Tanaka Masaru, Szabó Ágnes, Vécsei László
HUN-REN-SZTE Neuroscience Research Group, Hungarian Research Network, University of Szeged (HUN-REN-SZTE), Danube Neuroscience Research Laboratory, Tisza Lajos krt. 113, H-6725 Szeged, Hungary.
Department of Neurology, Albert Szent-Györgyi Medical School, University of Szeged, Semmelweis u. 6, H-6725 Szeged, Hungary.
Int J Mol Sci. 2024 Nov 27;25(23):12767. doi: 10.3390/ijms252312767.
The tryptophan-kynurenine (KYN) pathway has long been recognized for its essential role in generating metabolites that influence various physiological processes. Traditionally, these metabolites have been categorized into distinct, often opposing groups, such as pro-oxidant versus antioxidant, excitotoxic/neurotoxic versus neuroprotective. This dichotomous framework has shaped much of the research on conditions like neurodegenerative and neuropsychiatric disorders, as well as cancer, where metabolic imbalances are a key feature. The effects are significantly influenced by various factors, including the concentration of metabolites and the particular cellular milieu in which they are generated. A molecule that acts as neuroprotective at low concentrations may exhibit neurotoxic effects at elevated levels. The oxidative equilibrium of the surrounding environment can alter the function of KYN from an antioxidant to a pro-oxidant. This narrative review offers a comprehensive examination and analysis of the contemporary understanding of KYN metabolites, emphasizing their multifaceted biological functions and their relevance in numerous physiological and pathological processes. This underscores the pressing necessity for a paradigm shift in the comprehension of KYN metabolism. Understanding the context-dependent roles of KYN metabolites is vital for novel therapies in conditions like Alzheimer's disease, multiple sclerosis, and cancer. Comprehensive pathway modulation, including balancing inflammatory signals and enzyme regulation, offers promising avenues for targeted, effective treatments.
色氨酸-犬尿氨酸(KYN)途径长期以来因其在生成影响各种生理过程的代谢产物方面的重要作用而被认可。传统上,这些代谢产物被分为不同的、通常相互对立的类别,如促氧化剂与抗氧化剂、兴奋性毒性/神经毒性与神经保护剂。这种二分法框架塑造了许多关于神经退行性疾病、神经精神疾病以及癌症等疾病的研究,在这些疾病中代谢失衡是一个关键特征。这些影响受到多种因素的显著影响,包括代谢产物的浓度以及它们产生的特定细胞环境。一种在低浓度下起神经保护作用的分子在浓度升高时可能会表现出神经毒性作用。周围环境的氧化平衡可以将KYN的功能从抗氧化剂改变为促氧化剂。这篇叙述性综述对当前对KYN代谢产物的理解进行了全面的审视和分析,强调了它们多方面的生物学功能以及它们在众多生理和病理过程中的相关性。这突出了在理解KYN代谢方面进行范式转变的迫切必要性。了解KYN代谢产物依赖于环境的作用对于阿尔茨海默病、多发性硬化症和癌症等疾病的新疗法至关重要。全面的途径调节,包括平衡炎症信号和酶调节,为靶向、有效的治疗提供了有前景的途径。
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