Lei Wang , Qiang Wang , Xiaoqing Wang , Chenyi Yang , Xinyi Wang , Huan Liu , Haiyun Wang
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In this study, we aim to explore the potential impact of IF on postoperative cognitive function in aged mice undergoing sevoflurane surgery through the preoperative implementation of IF measures. The findings indicate two weeks of IF leads to a significant enhancement of learning and memory capabilities in mice following surgery. The cognitive performance, as determined by the novel object recognition and Morris water maze tests, as well as the synaptic plasticity, as measured by in vivo electrophysiological recordings, has demonstrated marked improvements. Furthermore, the administration of IF markedly enhances the expression of synaptic-associated proteins in hippocampal neurons, concomitant with a decreasing expression of pro-inflammatory factors and a reduced density of microglial cells within the hippocampal brain region. To summarize, the results of this study indicate that IF may mitigate inflammation in the hippocampal area of the brain. 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The cognitive performance, as determined by the novel object recognition and Morris water maze tests, as well as the synaptic plasticity, as measured by in vivo electrophysiological recordings, has demonstrated marked improvements. Furthermore, the administration of IF markedly enhances the expression of synaptic-associated proteins in hippocampal neurons, concomitant with a decreasing expression of pro-inflammatory factors and a reduced density of microglial cells within the hippocampal brain region. To summarize, the results of this study indicate that IF may mitigate inflammation in the hippocampal area of the brain. 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引用次数: 0
摘要
接受外科手术的老年人经常面临术后认知功能障碍(POCD)的危险。先前的研究表明,七氟醚麻醉会加重神经炎症,从而进一步恶化老年患者的认知功能障碍状况。间歇性禁食(IF)将食物摄入限制在一个特定的时间窗口内,已被证实能改善神经性炎症引起的认知功能障碍。我们让 18 个月大的雄性小鼠在 0 周、1 周、2 周和 4 周的 24 小时内分别禁食 16 小时和 8 小时,然后在七氟醚麻醉下进行腹部探查。在这项研究中,我们旨在通过术前实施 IF 措施,探讨 IF 对接受七氟醚手术的老年小鼠术后认知功能的潜在影响。研究结果表明,两周的 IF 可显著增强小鼠术后的学习和记忆能力。通过新物体识别和莫里斯水迷宫测试测定的认知能力,以及通过体内电生理记录测定的突触可塑性都有明显改善。此外,服用 IF 还能显著增强海马神经元中突触相关蛋白的表达,同时减少促炎因子的表达,降低海马脑区小胶质细胞的密度。总之,这项研究的结果表明,IF 可减轻大脑海马区的炎症反应。此外,IF似乎还能防止七氟醚麻醉带来的认知障碍和突触可塑性损伤。
Intermittent fasting alleviates postoperative cognitive dysfunction by reducing neuroinflammation in aged mice
Elderly individuals undergoing surgical procedures are often confronted with the peril of experiencing postoperative cognitive dysfunction (POCD). Prior research has demonstrated the exacerbating effect of sevoflurane anesthesia on neuroinflammation, which can further deteriorate the condition of POCD in elderly patients. Intermittent fasting (IF) restricts food consumption to a specific time window and has been demonstrated to ameliorate cognitive dysfunction induced by neuropathic inflammation. We subjected 18-month-old male mice to 16 hours of fasting and 8 hours of unrestricted eating over a 24-hour period for 0, 1, 2, and 4 weeks, followed by abdominal exploration under sevoflurane anesthesia. In this study, we aim to explore the potential impact of IF on postoperative cognitive function in aged mice undergoing sevoflurane surgery through the preoperative implementation of IF measures. The findings indicate two weeks of IF leads to a significant enhancement of learning and memory capabilities in mice following surgery. The cognitive performance, as determined by the novel object recognition and Morris water maze tests, as well as the synaptic plasticity, as measured by in vivo electrophysiological recordings, has demonstrated marked improvements. Furthermore, the administration of IF markedly enhances the expression of synaptic-associated proteins in hippocampal neurons, concomitant with a decreasing expression of pro-inflammatory factors and a reduced density of microglial cells within the hippocampal brain region. To summarize, the results of this study indicate that IF may mitigate inflammation in the hippocampal area of the brain. Furthermore, IF appears to provide a safeguard against cognitive impairment and synaptic plasticity impairment brought on by sevoflurane anesthesia.
期刊介绍:
The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.