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On the horizon.. THH + DMT

Migrated topic.
WOOPS.. accidentally made a double post. Here was my last post:

Yeah, that is a good idea. SWIM has some passionflower, but that's it. He's read that several species of passion flower contain harmala alkaloids. Can anyone here confirm that? Could passion flower sufice (with 100mg of oral THH) in activating oral DMT?

From what I've been able to find; the harmine and harmaline content is extremely low in passion flower and would require way too high of a dose. I'm assuming this is probably true, but does anyone else know?
 
Yes, passionflower will work for sure, but the dose required is something like 40 timees that used for peganum harmala.

Look at this quote from Gracie and Zarkov

Three Beta-Carboline Containing Plants As Potentiators of Synthetic DMT and Other Indole Psychedelics

a technical note from the underground by Gracie and Zarkov

WARNING: This paper is aimed at the serious student and/or researcher of psychedelic substances. Unlike many of our more popularly oriented articles and papers we do not intend it for our recreationally inclined friends on the psychedelic underground. Given the diets and drug habits of most contemporary "heads", the use of MAO inhibitors could easily result in serious physical complications (LIKE DEATH). Additionally, these states are so intense that unless you are crazy enough to regard 50mg of DMT or 7.5 grams of potent stropharia mushrooms as the beginning of a good time, these mixes are definitely NOT FOR YOU.

[60Ron's note: it has since been found that the harmala alkaloids are RIMAs which do not require special diets. RIMAs area a subset of monoamine oxidase inhibitors (MAOIs) that inhibit only isoenzyme A and are reversible. They are displaced from monoamine oxidase in the presence of tyramine, rather than inhibiting its breakdown in the liver as general MAOIs do. That's why no special diet is needed. A special low tyramine diet is needed for normal MAOI compounds. The main danger in using a RIMA is the possible drug interactions they may cause. Always check that a RIMA is safe to use with a specific drug before mixing the two drugs. RIMAs are safe to mix with DMT and most other hallucinogens (even mescaline is relatively safe to mix with RIMAs because they primarily affect MAO A and not MAO B)]

The content of this technical note will, we hope, provide researchers interested in the beta-carboline/tryptamine combinations with some "hard empirical facts" combined with our musings. Hopefully, these will spawn new ideas for further experiments in this very exciting and very confusing area of psychedelic research.

SUMMARY

The purpose of this paper is to summarize our current work with three beta- carboline, Harmala alkaloid-containing plants, i.e.,

* Passiflora incarnata (passion flower)
* Peganum harmala (syrian rue)
* Banisteriopsis caapi (principal ingredient in yage)

Specifically, we wish to report on the phenomena and comparitive activity when extracts of each of these plants are smoked in conjunction with DMT.

SOURCES OF THE PLANT MATERIAL

The passion flower was purchased as dried, whole, chopped plant material from an herb store. The seeds of the syrian rue were purchased from a specialty seed service. No attempt was made to ascertain the origin of the plant material. The Banisteriopsis caapi was obtained from a private plantation in Hawaii. The caapi arrived cut into lengths of about one foot long, and ranged in diameter from about one quarter of an inch to one half inch. The original plant specimens had been collected in the Amazon by the grower.

EXTRACTION TECHNIQUES

We used the same extraction technique for all three plants. We had developed this technique for smoking the passion flower to potentiate Psilocybin mushrooms (see below) and wished to have the data from this set of expriments to be comparable. The technique was a two-stage extraction. The first extraction used was a boiling alcohol (we used vodka) and water infusion followed by a second extraction using boiled distilled water. Each infusion was boiled for several hours. A "slow cooker" is ideal for this. In the case of the caapi, the bark was peeled off in strips first. For the syrian rue, we first ground the seeds very fine. For both the passion flower and the caapi, the second extract was essentially clear and seemed unnecessary. However, in the case of the syrian rue, the second extract was a bright cloudy yellow which may indicate harmine in solution.

The plant material was strained and compressed after each extraction. The liquids from the from the two extractions were combined and dried using low heat on the slow cooker. The result was a brown caramally mass for both the passion flower and the caapi. The weight was about 20% of the original for the passion flower and the rue, and about 45% for the caapi. Except in the case of the passion flower, we cannot see any clear advantages of extraction over that of smoking the original plant material due to the relatively minor concentration of the amount needed to smoke. A plain water infusion would also seem to be just as effective in removing the harmine and would result in less of the other plant components being extracted.

