Neurophysiology Unit, Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Department of Anesthesiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Eur J Neurosci. 2021 Nov;54(9):7006-7047. doi: 10.1111/ejn.15474. Epub 2021 Oct 25.
Neurological disorders following brain injuries and neurodegeneration are on the rise worldwide and cause disability and suffering in patients. It is crucial to explore novel neuroprotectants. Dexmedetomidine, a selective α2-adrenoceptor agonist, is commonly used for anxiolysis, sedation and analgesia in clinical anaesthesia and critical care. Recent studies have shown that dexmedetomidine exerts protective effects on multiple organs. This review summarized and discussed the current neuroprotective effects of dexmedetomidine, as well as the underlying mechanisms. In preclinical studies, dexmedetomidine reduced neuronal injury and improved functional outcomes in several models, including hypoxia-induced neuronal injury, ischaemic-reperfusion injury, intracerebral haemorrhage, post-traumatic brain injury, anaesthetic-induced neuronal injury, substance-induced neuronal injury, neuroinflammation, epilepsy and neurodegeneration. Several mechanisms are associated with the neuroprotective function of dexmedetomidine, including neurotransmitter regulation, inflammatory response, oxidative stress, apoptotic pathway, autophagy, mitochondrial function and other cell signalling pathways. In summary, dexmedetomidine has the potential to be a novel neuroprotective agent for a wide range of neurological disorders.
脑损伤和神经退行性疾病引起的神经紊乱在全球范围内呈上升趋势,给患者带来残疾和痛苦。探索新型神经保护剂至关重要。右美托咪定是一种选择性α2-肾上腺素受体激动剂,常用于临床麻醉和重症监护中的焦虑、镇静和镇痛。最近的研究表明,右美托咪定对多种器官具有保护作用。本综述总结和讨论了右美托咪定目前的神经保护作用及其潜在机制。在临床前研究中,右美托咪定在多种模型中减轻了神经元损伤并改善了功能结局,包括缺氧诱导的神经元损伤、缺血再灌注损伤、脑出血、创伤性脑损伤、麻醉诱导的神经元损伤、物质诱导的神经元损伤、神经炎症、癫痫和神经退行性变。几种机制与右美托咪定的神经保护功能相关,包括神经递质调节、炎症反应、氧化应激、细胞凋亡通路、自噬、线粒体功能和其他细胞信号通路。总之,右美托咪定有可能成为广泛的神经紊乱的新型神经保护剂。