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右美托咪定可否被重新用作神经胶质淋巴系统增强剂?

Could dexmedetomidine be repurposed as a glymphatic enhancer?

机构信息

Individualized Drug Therapy Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Department of Pharmacology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Perioperative Services, Intensive Care and Pain Medicine, Turku University Hospital, Turku, Finland.

出版信息

Trends Pharmacol Sci. 2022 Dec;43(12):1030-1040. doi: 10.1016/j.tips.2022.09.007. Epub 2022 Oct 21.

Abstract

Cerebrospinal fluid (CSF) flows through the central nervous system (CNS) via the glymphatic pathway to clear the interstitium of metabolic waste. In preclinical studies, glymphatic fluid flow rate increases with low central noradrenergic tone and slow-wave activity during natural sleep and general anesthesia. By contrast, sleep deprivation reduces glymphatic clearance and leads to intracerebral accumulation of metabolic waste, suggesting an underlying mechanism linking sleep disturbances with neurodegenerative diseases. The selective α-adrenergic agonist dexmedetomidine is a sedative drug that induces slow waves in the electroencephalogram, suppresses central noradrenergic tone, and preserves glymphatic outflow. As recently developed dexmedetomidine formulations enable self-administration, we suggest that dexmedetomidine could serve as a sedative-hypnotic drug to enhance clearance of harmful waste from the brain of those vulnerable to neurodegeneration.

摘要

脑脊液(CSF)通过脑淋巴系统在中枢神经系统(CNS)中流动,以清除间质中的代谢废物。在临床前研究中,脑淋巴液的流动速率在自然睡眠和全身麻醉期间随着中枢去甲肾上腺素能张力降低和慢波活动增加而增加。相比之下,睡眠剥夺会降低脑淋巴液的清除率,并导致脑内代谢废物的积累,这表明睡眠障碍与神经退行性疾病之间存在潜在的机制联系。选择性α-肾上腺素能激动剂右美托咪定是一种镇静药物,可在脑电图中诱导慢波,抑制中枢去甲肾上腺素能张力,并保留脑淋巴液的流出。由于最近开发的右美托咪定配方能够自我给药,因此我们认为右美托咪定可以作为镇静催眠药物,增强易发生神经退行性变的人群大脑中有害废物的清除。

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