NAD plus therapy in age-related degenerative disorders: A benefit/risk analysis

被引:66
作者
Braidy, Nady [1 ]
Liu, Yue [1 ]
机构
[1] Univ New South Wales, Ctr Hlth Brain Ageing, Sch Psychiat, Sydney, NSW, Australia
基金
澳大利亚研究理事会;
关键词
NAD; Nicotinamide; Ageing; Oxidative stress; Cellular energetics; NICOTINAMIDE ADENINE-DINUCLEOTIDE; RADIATION-INDUCED IMMUNOSUPPRESSION; FATTY LIVER-DISEASE; WATER MAZE PERFORMANCE; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; ENERGY-METABOLISM; KYNURENIC ACID; MOUSE MODEL; DNA-DAMAGE;
D O I
10.1016/j.exger.2020.110831
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Nicotinamide adenine dinucleotide (NAD +) is an essential pyridine nucleotide that is present in all living cells. NAD + acts as an important cofactor and substrate for a multitude of biological processes including energy production, DNA repair, gene expression, calcium-dependent secondary messenger signalling and immunoregulatory roles. The de novo synthesis of NAD + is primarily dependent on the kynurenine pathway (KP), although NAD + can also be recycled from nicotinic acid (NA), nicotinamide (NAM) and nicotinamide riboside (NR). NAD + levels have been reported to decline during ageing and age-related diseases. Recent studies have shown that raising intracellular NAD + levels represents a promising therapeutic strategy for age-associated degenerative diseases in general and to extend lifespan in small animal models. A systematic review of the literature available on Medline, Embase and Pubmed was undertaken to evaluate the potential health and/or longevity benefits due to increasing NAD + levels. A total of 1545 articles were identified and 147 articles (113 preclinical and 34 clinical) met criteria for inclusion. Most studies indicated that the NAD + precursors NAM, NR, nicotinamide mononucleotide (NMN), and to a lesser extent NAD + and NADH had a favourable outcome on several age-related disorders associated with the accumulation of chronic oxidative stress, inflammation and impaired mitochondrial function. While these compounds presented with a limited acute toxicity profile, evidence is still quite limited and long-term human clinical trials are still nascent in the current literature. Potential risks in raising NAD + levels in various clinical disorders using NAD + precursors include the accumulation of putative toxic metabolites, tumorigenesis and promotion of cellular senescence. Therefore, NAD + metabolism represents a promising target and further studies are needed to recapitulate the preclinical benefits in human clinical trials.
引用
收藏
页数:22
相关论文
共 208 条
[1]   Neuroinflammation, Oxidative Stress and the Pathogenesis of Alzheimer's Disease [J].
Agostinho, Paula ;
Cunha, Rodrigo A. ;
Oliveira, Catarina .
CURRENT PHARMACEUTICAL DESIGN, 2010, 16 (25) :2766-2778
[2]   An open-label, non-randomized study of the pharmacokinetics of the nutritional supplement nicotinamide riboside (NR) and its effects on blood NAD plus levels in healthy volunteers [J].
Airhart, Sophia E. ;
Shireman, Laura M. ;
Risler, Linda J. ;
Anderson, Gail D. ;
Gowda, G. A. Nagana ;
Raftery, Daniel ;
Tian, Rong ;
Shen, Danny D. ;
O'Brien, Kevin D. .
PLOS ONE, 2017, 12 (12)
[3]   Nicotinamide adenine dinucleotide (NADH) in patients with chronic fatigue syndrome [J].
Alegre, J. ;
Roses, J. M. ;
Javierre, C. ;
Ruiz-Baques, A. ;
Segundo, M. J. ;
Fernandez de Sevilla, T. .
REVISTA CLINICA ESPANOLA, 2010, 210 (06) :284-288
[4]  
Alenzi FQ, 2009, IRAN J ALLERGY ASTHM, V8, P11, DOI 08.01/ijaai.1118
[5]   Inhibition of the Kynurenine-NAD+ Pathway Leads to Energy Failure and Exacerbates Apoptosis in Pneumococcal Meningitis [J].
Bellac, Caroline L. ;
Coimbra, Roney S. ;
Christen, Stephan ;
Leib, Stephen L. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (11) :1096-1104
[6]  
Bellamine A., 2019, FASEB J, V33
[7]   Poly(ADP-ribosyl)ation inhibitors:: Promising drug candidates for a wide variety of pathophysiologic conditions [J].
Beneke, S ;
Diefenbach, J ;
Bürkle, A .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (06) :813-818
[8]   Pre-B-cell colony-enhancing factor exerts a neuronal protection through its enzymatic activity and the reduction of mitochondrial dysfunction in in vitro ischemic models [J].
Bi, Jing ;
Li, Hailong ;
Ye, Shui Qing ;
Ding, Shinghua .
JOURNAL OF NEUROCHEMISTRY, 2012, 120 (02) :334-346
[9]   Dynamic changes in N-methyl-D-aspartate receptors after closed head injury in mice:: Implications for treatment of neurological and cognitive deficits [J].
Biegon, A ;
Fry, PA ;
Paden, CM ;
Alexandrovich, A ;
Tsenter, J ;
Shohami, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :5117-5122
[10]  
Birkmayer J.G.D., 2002, WIEN MED WOCHENSCHR, V152, P450