MnSOD Mimetics in Therapy: Exploring Their Role in Combating Oxidative Stress-Related Diseases

被引:1
|
作者
Grujicic, Jovan [1 ,2 ]
Allen, Antino R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Arkansas Med Sci, Div Radiat Hlth, Little Rock, AR 72205 USA
[2] Univ Arkansas Med Sci, Dept Pharmacol & Toxicol, Little Rock, AR 72205 USA
[3] Univ Arkansas Med Sci, Dept Pharmaceut Sci, Little Rock, AR 72205 USA
[4] Univ Arkansas Med Sci, Neurobiol & Dev Sci, Little Rock, AR 72205 USA
关键词
manganese superoxide dismutase (MnSOD); MnSOD mimetics; oxidative stress; reactive oxygen species (ROS); Mn porphyrins; Mn salens; MitoQ10; nitroxides; mangafodipir; mitochondria-targeted antioxidants; MANGANESE SUPEROXIDE-DISMUTASE; INDUCED PERIPHERAL NEUROPATHY; NF-KAPPA-B; ESCHERICHIA-COLI; SOD MIMICS; MITOCHONDRIA; PORPHYRIN; ANTIOXIDANT; ACTIVATION; MANGAFODIPIR;
D O I
10.3390/antiox13121444
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
Reactive oxygen species (ROS) are double-edged swords in biological systems-they are essential for normal cellular functions but can cause damage when accumulated due to oxidative stress. Manganese superoxide dismutase (MnSOD), located in the mitochondrial matrix, is a key enzyme that neutralizes superoxide radicals (O2 center dot-), maintaining cellular redox balance and integrity. This review examines the development and therapeutic potential of MnSOD mimetics-synthetic compounds designed to replicate MnSOD's antioxidant activity. We focus on five main types: Mn porphyrins, Mn salens, MitoQ10, nitroxides, and mangafodipir. These mimetics have shown promise in treating a range of oxidative stress-related conditions, including cardiovascular diseases, neurodegenerative disorders, cancer, and metabolic syndromes. By emulating natural antioxidant defenses, MnSOD mimetics offer innovative strategies to combat diseases linked to mitochondrial dysfunction and ROS accumulation. Future research should aim to optimize these compounds for better stability, bioavailability, and safety, paving the way for their translation into effective clinical therapies.
引用
收藏
页数:23
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