Hip
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Great posts, @manna, very interesting and informative.
This again I find extremely interesting: the fact that ME/CFS symptoms can disappear for a few days after taking ayahuasca.
If the same effect could be obtained from some non-psychedelic drug which mimicked the relevant biochemical actions of DMT, and that non-psychedelic drug could be taken every day without tolerance build-up, then you would have a highly effective ME/CFS treatment, that would make all your ME/CFS symptoms disappear.
Of course, it may be that all the benefits of DMT for ME/CFS come from agonism of the very same receptors that produce a psychedelic effect, and in which case, it might be hard to separate the beneficial effects for ME/CFS from the psychedelic effects.
Would you say that your ME/CFS symptoms completely disappeared in these few days after ayahuasca, or was more like you were 80% or 90% in remission in those few days?
Do you mean it felt like the nerves in your body, your hands, arms, legs, etc, were tingling, or sort of more sensitive to tactile sensation? (I noticed that the virus which triggered my ME/CFS also seemed to permanently reduce the tactile sensitivity of the skin of my entire body).
By the way, the central nervous system (CNS) is the brain and spine; the nerves issuing from the brain and spine and running into the body are the peripheral nervous system.
Duly noted.
As I guess many here know, Banisteriopsis caapi (ayahuasca) contains beta-carbolines (specifically harmine, harmaline and tetrahydroharmine) which are MAO inhibitors. In the ayahuasca brew, Banisteriopsis caapi is mixed with a DMT-containing plant like Psychotria viridis (chacruna), and these MAO inhibitors prevent the DMT from being destroyed in the stomach by a stomach enzyme called monoamine oxidase A (MAO-A), which is found in the lining of the stomach. That is why orally taken Psychotria viridis has no psychedelic effects on its own, until mixed with Banisteriopsis caapi. More about ayahuasca biochemistry here.
But as well as being MAO inhibitors, the harmine, harmaline and tetrahydroharmine found in Banisteriopsis caapi also have their own psychedelic effects.
When I read some stories of ayahuasca temporarily putting all ME/CFS symptoms into remission, it occurred to me that it might be the harmine, harmaline or tetrahydroharmine in the ayahuasca brew, rather than the DMT, which is responsible (or partly responsible) for the benefits that ayahuasca has for ME/CFS.
You also get harmine, harmaline and tetrahydroharmine in Syrian rue seeds, so I decided to try some of these seeds, to see what effect they might have on my ME/CFS symptoms.
For a psychedelic trip, the dose of Syrian rue seeds is around 3 to 6 grams (ref: here). So I started with microdoses of 50 mg of Syrian rue seeds. This was fine (though no benefits observed), but when I worked up to a 200 mg dose, it started to make me feel mentally uneasy with very mild psychosis feelings, so I thought it would be best to drop my Syrian rue seed experiments.
I read that there are differences between Syrian rue seeds and Banisteriopsis caapi though: Syrian rue seeds has mostly harmaline, a bit of harmine and very little tetrahydroharmine. Banisteriopsis caapi has mostly harmine, and some harmaline and tetrahydroharmine.
Incidentally, in rats, harmaline increases the level of soluble guanylate cyclase, the only known nitric oxide receptor. So harmaline I think might have an effect equivalent to increasing nitric oxide levels.
Harmaline in large doses though is neurotoxic to Purkinje cells in the brain.
Note that it is essential to observe tyramine dietary restrictions before taking Syrian Rue seeds or Banisteriopsis caapi, at least in high doses.
I take it that it's the DMT-containing plants like Psychotria viridis that will be banned from sale, rather than Banisteriopsis caapi, which contains no DMT.
That is one aspect of ayahuasca / DMT that does interest me, the potential for a sort of spiritual purification and general raising of consciousness. I found the ME/CFS really reduced my spiritual and religious sensibilities (due to some biochemical factor in the brain, I believe)
Though I doubt if I would pluck up the courage to do a full ayahuasca / DMT session, given my fear of bring back the mild psychosis symptoms I had a few years ago.
Do you think a series of ayahuasca / DMT microdoses, say one taken every week for many months, would have the same spiritual benefits. Or is there no substitute for the full trip?
I did Ayahuasca and successfully broke through on about a dozen occasions. Often I would think "that's it I'm healed" only for it to return a few days later.
This again I find extremely interesting: the fact that ME/CFS symptoms can disappear for a few days after taking ayahuasca.
If the same effect could be obtained from some non-psychedelic drug which mimicked the relevant biochemical actions of DMT, and that non-psychedelic drug could be taken every day without tolerance build-up, then you would have a highly effective ME/CFS treatment, that would make all your ME/CFS symptoms disappear.
