Sleep-related disorders affect a significant portion of the global population. The nociceptin/orphanin FQ (N/OFQ) peptide (NOP) receptor has become a promising candidate for the development of innovative drugs to treat sleep disorders. In this study, we conducted an in-depth pharmacological characterization of sunobinop, a selective NOP receptor partial agonist already under clinical evaluation for treating multiple conditions including insomnia, using a wide range of in vitro and ex vivo methodologies. Sunobinop exhibited partial agonist activity in calcium mobilization, NOP − G protein interaction, label-free bioimpedance, and cAMP inhibition assays. Notably, it demonstrated competitive antagonism in the NOP – β-Arrestin 2 recruitment and ex vivo electrically stimulated mouse Vas Deferens, assays characterized by low amplification. The findings reported here confirm and extend the characterization of sunobinop as a tool for studying NOP receptor pharmacology providing new insights into its mode of action, relevant to its clinical evaluation.

In vitro pharmacological evaluation of the novel NOP receptor partial agonist sunobinop / Camilotto, Riccardo; Malfacini, Davide; Pola, Pietro; Morrone, Erika; Frezza, Alessia; Ramalingam, Rahul; Sturaro, Chiara; Pacifico, Salvatore; Ruzza, Chiara; Guerrini, Remo; Whiteside, Garth; Calo', Girolamo. - In: BIOCHEMICAL PHARMACOLOGY. - ISSN 1873-2968. - ELETTRONICO. - 238:(2025), pp. 116972.0-116972.0. [10.1016/j.bcp.2025.116972]

In vitro pharmacological evaluation of the novel NOP receptor partial agonist sunobinop

Calo', Girolamo
2025

Abstract

Sleep-related disorders affect a significant portion of the global population. The nociceptin/orphanin FQ (N/OFQ) peptide (NOP) receptor has become a promising candidate for the development of innovative drugs to treat sleep disorders. In this study, we conducted an in-depth pharmacological characterization of sunobinop, a selective NOP receptor partial agonist already under clinical evaluation for treating multiple conditions including insomnia, using a wide range of in vitro and ex vivo methodologies. Sunobinop exhibited partial agonist activity in calcium mobilization, NOP − G protein interaction, label-free bioimpedance, and cAMP inhibition assays. Notably, it demonstrated competitive antagonism in the NOP – β-Arrestin 2 recruitment and ex vivo electrically stimulated mouse Vas Deferens, assays characterized by low amplification. The findings reported here confirm and extend the characterization of sunobinop as a tool for studying NOP receptor pharmacology providing new insights into its mode of action, relevant to its clinical evaluation.
2025
238
0
0
Goal 3: Good health and well-being
Camilotto, Riccardo; Malfacini, Davide; Pola, Pietro; Morrone, Erika; Frezza, Alessia; Ramalingam, Rahul; Sturaro, Chiara; Pacifico, Salvatore; Ruzza,...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1460133
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