Literature Review on the Therapeutic Potential of NAMPT in Brain Diseases

Authors

Abstract

Nicotinamide Phosphoribosyl transferase (NAMPT) is an important enzyme in the biosynthesis NAD+ and the byproduct nicotinamide mononucleotide (NMN) is also a vital intermediate in NAD+ synthesis. More importantly, the enzyme has been found to have therapeutic potential in the management and treatment of brain diseases such as stroke, depression, and cerebral ischemic injury. In this review, we looked critically at studies that have sought to explore the activities of NAMPT in the brain, the relevant pathways, the byproducts, and precursors of NAMPT with the hope to utilizing the knowledge gotten from the studies to project the possibility of utilizing the enzyme as a better way to treat brain diseases. The enzyme is projected to have a double-edged influence on cell processes and aging Likewise, it has neuroprotective advantages in neurons that express them. More scientific studies have shown that NAMPT is involved in the chain of activities involved in preventing depression. This review further elaborates on the therapeutic potentials of NAMPT, and also seeks to recommend further studies in this field to be carried out on a regular basis due to its promising potential.

Keywords: NAMPT; Brain; Therapeutic potential; Diseases; NAD; Cerebral ischemic injury, Stroke

Keywords:

NAMPT, Brain, Therapeutic potential, Diseases, NAD, Cerebral ischemic injury, Stroke

DOI

https://doi.org/10.22270/jddt.v13i6.5854

Author Biographies

Joel Oluwamurewa Olayemi, Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Nebechukwu William Eneh, Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Etinosa Bright Ovabor, Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Hauwa-Kulu Saidu Arome, Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Hajara Shitu Mohammed, Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

Department of Physical and Life Sciences, National Space Research and Development Agency (NASRDA), Airport Road, FCT, Abuja, 900104

References

Wang P, Miao CY, NAMPT as a therapeutic target against stroke, Trends; Pharmacol Sci, 2015; 36:891-905. https://doi.org/10.1016/j.tips.2015.08.012

Wang P, Xu TY, Guan YF, Tian WW, Viollet B, Yao-Cheng R, et al., Nicotinamide phosphoribosyltransferase protects against ischemic stroke through SIRT1-dependent adenosine monophosphate-activated kinase pathway, Ann Neurol J, 2015; 69:360-374. https://doi.org/10.1002/ana.22236

Fukuhara A, Matsuda M, Nishizawa M, Segawa K, Tanaka M, Visfatin: a protein secreted by visceral fat that mimics the effects of insulin, J Science, 2005; 307: 426-430. https://doi.org/10.1126/science.1097243

Kitani T, Okuno S, Fujisawa H, Growth phase-dependent changes in the subcellular localization of pre-B-cell colony-enhancing factor, FEBS Lett, 2003; 544:74-78. https://doi.org/10.1016/S0014-5793(03)00476-9

Garten A, Petzold S, Korner A, Imai S, Kiess W, Nampt: linking NAD biology, metabolism and cancer, Trends; Endocrinol Metab, 2009; 20: 130-138. https://doi.org/10.1016/j.tem.2008.10.004

Rongvaux A, Shea RJ, Mulks MH, Gigot D, Urbain J, Leo O, et al., Pre-B-cell colony-enhancing factor, whose expression is up-regulated in activated lymphocytes, is a nicotinamide phosphoribosyltransferase, a cytosolic enzyme involved in NAD biosynthesis, Eur J Immunol, 2002; 32:3225-3234. https://doi.org/10.1002/1521-4141(200211)32:11<3225::AID-IMMU3225>3.0.CO;2-L

Yoshino J, Mills KF, Yoon MJ, Imai S, Nicotinamide mononucleotide, a key NAD(+) intermediate, treats the pathophysiology of diet- and age-induced diabetes in mice, Cell Metab, 2001; 14:528-536. https://doi.org/10.1016/j.cmet.2011.08.014

Nakahata Y, Sahar S, Astarita G, Kaluzova M, Sassone-Corsi P, Circadian control of the NAD+ salvage pathway by CLOCK-SIRT1, Science Journal, 2009; 324:654-657. https://doi.org/10.1126/science.1170803

Liu Y, Zhang R, Yan K, Chen F, Huang W, Liu V, et al., Mesenchymal stem cells inhibit lipopolysaccharide-induced inflammatory responses of BV2 microglial cells through TSG-6, Journal of Neuroinflammation, 2012; 11:135. https://doi.org/10.1186/1742-2094-11-135

Johnson RW and Jurgens HA Dysregulated neuronal-microglial cross-talk during aging, stress and inflammation Exp Neurol, 2012; 233: 40-48. https://doi.org/10.1016/j.expneurol.2010.11.014

Moschen AR, Gerner RR, Tilg H, Pre-B cell colony enhancing factor/ NAMPT/visfatin in inflammation and obesity-related disorders, Curr Pharm Des, 2010; 16: 1913-1920. https://doi.org/10.2174/138161210791208947

Chen X, Zhao S, Song Y, Shi Y, Leak RK, Cao G, The role of nicotinamide phosphoribosyltransferase in cerebral ischemia, Curr Top Med Chem, 2015b; 15:2211-2221. https://doi.org/10.2174/1568026615666150610142234

