Defined radio wave frequencies attenuate the head-twitch response in mice elicited by (±)-2,5-dimethoxy-4-iodoamphetamine.
Mary O Vu, B Michael Butters, Clinton E Canal, Xavier A Figueroa
Electromagnetic biology and medicine October 1, 2024 DOI: 10.1080/15368378.2024.2418552 via PubMed
Summary
AI-generated from the abstractA newly developed electromagnetic signal derived from the serotonin 2 receptor agonist DOI, converted into a playable WAV file, significantly reduced the head-twitch response in mice—a behavioral proxy for psychedelic effects—when administered alongside DOI. The effect was specific: a scrambled version of the signal did not alter the response. The findings suggest that defined electromagnetic signals could potentially modulate the psychoactive effects of serotonergic psychedelics, offering a new strategy to mitigate the heightened anxiety associated with psychedelic therapy. The authors discuss possible mechanisms and connections to prior work showing electromagnetic signals' efficacy in treating pain and cancer.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Mice |
| Keywords | 5-ht2a Electromagnetic Psychedelic Signal radio frequency Therapeutic |
| Citations | 1 |
| Key finding | An electromagnetic signal derived from the 5-HT2R agonist DOI significantly attenuated the DOI-elicited head-twitch response in mice, indicating potential modulation of psychedelic effects. |
Abstract
Results from clinical trials show that serotonergic psychedelics have efficacy in treating psychiatric disorders, where currently approved pharmacotherapies are inadequate. Developing psychedelic medicines, however, comes with unique challenges, such as tempering heightened anxiety associated with the psychedelic experience. We conceived a new strategy to potentially mitigate psychedelic effects with defined electromagnetic signals (ES). We recorded the electromagnetic fields emitted by the serotonin 2 receptor (5-HT2R) agonist (±)-2,5-dimethoxy-4-iodoamphetamine (DOI) and converted them to a playable WAV file. We then exposed the DOI WAV ES to mice to assess its effects on the DOI-elicited, 5-HT2AR dependent head-twitch response (HTR). The DOI WAV signal significantly attenuated the HTR in mice elicited by 0.1 and 0.3 mg/kg subcutaneous DOI (p < 0.05 and p < 0.01, respectively). A scrambled WAV signal did not affect the DOI-elicited HTR, suggesting specificity of the DOI WAV signal. These results provide evidence that defined ES could modulate the psychoactive effects of serotonergic psychedelics. We discuss putative explanations for the distinct effects of the DOI WAV signal in the context of previous studies that demonstrate ES's efficacy for treating other conditions, including pain and cancer.