Age‐dependent decline of NAD+ - universal truth or confounded consensus?

Research output: Contribution to journalReviewResearchpeer-review

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Age‐dependent decline of NAD+ - universal truth or confounded consensus? / Peluso, A. Augusto; Damgaard, Mads V.; Mori, Marcelo A.S.; Treebak, Jonas T.

In: Nutrients, Vol. 14, No. 1, 101, 2021.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Peluso, AA, Damgaard, MV, Mori, MAS & Treebak, JT 2021, 'Age‐dependent decline of NAD+ - universal truth or confounded consensus?', Nutrients, vol. 14, no. 1, 101. https://doi.org/10.3390/nu14010101

APA

Peluso, A. A., Damgaard, M. V., Mori, M. A. S., & Treebak, J. T. (2021). Age‐dependent decline of NAD+ - universal truth or confounded consensus? Nutrients, 14(1), [101]. https://doi.org/10.3390/nu14010101

Vancouver

Peluso AA, Damgaard MV, Mori MAS, Treebak JT. Age‐dependent decline of NAD+ - universal truth or confounded consensus? Nutrients. 2021;14(1). 101. https://doi.org/10.3390/nu14010101

Author

Peluso, A. Augusto ; Damgaard, Mads V. ; Mori, Marcelo A.S. ; Treebak, Jonas T. / Age‐dependent decline of NAD+ - universal truth or confounded consensus?. In: Nutrients. 2021 ; Vol. 14, No. 1.

Bibtex

@article{ffaac53effcc43d58beef804e12bf7d9,
title = "Age‐dependent decline of NAD+ - universal truth or confounded consensus?",
abstract = "Nicotinamide adenine dinucleotide (NAD+) is an essential molecule involved in various metabolic reactions, acting as an electron donor in the electron transport chain and as a co‐factor for NAD+ ‐dependent enzymes. In the early 2000s, reports that NAD+ declines with aging introduced the notion that NAD+ metabolism is globally and progressively impaired with age. Since then, NAD+ became an attractive target for potential pharmacological therapies aiming to increase NAD+ levels to promote vitality and protect against age‐related diseases. This review summarizes and discusses a collection of studies that report the levels of NAD+ with aging in different species (i.e., yeast, C. elegans, rat, mouse, monkey, and human), to determine whether the notion that overall NAD+ levels decrease with aging stands true. We find that, despite systematic claims of overall changes in NAD+ levels with aging, the evidence to support such claims is very limited and often restricted to a single tissue or cell type. This is particularly true in humans, where the development of NAD+ levels during aging is still poorly characterized. There is a need for much larger, preferably longitudinal, studies to assess how NAD+ levels develop with aging in various tissues. This will strengthen our conclusions on NAD metabolism during aging and should provide a foundation for better pharmacological targeting of relevant tissues.",
keywords = "Aging, C. elegans, Human, Monkey, Mouse, NAD, Rat, Yeast",
author = "Peluso, {A. Augusto} and Damgaard, {Mads V.} and Mori, {Marcelo A.S.} and Treebak, {Jonas T.}",
note = "Publisher Copyright: {\textcopyright} 2021 by the author. Licensee MDPI, Basel, Switzerland.",
year = "2021",
doi = "10.3390/nu14010101",
language = "English",
volume = "14",
journal = "Nutrients",
issn = "2072-6643",
publisher = "M D P I AG",
number = "1",

}

RIS

TY - JOUR

T1 - Age‐dependent decline of NAD+ - universal truth or confounded consensus?

AU - Peluso, A. Augusto

AU - Damgaard, Mads V.

AU - Mori, Marcelo A.S.

AU - Treebak, Jonas T.

N1 - Publisher Copyright: © 2021 by the author. Licensee MDPI, Basel, Switzerland.

PY - 2021

Y1 - 2021

N2 - Nicotinamide adenine dinucleotide (NAD+) is an essential molecule involved in various metabolic reactions, acting as an electron donor in the electron transport chain and as a co‐factor for NAD+ ‐dependent enzymes. In the early 2000s, reports that NAD+ declines with aging introduced the notion that NAD+ metabolism is globally and progressively impaired with age. Since then, NAD+ became an attractive target for potential pharmacological therapies aiming to increase NAD+ levels to promote vitality and protect against age‐related diseases. This review summarizes and discusses a collection of studies that report the levels of NAD+ with aging in different species (i.e., yeast, C. elegans, rat, mouse, monkey, and human), to determine whether the notion that overall NAD+ levels decrease with aging stands true. We find that, despite systematic claims of overall changes in NAD+ levels with aging, the evidence to support such claims is very limited and often restricted to a single tissue or cell type. This is particularly true in humans, where the development of NAD+ levels during aging is still poorly characterized. There is a need for much larger, preferably longitudinal, studies to assess how NAD+ levels develop with aging in various tissues. This will strengthen our conclusions on NAD metabolism during aging and should provide a foundation for better pharmacological targeting of relevant tissues.

AB - Nicotinamide adenine dinucleotide (NAD+) is an essential molecule involved in various metabolic reactions, acting as an electron donor in the electron transport chain and as a co‐factor for NAD+ ‐dependent enzymes. In the early 2000s, reports that NAD+ declines with aging introduced the notion that NAD+ metabolism is globally and progressively impaired with age. Since then, NAD+ became an attractive target for potential pharmacological therapies aiming to increase NAD+ levels to promote vitality and protect against age‐related diseases. This review summarizes and discusses a collection of studies that report the levels of NAD+ with aging in different species (i.e., yeast, C. elegans, rat, mouse, monkey, and human), to determine whether the notion that overall NAD+ levels decrease with aging stands true. We find that, despite systematic claims of overall changes in NAD+ levels with aging, the evidence to support such claims is very limited and often restricted to a single tissue or cell type. This is particularly true in humans, where the development of NAD+ levels during aging is still poorly characterized. There is a need for much larger, preferably longitudinal, studies to assess how NAD+ levels develop with aging in various tissues. This will strengthen our conclusions on NAD metabolism during aging and should provide a foundation for better pharmacological targeting of relevant tissues.

KW - Aging

KW - C. elegans

KW - Human

KW - Monkey

KW - Mouse

KW - NAD

KW - Rat

KW - Yeast

U2 - 10.3390/nu14010101

DO - 10.3390/nu14010101

M3 - Review

C2 - 35010977

AN - SCOPUS:85121723793

VL - 14

JO - Nutrients

JF - Nutrients

SN - 2072-6643

IS - 1

M1 - 101

ER -

ID: 288857496