Literature DB >> 18020963

NAD+/NADH and NADP+/NADPH in cellular functions and cell death: regulation and biological consequences.

Weihai Ying1.   

Abstract

Accumulating evidence has suggested that NAD (including NAD+ and NADH) and NADP (including NADP+ and NADPH) could belong to the fundamental common mediators of various biological processes, including energy metabolism, mitochondrial functions, calcium homeostasis, antioxidation/generation of oxidative stress, gene expression, immunological functions, aging, and cell death: First, it is established that NAD mediates energy metabolism and mitochondrial functions; second, NADPH is a key component in cellular antioxidation systems; and NADH-dependent reactive oxygen species (ROS) generation from mitochondria and NADPH oxidase-dependent ROS generation are two critical mechanisms of ROS generation; third, cyclic ADP-ribose and several other molecules that are generated from NAD and NADP could mediate calcium homeostasis; fourth, NAD and NADP modulate multiple key factors in cell death, such as mitochondrial permeability transition, energy state, poly(ADP-ribose) polymerase-1, and apoptosis-inducing factor; and fifth, NAD and NADP profoundly affect aging-influencing factors such as oxidative stress and mitochondrial activities, and NAD-dependent sirtuins also mediate the aging process. Moreover, many recent studies have suggested novel paradigms of NAD and NADP metabolism. Future investigation into the metabolism and biological functions of NAD and NADP may expose fundamental properties of life, and suggest new strategies for treating diseases and slowing the aging process.

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Year:  2008        PMID: 18020963     DOI: 10.1089/ars.2007.1672

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  456 in total

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Journal:  Antioxid Redox Signal       Date:  2012-02-03       Impact factor: 8.401

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Authors:  W Ying; Z-G Xiong
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Journal:  Glia       Date:  2017-12-08       Impact factor: 7.452

Review 7.  Mitochondrial dysfunction and NAD(+) metabolism alterations in the pathophysiology of acute brain injury.

Authors:  Katrina Owens; Ji H Park; Rosemary Schuh; Tibor Kristian
Journal:  Transl Stroke Res       Date:  2013-08-10       Impact factor: 6.829

8.  Two-photon autofluorescence dynamics imaging reveals sensitivity of intracellular NADH concentration and conformation to cell physiology at the single-cell level.

Authors:  Qianru Yu; Ahmed A Heikal
Journal:  J Photochem Photobiol B       Date:  2008-12-25       Impact factor: 6.252

9.  TIR Domain Proteins Are an Ancient Family of NAD+-Consuming Enzymes.

Authors:  Kow Essuman; Daniel W Summers; Yo Sasaki; Xianrong Mao; Aldrin Kay Yuen Yim; Aaron DiAntonio; Jeffrey Milbrandt
Journal:  Curr Biol       Date:  2018-01-25       Impact factor: 10.834

10.  Differential correlations between changes to glutathione redox state, protein ubiquitination, and stress-inducible HSPA chaperone expression after different types of oxidative stress.

Authors:  Pierre-Marie Girard; Nathalie Peynot; Jean-Marc Lelièvre
Journal:  Cell Stress Chaperones       Date:  2018-05-12       Impact factor: 3.667

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