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Molecular design of a therapeutic LSD analogue with reduced hallucinogenic potential

Jeremy R Tuck, Lee E. Dunlap, Yara A Khatib, Cassandra J. Hatzipantelis, Sammy Weiser Novak, Rachel M Rahn, Alexis R Davis, Adam Mosswood, Anna M M Vernier, Ethan M Fenton, Isak K Aarrestad, Robert J Tombari, Samuel J Carter, Zachary Deane, Yuning Wang, Arlo Sheridan, Monica A. Gonzalez, Arabo A. Avanes, Noel A Powell, Milan Chytil, Sharon Engel, James C Fettinger, Amaya R Jenkins, William A Carlezon, Alex S Nord, Brian D Kangas, Kurt Rasmussen, Conor Liston, Uri Manor, David E. Olson

Proceedings of the National Academy of Sciences April 14, 2025 DOI: 10.1073/pnas.2416106122 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Preclinical study Peer reviewed
Population Rodents (rats and/or mice, implied by behavioral assays)
Intervention (+)-JRT
Topics LSD Neuroplasticity
Keywords Neuropsychiatric disease Nonhallucinogenic Psychedelics hallucinogens Entheogens Psychoactive drugs Psychological medicine Behavioral health Neuroscience brain research Neural science Neurobiology Drug development pharmaceutical
Citations 32
Key points The nonhallucinogenic LSD analogue (+)-JRT promotes cortical spinogenesis and produces therapeutic effects in behavioral assays relevant to depression and cognition without exacerbating psychosis-related signatures.

Abstract

Decreased dendritic spine density in the cortex is a key pathological feature of neuropsychiatric diseases including depression, addiction, and schizophrenia (SCZ). Psychedelics possess a remarkable ability to promote cortical neuron growth and increase spine density; however, these compounds are contraindicated for patients with SCZ or a family history of psychosis. Here, we report the molecular design and de novo total synthesis of (+)-JRT, a structural analogue of lysergic acid diethylamide (LSD) with lower hallucinogenic potential and potent neuroplasticity-promoting properties. In addition to promoting spinogenesis in the cortex, (+)-JRT produces therapeutic effects in behavioral assays relevant to depression and cognition without exacerbating behavioral and gene expression signatures relevant to psychosis. This work underscores the potential of nonhallucinogenic psychoplastogens for treating diseases where the use of psychedelics presents significant safety concerns.

Comparable studies

Other preclinical and animal studies on LSD, most cited first.

Study Year Design Participants
Transcriptome Fingerprints Distinguish Hallucinogenic and Nonhallucinogenic 5-Hydroxytryptamine 2A Receptor Agonist Effects in Mouse Somatosensory Cortex Human embryonic kidney 293 cells stably expressing 5-HT2ARs; wild-type and 5-HT2AR... 2003 Experimental study
Evidence for a central 5‐hydroxytryptamine receptor stimulation by lysergic acid diethylamide Rats 1968 Experimental study
Psychedelics, but Not Ketamine, Produce Persistent Antidepressant-like Effects in a Rodent Experimental System for the Study of Depression Rats 2020 Preclinical study
Lysergic acid diethylamide (LSD) promotes social behavior through mTORC1 in the excitatory neurotransmission Male mice 2021 Multidisciplinary experimental study with in vivo electrophysiology, optogenetics, behavioral paradigms, molecular biology, and conditional knockout mice
A non-hallucinogenic LSD analog with therapeutic potential for mood disorders. Mice and cultured rat cortical neurons 2023 Preclinical study

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