美金刚
加兰他明
多奈哌齐
竞争对手
老年斑
疾病
τ蛋白
医学
药理学
阿尔茨海默病
痴呆
高磷酸化
早老素
神经科学
心理学
内科学
化学
生物化学
激酶
作者
Teresa Pardo-Moreno,Anabel González-Acedo,Antonio Rivas-Domínguez,Victoria García‐Morales,Francisco García-Cozar,Juan José Ramos‐Rodríguez,Lucia Melguizo‐Rodríguez
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-05-24
卷期号:14 (6): 1117-1117
被引量:75
标识
DOI:10.3390/pharmaceutics14061117
摘要
Alzheimer's disease (AD) is the most common cause of dementia. The pathophysiology of this disease is characterized by the accumulation of amyloid-β, leading to the formation of senile plaques, and by the intracellular presence of neurofibrillary tangles based on hyperphosphorylated tau protein. In the therapeutic approach to AD, we can identify three important fronts: the approved drugs currently available for the treatment of the disease, which include aducanumab, donepezil, galantamine, rivastigmine, memantine, and a combination of memantine and donepezil; therapies under investigation that work mainly on Aβ pathology and tau pathology, and which include γ-secretase inhibitors, β-secretase inhibitors, α-secretase modulators, aggregation inhibitors, metal interfering drugs, drugs that enhance Aβ clearance, inhibitors of tau protein hyperphosphorylation, tau protein aggregation inhibitors, and drugs that promote the clearance of tau, and finally, other alternative therapies designed to improve lifestyle, thus contributing to the prevention of the disease. Therefore, the aim of this review was to analyze and describe current treatments and possible future alternatives in the therapeutic approach to AD.
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