Interactions Between the Ubiquitin-Proteasome System, Nrf2, and the Cannabinoidome as Protective Strategies to Combat Neurodegeneration: Review on Experimental Evidence.

IF 2.9 3区 医学 Q2 NEUROSCIENCES Neurotoxicity Research Pub Date : 2024-02-23 DOI:10.1007/s12640-024-00694-3
Luis Angel Monsalvo-Maraver, Enid A Ovalle-Noguez, Jade Nava-Osorio, Marisol Maya-López, Edgar Rangel-López, Isaac Túnez, Alexey A Tinkov, Yousef Tizabi, Michael Aschner, Abel Santamaría
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Abstract

Neurodegenerative disorders are chronic brain diseases that affect humans worldwide. Although many different factors are thought to be involved in the pathogenesis of these disorders, alterations in several key elements such as the ubiquitin-proteasome system (UPS), the nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway, and the endocannabinoid system (ECS or endocannabinoidome) have been implicated in their etiology. Impairment of these elements has been linked to the origin and progression of neurodegenerative disorders, while their potentiation is thought to promote neuronal survival and overall neuroprotection, as proved with several experimental models. These key neuroprotective pathways can interact and indirectly activate each other. In this review, we summarize the neuroprotective potential of the UPS, ECS, and Nrf2 signaling, both separately and combined, pinpointing their role as a potential therapeutic approach against several hallmarks of neurodegeneration.

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泛素-蛋白酶体系统、Nrf2 和大麻素组之间的相互作用是对抗神经退行性变的保护性策略:实验证据综述》。
神经退行性疾病是影响全球人类的慢性脑部疾病。尽管有许多不同的因素被认为参与了这些疾病的发病机制,但泛素蛋白酶体系统(UPS)、红细胞核因子 2 相关因子 2(Nrf2)信号通路和内源性大麻素系统(ECS 或内源性大麻素组)等几个关键因素的改变已被认为与这些疾病的病因有关。这些因素的损伤与神经退行性疾病的起源和发展有关,而这些因素的增强被认为能促进神经元的存活和整体神经保护,这一点已在多个实验模型中得到证实。这些关键的神经保护途径可以相互作用并间接激活对方。在这篇综述中,我们总结了 UPS、ECS 和 Nrf2 信号传导的神经保护潜能,无论是单独使用还是结合使用,并指出它们作为一种潜在的治疗方法对神经退行性病变的几种特征所起的作用。
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来源期刊
Neurotoxicity Research
Neurotoxicity Research 医学-神经科学
CiteScore
7.70
自引率
5.40%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Neurotoxicity Research is an international, interdisciplinary broad-based journal for reporting both basic and clinical research on classical neurotoxicity effects and mechanisms associated with neurodegeneration, necrosis, neuronal apoptosis, nerve regeneration, neurotrophin mechanisms, and topics related to these themes. Published papers have focused on: NEURODEGENERATION and INJURY Neuropathologies Neuronal apoptosis Neuronal necrosis Neural death processes (anatomical, histochemical, neurochemical) Neurodegenerative Disorders Neural Effects of Substances of Abuse NERVE REGENERATION and RESPONSES TO INJURY Neural Adaptations Neurotrophin mechanisms and actions NEURO(CYTO)TOXICITY PROCESSES and NEUROPROTECTION Excitatory amino acids Neurotoxins, endogenous and synthetic Reactive oxygen (nitrogen) species Neuroprotection by endogenous and exogenous agents Papers on related themes are welcome.
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