Literature DB >> 17127427

NAD+ and NADH in brain functions, brain diseases and brain aging.

Weihai Ying1.   

Abstract

Numerous studies have suggested that NAD+ and NADH mediate multiple major biological processes, including calcium homeostasis, energy metabolism, mitochondrial functions, cell death and aging. In particular, NAD+ and NADH have emerged as novel, fundamental regulators of calcium homeostasis. It appears that most of the components in the metabolic pathways of NAD+ and NADH, including poly(ADP-ribose), ADP-ribose, cyclic ADP-ribose, O-acetyl-ADP-ribose, nicotinamide and kynurenine, can produce significant biological effects. This exquisiteness of NAD+ and NADH metabolism could epitomize the exquisiteness of life, through which we may grasp the intrinsic harmony life has evolved to produce. The exquisiteness also suggests a central regulatory role of NAD+ and NADH in life. It is tempted to propose that NAD+ and NADH, together with ATP and Ca2+, constitute a Central Regulatory Network of life. Increasing evidence has also suggested that NAD+ and NADH play important roles in multiple biological processes in brains, such as neurotransmission and learning and memory. NAD+ and NADH may also mediate brain aging and the tissue damage in various brain illnesses. Our latest studies have suggested that NADH can be transported across the plasma membranes of astrocytes, and that NAD+ administration can markedly decrease ischemic brain injury. Based on this information, it is proposed that NAD+ and NADH are fundamental mediators of brain functions, brain senescence and multiple brain diseases. Because numerous properties of NAD+ and NADH remain unclear, future studies regarding NAD+ and NADH may expose some fundamental mechanisms underlying brain functions, brain pathologies and brain aging.

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Year:  2007        PMID: 17127427     DOI: 10.2741/2194

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  38 in total

Review 1.  Oxidative stress and NAD+ in ischemic brain injury: current advances and future perspectives.

Authors:  W Ying; Z-G Xiong
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

2.  Inositol 1,4,5-triphosphate receptors and NAD(P)H mediate Ca2+ signaling required for hypoxic preconditioning of hippocampal neurons.

Authors:  P E Bickler; C S Fahlman; J Gray; W McKleroy
Journal:  Neuroscience       Date:  2009-02-13       Impact factor: 3.590

Review 3.  Multifunctional roles of NAD⁺ and NADH in astrocytes.

Authors:  Franziska Wilhelm; Johannes Hirrlinger
Journal:  Neurochem Res       Date:  2012-04-03       Impact factor: 3.996

4.  Malate-Aspartate Shuttle Inhibitor Aminooxyacetate Acid Induces Apoptosis and Impairs Energy Metabolism of Both Resting Microglia and LPS-Activated Microglia.

Authors:  Heyu Chen; Caixia Wang; Xunbin Wei; Xianting Ding; Weihai Ying
Journal:  Neurochem Res       Date:  2015-05-22       Impact factor: 3.996

Review 5.  Current perspectives on the link between neuroinflammation and neurogenesis.

Authors:  Brian Wang; Kunlin Jin
Journal:  Metab Brain Dis       Date:  2014-03-13       Impact factor: 3.584

Review 6.  NAD+ metabolism and oxidative stress: the golden nucleotide on a crown of thorns.

Authors:  Hassina Massudi; Ross Grant; Gilles J Guillemin; Nady Braidy
Journal:  Redox Rep       Date:  2012       Impact factor: 4.412

7.  Malate-aspartate shuttle inhibitor aminooxyacetic acid blocks lipopolysaccharides-induced activation of BV2 microglia.

Authors:  Wangsong Shang; Xunbin Wei; Weihai Ying
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2017-04-15

8.  Structure and function of an ADP-ribose-dependent transcriptional regulator of NAD metabolism.

Authors:  Nian Huang; Jessica De Ingeniis; Luca Galeazzi; Chiara Mancini; Yuri D Korostelev; Alexandra B Rakhmaninova; Mikhail S Gelfand; Dmitry A Rodionov; Nadia Raffaelli; Hong Zhang
Journal:  Structure       Date:  2009-07-15       Impact factor: 5.006

9.  In vivo monitoring of cellular energy metabolism using SoNar, a highly responsive sensor for NAD(+)/NADH redox state.

Authors:  Yuzheng Zhao; Aoxue Wang; Yejun Zou; Ni Su; Joseph Loscalzo; Yi Yang
Journal:  Nat Protoc       Date:  2016-06-30       Impact factor: 13.491

10.  Aralar plays a significant role in maintaining the survival and mitochondrial membrane potential of BV2 microglia.

Authors:  Caixia Wang; Jie Zhang; Mingchao Zhang; Heyu Chen; Weihai Ying
Journal:  Int J Physiol Pathophysiol Pharmacol       Date:  2015-08-15
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