Chen-Xiang C, Jing H, Ga-Qi T, Jia-Ting L, Xiang X, Bing Z, et al., NAMPT Inhibitor Protects Ischemic Neuronal Injury In Rat Brain Via Anti-Neuroinflammation, J Neuroscience, 2017; 356; 193-206. https://doi.org/10.1016/j.neuroscience.2017.05.022

Esposito E, Impellizzeri D, Mazzon E, Fakhfouri G, Rahimian R, Travelli C, Tron GC, Genazzani AA, Cuzzocrea S, The NAMPT inhibitor FK866 reverts the damage in spinal cord injury, J Neuroinflammation, 2012; 9:66. https://doi.org/10.1186/1742-2094-9-66

Bi J, Li H, Ye SQ, Ding S, 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 Neurochem, 2012; 120:334-346. https://doi.org/10.1111/j.1471-4159.2011.07566.x

Curat CA, Wegner V, Sengenes C, Miranville A, Tonus C, Busse R, et al., Macrophages in human visceral adipose tissue: increased accumulation in obesity and a source of resistin and visfatin, Diabetologia, 2016; 49: 744-747. https://doi.org/10.1007/s00125-006-0173-z

Garten A, Petzold S, Barnikol-Oettler A, Korner A, Thasler WE, Kratzsch J, Nicotinamide phosphoribosyltransferase (NAMPT/PBEF/visfatin) is constitutively released from human hepatocytes, Biochem Biophys Res Commun, 2010, 391: 376-381. https://doi.org/10.1016/j.bbrc.2009.11.066

Presumey J, Courties G, Louis-Plence P, Escriou V, Scherman D, Pers YM, et al., Nicotinamide phosphoribosyltransferase/visfatin expression by inflammatory monocytes mediates arthritis pathogenesis, Ann Rheum Dis, 2013; 72:1717-1724. https://doi.org/10.1136/annrheumdis-2012-202403

Halvorsen B, Espeland MZ, Andersen, GO Yndestad A, Sagen EL, Imai S, et al., NAD+ and sirtuins in aging and disease, Trends Cell Biol, 2014, 24:464-471. https://doi.org/10.1016/j.tcb.2014.04.002

Kim HD, Hesterman J, Call T, Magazu S, Keeley E, Armenta K., et al, SIRT1 mediates depression-like behaviors in the nucleus accumbens, J. Neurosci, 2016; 36, 8441-8452. https://doi.org/10.1523/JNEUROSCI.0212-16.2016

Covarrubias AJ, Perrone R, Grozio A, Verdin E, NAD+ metabolism and its roles in cellular processes during aging, Nat. Rev. Mol. Cell Biol, 2021, 22:119-141. https://doi.org/10.1038/s41580-020-00313-x

Imai S, Guarente L, NAD+ and sirtuins in aging and disease, Trends Cell Biol, 2014, 24(8):464-71. https://doi.org/10.1016/j.tcb.2014.04.002

Zhu Y, Xu P, Huang X, Shuai S, Liu L, Zhang S, Zhao R, et al., From Rate-Limiting Enzyme to Therapeutic Target: The Promise of NAMPT in Neurodegenerative Diseases, Front Pharmacol, 2022; 12;13:920113. https://doi.org/10.3389/fphar.2022.920113

Weng JF, Chen J, Hong WC, Plasma visfatin, associated with a genetic polymorphism -1535C>T, is correlated with C-reactive protein in Chinese Han patients with traumatic brain injury, Peptides, 2013, 40:8-12. https://doi.org/10.1016/j.peptides.2012.12.017

Chen X, Shangfeng Z, Yang S, Yejie S, Rehana L, and Guodong C, Nicotinamidephosphoribosyltransferase and cerebral ischemia, Curr Top Med Chem, 2015; 15(21): 2211-2221. https://doi.org/10.2174/1568026615666150610142234

Wang SN, Miao CY, Targeting NAMPT as a therapeutic strategy against stroke, Stroke Vasc Neurol, 2019; 4(2):83-89. https://doi.org/10.1136/svn-2018-000199

Zhang XQ, Lu JT, Jiang WX, Lu YB, Wu M, Wei EQ, Zhang WP, Tang C, NAMPT inhibitor and metabolite protect mouse brain from cryoinjury through distinct mechanisms, J Neuroscience, 2015; 291:230-240. https://doi.org/10.1016/j.neuroscience.2015.02.007

Published

2023-06-15
Statistics
Abstract Display: 333
PDF Downloads: 450
PDF Downloads: 76

How to Cite

1.
Olayemi JO, Eneh NW, Ovabor EB, Arome H-KS, Mohammed HS. Literature Review on the Therapeutic Potential of NAMPT in Brain Diseases. J. Drug Delivery Ther. [Internet]. 2023 Jun. 15 [cited 2026 Jan. 27];13(6):172-4. Available from: https://jddtonline.info/index.php/jddt/article/view/5854

How to Cite

1.
Olayemi JO, Eneh NW, Ovabor EB, Arome H-KS, Mohammed HS. Literature Review on the Therapeutic Potential of NAMPT in Brain Diseases. J. Drug Delivery Ther. [Internet]. 2023 Jun. 15 [cited 2026 Jan. 27];13(6):172-4. Available from: https://jddtonline.info/index.php/jddt/article/view/5854