4.6 Review

Recent Advances in the Inhibition of p38 MAPK as a Potential Strategy for the Treatment of Alzheimer's Disease

期刊

MOLECULES
卷 22, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/molecules22081287

关键词

p38 mitogen activated protein kinase (MAPK); kinase inhibitor; Alzheimer's disease; tau phosphorylation; neuroinflammation; amyloid beta

资金

  1. Basic Science Research Program grant through the National Research Foundation of Korea (NRF)
  2. Ministry of Science, ICT & Future Planning [NRF-2016R1A2B4015169]
  3. Korea Health Technology R & D Project through the Korea Health Industry Development Institute (KHIDI)
  4. Ministry of Health & Welfare, Republic of Korea [HI14C2203]
  5. Korea Health Promotion Institute [HI14C2203000016] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2016R1A2B4015169] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

P38 mitogen-activated protein kinase (MAPK) is a crucial target for chronic inflammatory diseases. Alzheimer's disease (AD) is characterized by the presence of amyloid plaques and neurofibrillary tangles in the brain, as well as neurodegeneration, and there is no known cure. Recent studies on the underlying biology of AD in cellular and animal models have indicated that p38 MAPK is capable of orchestrating diverse events related to AD, such as tau phosphorylation, neurotoxicity, neuroinflammation and synaptic dysfunction. Thus, the inhibition of p38 MAPK is considered a promising strategy for the treatment of AD. In this review, we summarize recent advances in the targeting of p38 MAPK as a potential strategy for the treatment of AD and envision possibilities of p38 MAPK inhibitors as a fundamental therapeutics for AD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据