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阿尔茨海默病中的5-羟色胺能调节剂:绝望状况下的一线希望

Serotonergic Modulators in Alzheimer's Disease: A Hope in the Hopeless Condition.

作者信息

Almohmadi Najlaa Hamed, Al-Kuraishy Hayder M, Al-Gareeb Ali I, Albuhadily Ali K, Fakhry Morkoss M, Alexiou Athanasios, Papadakis Marios, Batiha Gaber El-Saber

机构信息

Clinical Nutrition Department, College of Applied Medical Sciences, Umm Al-Qura University, Makkah, Saudi Arabia.

Department of Clinical Pharmacology and Medicine, College of Medicine, Mustansiriyah University, Baghdad, Iraq.

出版信息

Chem Biodivers. 2025 Aug;22(8):e202403401. doi: 10.1002/cbdv.202403401. Epub 2025 Jun 3.

Abstract

Alzheimer's disease (AD) is the main cause of dementia worldwide. AD is a progressive brain neurodegenerative disease due to genetic and environmental factors that induce a progressive accumulation of intracellular hyperphosphorylated tau protein and extracellular amyloid protein (Aβ). However, anti-AD medications cannot reverse the fundamental AD neuropathology due to amyloid plaques and related oxidative stress and inflammatory reactions. Thus, targeting other pathways might be reasonable in the management of AD. The serotonin (5-HT) neurotransmitter plays a crucial role in preventing neurodegeneration and related oxidative stress and inflammatory reactions. In addition, the serotonergic system is highly dysregulated in many neurodegenerative diseases, including AD. Deregulation of serotonin synthesis and its receptors is involved in the pathogenesis of AD. Therefore, this review aims to discuss how the serotonergic system is affected in AD, and how 5-HT modulators can reverse AD neuropathology and alleviate the associated neuropsychiatric disorders in AD patients.

摘要

阿尔茨海默病(AD)是全球痴呆的主要病因。AD是一种进行性脑神经退行性疾病,由遗传和环境因素引起,导致细胞内过度磷酸化的tau蛋白和细胞外淀粉样蛋白(Aβ)逐渐积累。然而,抗AD药物无法逆转由淀粉样斑块以及相关氧化应激和炎症反应导致的AD基本神经病理学改变。因此,针对其他途径来治疗AD可能是合理的。血清素(5-HT)神经递质在预防神经退行性变以及相关氧化应激和炎症反应中起着关键作用。此外,血清素能系统在包括AD在内的许多神经退行性疾病中高度失调。血清素合成及其受体的失调与AD的发病机制有关。因此,本综述旨在探讨血清素能系统在AD中是如何受到影响的,以及5-HT调节剂如何逆转AD神经病理学改变并减轻AD患者相关的神经精神障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c474/12351446/327006323bee/CBDV-22-e202403401-g003.jpg

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