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NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota
The oxidized form of nicotinamide adenine dinucleotide (NAD+) is a critical metabolite for living cells. NAD+ may act either as a cofactor for many cellular reactions as well as a coenzyme for different NAD+-consuming enzymes involved in the physiological homeostasis of different organs and systems....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346866/ https://www.ncbi.nlm.nih.gov/pubmed/37447318 http://dx.doi.org/10.3390/nu15132992 |
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author | Niño-Narvión, Julia Rojo-López, Marina Idalia Martinez-Santos, Patricia Rossell, Joana Ruiz-Alcaraz, Antonio J. Alonso, Núria Ramos-Molina, Bruno Mauricio, Didac Julve, Josep |
author_facet | Niño-Narvión, Julia Rojo-López, Marina Idalia Martinez-Santos, Patricia Rossell, Joana Ruiz-Alcaraz, Antonio J. Alonso, Núria Ramos-Molina, Bruno Mauricio, Didac Julve, Josep |
author_sort | Niño-Narvión, Julia |
collection | PubMed |
description | The oxidized form of nicotinamide adenine dinucleotide (NAD+) is a critical metabolite for living cells. NAD+ may act either as a cofactor for many cellular reactions as well as a coenzyme for different NAD+-consuming enzymes involved in the physiological homeostasis of different organs and systems. In mammals, NAD+ is synthesized from either tryptophan or other vitamin B3 intermediates that act as NAD+ precursors. Recent research suggests that NAD+ precursors play a crucial role in maintaining the integrity of the gut barrier. Indeed, its deficiency has been associated with enhanced gut inflammation and leakage, and dysbiosis. Conversely, NAD+-increasing therapies may confer protection against intestinal inflammation in experimental conditions and human patients, with accumulating evidence indicating that such favorable effects could be, at least in part, mediated by concomitant changes in the composition of intestinal microbiota. However, the mechanisms by which NAD+-based treatments affect the microbiota are still poorly understood. In this context, we have focused specifically on the impact of NAD+ deficiency on intestinal inflammation and dysbiosis in animal and human models. We have further explored the relationship between NAD+ and improved host intestinal metabolism and immunity and the composition of microbiota in vivo. Overall, this comprehensive review aims to provide a new perspective on the effect of NAD+-increasing strategies on host intestinal physiology. |
format | Online Article Text |
id | pubmed-10346866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103468662023-07-15 NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota Niño-Narvión, Julia Rojo-López, Marina Idalia Martinez-Santos, Patricia Rossell, Joana Ruiz-Alcaraz, Antonio J. Alonso, Núria Ramos-Molina, Bruno Mauricio, Didac Julve, Josep Nutrients Review The oxidized form of nicotinamide adenine dinucleotide (NAD+) is a critical metabolite for living cells. NAD+ may act either as a cofactor for many cellular reactions as well as a coenzyme for different NAD+-consuming enzymes involved in the physiological homeostasis of different organs and systems. In mammals, NAD+ is synthesized from either tryptophan or other vitamin B3 intermediates that act as NAD+ precursors. Recent research suggests that NAD+ precursors play a crucial role in maintaining the integrity of the gut barrier. Indeed, its deficiency has been associated with enhanced gut inflammation and leakage, and dysbiosis. Conversely, NAD+-increasing therapies may confer protection against intestinal inflammation in experimental conditions and human patients, with accumulating evidence indicating that such favorable effects could be, at least in part, mediated by concomitant changes in the composition of intestinal microbiota. However, the mechanisms by which NAD+-based treatments affect the microbiota are still poorly understood. In this context, we have focused specifically on the impact of NAD+ deficiency on intestinal inflammation and dysbiosis in animal and human models. We have further explored the relationship between NAD+ and improved host intestinal metabolism and immunity and the composition of microbiota in vivo. Overall, this comprehensive review aims to provide a new perspective on the effect of NAD+-increasing strategies on host intestinal physiology. MDPI 2023-06-30 /pmc/articles/PMC10346866/ /pubmed/37447318 http://dx.doi.org/10.3390/nu15132992 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Niño-Narvión, Julia Rojo-López, Marina Idalia Martinez-Santos, Patricia Rossell, Joana Ruiz-Alcaraz, Antonio J. Alonso, Núria Ramos-Molina, Bruno Mauricio, Didac Julve, Josep NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title | NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title_full | NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title_fullStr | NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title_full_unstemmed | NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title_short | NAD+ Precursors and Intestinal Inflammation: Therapeutic Insights Involving Gut Microbiota |
title_sort | nad+ precursors and intestinal inflammation: therapeutic insights involving gut microbiota |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10346866/ https://www.ncbi.nlm.nih.gov/pubmed/37447318 http://dx.doi.org/10.3390/nu15132992 |
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