Psychedelic drug ayahuasca could treat PTSD, early studies hint. But exactly how it works isn't clear.
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Emerging scientific investigations indicate that the psychedelic beverage ayahuasca might provide substantial relief for individuals suffering from post-traumatic stress disorder (PTSD). Despite these promising preliminary findings, the specific biological mechanisms by which the substance functions remain largely unclear to the broader medical community. The profound personal journey of Kegan Gill, a former U.S. Navy fighter pilot known by the callsign "Smurf," offers a stark illustration of the devastating severity of PTSD and the urgent necessity for effective therapeutic interventions. In 2014, while piloting an F/A-18 Super Hornet, Gill encountered a catastrophic engine failure. The aircraft plunged into a steep dive, accelerating to speeds of 695 miles per hour, or 1,118 kilometers per hour. Gill ejected from the jet mere moments before it crashed into the ground. Although he survived the traumatic event, the physical toll was immense, including broken limbs, a shattered neck, and a severe brain injury.
Medical professionals eventually diagnosed Gill with delayed-onset PTSD, a condition that effectively ended his military aviation career. He described the impact of the disorder as hitting his career "like a warhead." As his professional identity crumbled, Gill lost his sense of purpose, feeling an overwhelming wave of shame for having disappointed the people who had supported him. The psychological stress became so unmanageable that he contemplated suicide. Despite receiving various medications, his life spiraled out of control. He spent forty consecutive days and nights in a Veterans Affairs inpatient psychiatric facility. Upon his discharge, Gill described his mental state as that of "a broken shell of a man in a drug-induced stupor."
However, Gill's narrative did not conclude with despair. He connected with the Heroic Hearts Project (HHP), a nonprofit organization that facilitates supervised psychedelic therapy retreats for veterans and their spouses in international locations. In Peru, Gill underwent treatment involving ayahuasca, a psychoactive beverage brewed from specific Amazonian plants. He attributes this transformative experience to initiating his path toward healing. The HHP has successfully hosted more than 1,100 veterans and spouse partners through these retreat programs. These gatherings aim to reduce or completely eliminate PTSD symptoms while significantly improving the overall quality of life for participants. Most retreats utilize ayahuasca, a drink with deep roots in the traditional ceremonies of Indigenous Amazonian communities. Because ayahuasca is classified as a Schedule I controlled substance in the United States, these ceremonies are legally conducted in countries where such practices are permitted.
While numerous individuals have shared anecdotal accounts of the benefits derived from ayahuasca, rigorous scientific research on its efficacy has not yet matched the extensive studies conducted on other psychedelics, such as MDMA and psilocybin. Only a limited number of small-scale studies have specifically investigated ayahuasca as a treatment for PTSD. Notably, none of these studies were placebo-controlled, randomized clinical trials. Such rigorous trials are considered the gold standard for definitively proving that a specific drug is effective. Without this level of evidence, it remains difficult to ascertain whether ayahuasca actually reduces PTSD symptoms or if the improvements are attributed to other variables, such as concurrent therapy or the supportive environment of the retreat itself.
Complicating the scientific inquiry further is the chemical composition of the ayahuasca brew. This plant-based mixture contains two primary components: the potent psychoactive chemical DMT (N,N-Dimethyltryptamine) and beta-carbolines. The concentration of these ingredients fluctuates significantly between different batches of the brew. This inconsistency makes it extremely challenging to create a standardized, repeatable dose required for strict clinical trials. In contrast, MDMA and psilocybin are single, distinct molecules. They can be synthesized in laboratories and packaged as pure, consistent pills or capsules, making them far easier to utilize in a controlled research setting. Furthermore, pharmaceutical companies face substantial obstacles when attempting to secure patents on ayahuasca, a natural plant concoction. This lack of patent protection reduces the financial incentive for the massive private investment necessary to fund large-scale clinical trials.
"It is probably never going to be a treatment in the traditional sense in the United States because it is a plant concoction," explained Gregory Fonzo, a clinical psychologist and co-director of the Charmaine and Gordon McGill Center for Psychedelic Research and Therapy at the University of Texas at Austin's Dell Medical School.
