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Rising Star
Thought it would be good to post an updated post on this old topic, drawing from classic old and new literature:
From page 61 of "Ayahuasca Analogues" (1994) by Jonathan Ott:
hxxp://ibogaine.mindvox.com/articles/pharmahuasca-anahuasca-vinho-da-jurema/
In 1997 he wrote (from above link):
From "Articulations, On the Utilisation and Meanings of Psychedelics" (2015) by Julian Palmer:
From page 61 of "Ayahuasca Analogues" (1994) by Jonathan Ott:
His book is rare to find and retails for over two hundred dollars from book collectors, but read back when it was in print. I should also mention that back in the day, Ott knew very little about tetrahydroharmine or thh in caapi. Many people forget that it is the 2nd biggest alkaloid in caapi, and plays a huge role. I would suggest sticking with real caapi vs harmine only in dreams.On a 5 point potency scale,
1 = non-entheogenic stimulation
2 = entheogenic threshold
3 = mild trip
4 = moderately-strong trip
5 = technical knockout of the ego
Experiment 3 with Ayahuasquero in Equador: 50 psychotria viridis leaves per dose, thrice extracted with water and boiled down to 700ml with caapi. I received about 50ml. The potion was far from delectable and we were all give a piece of ginger to kill the taste. This time there was no question that the potion was powerfully entheogenic. Within a hour I experienced vivid visions and synaesthesia, with a pronounced auditory component. Very euphoric and quite powerful dmt effects lasted for some 2 hours, after which I slept easily and soundly.
Experiment 13 consisted of 188mg harmine hcl (160mg freebase) (2.0mg/kg) with 40mg dmt freebase (0.5mg/kg) mixed together & ingested as a single pharmahuasca capsule. Indeed, this evoked a proportionally stronger dmt effect with first signs evident only 20 minutes after ingesting and the peak attained at 1:30, maintaining a plateau until 2:40, with clearly diminishing effects at the 3 hour point, and no effects at all by the fourth hour. This was a 3 on a scale of 1 to 5, representing a "mild trip."
Experiment 20 consisted of 188mg harmine hcl (160mg freebase) (2.0mg/kg) with 50mg dmt freebase (0.63mg/kg) mixed together & ingested as a single gelatin pharmahuasca capsule. This was between a "3" and a "4" on a scale of 1 to 5. It was between a mild and moderately strong trip.
Experiment 21 consisted of 188mg harmine hcl (160mg freebase) (2.0mg/kg) with 60mg dmt freebase (0.75mg/kg) mixed together & ingested as a single gelatin pharmahuasca capsule. This represented a "4" on a scale of 1 to 5. It was a moderately-strong trip.
Pharmahuasca, Anahuasca and Vinho da Jurema
Pharmahuasca, Anahuasca and Vinho da Jurema
ibogaine.mindvox.com
In 1997 he wrote (from above link):
I have tested doses as high as 160 mg DMT [2.0 mg/kgl, experiencing progressively more intense psychotropic effects, but always with the same approximate pharmacodynamics, quite similar to what I have enjoyed with genuine Amazonian ayahuasca potions in Brasil, Ecuador and Perú:
– 45 minutes to an hour incubation period; the effects quickly building to a peak by 1: 15 and maintaining a plateau for 45 minutes to an hour; followed by about an hour of diminishing effects; the experience usually all but over around the 3 hour point.
In no case have I ever experienced nausea in pharmahuasca experiments, although I have weathered nausea and episodes of vomiting provoked by genuine ayahuasca in Amazonia.
In any case, I generally eat little or nothing on the day of ingestion.
During the experimental series, I always allowed roughly a minimum of a week to elapse between the individual experiments.
From "Articulations, On the Utilisation and Meanings of Psychedelics" (2015) by Julian Palmer:
A sample experiment from "Ayahuasca Analogues" page 58:Modern day researchers, spearheaded by people such as myself, have realized that Jonathan Ott's calculations fall short of what most explorers need for a truly visionary experience. Even with a strong harmine/Banisteriopsis caapi dosage, 30-60mg of dmt is not sufficient to produce significant visionary effects in most people. So if fact, a dosage of 30-40mg of dmt is where tryptamine-like effects just begin to occur for most people, and 10-25mg dmt is not really noticeable above the gentle psychoactive effects of the harmine.
Each person is different and for some rare individuals, 30-40mg may be about as much dmt as they wish to take--but most people need at least 60-80mg for sufficient psychoactive effects and even at this dosage, you generally cannot expect a full-blown visionary experience, even when using a strong dose of 4 grams of syrian rue or 100 grams of strong caapi vine. Also, it should be pointed out that going beyond 4 grams of syrian rue (around 200-280mg of harmaline) or 100 grams of strong caapi vine (150--250mg of harmine) can increase the negative effects of these beta-carbolines--which include a feeling of heaviness, pressure in the head, inability to walk properly, more purging and perhaps more of an emphasis on bodily processes.
An oral dosage of 100mg of dmt is where the visionary qualities really begin to occur, for most people say when they are taking 3 grams of syrian rue or 80 grams of strong vine, and in context, 40-60 grams of strong vine is enough to fully mao inhibit most people.
I would say to neophyte explorers to tread carefully, and to slowly increase your dmt dosage in increments: perhaps starting at 60mg, going to 100mg, then 150mg. Some people are going to find 100mg of dmt to be exceedingly strong, and it will perhaps give them an experience they did not feel ready for.
It came to my attention after an embarrassing number of years, that taking freebase crystal DMT orally was not as potent, colourful, or clear as taking the equivalent amount of DMT in a tea that was brewed from the plant. For many years, I couldn't see how there could be a difference, but after doing some comparisons, it was obvious that the tea was much better, and the experiences resulting from the crystalline extract were inferior.
You could take twice or even three times as much DMT crystal as the equivalent in brew, and the experience from the crystal would never be as bright or full as that from the tea. Why could this be?
With extracted dmt, with chemicals used it would appear that some dimensions and qualities of the tryptamine molecules are compromised. Also, there is the factor of isolating the alkaloids from the rest of the plant. For example, there are very few people who say that extracted pure mescaline from the cactus is as potent of full bodied compared to when they take the tea made from the cactus flesh.
When making a tea from the whole plant, you are extracting the essence of the plant intelligence from its very flesh, not just isolating the alkaloids. In the alchemic method "Spagyrics" developed by Paracelsus, often considered the father of modern medicine, the ashes of the plant are commonly burnt and then blended back into an alcohol-extracted tincture. Friends who have experimented with this procedure report that a Spagyric tincture of Ayahuasca is much more potent than a normal tea prepared from the same amount of Ayahuasca vine.