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阿尔茨海默病治疗策略的进展:从药用植物到纳米技术。

Advances on Therapeutic Strategies for Alzheimer's Disease: From Medicinal Plant to Nanotechnology.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Shaqra University, Shaqra 11961, Saudi Arabia.

Synthetic Unit, Department of Photochemistry, Chemical Industries Research Institute, National Research Centre, Cairo 12622, Egypt.

出版信息

Molecules. 2022 Jul 28;27(15):4839. doi: 10.3390/molecules27154839.

Abstract

Alzheimer's disease (AD) is a chronic dysfunction of neurons in the brain leading to dementia. It is characterized by gradual mental failure, abnormal cognitive functioning, personality changes, diminished verbal fluency, and speech impairment. It is caused by neuronal injury in the cerebral cortex and hippocampal area of the brain. The number of individuals with AD is growing at a quick rate. The pathology behind AD is the progress of intraneuronal fibrillary tangles, accumulation of amyloid plaque, loss of cholinergic neurons, and decrease in choline acetyltransferase. Unfortunately, AD cannot be cured, but its progression can be delayed. Various FDA-approved inhibitors of cholinesterase enzyme such as rivastigmine, galantamine, donepezil, and NDMA receptor inhibitors (memantine), are available to manage the symptoms of AD. An exhaustive literature survey was carried out using SciFinder's reports from Alzheimer's Association, PubMed, and Clinical Trials.org. The literature was explored thoroughly to obtain information on the various available strategies to prevent AD. In the context of the present scenario, several strategies are being tried including the clinical trials for the treatment of AD. We have discussed pathophysiology, various targets, FDA-approved drugs, and various drugs in clinical trials against AD. The goal of this study is to shed light on current developments and treatment options, utilizing phytopharmaceuticals, nanomedicines, nutraceuticals, and gene therapy.

摘要

阿尔茨海默病(AD)是一种大脑神经元的慢性功能障碍,导致痴呆。其特征为逐渐出现精神衰竭、认知功能异常、人格改变、言语流畅性下降和言语障碍。它是由大脑皮层和海马区的神经元损伤引起的。AD 患者的数量正在迅速增长。AD 的病理学是神经元内纤维缠结的进展、淀粉样斑块的积累、胆碱能神经元的丧失和胆碱乙酰转移酶的减少。不幸的是,AD 无法治愈,但可以延缓其进展。有多种 FDA 批准的胆碱酯酶抑制剂,如利伐斯的明、加兰他敏、多奈哌齐和 NMDA 受体抑制剂(美金刚),可用于治疗 AD 症状。利用来自阿尔茨海默病协会、PubMed 和 ClinicalTrials.gov 的 SciFinder 报告,进行了全面的文献调查。深入探讨了文献,以获取有关预防 AD 的各种现有策略的信息。在当前情况下,正在尝试几种策略,包括 AD 的治疗临床试验。我们讨论了病理生理学、各种靶点、FDA 批准的药物以及针对 AD 的临床试验中的各种药物。本研究的目的是利用植物药、纳米医学、营养保健品和基因治疗,阐明当前的发展和治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21aa/9369981/ba2c3c44f186/molecules-27-04839-g001.jpg

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