Despite these formidable challenges, some researchers are actively working to quantify the drug's impact on PTSD symptoms. The research division of the HHP designed and conducted an observational study that tracked 58 veterans between the years 2021 and 2024. During this period, forty-five veterans attended an ayahuasca retreat, while thirteen attended a psilocybin retreat. Scientists meticulously tracked changes in the participants' mental health before and after their psychedelic experiences. They discovered that participants in both groups demonstrated an average 29% reduction in depression symptoms and a 26% reduction in PTSD symptoms. Participants also reported notable improvements in anxiety, sleep quality, emotional well-being, and overall quality of life.
"We only took veterans who met criteria for having PTSD, and more than 80% of them no longer met that criteria anymore," stated neuroscientist Grace Blest-Hopley, the director of research for the HHP. To investigate these findings further, Fonzo is collaborating with the HHP to lead a new study. This study will examine the brain responses of combat veterans with PTSD and analyze how these neural patterns change following ayahuasca treatment.
The researchers in Texas are collecting brain imaging data, clinical information, blood measurements, and electroencephalographic (EEG) recordings from veterans before and after they attend an ayahuasca retreat. The EEG data offers a method to identify objective, biological markers associated with PTSD. The scientists aim to recruit 40 participants for this study, which Fonzo estimates will likely require another year to complete.
In the HHP observational study, both the ayahuasca and psilocybin groups exhibited a reduction in symptoms following treatment. However, ayahuasca appeared to be slightly more effective in certain metrics. The researchers cautioned that the study was not specifically designed to directly compare the efficacy of the two treatments. Fonzo hypothesizes that both compounds operate through a two-phase process. In the first phase, the psychedelics disrupt the rigid psychological patterns that individuals are often stuck in, effectively "shaking up the snow globe." The second phase is characterized by an enhancement of neuroplasticity. Neuroplasticity refers to the brain's remarkable ability to forge new connections between neurons. This second phase can persist for several weeks.
"That creates an opportunity for people to glean and consolidate insights and reshape their brain in a way that is more conducive to mental health," Fonzo explained. To achieve this effect, both psilocybin and DMT, the primary active component of ayahuasca, activate the serotonin 2A receptor in the brain. However, the ayahuasca brew also contains beta-carbolines. These compounds boost the levels of key mood-regulating chemicals, such as serotonin and norepinephrine, in both the body and the brain. Additionally, the DMT in ayahuasca targets unique receptors, such as the "sigma-1 receptor," leading to a broader and more complex effect on brain chemistry than is observed with psilocybin alone. Nevertheless, research on ayahuasca remains in its early stages, making it difficult to isolate how other aspects of the retreat experience influence the drug's effectiveness.
New research suggests that psychedelics may rewire the brain to treat PTSD, and scientists are only beginning to understand the intricate process. Studies indicate that MDMA and psilocybin may restore neural flexibility in people with PTSD, helping the brain unlearn fear responses and relearn safety. For instance, HHP retreats place a strong emphasis on processing and integrating the psychedelic experience. This integration process often includes therapy, community support, and necessary lifestyle changes. "If you just do the medicine and then come out and carry on as normal and don't make some changes, our brains will just go back to how they were before," Blest-Hopley theorized.
Gill agrees with this assessment. He feels that ayahuasca shattered the darkness he had been living in and fundamentally changed him at his core. However, he began to heal after that experience by focusing on sleep, nutrition, exercise, reconnection with nature and community, and meditation. Now an ultra-endurance athlete, motivational speaker, and coach who has authored a book about his experiences, Gill seeks to offer inspiration to anyone facing seemingly insurmountable challenges. "I was able to regrow myself from within," Gill said. "Now, I get to be the father, husband, son, and friend that I was always meant to be."
The journey of the Heroic Hearts Project and the research led by institutions like the University of Texas underscores a critical shift in how the medical community approaches traumatic stress. While ayahuasca remains a complex subject due to legal restrictions and chemical variability, the personal testimonies and emerging data provide a compelling argument for further investigation. The combination of ancient healing traditions with modern neuroscientific research offers a hopeful outlook for veterans and others struggling with the invisible wounds of war. As the field continues to evolve, the distinction between anecdotal evidence and clinical proof will become increasingly important, ensuring that treatments are both safe and effective for those in need.