4.7 Article

Meridianins Rescue Cognitive Deficits, Spine Density and Neuroinflammation in the 5xFAD Model of Alzheimer's Disease

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.791666

关键词

microglia; GSK3 beta; learning; memory; astrocytes

资金

  1. Ministerio de Ciencia, Innovacion y Universidades [RTI2018-094678-A-I00]
  2. [MDM-2017-0729]
  3. [RYC-2016-19466]

向作者/读者索取更多资源

In this study, we found that meridianins can inhibit neural GSK3 beta in the 5xFAD mouse model and such inhibition leads to improvements in cognitive function and neuroinflammation.
Glycogen synthase kinase 3 beta (GSK3 beta) is a core protein, with a relevant role in many neurodegenerative disorders including Alzheimer's disease. The enzyme has been largely studied as a potential therapeutic target for several neurological diseases. Unfortunately, preclinical and clinical studies with several GSK3 beta inhibitors have failed due to many reasons such as excessive toxicity or lack of effects in human subjects. We previously reported that meridianins are potent GSK3 beta inhibitors without altering neuronal viability. In the present work, we examine whether meridianins are capable to inhibit neural GSK3 beta in vivo and if such inhibition induces improvements in the 5xFAD mouse model of Alzheimer's Disease. Direct administration of meridianins in the third ventricle of 5xFAD mice induced robust improvements of recognition memory and cognitive flexibility as well as a rescue of the synaptic loss and an amelioration of neuroinflammatory processes. In summary, our study points out meridianins as a potential compound to treat neurodegenerative disorders associated with an hyperactivation of GSK3 beta such as Alzheimer's disease.

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