Of course, it may be that all the benefits of DMT for ME/CFS come from agonism of the very same receptors that produce a psychedelic effect, and in which case, it might be hard to separate the beneficial effects for ME/CFS from the psychedelic effects.
Would you say that your ME/CFS symptoms completely disappeared in these few days after ayahuasca, or was more like you were 80% or 90% in remission in those few days?
I felt the affect of psychadelics was largely on my Central Nervous System (which is everywhere yes?) and bringing more electricity, if that's the right word, into it.
Do you mean it felt like the nerves in your body, your hands, arms, legs, etc, were tingling, or sort of more sensitive to tactile sensation? (I noticed that the virus which triggered my ME/CFS also seemed to permanently reduce the tactile sensitivity of the skin of my entire body).
By the way, the central nervous system (CNS) is the brain and spine; the nerves issuing from the brain and spine and running into the body are the peripheral nervous system.
On psylocibin, I did find this helpful some of the time but also it unfortunately induced 2 psychotic breaks. Apparently this is fairly common with succeptible people. I would advise caution with it. Microdosing is probably the way to go and supposedly not more than once every 4-5 days.
Duly noted.
Caapi leaf is quite a nice relaxing and safe way to get a slight psychadelic lift.
As I guess many here know, Banisteriopsis caapi (ayahuasca) contains beta-carbolines (specifically harmine, harmaline and tetrahydroharmine) which are MAO inhibitors. In the ayahuasca brew, Banisteriopsis caapi is mixed with a DMT-containing plant like Psychotria viridis (chacruna), and these MAO inhibitors prevent the DMT from being destroyed in the stomach by a stomach enzyme called monoamine oxidase A (MAO-A), which is found in the lining of the stomach. That is why orally taken Psychotria viridis has no psychedelic effects on its own, until mixed with Banisteriopsis caapi. More about ayahuasca biochemistry here.
But as well as being MAO inhibitors, the harmine, harmaline and tetrahydroharmine found in Banisteriopsis caapi also have their own psychedelic effects.
When I read some stories of ayahuasca temporarily putting all ME/CFS symptoms into remission, it occurred to me that it might be the harmine, harmaline or tetrahydroharmine in the ayahuasca brew, rather than the DMT, which is responsible (or partly responsible) for the benefits that ayahuasca has for ME/CFS.
You also get harmine, harmaline and tetrahydroharmine in Syrian rue seeds, so I decided to try some of these seeds, to see what effect they might have on my ME/CFS symptoms.
For a psychedelic trip, the dose of Syrian rue seeds is around 3 to 6 grams (ref: here). So I started with microdoses of 50 mg of Syrian rue seeds. This was fine (though no benefits observed), but when I worked up to a 200 mg dose, it started to make me feel mentally uneasy with very mild psychosis feelings, so I thought it would be best to drop my Syrian rue seed experiments.
I read that there are differences between Syrian rue seeds and Banisteriopsis caapi though: Syrian rue seeds has mostly harmaline, a bit of harmine and very little tetrahydroharmine. Banisteriopsis caapi has mostly harmine, and some harmaline and tetrahydroharmine.
Incidentally, in rats, harmaline increases the level of soluble guanylate cyclase, the only known nitric oxide receptor. So harmaline I think might have an effect equivalent to increasing nitric oxide levels.
Harmaline in large doses though is neurotoxic to Purkinje cells in the brain.
Note that it is essential to observe tyramine dietary restrictions before taking Syrian Rue seeds or Banisteriopsis caapi, at least in high doses.
In the UK it is currently legal to buy but not to brew. By April it will be illegal to buy as well.
I take it that it's the DMT-containing plants like Psychotria viridis that will be banned from sale, rather than Banisteriopsis caapi, which contains no DMT.
this sort of spiritual healing that occurs during Ayahuasca can have the most proifound affects and results as you are left to see your situation in a much clearer light. Longterm chronic illness can bring you down in ways that you're so used to that you don't really notice as being other than normality.
That is one aspect of ayahuasca / DMT that does interest me, the potential for a sort of spiritual purification and general raising of consciousness. I found the ME/CFS really reduced my spiritual and religious sensibilities (due to some biochemical factor in the brain, I believe)
Though I doubt if I would pluck up the courage to do a full ayahuasca / DMT session, given my fear of bring back the mild psychosis symptoms I had a few years ago.
Do you think a series of ayahuasca / DMT microdoses, say one taken every week for many months, would have the same spiritual benefits. Or is there no substitute for the full trip?
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