The syrian rue extract was the most interesting. It actually had long, thin, yellowish crystals in a brownish, red, hard, clear matrix which was not at all gooey like the other two extracts. This is not surprising given the assumed concentration of beta-carboline alkaloids. Based on our rough averaging from a variety of sources, our up-front beta-carboline concentration estimates for the plant materials were as follows:

Code:
Plant               % beta-carbolines       Ratio (Syrian rue=1)
-----               -----------------       --------------------
Rue                      2.0%  - 4.0%               1
Caapi                    0.1%                      20
Passion flower           0.05% - 0.1%              40

USAGE

In each case we smoked the extract until we had reached subjectively the same high. As with our previous work with the passion flower extract, smoking significant amounts above this did not seem to get one any higher, but just intensified the physical symptoms and one felt increasingly sick. So far, only with the passion flower have we experimented with an oral dose. Oral infusions of the other plants are planned for our fall 1985 series of experiments.

The plant material is smoked with a match, lighter or torch in such a way to promote the boiling of the material, rather than burning it. This seems to yield the most effective high. The highly concentrated rue extract lends itself nicely to smoking in a "hash oil" pipe with the flame heating the bowl on the outside.

THE HIGH

The high is not particularly psychedelic or hallucinogenic. One feels calm. This calming effect is particularly noted by an observer as a significant change in facial expression and tone of voice. The limbs become heavy and lethargic and visibly tremble. Hypersalivation occurs, particularly at the back of the mouth, making for a particularly smooth smoke. A slight irritation of urethra and anus is sometimes reported. At higher dosages, dizziness and nausea sets in with very little increase in the high. Closed eye imagery is at best hypnagogic. That is to say, faint, moving outlines can be discerned with closed eyes. If one has a particularly vivid imagination, ghostly outlines of figures can be discerned. The more literal minded just see shifting blobs of light and dark. No one who has experienced DMT or high dose mushrooms would ever call them visions.

The high comes on and stabilizes after about 5 to 10 minutes from smoking. As mentioned before, it is very difficult to get higher by smoking more. If one stops at this point, the most noticable thing would be a calm and unapprehensive state. We take particular note of this diminishing of apprehensions since we are always apprehensive before we smoke DMT so its dimunition or absence is very noticable.

The passion flower is mentally the foggiest high, but curiously has the strongest "antidepresant" effect. This may be related to the overall mix of alkaloids in the passion flower (see below). The syrian rue was the clearest, cleanest high with the caapi being, subjectively in between. The caapi had the least "antidepressant" effect.

Sage ratios of the original plant material smoked for subjectively reaching the same level of high is roughly estimated as follows:

Code:
    Plant               Dosage Ratio
    -----               ------------
    Rue                      1
    Caapi                   12
    Passion flower          20

The dosage ratio is based on the mass of the original plant material. That is to say, to get as high as smoking one ounce of syrian rue, would require smoking 12 onces of caapi, or over two kilograms of passion flower.

Curiously, although various field researchers estimate beta-carboline dosage in native brews to range between 300 to 500mg, in our dosage we only needed dosages in the 50mg range. As noted above, increasing the dosage did not increase the high but only aggravated the physical symptoms. Even when tryptamines were taken later in addition, increasing the dosage past this point did not significantly alter the combined trip. It was as if there was some "switch" in the brain which, with sufficient beta-carbolines, was set from "off" to "on" and no further action could take place. We do not rule out the possibility of a second 'switch' as the 300-500mg range that we might have missed.

TRYPTAMINE COMBINATIONS

For comparison purposes, each of the plant materials was smoked according to the above method. Approximately 10 minutes after this plant-material-high stabilized, 15mg of DMT was smoked. One of us would go through the entire procedure while the other kept notes and timings.

The following consistent effects were observed:

* The overall impact of the trip was heightened far above the normally only threshold effects of a 15mg dose of DMT. Subjectively, the dose felt more like 35-45mg or roughly tripled in intensity.

* The overall length of the DMT 'flash' and subsequent patterns was lengthened. The 'flash' of visions which is normally 2 to 3 minutes at a 40mg dosage, was about 6 minutes with the beta-carboline predosing at 15mg of DMT. The total period of intense closed eye imagery, normally less than 5 to 7 minutes (including the flash) was extended uniformly to about 9 minutes with an additional 10 minute slowly decreasing tail of closed eye patterns.

