Rick Strassman | |
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Born | |
Nationality | American |
Education | |
Alma mater | Albert Einstein College of Medicine |
Known for | DMT: The Spirit Molecule |
Scientific career | |
Fields |
Rick Strassman is an American clinical associate professor of psychiatry at the University of New Mexico School of Medicine. He has held a fellowship in clinical psychopharmacology research at the University of California San Diego and was Professor of Psychiatry for eleven years at the University of New Mexico. [1] After 20 years of intermission, Strassman was the first person in the United States to undertake human research with psychedelic, hallucinogenic, or entheogenic substances with his research on N,N-dimethyltryptamine, also known as DMT. He is also the author of DMT: The Spirit Molecule , which summarizes his academic research into DMT and other experimental studies of it, and includes his own reflections and conclusions based on this research.
Strassman was born in Los Angeles, California, on February 8, 1952, to a Conservative Jewish family. [1] [2] [3] He graduated from Ulysses S. Grant High School in Van Nuys in 1969. He studied zoology at Pomona College in Claremont for two years before transferring to Stanford University, where he graduated with departmental honors in biological sciences in 1973. He continued laboratory research at Stanford before attending Albert Einstein College of Medicine of Yeshiva University in New York, where he graduated with an M.D. with departmental honors, specializing in psychiatry. He began his general psychiatry residency at the University of California, Davis, where he received the Sandoz Award for outstanding graduating resident in 1981. From 1982 to 1983, he trained as a fellow in clinical psychopharmacology research at the University of California, San Diego. He then served on the clinical faculty in the psychiatry department at UC Davis Medical Center, before becoming an assistant professor in the psychiatry department at the University of New Mexico School of Medicine in Albuquerque in 1984. At UNM, Strassman researched the function of the pineal gland. His research group documented the first known role of melatonin in humans. He became clinical associate professor of psychiatry in 1991. He has published over 40 peer-reviewed scientific articles on psychopharmacology, neurology, psychiatry, neuroendocrinology and neuropsychopharmacology.
As an undergraduate at Stanford, working in the developmental biology laboratory of Norman K. Wessells, Strassman developed a new model for growing embryonic avian dorsal root ganglion neurons, suspended in a semi-solid agar matrix, thus allowing three-dimensional assessment of growing patterns. [4] Using this model, he discovered a nonrandom pattern of growth of the leading edge of these cells. [5]
Strassman's interest in the human biology of altered states of consciousness led him to study the pineal gland hormone melatonin in the 1980s, at which time there were suggestive data regarding its psychoactive effects. This research took place at the University of New Mexico's School of Medicine in Albuquerque, where he became a tenured associate professor of psychiatry. He first developed a model of all-night suppression of melatonin by all-night bright light. He then established a successful exogenous melatonin infusion protocol that replicated endogenous melatonin levels in the bright-light conditions. [6] All-night bright-light suppression of melatonin suppressed the normal trough of body temperature seen between 3-4 a.m., the time of maximum melatonin levels. Exogenous infusion of melatonin, replicating endogenous levels in the bright-light condition (in which endogenous melatonin was suppressed) reestablished the normal core body temperature trough. [7] But melatonin's psychoactive effects were only sedative, leading him to focus on DMT in his future work.
From 1990 to 1995, Strassman led a government-funded clinical research team at the University of New Mexico studying the effects of N,N-dimethyltryptamine, also known as DMT, on human subjects in experimental conditions. The research continued from his work on melatonin.
Strassman's studies between 1990 and 1995 aimed to experimentally investigate DMT's effects. DMT is a powerful psychedelic drug found in hundreds of plants and every mammal that has been studied.[ citation needed ] It is made primarily in mammalian brains [8] as well as lung tissue and is related to serotonin and melatonin.
