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ω-3脂肪酸的神经保护作用:对抗阿尔茨海默病

Neuroprotective Role of Omega-3 Fatty Acids: Fighting Alzheimer's Disease.

作者信息

Chávez-Castillo Mervin, Gotera María Paula, Duran Pablo, Díaz María P, Nava Manuel, Cano Clímaco, Díaz-Camargo Edgar, Cano Gabriel, Cano Raquel, Rivera-Porras Diego, Bermúdez Valmore

机构信息

Endocrine and Metabolic Diseases Research Center, School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.

Facultad de Ciencias Jurídicas y Sociales, Universidad Simón Bolívar, Cúcuta 540006, Colombia.

出版信息

Molecules. 2025 Jul 22;30(15):3057. doi: 10.3390/molecules30153057.

Abstract

Alzheimer's disease (AD) is one of the main causes of dementia, with an exponential increment in its incidence as years go by. However, since pathophysiological mechanisms are complex and multifactorial, therapeutic strategies remain inconclusive and only provide symptomatic relief to patients. In order to solve this problem, new strategies have been investigated over recent years for AD treatment. This field has been reborn due to epidemiological and preclinical findings that demonstrate the fact that omega-3 polyunsaturated fatty acids (ω-3 PUFAs) can be promising therapeutic agents because of their anti-inflammatory, antioxidant, and neurogenic-promoting activities, thus allowing us to classify these molecules as neuroprotectors. Similarly, ω-3 PUFAs perform important actions in the formation of characteristic AD lesions, amyloid-β plaques (Aβ) and neurofibrillary tangles, reducing the development of these structures. Altogether, the aforementioned actions hinder cognitive decline and possibly reduce AD development. In addition, ω-3 PUFAs modulate the inflammatory response by inhibiting the production of pro-inflammatory molecules and promoting the synthesis of specialised pro-resolving mediators. Consequently, the present review assesses the mechanisms by which ω-3 PUFAs can act as therapeutic molecules and the effectiveness of their use in patients. Clinical evidence so far has shown promising results on ω-3 PUFA effects, both in animal and epidemiological studies, but remains contradictory in clinical trials. More research on these molecules and their neuroprotective effects in AD is needed, as well as the establishment of future guidelines to obtain more reproducible results on this matter.

摘要

阿尔茨海默病(AD)是痴呆症的主要病因之一,其发病率随时间呈指数增长。然而,由于病理生理机制复杂且多因素,治疗策略仍无定论,仅能为患者提供症状缓解。为了解决这一问题,近年来人们对AD治疗的新策略进行了研究。由于流行病学和临床前研究结果表明,ω-3多不饱和脂肪酸(ω-3 PUFAs)因其抗炎、抗氧化和促进神经生成的活性,有望成为治疗药物,从而使我们能够将这些分子归类为神经保护剂,该领域得以重生。同样,ω-3 PUFAs在特征性AD病变淀粉样β斑块(Aβ)和神经纤维缠结的形成中发挥重要作用,减少这些结构的发展。总之,上述作用阻碍认知能力下降,并可能减少AD的发展。此外,ω-3 PUFAs通过抑制促炎分子的产生和促进特异性促解决介质的合成来调节炎症反应。因此,本综述评估了ω-3 PUFAs作为治疗分子的作用机制及其在患者中的使用效果。迄今为止的临床证据表明,ω-3 PUFAs的作用在动物和流行病学研究中均显示出有希望的结果,但在临床试验中仍存在矛盾。需要对这些分子及其在AD中的神经保护作用进行更多研究,并制定未来指南,以便在这一问题上获得更可重复的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a0/12348196/3f87e04e6b43/molecules-30-03057-g001.jpg

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