* The auditory effects were so pronounced as to be almost overwhelming on several occasions. In fact, the auditory effects were stronger than even extremely high dose trips where we had smoked 50 to 70mg of DMT all at once. The initial sounds, the so-called 'carrier wave' or opening buzz that has been described as 'tearing plastic' was greatly amplified. The DMT 'music' which we describe as a xylophone-type sound which accompanies the visions was extremely loud and seemed to keep coming on to the point where it became disturbing on several trips.

* The basic 'jeweled dome' or 'chrysanthemum' pattern, seen after the 'vision flash' was fractured or separated. Instead of a uniform circular pattern, there seemed to be distinctive left and right halves of the pattern with a new, hard to describe pattern in the middle. The overall effect of the patterns seemed to us more mushroom-like, although we would be hard pressed to give a detailed explaination of why we felt this way.

* Similarly, the visions seemed to unfold in a more leisurely fashion. Again, we were reminded of the mushroom. While the DMT effect still hits fast and hard, the rushed 'million things at once' feeling of DMT smoked alone is quite muted.

* The colors of the pattern are also shifted as compard to DMT alone. Again, since we can't accurately describe colors in the first place, it is hard to pin down, but it could be characterized as less primary or jewel-like, with fewer or less saturated colors than DMT alone.

* Finally, when one comes out of the vision state, the 'woozey' feeling is quite pronounced for an additional 10 minutes or so. This feeling was very reminicent of the mushroom 'knock-down'.

The content of the visions was also altered. There were fewer "alien, self- transforming, elf-machines" and more visions of recognizable things. Strange animals and hooded figures marched on a bas relief procession. Griffin-like monsters rhythmically changed into beautiful naked women and back. The feeling tone was serious, unlike the playfulness or cheerful even though quite terrifying hilarity of the "self-transforming elf machines" experienced on DMT alone. The intensity was altered. We hesitate to say increase, since DMT is intense by itself, but the change in feeling tone, the more serious, almost personally directed information of the trance, subjectively made the trip more intense. On one trip, one of us made ocntact with a highly serious, palpable entity whose message could be quite simply summarized as "Are you sure you want to get into this? This is far more extreme than what you have done before. It is the path to destruction of gnosis!"

Subjectivelly, we preferred the syrian rue to potentiate DMT. It gave the cleanest, most intense high. While we have never taken true Ayahuasca, detailed discussion of some of the trip's contents with someone who has significant experience with that brew, confirmed that the trip content was like a short ayahuasca trip.

The passion flower was the least desirable potentiator. (Probably due to low harmine content in proportion to the total bet-carboline content.) The amount needed for effective tryptamine potentiation left us foggy and somewhat sick. Furthermore the MAO effects lingered for two to three days. The caapi's effects were, again, in between.

Anomalous Observations

This brings us to a curious set of observations. First, although the literature would indicate that the harmine MAO inhibition should be reversed in about five hours, the effects from all of the smoked plant material continued for at least 24 to 48 hours. That is to say, clear potentiation was noticed after this amount of time had elapsed. We hypothesize that this effect is due primarily to beta-carbolines other than harmine present in the plant material which, while qualitatively weaker as MAO inhibitors, may have a duration of effect which is much longer. However, we have reason to believe that something additional, due to tryptamines, may be happening.

Once we had taken 7.5 grams of very potent dried Stropharia. We were interested in making contact with the 'voice in the head' phenomenon. We potentiated the mushrooms by each smoking about 750 grams (!) of passion flower (reduced as described above) starting about 30 minutes after eating the mushrooms. The potentiation was quite overwhelming. After smoking about one quarter of the plant material, each fresh lungful brought on, within seconds, powerful "starburst" and "intersecting lightning bolt" hallucinations which, with eyes opened, obscured a well-lit room. The voice phenomenon was loud and clear and very unsettling (the content of the trip has been described in High Frontiers, Issue 2). Before the trip we had attempted on several occasions to invoke the voice phenomenon with the same mushrooms at dosages of up to 10 grams, to no avail. But, even more curiously, effects such as clear instance of MAO inhibition, voices in the head, visions (with both closed and opened eyes) and finally at the end of the period, clear potentiation of another psychedelic (LSD) occurred at discrete short intervals over a period of 14 days! We realize that this sounds unbelievable, however it did happen. It is our opinion that particular long-term effects can be initiated by large combined doses of tyrptamines and beta-carbolines that cannot be adequately explained using current models of brain chemistry.

Additionally, since that rather harrowing trip, the mushroom "voice" has been inescapable even on dosages as low as approximately one gram. As less spectacular long-term effects, we have also noticed this "locking in" or tuning-in effect with the beta-carboline/DMT combination. That is, effects that were previously elusive on DMT alone became easy to invoke once they have occurred in the combination.

