Targeting the orexin/hypocretin system for the treatment of neuropsychiatric and neurodegenerative diseases: From animal to clinical studies

•Dual orexin receptor antagonists have been approved for the treatment of insomnia.•Stress-related disorders entail a dysregulation of the orexin system.•Blockade of orexin receptors is a potential target for addictive disorders.•Orexinergic system is disturbed in various neurodegenerative diseases....

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Veröffentlicht in:Frontiers in neuroendocrinology 2023-04, Vol.69, p.101066-101066, Article 101066
Hauptverfasser: Ten-Blanco, Marc, Flores, África, Cristino, Luigia, Pereda-Pérez, Inmaculada, Berrendero, Fernando
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Sprache:eng
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Zusammenfassung:•Dual orexin receptor antagonists have been approved for the treatment of insomnia.•Stress-related disorders entail a dysregulation of the orexin system.•Blockade of orexin receptors is a potential target for addictive disorders.•Orexinergic system is disturbed in various neurodegenerative diseases.•New drugs based on orexins will be probably developed in the near future. Orexins (also known as hypocretins) are neuropeptides located exclusively in hypothalamic neurons that have extensive projections throughout the central nervous system and bind two different G protein-coupled receptors (OX1R and OX2R). Since its discovery in 1998, the orexin system has gained the interest of the scientific community as a potential therapeutic target for the treatment of different pathological conditions. Considering previous basic science research, a dual orexin receptor antagonist, suvorexant, was the first orexin agent to be approved by the US Food and Drug Administration to treat insomnia. In this review, we discuss and update the main preclinical and human studies involving the orexin system with several psychiatric and neurodegenerative diseases. This system constitutes a nice example of how basic scientific research driven by curiosity can be the best route to the generation of new and powerful pharmacological treatments.
ISSN:0091-3022
1095-6808
DOI:10.1016/j.yfrne.2023.101066