核iferine 对高脂饮食诱发的肥胖小鼠认知功能障碍的神经保护作用:胰岛素抵抗、神经炎症和氧化应激的作用

IF 7.4 Q1 FOOD SCIENCE & TECHNOLOGY Food frontiers Pub Date : 2024-02-08 DOI:10.1002/fft2.365
Xiangyang Zhu, Rili Hao, Xi-Qian Lv, Jing Su, Dapeng Li, Chen Zhang
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引用次数: 0

摘要

高脂饮食(HFD)会引发机体氧化应激、胰岛素抵抗(IR)和炎症反应,从而导致认知功能障碍。本研究旨在阐明核iferine对高脂饮食诱导的胰岛素抵抗和肥胖小鼠中枢神经系统认知功能障碍的影响,并进一步确定其可能的内在机制。在行为实验中,服用纽iferine可增加小鼠的总移动距离、进入开放臂的次数、开放停留时间和交替次数,同时缩短逃逸潜伏期。神经营养因子BDNF和突触功能蛋白SYN、SNAP-25和PSD-95的表达量增加证明,母核碱抑制了HFD诱导的突触结构损伤。此外,荧光素还能通过IRS/PI3K/AKT途径有效改善HFD诱导的IR,通过AMPK/SIRT1途径减轻HFD诱导的神经损伤,并通过Aβ-tau-神经炎症轴改善认知障碍。因此,褐藻素可能是一种新的食物来源神经保护剂,可用于对抗高频分解诱导的损伤。
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Neuroprotective effects of nuciferine on high‐fat diet‐induced cognitive dysfunction in obese mice: Role of insulin resistance, neuroinflammation, and oxidative stress
High‐fat diets (HFDs) trigger oxidative stress, insulin resistance (IR), and inflammatory responses in the body, leading to cognitive dysfunction. This study aimed to elucidate the effects of nuciferine on HFD‐induced IR and cognitive impairment in the central nervous system of obese mice and further identify the possible underlying mechanisms. In behavioral experiments, nuciferine administration increased the total distance moved, the number of times mice entered the open arm, the duration of open dwell time, and the number of alternations while shortening the latency to escape. Nuciferine suppressed HFD‐induced synaptic structure damage, as evidenced by the increased expressions of neurotrophic factor BDNF and synaptic function proteins SYN, SNAP‐25, and PSD‐95. In addition, nuciferine effectively ameliorated HFD‐induced IR by IRS/PI3K/AKT pathway, alleviated HFD‐induced neurological damage through AMPK/SIRT1 pathway, and improved cognitive impairment via the Aβ‐tau‐neuroinflammation axis. Therefore, nuciferine could be a new food‐derived neuroprotective agent to counteract HFD‐induced damage.
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