Behavioral and Cognitive Improvement Induced by Novel Imidazoline I<inf>2</inf> Receptor Ligands in Female SAMP8 Mice

Christian Griñán-Ferré, Foteini Vasilopoulou, Sònia Abás, Sergio Rodríguez-Arévalo, Andrea Bagán, Francesc X. Sureda, Belén Pérez, Luis F. Callado, Jesús A. García-Sevilla, M. Julia García-Fuster, Carmen Escolano, Mercè Pallàs

Research output: Contribution to journalArticleResearch

9 Citations (Scopus)


© 2018, The American Society for Experimental NeuroTherapeutics, Inc. As populations increase their life expectancy, age-related neurodegenerative disorders such as Alzheimer’s disease have become more common. I2-Imidazoline receptors (I2-IR) are widely distributed in the central nervous system, and dysregulation of I2-IR in patients with neurodegenerative diseases has been reported, suggesting their implication in cognitive impairment. This evidence indicates that high-affinity selective I2-IR ligands potentially contribute to the delay of neurodegeneration. In vivo studies in the female senescence accelerated mouse-prone 8 mice have shown that treatment with I2-IR ligands, MCR5 and MCR9, produce beneficial effects in behavior and cognition. Changes in molecular pathways implicated in oxidative stress, inflammation, synaptic plasticity, and apoptotic cell death were also studied. Furthermore, treatments with these I2-IR ligands diminished the amyloid precursor protein processing pathway and increased Aβ degrading enzymes in the hippocampus of SAMP8 mice. These results collectively demonstrate the neuroprotective role of these new I2-IR ligands in a mouse model of brain aging through specific pathways and suggest their potential as therapeutic agents in brain disorders and age-related neurodegenerative diseases.
Original languageEnglish
Pages (from-to)416-431
Publication statusPublished - 15 Apr 2019


  • (2-imidazolin-4-yl)phosphonates
  • Aging
  • Behavior
  • Cognition
  • Imidazoline I receptors 2
  • Neurodegeneration
  • Neuroprotection


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