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犬尿氨酸途径在神经退行性疾病氧化应激中的作用。

Role of Kynurenine Pathway in Oxidative Stress during Neurodegenerative Disorders.

机构信息

Department of Pharmacodynamics, Medical University of Bialystok, Mickiewicza 2c, 15-222 Bialystok, Poland.

Department of Monitored Pharmacotherapy, Medical University of Bialystok, Mickiewicza 2c, 15-222 Bialystok, Poland.

出版信息

Cells. 2021 Jun 26;10(7):1603. doi: 10.3390/cells10071603.

Abstract

Neurodegenerative disorders are chronic and life-threatening conditions negatively affecting the quality of patients' lives. They often have a genetic background, but oxidative stress and mitochondrial damage seem to be at least partly responsible for their development. Recent reports indicate that the activation of the kynurenine pathway (KP), caused by an activation of proinflammatory factors accompanying neurodegenerative processes, leads to the accumulation of its neuroactive and pro-oxidative metabolites. This leads to an increase in the oxidative stress level, which increases mitochondrial damage, and disrupts the cellular energy metabolism. This significantly reduces viability and impairs the proper functioning of central nervous system cells and may aggravate symptoms of many psychiatric and neurodegenerative disorders. This suggests that the modulation of KP activity could be effective in alleviating these symptoms. Numerous reports indicate that tryptophan supplementation, inhibition of KP enzymes, and administration or analogs of KP metabolites show promising results in the management of neurodegenerative disorders in animal models. This review gathers and systematizes the knowledge concerning the role of metabolites and enzymes of the KP in the development of oxidative damage within brain cells during neurodegenerative disorders and potential strategies that could reduce the severity of this process.

摘要

神经退行性疾病是慢性且危及生命的疾病,会降低患者的生活质量。这些疾病通常具有遗传背景,但氧化应激和线粒体损伤似乎至少部分导致了它们的发生。最近的报告表明,伴随神经退行性过程的促炎因子的激活会导致犬尿氨酸途径(KP)的激活,从而导致其神经活性和促氧化代谢物的积累。这会导致氧化应激水平的增加,从而增加线粒体损伤,并破坏细胞能量代谢。这会显著降低细胞活力,损害中枢神经系统细胞的正常功能,并可能加重许多精神疾病和神经退行性疾病的症状。这表明调节 KP 活性可能有助于缓解这些症状。许多报告表明,色氨酸补充、KP 酶的抑制以及 KP 代谢物的给药或类似物在动物模型的神经退行性疾病的治疗中显示出良好的效果。这篇综述汇集并系统化了关于 KP 代谢物和酶在神经退行性疾病期间脑细胞内氧化损伤发展中的作用以及可能减轻该过程严重程度的潜在策略的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc2e/8306609/e531ae18e55a/cells-10-01603-g001.jpg

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