New Study: This Plant-Based Beverage Could Be the Key to Treating Trauma-Related Disorders

Ayahuasca Brew on Drum
A review consolidates evidence on ayahuasca’s effects on fear, anxiety, and emotional processing, emphasizing its therapeutic potential for PTSD and anxiety disorders while calling for more clinical trials.
A new analysis summarizes a decade of research on the effects of a psychedelic brew on anxiety and trauma responses.

With the rising interest in psychedelic medicine, researchers have compiled a decade of evidence to explore how ayahuasca impacts fear and anxiety in the brain. A recent review in Psychedelics brings together insights from molecular studies, animal experiments, and human clinical trials, providing a comprehensive understanding of how this traditional Amazonian brew influences emotional processing and memory systems.

The analysis, led by Lorena Terene Lopes Guerra and colleagues at the University of São Paulo, examines the growing body of evidence about ayahuasca’s complex interactions with brain systems involved in emotional processing and memory, with particular focus on its effects through two distinct serotonin receptor systems.

Insights from Serotonin Receptors

“Understanding how signals coordinate the processes in cells, tissues, and organs is fundamental to grasping ayahuasca’s potential therapeutic applications,” explains Dr. Rafael Guimarães dos Santos, one of the review’s authors. “By examining evidence across multiple levels – from receptor interactions to clinical outcomes – we can better understand how this traditional medicine might help treat anxiety and trauma-related disorders.”

Plasticity Promoting Mechanisms Triggered by Dimethyltryptamine and β Carboline
Plasticity-promoting mechanisms triggered by dimethyltryptamine (DMT) and β-carboline (BC). (A) DMT and BC-induced increase in cortical plasticity are linked to enhanced BDNF levels, although this might result from the activation of different receptors. (B) Increased hippocampal plasticity and neurogenesis induced by DMT and BC rely on different molecular pathways. 5HT2A: serotonergic receptor 2A subtype; BC: β-carboline; BDNF: brain-derived neurotrophic factor;DMT: N,N-dimethyltryptamine; SIGMA1: sigma receptor subtype 1. Credit: Rafael Guimarães dos Santos
The review synthesizes evidence showing that ayahuasca’s effects involve a delicate balance between two serotonin receptor types: 5-HT2A and 5-HT1A. This dual action appears crucial for understanding both the immediate effects of ayahuasca and its potential long-term therapeutic benefits.

Key Findings on Emotional Processing and Memory

Key findings from the reviewed literature include:

  • Ayahuasca’s main component, DMT, acts primarily through 5-HT2A receptors to influence emotional processing
  • The brew’s β-carboline compounds may work through different mechanisms to affect memory and anxiety
  • Clinical studies suggest specific effects on fear extinction and emotional processing
  • Brain imaging studies show ayahuasca modulates activity in regions crucial for emotional regulation

The synthesis of available evidence raises important questions about ayahuasca’s therapeutic potential. Can the timing of ayahuasca administration be optimized for treating specific conditions? Might different preparations of ayahuasca be more effective for different therapeutic purposes? How do individual differences in receptor systems affect treatment outcomes?

Current evidence reviewed suggests ayahuasca might be particularly promising for treating PTSD and anxiety disorders. However, Dr. dos Santos emphasizes the need for more controlled clinical trials: “While the preclinical and observational evidence is encouraging, we need more rigorous clinical studies to understand the optimal therapeutic applications.”

The review also examines safety considerations and the importance of controlled settings for therapeutic use, noting that ayahuasca’s complex nature requires careful consideration of individual patient factors.

Reference: “Effects of ayahuasca on fear and anxiety: cross-talk between 5HT1A and 5HT2A receptors” by Lorena Terene Lopes Guerra, Rafael Guimarães dos Santos and Jaime Eduardo Cecilio Hallak, 10 December 2024, Psychedelics.
DOI: 10.61373/pp024i.0037; (credit: https://scitechdaily.com/)

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