NOTE: We understand from conversations with other investigators that this approach of first taking the mushrooms and then smoking the beta-carboline material when mushroom effects begin to come on to be the most efficacious approach.

Another curious observation is the "9 minute barrier". So far, we have not been successful in causing the DMT imagery to last longer than 9 minutes, irrespective of the dosage, or the type of underlying predose plant material. To make matters more interesting in our experiments with DMT and MDA (which is also a mild MAO inhibitor) the DMT effects are again lengthened to about 9 minutes. Yet ayahuasca produces a trip which lasts for several hours. At present we have no explaination, especially since much of the active components in the orally consumed brews are inactivated in the stomach and intestines or not absorbed.

In experiments in which we have predosed ourselves with DMT and then taken another psychedelic several hour later, we have noted very discernible (MDA) to dramatic (mushrooms or LSD) effects when the second substance is taken as much as 8 hours after the DMT. Again, this is hard to explain since the total DMT experience should only last about one hour. However, when we smoked DMT and after the flash smoked the beta-carboline plant material we were unable to cause any clear DMT imagery. What did happen was an immediate feeling of depression, almost exactly opposite the effect on mood of DMT.

One final hard-to-explain phenomenon. On about one quarter of the trips, after coming out of the trance and with our condition stabilized (or at least so we felt) about 20 minutes after smoking DMT, we experienced a rush of "information" into our minds with no other psychedelic effects. That is to say, without any visual, physical or auditory shift, we suddenly possessed, in our minds, a complex, detailed and lengthy thought with no idea where it had come from and the conviction that it had not existed in our heads, even in fragments, an instant before. The content of each of these thoughts was bizarre and had to do with directions on how to accomplish activities that are normally regarded as supernatural, impossible and/or crazy. Furthermore, the content of the thought was encouraging us to attempt these feats! While we have no first hand experience with schizophrenics (other than some Berkeley street people) our reading of the literature caused us to conclude that this type of phenomenon would be considered a clear instance of schizophrenic thinking.

Beta-Carbolone Potentiation of LSD

We have also experimented with potentiation of LSD by beta-carboline containing plants. Generically, the effects follow the same patterns. Subjectively, the dose feels three to four times more potent than it actually is. The closed eye imagery is greatly enhanced with circular highly visible bright imagery visible on only 25 [sic] micrograms. On higher doses (150-200 micrograms) there was a feeling of an ancestral presence (we have never felt an outside presence on LSD alone in over several hundred acid trips but we have found it quite common when LSD is combined with another psychedelic).

The closed-eye patterns were "almost visions". That is to say they were clearer than hypnagogic imagery but not as overwhelming or clear as DMT visions. The visuals were more like clear dream imagery. The mood elevation was quite astounding. At one point one of us shouted "You couldn't possibly have a bad trip on this stuff." There were no mood swings and the buoyant elation slowly receded to baseline over the course of the trip.

Tentative Conclusions and Suggestions for Further Research

To restate the obvious, indole psychedelics taken in a state of MAO inhibition are much more intense and qualitatively different than when taken alone. We believe that these combinations offer numerous fruitful avenues for further research.

Additionally, we find the syrian rue seeds to be a convenient, concentrated and easily obtainable source of beta-carbolines that can serve as a substitute for the more exotic, difficult to obtain, Banisteriopsis caapi.

Clearly, our next area of research should be in the area of "synthetic Ayahuasca". That is, trying to perfect an orally administered mixture of syrian rue and synthetic DMT that qualitatively behaves like the South American plant brews.

Additional work should be done with the smoked mixtures to investigate the "9 minute barrier" and to provide more qualitative mixtures for some future beta-carboline/tryptamine cookbook.

Finally, we hope that the information in this article might be correlated with the work of other researchers to suggest entirely new areas for research and to provide explainations for some of these phenomena.

Stay High and Stay Free,
Gracie and Zarkov
 
Thanks for the post ron.
SWIM actually obtained some more THH, and is preparing to take 200mg with 25mg of DMT mixed into a glass of water.

SWIM wants to know if it matters what state your DMT is in when consuming orally. He's searched for the info and is still unsure. The reason he wants to know is because the DMT was given to him by another friend, so he isn't exactly sure what state it is in. Does it matter?

Should SWIM consider getting food grade citric acid to add to the drink?
 
It's best if the DMT is a water soluble salt and not freebase. Just put the DMT in some lemonade or orange juice. They contain a ton of citric acid. Lemon gets its flavor from d-limonene and citric acid. It's a great source of citric acid. If it's freebase then it will form DMT citrate which works very well.

