Improvement of cognitive function in Alzheimer's disease model mice by genetic and pharmacological inhibition of the EP 4 receptor

Tatsuya Hoshino, Takushi Namba, Masaya Takehara, Naoya Murao, Takahide Matsushima, Yukihiko Sugimoto, Shuh Narumiya, Toshiharu Suzuki, Tohru Mizushima

研究成果: Article

22 引用 (Scopus)

抜粋

Amyloid-β peptide (Aβ), which is generated by the β- and γ-secretase-mediated proteolysis of β-amyloid precursor protein (APP), plays an important role in the pathogenesis of Alzheimer's disease (AD). We recently reported that prostaglandin E 2 (PGE 2) stimulates the production of Aβ through both EP 2 and EP 4 receptors and that activation of the EP 4 receptor stimulates Aβ production through endocytosis and activation of γ-secretase. We here found that transgenic mice expressing mutant APP (APP23) mice showed a greater or lesser apparent cognitive deficit when they were crossed with mice lacking EP 2 or EP 4 receptors, respectively. Mice lacking the EP 4 receptor also displayed lower levels of Aβ plaque deposition and less neuronal and synaptic loss than control mice. Oral administration of a specific EP 4 receptor antagonist, AE3-208 to APP23 mice, improved their cognitive performance, as well as decreasing brain levels of Aβ and suppressing endocytosis and activation of γ-secretase. Taken together, these results suggest that inhibition of the EP 4 receptor improves the cognitive function of APP23 mice by suppressing Aβ production and reducing neuronal and synaptic loss. We therefore propose that EP 4 receptor antagonists, such as AE3-208, could be therapeutically beneficial for the prevention and treatment of AD.

元の言語English
ページ(範囲)795-805
ページ数11
ジャーナルJournal of Neurochemistry
120
発行部数5
DOI
出版物ステータスPublished - 2012 3 1

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

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    Hoshino, T., Namba, T., Takehara, M., Murao, N., Matsushima, T., Sugimoto, Y., Narumiya, S., Suzuki, T., & Mizushima, T. (2012). Improvement of cognitive function in Alzheimer's disease model mice by genetic and pharmacological inhibition of the EP 4 receptor. Journal of Neurochemistry, 120(5), 795-805. https://doi.org/10.1111/j.1471-4159.2011.07567.x