Calabrese Vittorio, Wenzel Uwe, Piccoli Tommaso, Jacob Ursula M, Nicolosi Lidia, Fazzolari Giovanni, Failla Gabriella, Fritsch Tilman, Osakabe Naomi, Calabrese Edward J
Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy.
Institut für Ernährungswissenschaft, Justus Liebig Universitat Giessen, Germany.
Open Med (Wars). 2024 Jun 17;19(1):20240986. doi: 10.1515/med-2024-0986. eCollection 2024.
Mitochondria-derived reactive oxygen species production at a moderate physiological level plays a fundamental role in the anti-aging signaling, due to their action as redox-active sensors for the maintenance of optimal mitochondrial balance between intracellular energy status and hormetic nutrients. Iron regulatory protein dysregulation, systematically increased iron levels, mitochondrial dysfunction, and the consequent oxidative stress are recognized to underlie the pathogenesis of multiple neurodegenerative diseases, such as Parkinson's disease and Alzheimer's disease. Central to their pathogenesis, Nrf2 signaling dysfunction occurs with disruption of metabolic homeostasis. We highlight the potential therapeutic importance of nutritional polyphenols as substantive regulators of the Nrf2 pathway. Here, we discuss the common mechanisms targeting the Nrf2/vitagene pathway, as novel therapeutic strategies to minimize consequences of oxidative stress and neuroinflammation, generally associated to cognitive dysfunction, and demonstrate its key neuroprotective and anti-neuroinflammatory properties, summarizing pharmacotherapeutic aspects relevant to brain pathophysiology.
适度生理水平的线粒体衍生活性氧生成在抗衰老信号传导中起着基础性作用,这是因为它们作为氧化还原活性传感器,在维持细胞内能量状态与促有丝分裂营养素之间的最佳线粒体平衡方面发挥作用。铁调节蛋白失调、系统性铁水平升高、线粒体功能障碍以及随之而来的氧化应激被认为是多种神经退行性疾病(如帕金森病和阿尔茨海默病)发病机制的基础。在其发病机制的核心,Nrf2信号功能障碍伴随着代谢稳态的破坏而发生。我们强调营养多酚作为Nrf2途径实质性调节剂的潜在治疗重要性。在此,我们讨论靶向Nrf2/维他基因途径的共同机制,作为尽量减少通常与认知功能障碍相关的氧化应激和神经炎症后果的新治疗策略,并展示其关键的神经保护和抗神经炎症特性,总结与脑病理生理学相关的药物治疗方面。