As a result of his research, Strassman came to call DMT the "spirit molecule" because its effects include many features of religious experience, such as visions, voices, disembodied consciousness, powerful emotions, novel insights, and feelings of overwhelming significance. During the project's five years, he administered approximately 400 doses of DMT to nearly 60 human volunteers. [9] [10] Strassman was the first in 20 years to legally administer psychedelics to people in the United States, and his research has widely been regarded as kicking off the "psychedelic renaissance", in which many psychedelic compounds have begun to be scientifically studied for the first time since the early 1970s. [11] [12]
Strassman characterized DMT's biological and psychological effects in his first set of dose-response studies, effects consistent with activation of central and/or peripheral serotonin receptors. [13] His team published a companion article describing the psychological effects and preliminary results of a new rating scale, the Hallucinogen Rating Scale, or HRS. [14] Researchers have widely accepted the HRS as a sensitive and specific measure of the psychological effects of a wide variety of psychoactive substances, with over 45 articles documenting its use as of mid-2015.[ citation needed ] A follow-up study demonstrated lack of tolerance of the psychological effects of repeated closely spaced doses of DMT, making it unique among classical psychedelics. [15]
More than half of Strassman's volunteers reported profound encounters/interaction with nonhuman beings while in a dissociated state. Strassman has conjectured that when a person is approaching death or possibly when in a dream state, the body releases a relatively large amount of DMT, mediating some of the imagery survivors of near-death experiences report. But there are no data correlating endogenous DMT activity to non-drug-related altered states of consciousness. [16] He also has theorized that the pineal gland may form DMT under certain conditions. In 2013 researchers first reported DMT in the pineal gland microdialysate of rodents. [17]
Strassman has detailed his research in his book DMT: The Spirit Molecule, and co-produced a 2010 documentary film of the same name based on this book. [18] He has also conducted similar research on psilocybin, a psychedelic alkaloid found in hallucinogenic mushrooms. In unpublished studies, he administered doses of up to 1.1 mg/kg, nearly three times the doses considered "psychedelic" in contemporary clinical research with this compound. [19] [ citation needed ]
Inspired by visions he had when he took LSD in the early 1970s, Strassman began studying Buddhism as a young man. He trained for 20 years in Zen Buddhism, received lay ordination in a Western Buddhist order, and led a meditation group of the order. But his work with DMT led him to feel Buddhist models may not be the most suitable way for us to explain and integrate the spiritual dimensions of the DMT experience:
I worked through various models' methods of understanding the DMT volunteers' experiences, and found them wanting. The Buddhist psychological model didn't comport with the data—the "more real than real" element of volunteers' experiences (Buddhism proposes these phenomena are all generated by the mind, rather than "real" observations of external reality); [this] did nothing to suggest a satisfactory evolutionary explanation for the presence of DMT in the human body. [2]
Strassman suggests that DMT experiences may most closely resemble those found in the Hebrew Bible's model of prophecy:
The Hebrew Bible's model of prophecy is appealing because it comports well with the reports of the DMT volunteers. One's sense of self is maintained, there is an external free-standing independent-of-the-observer spiritual world. One relates to the content of the experience, rather than being dissolved into it. [2]
Some of Strassman's experimental participants say that other entities can resemble creatures more like insects and aliens than anything in the Bible. [20] As a result, Strassman wrote that these experiences of his experimental participants "also left me feeling confused and concerned about where the spirit molecule was leading us. It was at this point that I began to wonder if I was getting in over my head with this research." [21] He has also hypothesized that endogenous DMT experiences could be the cause of alien abduction experiences. [21]
N,N-Dimethyltryptamine is a substituted tryptamine that occurs in many plants and animals, including humans, and which is both a derivative and a structural analog of tryptamine. DMT is used as a psychedelic drug and prepared by various cultures for ritual purposes as an entheogen.
Psilocybin, also known as 4-phosphoryloxy-N,N-dimethyltryptamine (4-PO-DMT), and formerly sold under the brand name Indocybin, is a naturally occurring psychedelic prodrug compound produced by more than 200 species of fungi. Psilocybin is itself biologically inactive but is quickly converted by the body to psilocin, which has mind-altering effects similar, in some aspects, to those of other classical psychedelics. Effects include euphoria, visual and mental hallucinations, changes in perception, a distorted sense of time, and perceived spiritual experiences. It can also cause adverse reactions such as nausea and panic attacks.
