没食子酸通过抗氧化作用改善睡眠剥夺引起的认知障碍。

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Experimental Neurobiology Pub Date : 2023-08-31 DOI:10.5607/en23015
Xiaogang Pang, Yifan Xu, Shuoxin Xie, Tianshu Zhang, Lin Cong, Yuchen Qi, Lubing Liu, Qingjun Li, Mei Mo, Guimei Wang, Xiuwei Du, Hui Shen, Yuanyuan Li
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摘要

睡眠剥夺(SD)对中枢神经系统有着深远的影响,导致一系列情绪障碍,包括抑郁和焦虑。尽管如此,睡眠剥夺期间神经元活动的动态变化尚未得到广泛研究。而一些研究人员提出,睡眠不足会减少神经元活动,从而导致抑郁症。其他人认为,短期睡眠不足会增强神经元活动和树突棘密度,可能产生抗抑郁作用。在本研究中,使用双光子显微镜在体内每隔24小时检测清醒SD小鼠前扣带皮层(ACC)神经元的钙瞬变。观察到SD降低了Ca2+瞬变的频率和幅度,同时增加了不活动神经元的比例。睡眠剥夺停止后,神经元钙瞬变表现为逐渐恢复。此外,全细胞膜片钳记录显示,SD后自发兴奋性突触后电流(sEPSC)的频率显著降低。该研究还评估了几个氧化应激参数,发现睡眠剥夺显著升高了丙二醛(MDA)水平,同时降低ACC中核因子-红系2相关因子2(Nrf2)的表达和超氧化物歧化酶(SOD)的活性。重要的是,没食子酸(GA)的给药显著减轻了ACC神经元中钙瞬变的下降。GA还被证明可以减轻大脑中的氧化应激,改善睡眠不足引起的认知障碍。这些发现表明,ACC神经元的钙瞬变在睡眠剥夺过程中持续下降,这一过程是可逆的。GA可能是预防和治疗睡眠剥夺引起的认知障碍的潜在候选药物。
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Gallic Acid Ameliorates Cognitive Impairment Caused by Sleep Deprivation through Antioxidant Effect.

Sleep deprivation (SD) has a profound impact on the central nervous system, resulting in an array of mood disorders, including depression and anxiety. Despite this, the dynamic alterations in neuronal activity during sleep deprivation have not been extensively investigated. While some researchers propose that sleep deprivation diminishes neuronal activity, thereby leading to depression. Others argue that short-term sleep deprivation enhances neuronal activity and dendritic spine density, potentially yielding antidepressant effects. In this study, a two-photon microscope was utilized to examine the calcium transients of anterior cingulate cortex (ACC) neurons in awake SD mice in vivo at 24-hour intervals. It was observed that SD reduced the frequency and amplitude of Ca2+ transients while increasing the proportions of inactive neurons. Following the cessation of sleep deprivation, neuronal calcium transients demonstrated a gradual recovery. Moreover, whole-cell patch-clamp recordings revealed a significant decrease in the frequency of spontaneous excitatory post-synaptic current (sEPSC) after SD. The investigation also assessed several oxidative stress parameters, finding that sleep deprivation substantially elevated the level of malondialdehyde (MDA), while simultaneously decreasing the expression of Nuclear Factor erythroid 2-Related Factor 2 (Nrf2) and activities of Superoxide dismutase (SOD) in the ACC. Importantly, the administration of gallic acid (GA) notably mitigated the decline of calcium transients in ACC neurons. GA was also shown to alleviate oxidative stress in the brain and improve cognitive impairment caused by sleep deprivation. These findings indicate that the calcium transients of ACC neurons experience a continuous decline during sleep deprivation, a process that is reversible. GA may serve as a potential candidate agent for the prevention and treatment of cognitive impairment induced by sleep deprivation.

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来源期刊
Experimental Neurobiology
Experimental Neurobiology Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.30
自引率
4.20%
发文量
29
期刊介绍: Experimental Neurobiology is an international forum for interdisciplinary investigations of the nervous system. The journal aims to publish papers that present novel observations in all fields of neuroscience, encompassing cellular & molecular neuroscience, development/differentiation/plasticity, neurobiology of disease, systems/cognitive/behavioral neuroscience, drug development & industrial application, brain-machine interface, methodologies/tools, and clinical neuroscience. It should be of interest to a broad scientific audience working on the biochemical, molecular biological, cell biological, pharmacological, physiological, psychophysical, clinical, anatomical, cognitive, and biotechnological aspects of neuroscience. The journal publishes both original research articles and review articles. Experimental Neurobiology is an open access, peer-reviewed online journal. The journal is published jointly by The Korean Society for Brain and Neural Sciences & The Korean Society for Neurodegenerative Disease.
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