischemia-reperfusion, Nitric oxide, Nitrite, Oxidative burst, Respirometry
|keywords=Hippocampus, Ischemia-reperfusion, Nitric oxide, Nitrite, Oxidative burst, Respirometry
|editor=[[Plangger M]]
|editor=[[Plangger M]]
|mipnetlab=PT Coimbra Laranjinha J
}}
}}
{{Labeling
{{Labeling

Revision as of 17:20, 23 November 2022

Publications in the MiPMap
Dias C, Lourenço CF, Laranjinha J, Ledo A (2022) Modulation of oxidative neurometabolism in ischemia/reperfusion by nitrite. https://doi.org/10.1016/j.freeradbiomed.2022.11.021

Β» Free Radic Biol Med [Epub ahead of print]. PMID: 36403737 Open Access

Dias C, Lourenco CF, Laranjinha J, Ledo A (2022) Free Radic Biol Med

Abstract: Nitrite has been viewed in the past essentially as an inert metabolic endpoint of nitric oxide (β€’NO). However, it has become evident that, under certain conditions, nitrite can be a source of β€’NO. In the brain, this alternative source of β€’NO production independent of nitric oxide synthase activity may be particularly relevant in ischemia/reperfusion (I/R), where low oxygen availability limits enzymatic production of β€’NO. Notably, in vivo concentration of nitrite can be easily increased with diet, through the ingestion of nitrate-rich foods, opening the window for a therapeutic intervention based on diet. Considering the modulation of mitochondrial respiration by β€’NO, we have hypothesized that the protective action of nitrite in I/R may also result from modulation of mitochondrial function. We used high-resolution respirometry to evaluate the effects of nitrite in two in vitro models of I/R. In both cases, an increase in oxygen flux was observed following reoxygenation, a phenomenon that has been coined "oxidative burst". The amplitude of this "oxidative burst" was decreased by nitrite in a concentration-dependent manner. Additionally, a pilot in vivo study in which animals received a nitrate-rich diet as a strategy to increase circulating and tissue levels of nitrite also revealed that the "oxidative burst" was decreased in the nitrate-treated animals. These results may provide mechanistic support to the observation of a protective effect of nitrite in situations of brain ischemia. β€’ Keywords: Hippocampus, Ischemia-reperfusion, Nitric oxide, Nitrite, Oxidative burst, Respirometry β€’ Bioblast editor: Plangger M β€’ O2k-Network Lab: PT Coimbra Laranjinha J


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2022-11 

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