Arc wrote:Maksutov, you were too quick on the keyboard for me. I truncated the original post above because the chemical structure graphics did not display properly. Might try again later. The structure that did display properly is DMT.Maksutov wrote:https://en.wikipedia.org/wiki/Marsh_Chapel_Experiment
The Marsh Chapel Experiment, also called the "Good Friday Experiment", was a 1962 experiment conducted on Good Friday at Boston University's Marsh Chapel. Walter N. Pahnke, a graduate student in theology at Harvard Divinity School, designed the experiment under the supervision of Timothy Leary, Richard Alpert, and the Harvard Psilocybin Project.[1] Pahnke's experiment investigated whether psilocybin (the active principle in psilocybin mushrooms) would act as a reliable entheogen in religiously predisposed subjects.[2]
Upon ingestion, psilocybin is rapidly converted to psilocin, which is the hallucinogenic agent. Psilocin is 4-hydroxy DMT. That is, DMT with a hydoxy group added in the 4 position on the benzene ring.
LSD, DMT, psilocybin (psilocin), and 5-methoxy DMT are tryptophan based hallucinogens that exert their activity via a group of receptors for the neurotransmitter serotonin (5-hydroxy tryptamine).
Several popular pharmaceuticals for treating depression, anxiety and mood disorders, including Paxil, Prozac and Zoloft, are selective serotonin re-uptake inhibitors (SSRIs). These act to increase the amount of available serotonin in the brain. They can substantially improve mood and affect.
As Gadianton and DrW indicated, it's all down to the "blind forces of atoms".
I find it difficult to fit the "soul" into a scientific discussion.
