Signalling Pathways Involved in Microglial Activation in Alzheimer's Disease and Potential Neuroprotective Role of Phytoconstituents.

IF 2.7 4区 医学 Q3 NEUROSCIENCES CNS & neurological disorders drug targets Pub Date : 2024-01-01 DOI:10.2174/1871527322666221223091529
Mohd Uzair Ali, Laiba Anwar, Mohd Humair Ali, Mohammad Kashif Iqubal, Ashif Iqubal, Sanjula Baboota, Javed Ali
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Abstract

Alzheimer's disease (AD) is a commonly reported neurodegenerative disorder associated with dementia and cognitive impairment. The pathophysiology of AD comprises Aβ, hyperphosphorylated tau protein formation, abrupt cholinergic cascade, oxidative stress, neuronal apoptosis, and neuroinflammation. Recent findings have established the profound role of immunological dysfunction and microglial activation in the pathogenesis of AD. Microglial activation is a multifactorial cascade encompassing various signalling molecules and pathways such as Nrf2/NLRP3/NF-kB/p38 MAPKs/ GSK-3β. Additionally, deposited Aβ or tau protein triggers microglial activation and accelerates its pathogenesis. Currently, the FDA-approved therapeutic regimens are based on the modulation of the cholinergic system, and recently, one more drug, aducanumab, has been approved by the FDA. On the one hand, these drugs only offer symptomatic relief and not a cure for AD. Additionally, no targetedbased microglial medicines are available for treating and managing AD. On the other hand, various natural products have been explored for the possible anti-Alzheimer effect via targeting microglial activation or different targets of microglial activation. Therefore, the present review focuses on exploring the mechanism and associated signalling related to microglial activation and a detailed description of various natural products that have previously been reported with anti-Alzheimer's effect via mitigation of microglial activation. Additionally, we have discussed the various patents and clinical trials related to managing and treating AD.

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参与阿尔茨海默病小胶质细胞活化的信号通路及植物成分的潜在神经保护作用
阿尔茨海默病(AD)是一种常见的神经退行性疾病,与痴呆和认知障碍有关。阿尔茨海默病的病理生理学包括 Aβ、高磷酸化 tau 蛋白形成、突变胆碱能级联、氧化应激、神经元凋亡和神经炎症。最近的研究结果表明,免疫功能障碍和小胶质细胞活化在注意力缺失症的发病机制中扮演着重要角色。小胶质细胞活化是一个多因素级联过程,包括各种信号分子和途径,如 Nrf2/NLRP3/NF-kB/p38 MAPKs/ GSK-3β。此外,沉积的 Aβ 或 tau 蛋白会引发小胶质细胞活化并加速其发病。目前,美国食品和药物管理局批准的治疗方案均以调节胆碱能系统为基础,最近又有一种药物--阿杜单抗(aducanumab)获得了美国食品和药物管理局的批准。一方面,这些药物只能缓解症状,不能治愈注意力缺失症。此外,目前还没有治疗和控制注意力缺失症的靶向微神经胶质细胞药物。另一方面,人们已经探索了各种天然产品,以通过靶向小胶质细胞活化或小胶质细胞活化的不同靶点来发挥可能的抗老年痴呆作用。因此,本综述重点探讨了与小胶质细胞活化相关的机制和相关信号,并详细介绍了以前报道过的通过缓解小胶质细胞活化而具有抗阿尔茨海默氏症作用的各种天然产品。此外,我们还讨论了与管理和治疗阿兹海默症有关的各种专利和临床试验。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
158
审稿时长
6-12 weeks
期刊介绍: Aims & Scope CNS & Neurological Disorders - Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular targets involved in neurological and central nervous system (CNS) disorders e.g. disease specific proteins, receptors, enzymes, genes. CNS & Neurological Disorders - Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of CNS & neurological drug targets. The journal also accepts for publication original research articles, letters, reviews and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for neurological and CNS drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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