1. GPR40 receptor agonist TAK-875 improves cognitive deficits and reduces β-amyloid production in APPswe/PS1dE9 mice
- Author
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Zhao-Yan Cheng, Qing-Peng Xia, Ling He, Yu-Hui Hu, Chen Wang, and Chao Liu
- Subjects
Male ,Agonist ,endocrine system ,medicine.drug_class ,ADAM10 ,Mice, Transgenic ,Pharmacology ,Receptors, G-Protein-Coupled ,Protein kinase C signaling ,Amyloid beta-Protein Precursor ,Mice ,03 medical and health sciences ,0302 clinical medicine ,Free fatty acid receptor 1 ,Presenilin-1 ,Amyloid precursor protein ,Animals ,Humans ,Memory impairment ,Medicine ,Cognitive Dysfunction ,Sulfones ,Receptor ,Benzofurans ,Injections, Intraventricular ,Amyloid beta-Peptides ,Phospholipase C ,biology ,business.industry ,Brain ,030227 psychiatry ,Mice, Inbred C57BL ,biology.protein ,business ,030217 neurology & neurosurgery - Abstract
Alzheimer’s disease (AD) is an age-related neurodegenerative disease characterized by progressive cognitive dysfunction and memory impairment. G protein-coupled receptor 40 (GPR40) is expressed in brain in addition to periphery and is associated with cognitive function such as space orientation, memory, and learning. However, the effects and mechanisms of GPR40 agonist in improving the AD progression remain largely unknown. The present study aimed to investigate the therapeutic effects and mechanisms of a potent and selective GPR40 agonist TAK-875 on the APPswe/PS1dE9 mice. The results showed that intracerebroventricular administration of TAK-875 significantly rescued cognitive deficits in APPswe/PS1dE9 mice, and these effects may be mediated by the regulation of phospholipase C/protein kinase C signaling pathway, which enhanced α-secretase ADAM10 activity, promoted amyloid precursor protein non-amyloidogenic processing pathway, and reduced β-amyloid production. These results suggest that GPR40 may be a potential therapeutic target for AD, and GPR40 agonists may become promising AD drugs in the future.
- Published
- 2021