4.7 Review

Neuroprotection against Aminochrome Neurotoxicity: Glutathione Transferase M2-2 and DT-Diaphorase

期刊

ANTIOXIDANTS
卷 11, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/antiox11020296

关键词

glutathione; glutathione transferase; dopamine; Parkinson's disease; neuron; astrocytes; neuroprotection; aminochrome

资金

  1. ANID-STINT-CONICYT [CS2018-7940]
  2. Swedish Cancer Society and the Swedish Research Council [2015-04222]
  3. National Institute on Ageing of the National Institutes of Health [R01AG065209]
  4. Swedish Research Council [2015-04222] Funding Source: Swedish Research Council
  5. Vinnova [2015-04222] Funding Source: Vinnova

向作者/读者索取更多资源

Glutathione is an important antioxidant that plays a crucial role in cellular protection and detoxification. Aminochrome may trigger neurodegenerative processes in the nigrostriatal neurons, but the exact triggers are still unknown. There are protective mechanisms against aminochrome neurotoxicity in the brain.
Glutathione is an important antioxidant that plays a crucial role in the cellular protection against oxidative stress and detoxification of electrophilic mutagens, and carcinogens. Glutathione transferases are enzymes catalyzing glutathione-dependent reactions that lead to inactivation and conjugation of toxic compounds, processes followed by subsequent excretion of the detoxified products. Degeneration and loss of neuromelanin-containing dopaminergic neurons in the nigrostriatal neurons generally involves oxidative stress, neuroinflammation, alpha-synuclein aggregation to neurotoxic oligomers, mitochondrial dysfunction, protein degradation dysfunction, and endoplasmic reticulum stress. However, it is still unclear what triggers these neurodegenerative processes. It has been reported that aminochrome may elicit all of these mechanisms and, interestingly, aminochrome is formed inside neuromelanin-containing dopaminergic neurons during neuromelanin synthesis. Aminochrome is a neurotoxic ortho-quinone formed in neuromelanin synthesis. However, it seems paradoxical that the neurotoxin aminochrome is generated during neuromelanin synthesis, even though healthy seniors have these neurons intact when they die. The explanation of this paradox is the existence of protective tools against aminochrome neurotoxicity composed of the enzymes DT-diaphorase, expressed in these neurons, and glutathione transferase M2-2, expressed in astrocytes. Recently, it has been reported that dopaminergic neurons can be protected by glutathione transferase M2-2 from astrocytes, which secrete exosomes containing the protective enzyme.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据