{"title":"New Drug Research and Development for Alzheimer's Pathology: Present and Prospect.","authors":"Tao Wang","doi":"10.11919/j.issn.1002-0829.217045","DOIUrl":null,"url":null,"abstract":"<p><p>Cholinesterase inhibitors and N-methyl-D-aspartic receptor antagonists are currently the main treatments for Alzheimer's disease (AD), targeting the clinical symptoms of AD. β-amyloid (Aβ) deposition and the highly-phosphorylated Tau protein-induced neurofibrillary tangles are some of the common pathological features of AD. In the past 20 years, many new drugs that focus on the pathogenesis of Alzheimer's disease have been assessed in clinical trials. Drugs such as β-amyloid monoclonal antibody and gamma-secretase inhibitor target the Aβ pathological pathway. New drugs targeting the Tau pathological pathway inhibit the generation of neurofibrillary tangles and the Tau protein antibodies. But until now, none of these drugs has brought a fundamental breakthrough. This initial breakthrough may come out of China as there are several groups here which already have disease-modifying drugs in phase II and phase III of clinical trials.</p>","PeriodicalId":21886,"journal":{"name":"上海精神医学","volume":"29 4","pages":"237-239"},"PeriodicalIF":0.0000,"publicationDate":"2017-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/45/fb/sap-29-237.PMC5608996.pdf","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"上海精神医学","FirstCategoryId":"95","ListUrlMain":"https://doi.org/10.11919/j.issn.1002-0829.217045","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
Abstract
Cholinesterase inhibitors and N-methyl-D-aspartic receptor antagonists are currently the main treatments for Alzheimer's disease (AD), targeting the clinical symptoms of AD. β-amyloid (Aβ) deposition and the highly-phosphorylated Tau protein-induced neurofibrillary tangles are some of the common pathological features of AD. In the past 20 years, many new drugs that focus on the pathogenesis of Alzheimer's disease have been assessed in clinical trials. Drugs such as β-amyloid monoclonal antibody and gamma-secretase inhibitor target the Aβ pathological pathway. New drugs targeting the Tau pathological pathway inhibit the generation of neurofibrillary tangles and the Tau protein antibodies. But until now, none of these drugs has brought a fundamental breakthrough. This initial breakthrough may come out of China as there are several groups here which already have disease-modifying drugs in phase II and phase III of clinical trials.
胆碱酯酶抑制剂和n -甲基- d -天冬氨酸受体拮抗剂是目前治疗阿尔茨海默病(AD)的主要药物,针对的是AD的临床症状。β-淀粉样蛋白(Aβ)沉积和高度磷酸化的Tau蛋白诱导的神经原纤维缠结是AD的一些共同病理特征。在过去的20年里,许多着眼于阿尔茨海默病发病机制的新药已经在临床试验中进行了评估。β-淀粉样蛋白单克隆抗体和γ -分泌酶抑制剂等药物靶向Aβ病理通路。靶向Tau病理通路的新药抑制神经原纤维缠结和Tau蛋白抗体的产生。但直到现在,这些药物都没有带来根本性的突破。这个最初的突破可能来自中国,因为这里有几个小组已经在II期和III期临床试验中使用了改善疾病的药物。