The problem with freebase DMT is that it can get stuck in your esophagus or pass really fast through your stomach and never get converted to DMT HCl by the hydrochloric acid in the stomach. Also, sometimes the stomach might not secrete enough acid and can become slightly alkaline and so the DMT might not convert to DMT HCl even when staying in the stomach for extended periods of time. So it's always best to ingest it in salt form.
 
Phlux- said:
if u can smoke the spice u have then its freebase.

That's what I thought, but just wanted to make sure- and see if it made a difference. Thanks for all the information guys. SWIM is gonna give it a go some time in the near future. He has tickets to an OTT show in a week- he's been toying with the idea of taking a threshold dose before hand :shock:
 
TheNtt said:
Phlux- said:
if u can smoke the spice u have then its freebase.

That's what I thought, but just wanted to make sure- and see if it made a difference. Thanks for all the information guys. SWIM is gonna give it a go some time in the near future. He has tickets to an OTT show in a week- he's been toying with the idea of taking a threshold dose before hand :shock:

That's not completely correct. The bark does NOT contain freebase DMT and yet it is still smokeable as is. Some salts are smokeable as is and vaporize without decomposing. Others decompose with heat and aren't smokeable, and others become freebase when smoked.

For example, mescaline hydrochloride is smokeable. The entire salt gets vaporized as is. Freebase is more desirable usually because it absorbs faster when smoked and is usually more potent because of that. But freebase mescaline is an oil and difficult to smoke, so people use mescaline hydrochloride instead. Bufotenine hydrochloride is also smokeable, but freebase bufotenine is much better, and far more psychedelic.
 
So.. No one ever did try using sublingual THH to activate oral DMT?

I might try it.. I want to try DMT again at a lower dose.. all I have left is maybe 75 mg's or so of THH and maybe around 100 mg's of DMT or so.. but it's enough to probably get the sort of lower dose trip I want out of it.. Who knows, maybe it will activate it.. or maybe I should swallow all the THH and then mix maybe half or less of the DMT I have left into lemonade.. Think 75 mg's of THH will activate it? It's what I got. Maybe if I bought a supplement tincture from the local natural food store.. they had a Passionflower extract one time, I tried about half of the bottle in a shot and it did significantly brighten my vision and was very beta-carboline feeling..

Maybe if the sublingual doesn't work to activate DMT, I can then try smoking some spice while the DMT is still in effect.. I'm sorta bad at getting big hits with it, so maybe it'd allow a small hit to give me some visuals other than brighter colors.. I smoked a little bit ago, no MAOI or anything, and I got colors both times.. one time out of a bong I managed to get things melting somewhat and wavering like they were really hot air like coming off the road.. wavy..

Then if all else fails, I haven't tried sammiching the spice yet to smoke.. this might end up the best method for me.. if the smoke is mixed with a blend I'm used to, I will likely not feel as odd getting big hits.. Maybe the k2 blends from BBB that I've been enjoying.
 
I don't know that I can. I'm going to try the sandwich method today.. if it seems just as harsh and bad, I don't want to waste all the rest of my DMT vaporizing it and having half of it recondense in my favorite bong, making it smell bad and wasting it, or in a light bulb.. or burning it between herb and coughing while I'm coming up.. not fun for me..

If THH can activate it, I'd likely enjoy a trip about half the strength of my previous experience.
 
I'd bet the problem lies with your pipe or the method your are introducing the flame...
Cleanly vaped spice is not tough on the chest and you will hardly taste anything till its almost over.
 
Well I don't think that's the case.. I inhale the vapor and it doesn't hurt too bad, but I suddenly have a cough and then my lungs feel bad.. some people just aren't as good at smoking as others, if you can accept that. I'm really good at smoking many substances but DMT is rough for me out of a bulb..

Now, the thing is, I tried smoking some with the sandwich method.. I used a mullein based smoking blend I have had but don't use much because it doesn't do a lot on it's own, and I sammiched some DMT between.. I got it all in one hit, no cough or anything, and I got much further than I did with vaporizing it.. I think water filtering it combined with something else I'm more used to smoking is ideal for me.. takes the harshness out a bit.. I might try a breakthrough dose sometime soon, maybe even tonight, but this topic isn't really the best place to talk about smoking DMT without THH.. I'll let this topic die again or go back on-topic..

I might still try some sublingual THH before smoking, so if I do that I'll post.
 
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