Eman H Rashwan, Mohamed Elashal, Shaden A M Khalifa, Aida A Abd El-Wahed, Daijie Wang, Wesam M Hussein, Xiao-Ping Wang, Guiguang Cheng, Yahya Al Naggar, Haiyan Wang, Zhengxuan Wang, Lutfun Nahar, Zhiming Guo, Hesham R El-Seedi
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引用次数: 0
Abstract
Alzheimer's disease (AD) is one of the devastating diseases that has a high incidence without satisfactory preventive and curative strategies. The multi-targeted interventions become a promising alternative to address their complex pathogenesis. This narrative review searched PubMed/MEDLINE, Scopus, and Web of Science (January 2010-December 2025) to assess the therapeutic potential of honeybee products for AD management. The use of bee-derived compounds demonstrated neuroprotective advantages via known mechanisms. For instance, honey polyphenols reduce tau hyperphosphorylation and amyloid beta (Aβ) deposition through anti-inflammatory and antioxidant actions. Pinocembrin a compound of propolis, plays a role in nuclear factor kappa B (NF-B) suppression of microglial activation via its proteolytic degradation and even enhances synaptic plasticity. Phospholipase A2 and melittin inhibited the acetylcholinesterase activity by raising the level of brain-derived neurotrophic factor (BDNF). Royal jelly has a neurotrophic impact, proven to promote neuroprogenitor cell proliferation, while bee pollen enhances cognitive function via extracellular signal-regulated kinase- cyclic adenosine monophosphate response element-binding protein (ERK-CREB) signaling. Apilarnil can protect and stimulate nerves and possesses anti-inflammatory properties. Despite the notion that apitherapy has a promising role in the management of, challenges including standardization, bioavailability, and clinical validation, warrant more attention prior to the implication in the drug discovery field.
阿尔茨海默病(Alzheimer’s disease, AD)是一种发病率高、防治策略不理想的致命性疾病。多目标干预成为解决其复杂发病机制的一种有希望的替代方法。本综述检索了PubMed/MEDLINE、Scopus和Web of Science(2010年1月- 2025年12月),以评估蜜蜂产品对AD治疗的治疗潜力。蜜蜂衍生化合物的使用通过已知机制证明了神经保护的优势。例如,蜂蜜多酚通过抗炎和抗氧化作用减少tau过度磷酸化和β淀粉样蛋白(Aβ)沉积。pinonembrin是一种蜂胶化合物,它通过蛋白水解降解核因子κ B (NF-B)抑制小胶质细胞的激活,甚至增强突触的可塑性。磷脂酶A2和蜂毒素通过提高脑源性神经营养因子(BDNF)水平抑制乙酰胆碱酯酶活性。蜂王浆具有神经营养作用,被证明可以促进神经祖细胞增殖,而蜂花粉通过细胞外信号调节的激酶-环腺苷单磷酸反应元件结合蛋白(ERK-CREB)信号传导增强认知功能。阿非拉尼尔可以保护和刺激神经,并具有抗炎特性。尽管人们认为蜂疗在疾病管理中具有很好的作用,但包括标准化、生物利用度和临床验证在内的挑战值得更多的关注,而不是药物发现领域的影响。