TY - JOUR
T1 - The psychedelic phenethylamine 25C-NBF, a selective 5-HT2A agonist, shows psychoplastogenic properties and rapid antidepressant effects in male rodents
AU - Nadal-Gratacós, Núria
AU - Puigseslloses, Pol
AU - Guzmán, Laura
AU - Weiss, Nicola
AU - Pottie, Eline
AU - Riera-Colomer, Clara
AU - Lardeux, Virginie
AU - Thiriet, Nathalie
AU - Wang, Fu Hua
AU - Källsten, Liselott
AU - Pérez-Esteban, Irene
AU - Ketsela, Gabriel
AU - Margall, Joel
AU - Berzosa, Xavier
AU - Pubill, David
AU - Rodríguez-Arias, Marta
AU - Ettcheto, Miren
AU - Kehr, Jan
AU - Stove, Christophe
AU - Solinas, Marcello
AU - Sitte, Harald H.
AU - Escubedo, Elena
AU - López-Arnau, Raul
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/11/14
Y1 - 2025/11/14
N2 - Psychedelics have garnered significant interest for their therapeutic potential in mental health conditions such as depression, anxiety, and post-traumatic stress disorder. While research has primarily focused on well-studied psychedelics, phenethylamine derivatives have also gathered interest for their potential therapeutic applications. Thus, this study aims to investigate the pharmacological profile, safety and therapeutic potential of novel N-(2-fluorobenzyl) phenethylamine analogs (NBFs) of the 2C-X series—25C-NBF, 25B-NBF, and 25I-NBF. NBFs displayed high affinity and selectivity for the 5-HT2A receptor and demonstrated bias factors (defined in our study as the preference for Gq over β-arrestin pathways at 5-HT2A receptor) similar to that of 5-HT. Acute administration induced moderate head-twitch responses without affecting locomotion or pre-pulse inhibition. Our studies revealed no rewarding effects in mice nor reinforcing effects or changes in accumbal dopamine levels in rats after NBFs administration. Further characterization of 25C-NBF revealed psychoplastogenic effects (dendritogenesis, spinogenesis and increased Bdnf mRNA levels) both in vitro and in vivo. In addition, 25C-NBF reduced despair-like behavior in response to acute stress and exerted rapid antidepressant effects in a model of anhedonia-like behavior induced by chronic corticosterone administration. Taken together, these findings suggest that 25C-NBF, and further analogs, may hold potential as novel antidepressants with a rapid onset of action and a favorable safety profile in terms of no abuse potential or sensorimotor gating deficits.
AB - Psychedelics have garnered significant interest for their therapeutic potential in mental health conditions such as depression, anxiety, and post-traumatic stress disorder. While research has primarily focused on well-studied psychedelics, phenethylamine derivatives have also gathered interest for their potential therapeutic applications. Thus, this study aims to investigate the pharmacological profile, safety and therapeutic potential of novel N-(2-fluorobenzyl) phenethylamine analogs (NBFs) of the 2C-X series—25C-NBF, 25B-NBF, and 25I-NBF. NBFs displayed high affinity and selectivity for the 5-HT2A receptor and demonstrated bias factors (defined in our study as the preference for Gq over β-arrestin pathways at 5-HT2A receptor) similar to that of 5-HT. Acute administration induced moderate head-twitch responses without affecting locomotion or pre-pulse inhibition. Our studies revealed no rewarding effects in mice nor reinforcing effects or changes in accumbal dopamine levels in rats after NBFs administration. Further characterization of 25C-NBF revealed psychoplastogenic effects (dendritogenesis, spinogenesis and increased Bdnf mRNA levels) both in vitro and in vivo. In addition, 25C-NBF reduced despair-like behavior in response to acute stress and exerted rapid antidepressant effects in a model of anhedonia-like behavior induced by chronic corticosterone administration. Taken together, these findings suggest that 25C-NBF, and further analogs, may hold potential as novel antidepressants with a rapid onset of action and a favorable safety profile in terms of no abuse potential or sensorimotor gating deficits.
KW - Serotonin 5-ht2a
KW - Depression
KW - Receptors
KW - Drug
KW - Hallucinogens
KW - Derivatives
KW - Inhibition
KW - Challenges
KW - Psilocybin
KW - Addiction
UR - https://www.scopus.com/pages/publications/105021823240
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:001614394100001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1038/s41380-025-03341-1
DO - 10.1038/s41380-025-03341-1
M3 - Article
AN - SCOPUS:105021823240
SN - 1359-4184
JO - Molecular Psychiatry
JF - Molecular Psychiatry
ER -