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氧化应激相关神经退行性疾病中的神经保护作用:内源性大麻素系统调制的作用。

Neuroprotection in Oxidative Stress-Related Neurodegenerative Diseases: Role of Endocannabinoid System Modulation.

机构信息

1 Laboratory of Cardiovascular Physiology and Tissue Injury (LCPTI), National Institute on Alcohol Abuse and Alcoholism (NIAAA), National Institutes of Health (NIH) , Bethesda, Maryland.

2 Department of Surgery, Rutgers New Jersey Medical School , Newark, New Jersey.

出版信息

Antioxid Redox Signal. 2018 Jul 1;29(1):75-108. doi: 10.1089/ars.2017.7144. Epub 2017 Jul 18.

Abstract

SIGNIFICANCE

Redox imbalance may lead to overproduction of reactive oxygen and nitrogen species (ROS/RNS) and subsequent oxidative tissue damage, which is a critical event in the course of neurodegenerative diseases. It is still not fully elucidated, however, whether oxidative stress is the primary trigger or a consequence in the process of neurodegeneration. Recent Advances: Increasing evidence suggests that oxidative stress is involved in the propagation of neuronal injury and consequent inflammatory response, which in concert promote development of pathological alterations characteristic of most common neurodegenerative diseases.

CRITICAL ISSUES

Accumulating recent evidence also suggests that there is an important interplay between the lipid endocannabinoid system [ECS; comprising the main cannabinoid 1 and 2 receptors (CB1 and CB2), endocannabinoids, and their synthetic and metabolizing enzymes] and various key inflammatory and redox-dependent processes.

FUTURE DIRECTIONS

Targeting the ECS to modulate redox state-dependent cell death and to decrease consequent or preceding inflammatory response holds therapeutic potential in a multitude of oxidative stress-related acute or chronic neurodegenerative disorders from stroke and traumatic brain injury to Alzheimer's and Parkinson's diseases and multiple sclerosis, just to name a few, which will be discussed in this overview. Antioxid. Redox Signal. 29, 75-108.

摘要

意义

氧化还原失衡可能导致活性氧和氮物种(ROS/RNS)的过度产生,并随后导致氧化组织损伤,这是神经退行性疾病过程中的一个关键事件。然而,氧化应激是神经变性过程中的主要触发因素还是后果仍不完全清楚。最近的进展:越来越多的证据表明,氧化应激参与神经元损伤的传播和随后的炎症反应,这两者共同促进了大多数常见神经退行性疾病的病理改变的发展。

关键问题

越来越多的证据还表明,脂质内源性大麻素系统[由主要大麻素 1 和 2 受体(CB1 和 CB2)、内源性大麻素及其合成和代谢酶组成]与各种关键的炎症和依赖于氧化还原的过程之间存在重要的相互作用。

未来方向

针对内源性大麻素系统来调节氧化还原状态依赖性细胞死亡,并减少随后或之前的炎症反应,在多种与氧化应激相关的急性或慢性神经退行性疾病中具有治疗潜力,从中风和创伤性脑损伤到阿尔茨海默病和帕金森病以及多发性硬化症等等,仅举几例,本文将对此进行讨论。抗氧化。氧化还原信号。29,75-108。

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