Psychopharmacology is the scientific study of the effects drugs have on mood, sensation, thinking, behavior, judgment and evaluation, and memory. It is distinguished from neuropsychopharmacology, which emphasizes the correlation between drug-induced changes in the functioning of cells in the nervous system and changes in consciousness and behavior.
Psychedelics are a subclass of hallucinogenic drugs whose primary effect is to trigger non-ordinary mental states and a perceived "expansion of consciousness". Also referred to as classic hallucinogens or serotonergic hallucinogens, the term psychedelic is sometimes used more broadly to include various types of hallucinogens, such as those which are atypical or adjacent to psychedelia like salvia and MDMA, respectively.
Tryptophan (symbol Trp or W) is an α-amino acid that is used in the biosynthesis of proteins. Tryptophan contains an α-amino group, an α-carboxylic acid group, and a side chain indole, making it a polar molecule with a non-polar aromatic beta carbon substituent. Tryptophan is also a precursor to the neurotransmitter serotonin, the hormone melatonin, and vitamin B3 (niacin). It is encoded by the codon UGG.
The third eye is an invisible eye, usually depicted as located on the forehead, supposed to provide perception beyond ordinary sight. In Hinduism, the third eye refers to the ajna chakra. In both Hinduism and Buddhism, the third eye is said to be located around the middle of the forehead, slightly above the junction of the eyebrows, representing the enlightenment one achieves through meditation.
The pineal gland is a small endocrine gland in the brain of most vertebrates. It produces melatonin, a serotonin-derived hormone, which modulates sleep patterns following the diurnal cycles. The shape of the gland resembles a pine cone, which gives it its name. The pineal gland is located in the epithalamus, near the center of the brain, between the two hemispheres, tucked in a groove where the two halves of the thalamus join. It is one of the neuroendocrine secretory circumventricular organs in which capillaries are mostly permeable to solutes in the blood.
Melatonin, an indoleamine, is a natural compound produced by various organisms, including bacteria and eukaryotes. Its discovery in 1958 by Aaron B. Lerner and colleagues stemmed from the isolation of a substance from the pineal gland of cows that could induce skin lightening in common frogs. This compound was later identified as a hormone secreted in the brain during the night, playing a crucial role in regulating the sleep-wake cycle, also known as the circadian rhythm, in vertebrates.
Tryptamine is an indolamine metabolite of the essential amino acid, tryptophan. The chemical structure is defined by an indole—a fused benzene and pyrrole ring, and a 2-aminoethyl group at the second carbon. The structure of tryptamine is a shared feature of certain aminergic neuromodulators including melatonin, serotonin, bufotenin and psychedelic derivatives such as dimethyltryptamine (DMT), psilocybin, psilocin and others.
5-MeO-DMT (5-methoxy-N,N-dimethyltryptamine), also known as O-methylbufotenin or mebufotenin, is a psychedelic of the tryptamine family. It is found in a wide variety of plant species, and also is secreted by the glands of at least one toad species, the Colorado River toad. Like its close relatives dimethyltryptamine (DMT) and bufotenin (5-HO-DMT), it has been used as an entheogen in South America. Slang terms include Five-methoxy, the power, bufo, and toad venom.
Psychedelic therapy refers to the proposed use of psychedelic drugs, such as psilocybin, ayahuasca, LSD, psilocin, mescaline (peyote), DMT, 5-MeO-DMT,Ibogaine,MDMA, to treat mental disorders. As of 2021, psychedelic drugs are controlled substances in most countries and psychedelic therapy is not legally available outside clinical trials, with some exceptions.
Psilocin, also known as 4-hydroxy-N,N-dimethyltryptamine (4-OH-DMT), is a substituted tryptamine alkaloid and a serotonergic psychedelic. It is present in most psychedelic mushrooms together with its phosphorylated counterpart psilocybin. Psilocin is a Schedule I drug under the Convention on Psychotropic Substances. Acting on the serotonin 5-HT2A receptors, psilocin's psychedelic effects are directly correlated with the drug's occupancy at these receptor sites. The subjective mind-altering effects of psilocin are highly variable and are said to resemble those of lysergic acid diethylamide (LSD) and N,N-dimethyltryptamine (DMT).
