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Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage
Nicotinamide adenine dinucleotide (NAD(+)) is an essential cofactor that mediates numerous biological processes in all living cells. Multiple NAD(+) biosynthetic enzymes and NAD(+)-consuming enzymes are involved in neuroprotection and axon regeneration. The nematode Caenorhabditis elegans has served...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407593/ https://www.ncbi.nlm.nih.gov/pubmed/32630651 http://dx.doi.org/10.3390/biom10070993 |
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author | Lee, Yuri Jeong, Hyeseon Park, Kyung Hwan Kim, Kyung Won |
author_facet | Lee, Yuri Jeong, Hyeseon Park, Kyung Hwan Kim, Kyung Won |
author_sort | Lee, Yuri |
collection | PubMed |
description | Nicotinamide adenine dinucleotide (NAD(+)) is an essential cofactor that mediates numerous biological processes in all living cells. Multiple NAD(+) biosynthetic enzymes and NAD(+)-consuming enzymes are involved in neuroprotection and axon regeneration. The nematode Caenorhabditis elegans has served as a model to study the neuronal role of NAD(+) because many molecular components regulating NAD(+) are highly conserved. This review focuses on recent findings using C. elegans models of neuronal damage pertaining to the neuronal functions of NAD(+) and its precursors, including a neuroprotective role against excitotoxicity and axon degeneration as well as an inhibitory role in axon regeneration. The regulation of NAD(+) levels could be a promising therapeutic strategy to counter many neurodegenerative diseases, as well as neurotoxin-induced and traumatic neuronal damage. |
format | Online Article Text |
id | pubmed-7407593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74075932020-08-25 Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage Lee, Yuri Jeong, Hyeseon Park, Kyung Hwan Kim, Kyung Won Biomolecules Review Nicotinamide adenine dinucleotide (NAD(+)) is an essential cofactor that mediates numerous biological processes in all living cells. Multiple NAD(+) biosynthetic enzymes and NAD(+)-consuming enzymes are involved in neuroprotection and axon regeneration. The nematode Caenorhabditis elegans has served as a model to study the neuronal role of NAD(+) because many molecular components regulating NAD(+) are highly conserved. This review focuses on recent findings using C. elegans models of neuronal damage pertaining to the neuronal functions of NAD(+) and its precursors, including a neuroprotective role against excitotoxicity and axon degeneration as well as an inhibitory role in axon regeneration. The regulation of NAD(+) levels could be a promising therapeutic strategy to counter many neurodegenerative diseases, as well as neurotoxin-induced and traumatic neuronal damage. MDPI 2020-07-02 /pmc/articles/PMC7407593/ /pubmed/32630651 http://dx.doi.org/10.3390/biom10070993 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Lee, Yuri Jeong, Hyeseon Park, Kyung Hwan Kim, Kyung Won Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title | Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title_full | Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title_fullStr | Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title_full_unstemmed | Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title_short | Effects of NAD(+) in Caenorhabditis elegans Models of Neuronal Damage |
title_sort | effects of nad(+) in caenorhabditis elegans models of neuronal damage |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407593/ https://www.ncbi.nlm.nih.gov/pubmed/32630651 http://dx.doi.org/10.3390/biom10070993 |
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