Increased 5-HT 2A receptor signalling efficacy differentiates serotonergic psychedelics from non-psychedelics
OpenAlex – June 16, 2024
Source: OpenAlex
Summary
All tested psychedelics demonstrated unbiased, partial agonist activity at 5-HT 2A receptors. In a study involving SH-SY5Y cells (sample size not specified), eight psychedelics, including LSD and psilocin, were compared to non-psychedelics like lisuride and TBG. While none of the substances showed significant signalling bias, lisuride and TBG exhibited the lowest efficacy among all drugs, suggesting that the efficacy of 5-HT 2A receptor signalling, rather than biased signalling, explains why certain agonists lack psychedelic effects.
Abstract
ABSTRACT Background and Purpose Serotonergic psychedelic drugs are under renewed investigation for the potential treatment of several psychiatric disorders. While all serotonergic psychedelics have 5-HT 2A receptor activity, the explanation for why some 5-HT 2A receptor agonists are not psychedelic is unknown. To address this question, we investigated the 5-HT 2A receptor signalling bias and efficacy of a panel of psychedelics and non-psychedelics. Experimental Approach G -coupled (Ca 2+ and IP) and β-arrestin2 signalling effects of eight chemically diverse psychedelics (psilocin, 5-MeO-DMT, LSD, mescaline, 25B-NBOMe and DOI) and non-psychedelics (lisuride and TBG) were characterised using SH-SY5Y cells expressing recombinant human 5-HT 2A receptors. Measurements of signalling efficacy and bias were derived from dose-responses curves for each agonist, compared to 5-HT. Follow-up experiments sought to confirm the generality of findings using rat C6 cells expressing endogenous 5-HT 2A receptors. Key Results In SH-SY5Y cells, all psychedelics were partial agonists at both 5-HT 2A receptor signalling pathways and none showed significant signalling bias. In comparison, in SH-SY5Y cells the non-psychedelics lisuride and TBG were not distinguishable from psychedelics in terms of biased agonist properties, but both exhibited the lowest 5-HT 2A receptor signalling efficacy of all drugs tested, a result confirmed in C6 cells. Conclusion and Implications In summary, all psychedelics tested were unbiased, partial 5-HT 2A receptor agonists. Importantly, the non-psychedelics lisuride and TBG were discriminated from psychedelics, not through biased signalling but rather by relatively low efficacy. Thus, 5-HT 2A receptor signalling efficacy and not bias provides a possible explanation for why some 5-HT 2A receptor agonists are not psychedelic.