氧化应激作为神经退行性疾病中膜兴奋性过高的潜在机制
Oxidative Stress as a Potential Mechanism Underlying Membrane Hyperexcitability in Neurodegenerative Diseases.
作者信息
Pardillo-Díaz Ricardo, Pérez-García Patricia, Castro Carmen, Nunez-Abades Pedro, Carrascal Livia
机构信息
Biomedical Research and Innovation Institute of Cadiz (INIBICA), 11003 Cadiz, Spain.
Area of Physiology, School of Medicine, University of Cádiz, 11003 Cadiz, Spain.
出版信息
Antioxidants (Basel). 2022 Aug 2;11(8):1511. doi: 10.3390/antiox11081511.
Neurodegenerative diseases are characterized by gradually progressive, selective loss of anatomically or physiologically related neuronal systems that produce brain damage from which there is no recovery. Despite the differences in clinical manifestations and neuronal vulnerability, the pathological processes appear to be similar, suggesting common neurodegenerative pathways. It is well known that oxidative stress and the production of reactive oxygen radicals plays a key role in neuronal cell damage. It has been proposed that this stress, among other mechanisms, could contribute to neuronal degeneration and might be one of the factors triggering the development of these pathologies. Another common feature in most neurodegenerative diseases is neuron hyperexcitability, an aberrant electrical activity. This review, focusing mainly on primary motor cortex pyramidal neurons, critically evaluates the idea that oxidative stress and inflammation may be involved in neurodegeneration via their capacity to increase membrane excitability.
神经退行性疾病的特征是解剖学或生理学相关神经元系统逐渐进行性、选择性丧失,导致脑损伤且无法恢复。尽管临床表现和神经元易损性存在差异,但病理过程似乎相似,提示存在共同的神经退行性通路。众所周知,氧化应激和活性氧自由基的产生在神经元细胞损伤中起关键作用。有人提出这种应激与其他机制一起,可能导致神经元变性,并且可能是引发这些疾病发展 的因素之一。大多数神经退行性疾病的另一个共同特征是神经元过度兴奋,即异常的电活动。本综述主要关注初级运动皮层锥体神经元,批判性地评估氧化应激和炎症可能通过增加膜兴奋性而参与神经退行性变的观点。