Survived Abortion
Bluelighter
I have been taking Rhodiola Rosea (360mg SHR-5 extract) daily for about a week, and I am wondering if anyone in PD has tripped on a phenethylamine or tryptamine compound whilst taking this specific herb. It seems that it inhibits MAO types A and B, but I'm not sure to what extent (as compared to other MAOIs).
It's an amazing herb that gives a really lovely mood-lift with extra physical and mental drive, probably the greatest thing of this kind I've ever used. It feels very natural and smooth. And I don't really want to stop taking it, but I don't want to stop tripping either.
There was a study done to see how effective of an MAO inhibitor it is, but I don't how to interpret the results because I'm not a biochemist:
Can somebody interpret these figures for me, and maybe compare them to, say, harmala? I'm less worried about the 4-sub tryptamines, but more concerned about aMT and the phenethylamines like the 2Cs.
I've heard of people combining phens with MAOI before, and having to reduce the dose by around 3X. I've been looking through old threads, and found people mentioning combos such as mescaline + harmala, mescaline + selegiline, 2C-x + selegiline. Although those who have done this have reported it to be very potentiating and quite risky.
I've prepared some capsules of 2C-C at 12mg and 25mg to see how much the effects are potentiated at that low dose. I'll probably start even lower than this.
It's an amazing herb that gives a really lovely mood-lift with extra physical and mental drive, probably the greatest thing of this kind I've ever used. It feels very natural and smooth. And I don't really want to stop taking it, but I don't want to stop tripping either.
There was a study done to see how effective of an MAO inhibitor it is, but I don't how to interpret the results because I'm not a biochemist:
Monoamine oxidase inhibition by Rhodiola rosea L. roots.
Abstract
AIM OF THE STUDY: Rhodiola rosea L. (Crassulaceae) is traditionally used in Eastern Europe and Asia to stimulate the nervous system, enhance physical and mental performance, treat fatigue, psychological stress and depression. In order to investigate the influence of Rhodiola rosea L. roots on mood disorders, three extracts were tested against monoamine oxidases (MAOs A and B) in a microtitre plate bioassay.
MATERIALS AND METHODS: Methanol and water extracts gave the highest inhibitory activity against MAOs. Twelve compounds were then isolated by bioassay-guided fractionation using chromatographic methods. The structures were determined by 1H, 13C NMR and HR-MS.
RESULTS: The methanol and water extracts exhibited respectively inhibitions of 92.5% and 84.3% on MAO A and 81.8% and 88.9% on MAO B, at a concentration of 100 microg/ml. The most active compound (rosiridin) presented an inhibition over 80% on MAO B at a concentration of 10(-5) M (pIC50=5.38+/-0.05).
CONCLUSIONS: The present investigation demonstrates that Rhodiola rosea L. roots have potent anti-depressant activity by inhibiting MAO A and may also find application in the control of senile dementia by their inhibition of MAO B.
Can somebody interpret these figures for me, and maybe compare them to, say, harmala? I'm less worried about the 4-sub tryptamines, but more concerned about aMT and the phenethylamines like the 2Cs.
I've heard of people combining phens with MAOI before, and having to reduce the dose by around 3X. I've been looking through old threads, and found people mentioning combos such as mescaline + harmala, mescaline + selegiline, 2C-x + selegiline. Although those who have done this have reported it to be very potentiating and quite risky.
I've prepared some capsules of 2C-C at 12mg and 25mg to see how much the effects are potentiated at that low dose. I'll probably start even lower than this.
