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The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging
Nicotinamide adenine dinucleotide (NAD(+)) is an essential pyridine nucleotide that serves as an electron carrier in cellular metabolism and plays a crucial role in the maintenance of balanced redox homeostasis. Quantification of NAD(+):NADH and NADP(+):NADPH ratios are pivotal to a wide variety of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482912/ https://www.ncbi.nlm.nih.gov/pubmed/30124109 http://dx.doi.org/10.1089/rej.2018.2077 |
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author | Clement, James Wong, Matthew Poljak, Anne Sachdev, Perminder Braidy, Nady |
author_facet | Clement, James Wong, Matthew Poljak, Anne Sachdev, Perminder Braidy, Nady |
author_sort | Clement, James |
collection | PubMed |
description | Nicotinamide adenine dinucleotide (NAD(+)) is an essential pyridine nucleotide that serves as an electron carrier in cellular metabolism and plays a crucial role in the maintenance of balanced redox homeostasis. Quantification of NAD(+):NADH and NADP(+):NADPH ratios are pivotal to a wide variety of cellular processes, including intracellular secondary messenger signaling by CD38 glycohydrolases, DNA repair by poly(adenosine diphosphate ribose) polymerase (PARP), epigenetic regulation of gene expression by NAD-dependent histone deacetylase enzymes known as sirtuins, and regulation of the oxidative pentose phosphate pathway. We quantified changes in the NAD(+) metabolome in plasma samples collected from consenting healthy human subjects across a wide age range (20–87 years) using liquid chromatography coupled to tandem mass spectrometry. Our data show a significant decline in the plasma levels of NAD(+), NADP(+), and other important metabolites such as nicotinic acid adenine dinucleotide (NAAD) with age. However, an age-related increase in the reduced form of NAD(+) and NADP(+)—NADH and NADPH—and nicotinamide (NAM), N-methyl-nicotinamide (MeNAM), and the products of adenosine diphosphoribosylation, including adenosine diphosphate ribose (ADPR) was also reported. Whereas, plasma levels of nicotinic acid (NA), nicotinamide mononucleotide (NMN), and nicotinic acid mononucleotide (NAMN) showed no statistically significant changes across age groups. Taken together, our data cumulatively suggest that age-related impairments are associated with corresponding alterations in the extracellular plasma NAD(+) metabolome. Our future research will seek to elucidate the role of modulating NAD(+) metabolites in the treatment and prevention of age-related diseases. |
format | Online Article Text |
id | pubmed-6482912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-64829122019-04-26 The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging Clement, James Wong, Matthew Poljak, Anne Sachdev, Perminder Braidy, Nady Rejuvenation Res Original Articles Nicotinamide adenine dinucleotide (NAD(+)) is an essential pyridine nucleotide that serves as an electron carrier in cellular metabolism and plays a crucial role in the maintenance of balanced redox homeostasis. Quantification of NAD(+):NADH and NADP(+):NADPH ratios are pivotal to a wide variety of cellular processes, including intracellular secondary messenger signaling by CD38 glycohydrolases, DNA repair by poly(adenosine diphosphate ribose) polymerase (PARP), epigenetic regulation of gene expression by NAD-dependent histone deacetylase enzymes known as sirtuins, and regulation of the oxidative pentose phosphate pathway. We quantified changes in the NAD(+) metabolome in plasma samples collected from consenting healthy human subjects across a wide age range (20–87 years) using liquid chromatography coupled to tandem mass spectrometry. Our data show a significant decline in the plasma levels of NAD(+), NADP(+), and other important metabolites such as nicotinic acid adenine dinucleotide (NAAD) with age. However, an age-related increase in the reduced form of NAD(+) and NADP(+)—NADH and NADPH—and nicotinamide (NAM), N-methyl-nicotinamide (MeNAM), and the products of adenosine diphosphoribosylation, including adenosine diphosphate ribose (ADPR) was also reported. Whereas, plasma levels of nicotinic acid (NA), nicotinamide mononucleotide (NMN), and nicotinic acid mononucleotide (NAMN) showed no statistically significant changes across age groups. Taken together, our data cumulatively suggest that age-related impairments are associated with corresponding alterations in the extracellular plasma NAD(+) metabolome. Our future research will seek to elucidate the role of modulating NAD(+) metabolites in the treatment and prevention of age-related diseases. Mary Ann Liebert, Inc., publishers 2019-04-01 2019-04-23 /pmc/articles/PMC6482912/ /pubmed/30124109 http://dx.doi.org/10.1089/rej.2018.2077 Text en © James Clement et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Clement, James Wong, Matthew Poljak, Anne Sachdev, Perminder Braidy, Nady The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title | The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title_full | The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title_fullStr | The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title_full_unstemmed | The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title_short | The Plasma NAD(+) Metabolome Is Dysregulated in “Normal” Aging |
title_sort | plasma nad(+) metabolome is dysregulated in “normal” aging |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482912/ https://www.ncbi.nlm.nih.gov/pubmed/30124109 http://dx.doi.org/10.1089/rej.2018.2077 |
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