Skip to content

Repeated microdoses of LSD do not alter anxiety or boldness in zebrafish.

Ethan V Hagen, Melike Schalomon, Yanbo Zhang, Trevor J Hamilton

Scientific Reports February 22, 2024 DOI: 10.1038/s41598-024-54676-8 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Zebrafish (Danio rerio)
Intervention Lysergic acid diethylamide (LSD)
Dose 1.5 µg/L, 15 µg/L, 150 µg/L
Duration Acute and repeated 10-day exposure with seven-day withdrawal
Topics Microdosing Anxiety LSD
Keywords Psychedelics Behavioral neuroscience Animal research Pharmacology
Citations 11
Key findings Acute LSD exposure at 1.5, 15, and 150 µg/L reduced high mobility and velocity in zebrafish, but repeated 10-day treatment and withdrawal produced no significant behavioral differences from controls.

Abstract

The therapeutic use of lysergic acid diethylamide (LSD) has resurfaced in the last decade, prompting further scientific investigation into its effectiveness in many animal models. Zebrafish (Danio rerio) are a popular model organism in medical sciences and are used to examine the repeated administration of pharmacological compounds. Previous zebrafish research found acute LSD altered behaviour and cortisol levels at high (250 µg/L) but not low (5-100 µg/L) levels. In this study, we used a motion tracking system to record and analyze the movement patterns of zebrafish after acute and repeated 10-day LSD exposure (1.5 µg/L, 15 µg/L, 150 µg/L) and after seven days of withdrawal. The open-field and novel object approach tests were used to examine anxiety-like behaviour, boldness, and locomotion. In the acute experiments we observed a significant decrease in high mobility with 1.5 µg/L, 15 µg/L, and 150 µg/L of LSD compared to the control and a decrease in velocity with 1.5 and 15 µg/L. In repeated experiments, there were no significant differences in the levels of anxiety, boldness, or locomotion between all LSD groups and controls immediately after 10-day treatment or after withdrawal.

Comparable studies

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

Study Year Design Participants
Assessing the Potential Cardiovascular Risk of Microdosing the Psychedelic LSD in Mice Mice 2025 Animal study
A New Use for an Old Compound: Microdosing LSD to Reduce Fibromyalgia Symptoms Male and female mice with fibromyalgia-like symptoms 2026 Preclinical animal study

Explore topics

By condition and practice