Wang Cheng-Cheng, Kong Jing-Ya, Li Xiao-Yue, Yang Jin-Yue, Xue Chang-Hu, Yanagita Teruyoshi, Wang Yu-Ming
College of Food Science and Engineering, Ocean University of China, Qingdao, China.
Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology, Qingdao, China.
Front Aging Neurosci. 2022 Sep 16;14:964077. doi: 10.3389/fnagi.2022.964077. eCollection 2022.
The complex pathogenesis of Alzheimer's disease (AD) leads to a limited therapeutic effect; therefore, the combination of multiple bioactive ingredients may be more effective in improving AD due to synergistic effects. Based on the perspective of the sea-land combination, the effects of sea-derived Antarctic krill oil (AKO) combined with land-derived nobiletin (Nob) and L-theanine (The) on memory loss and cognitive deficiency were studied in senescence-accelerated prone 8 mice (SAMP8). The results demonstrated that AKO combined with The significantly increased the number of platform crossings in the Morris water maze test by 1.6-fold, and AKO combined with Nob significantly increased the preference index in a novel object recognition test. AKO exhibited synergistic effects with Nob and The in ameliorating recognition memory and spatial memory deficiency in SAMP8 mice, respectively. Further research of the mechanism indicated that AKO exhibited synergistic effects with Nob in suppressing β-amyloid (Aβ) aggregation, neurofibrillary tangles, and apoptosis and neuroinflammation, while the synergistic effects of AKO and The involved in synaptic plasticity and anti-neuroinflammation, which revealed that the combination was complex, not a mechanical addition. These findings revealed that the sea-land combination may be an effective strategy to treat and alleviate AD.
阿尔茨海默病(AD)复杂的发病机制导致治疗效果有限;因此,多种生物活性成分联合使用可能因协同作用而在改善AD方面更有效。基于海陆结合的视角,研究了海洋来源的南极磷虾油(AKO)与陆地来源的诺米林(Nob)和L-茶氨酸(The)联合使用对快速老化小鼠8(SAMP8)记忆丧失和认知缺陷的影响。结果表明,AKO与The联合使用在莫里斯水迷宫试验中使平台穿越次数显著增加了1.6倍,AKO与Nob联合使用在新物体识别试验中显著提高了偏好指数。AKO分别与Nob和The协同改善SAMP8小鼠的识别记忆和空间记忆缺陷。机制的进一步研究表明,AKO与Nob协同抑制β-淀粉样蛋白(Aβ)聚集、神经原纤维缠结以及细胞凋亡和神经炎症,而AKO和The的协同作用涉及突触可塑性和抗神经炎症,这表明这种联合是复杂的,而非机械相加。这些发现揭示了海陆结合可能是治疗和缓解AD的有效策略。