Emerging therapeutic opportunities of novel thiol-amides, NAC-amide (AD4/NACA) and thioredoxin mimetics (TXM-Peptides) for neurodegenerative-related disorders

被引:22
作者
Atlas, Daphne [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Life Sci, Dept Biol Chem, Neurochem, IL-91904 Jerusalem, Israel
关键词
Oxidative stress; Inflammation GSH; AD4; (NACA); TXM-CB3; Neurodegeneration; Aging; ROS; Inflammation; N-ACETYLCYSTEINE AMIDE; PROTEIN S-NITROSYLATION; LOW-MOLECULAR-WEIGHT; ALLERGIC AIRWAY DISEASE; BLOOD-BRAIN-BARRIER; FACTOR-KAPPA-B; OXIDATIVE STRESS; MITOCHONDRIAL BIOENERGETICS; MAMMALIAN THIOREDOXIN; INDUCED CYTOTOXICITY;
D O I
10.1016/j.freeradbiomed.2021.08.239
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding neurodegenerative diseases have challenged scientists for decades. It has become apparent that a decrease in life span is often correlated with the development of neurodegenerative disorders. Oxidative stress and the subsequent inflammatory damages appear to contribute to the different molecular and biochemical mechanisms associated with neurodegeneration. In this review, I examine the protective properties of novel amino acid based compounds, comprising the AD series (AD1-AD7) in particular N-acetylcysteine amide, AD4, also called NACA, and the series of thioredoxin mimetic (TXM) peptides, TXM-CB3-TXM-CB16. Designed to cross the blood-brain-barrier (BBB) and permeate the cell membrane, these antioxidant/anti-inflammatory compounds may enable effective treatment of neurodegenerative related disorders. The review addresses the molecular mechanism of cellular protection exhibited by these new reagents, focusing on the reversal of oxidative stress, mitochondrial stress, inflammatory damages, and prevention of premature cell death. In addition, it will cover the outlook of the clinical prospects of AD4/ NACA and the thioredoxin-mimetic peptides, which are currently in development.
引用
收藏
页码:120 / 141
页数:22
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