Bufotenin, also known as dimethylserotonin or as 5-hydroxy-N,N-dimethyltryptamine (5-HO-DMT), is a tryptamine derivative, more specifically, a dimethyltryptamine (DMT) analogue, related to the neurotransmitter serotonin. It is an alkaloid found in some species of mushrooms, plants and toads, especially the skin. It is also found naturally in the human body in small amounts.
Psilacetin, also known as O-acetylpsilocin or as 4-acetoxy-N,N-dimethyltryptamine, is a semi-synthetic serotonergic psychedelic drug that has been suggested by David Nichols to be a potentially useful alternative to psilocybin for pharmacological studies, as they are both believed to be prodrugs of psilocin. However, some users report that O-acetylpsilocin's subjective effects differ from those of psilocybin and psilocin. Additionally, some users prefer 4-AcO-DMT to natural psilocybin mushrooms due to feeling fewer adverse side effects such as nausea and heavy body load, which are more frequently reported in experiences involving natural mushrooms. It is the acetylated form of the psilocybin mushroom alkaloid psilocin and is a lower homolog of 4-AcO-MET, 4-AcO-DET, 4-AcO-MiPT and 4-AcO-DiPT.
Stephen István Szára was a Hungarian-American chemist and psychiatrist who made major contributions in the field of pharmacology.
A chronobiotic is an agent that can cause phase adjustment of the circadian rhythm. That is, it is a substance capable of therapeutically entraining or re-entraining long-term desynchronized or short-term dissociated circadian rhythms in mammals, or prophylactically preventing their disruption following an environmental insult such as is caused by rapid travel across several time zones. The most widely recognized chronobiotic is the hormone melatonin, secreted at night in both diurnal and nocturnal species.
Psychoplastogens are a group of small molecule drugs that produce rapid and sustained effects on neuronal structure and function, intended to manifest therapeutic benefit after a single administration. Several existing psychoplastogens have been identified and their therapeutic effects demonstrated; several are presently at various stages of development as medications including ketamine, MDMA, scopolamine, and the serotonergic psychedelics, including LSD, psilocin, DMT, and 5-MeO-DMT. Compounds of this sort are being explored as therapeutics for a variety of brain disorders including depression, addiction, and PTSD. The ability to rapidly promote neuronal changes via mechanisms of neuroplasticity was recently discovered as the common therapeutic activity and mechanism of action.
O-Acetylbufotenine, or bufotenine O-acetate, also known as 5-acetoxy-N,N-dimethyltryptamine (5-AcO-DMT) or O-acetyl-N,N-dimethylserotonin, is a synthetic tryptamine derivative and putative serotonergic psychedelic. It is the O-acetylated analogue of the naturally occurring peripherally selective serotonergic tryptamine bufotenine and is thought to act as a centrally penetrant prodrug of bufotenine.
A neurotransmitter prodrug, or neurotransmitter precursor, is a drug that acts as a prodrug of a neurotransmitter. A variety of neurotransmitter prodrugs have been developed and used in medicine. They can be useful when the neurotransmitter itself is not suitable for use as a pharmaceutical drug owing to unfavorable pharmacokinetic or physicochemical properties, for instance high susceptibility to metabolism, short elimination half-life, or lack of blood–brain barrier permeability. Besides their use in medicine, neurotransmitter prodrugs have also been used as recreational drugs in some cases.
A trip killer, or hallucinogen antidote, is a drug that aborts or reduces the effects of a hallucinogenic drug experience. As there are different types of hallucinogens that work in different ways, there are different types of trip killers. They can completely block or reduce the effects of hallucinogens or they can simply provide anxiety relief and sedation. Examples of trip killers, in the case of serotonergic psychedelics, include serotonin receptor antagonists, like antipsychotics and certain antidepressants, and benzodiazepines. Trip killers are sometimes used by recreational psychedelic users as a form of harm reduction to manage so-called bad trips, for instance difficult experiences with prominent anxiety. They can also be used clinically to manage effects of hallucinogens, like anxiety and psychomotor agitation, for instance in the emergency department.