The effect of psychedelic microdosing on animal behavior: A review with recommendations for the field
Rotem Petranker, Benjamin Tsang, Omer A. Syed
Neuroscience & Biobehavioral Reviews May 9, 2025 DOI: 10.1016/j.neubiorev.2025.106204 via OpenAlex
Summary
AI-generated from the abstractA narrative review of 12 studies on microdosing LSD, psilocybin, or DMT in rats, mice, and zebrafish found that microdosing caused little change in behaviors related to anxiety- and depressive-like states. The practice was well-tolerated across species, but specific safety concerns remain unaddressed. The authors recommend future research prioritize replication of existing findings, standardize methodologies, explore mescaline microdosing, examine sex-dependent effects, and extend studies to models of obsessive-compulsive disorder and post-traumatic stress disorder.
Study at a glance
| Characteristics | Narrative review Peer reviewed |
|---|---|
| Population | Rats, mice, and zebrafish |
| Interventions | LSD psilocybin DMT |
| Keywords | Animal testing Psychology Pharmacology |
| Citations | 3 |
| Key finding | Microdosing caused little change in anxiety- and depressive-like behaviors across three animal species. |
Abstract
Microdosing, the repeated use of psychedelic substances at low doses, is growing in popularity among recreational consumers. While this practice is associated with many benefits to mood, well-being and health, research in this area is in its early stages and predominantly centered on human applications. In this narrative review, we synthesize the findings from studies investigating the effects of microdosing on the behaviors of three animal species: rats, mice, and zebrafish. A total of 12 studies were identified that implemented a microdosing regimen of LSD, psilocybin, or DMT in these animal models. Overall, microdosing caused little changes in behaviors associated with anxiety- and depressive-like states. Moreover, while microdosing was well-tolerated across species, further research is needed to capture specific safety concerns. Finally, we critically appraise the studies included in this review based on their methodologies and discuss further avenues of research to advance the preclinical literature on psychedelic microdosing. Specifically, we recommend that future research prioritize the replication of existing findings to inform the development of robust study designs and dosing protocols, as well as establish standardized methodologies to enable effective comparisons across different animal models. Furthermore, future investigations should explore the therapeutic potential of mescaline microdosing, examine sex-dependent effects, and extend research to additional models of psychiatric conditions, including those related to obsessive-compulsive disorder and post-traumatic stress disorder.