Literature DB >> 33397266

Nicotinamide as a Foundation for Treating Neurodegenerative Disease and Metabolic Disorders.

Kenneth Maiese1.   

Abstract

Neurodegenerative disorders impact more than one billion individuals worldwide and are intimately tied to metabolic disease that can affect another nine hundred individuals throughout the globe. Nicotinamide is a critical agent that may offer fruitful prospects for neurodegenerative diseases and metabolic disorders, such as diabetes mellitus. Nicotinamide protects against multiple toxic environments that include reactive oxygen species exposure, anoxia, excitotoxicity, ethanolinduced neuronal injury, amyloid (Aß) toxicity, age-related vascular disease, mitochondrial dysfunction, insulin resistance, excess lactate production, and loss of glucose homeostasis with pancreatic β-cell dysfunction. However, nicotinamide offers cellular protection in a specific concentration range, with dosing outside of this range leading to detrimental effects. The underlying biological pathways of nicotinamide that involve the silent mating type information regulation 2 homolog 1 (Saccharomyces cerevisiae) (SIRT1), the mechanistic target of rapamycin (mTOR), AMP activated protein kinase (AMPK), and mammalian forkhead transcription factors (FoxOs) may offer insight for the clinical translation of nicotinamide into a safe and efficacious therapy through the modulation of oxidative stress, apoptosis, and autophagy. Nicotinamide is a highly promising target for the development of innovative strategies for neurodegenerative disorders and metabolic disease, but the benefits of this foundation depend greatly on gaining a further understanding of nicotinamide's complex biology. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Entities:  

Keywords:  AMP activated protein kinase (AMPK); Alzheimer's disease; FoxO; apoptosis; autophagy; dementia; diabetes mellitus; forkhead transcription factors; mechanistic target of rapamycin (mTOR); oxidative stress; silent mating type informationzzm321990regulation 2 homolog 1 (Saccharomyces cerevisiae) (SIRT1); sirtuin; stem cells.

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Year:  2021        PMID: 33397266      PMCID: PMC8254823          DOI: 10.2174/1567202617999210104220334

Source DB:  PubMed          Journal:  Curr Neurovasc Res        ISSN: 1567-2026            Impact factor:   1.990


  312 in total

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Review 6.  Sirtuins: critical regulators at the crossroads between cancer and aging.

Authors:  L R Saunders; E Verdin
Journal:  Oncogene       Date:  2007-08-13       Impact factor: 9.867

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Journal:  Nutrients       Date:  2020-04-05       Impact factor: 5.717

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Journal:  Int J Mol Med       Date:  2020-03-12       Impact factor: 4.101

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