somnilicious
Bluelighter
but wouldn't inhibition stop the CYP from converting the mitragynine to the more powerful 7-OH thus rendering it weaker.
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but wouldn't inhibition stop the CYP from converting the mitragynine to the more powerful 7-OH thus rendering it weaker.
I think 7ohm and mitragynine feel pretty different, some people prefer the mitra feeling and some others prefer the (generally red strain´s) 7-ohm feeling...but wouldn't inhibition stop the CYP from converting the mitragynine to the more powerful 7-OH thus rendering it weaker.
I read that it did awhile back but I don't remember where. I just say tickle because in my mind that's how it worked, I can't see why it wouldn't potentiate to the extreme extent it does or help with opioid withdrawal so much if it didn't have some affinity to the MOR.NIgella Sativa is a calcium channel blocker. It doesnt "tickle" the MOR. https://www.mdpi.com/2218-273X/12/1/20
Because it is a calcium channel blockerI read that it did awhile back but I don't remember where. I just say tickle because in my mind that's how it worked, I can't see why it wouldn't potentiate to the extreme extent it does or help with opioid withdrawal so much if it didn't have some affinity to the MOR.
According to this source: "It has been proved in many in vitro studies that calcium channels/blockers modulate the opioid receptors or release of endogenous opiopeptins in one or other way."
I'm not entirely sure how to interpret that but it sounds like it at least has some involvement in the MOR. It's particularly popular for people coming off kratom, it helps with opioid withdrawal in general but it seems to help with kratom withdrawal the most.
Reds are fermented. They are tied up wet into plastic bags air tight and left to rot in the sun for 3 days. However, when you compare alkaloid profile C of A's of the 3 main colors. the 7oh really doesnt differ, you are spot on thereI think "reds" containing more 7-ohm is mostly a myth. I heard something like, sun drying it so it gets all brown increases the 7-ohm by a slight amount but still not enough to really notice but I'm not sure. I never saw anything for sure about this. Maybe there is a proper sun drying method because a lot of vendors do it for so long it just renders the kratom very weak, which was the case with a vendor I previously used.
I tried a few of their reds and they were all impossible to get any effect from. But when I was new I had some like Bentuangie that definitely felt distinct and different. Weaker in a way but just, different. Like I could go into this half sleep lucid state on that one easily. So maybe there is truth to the sun drying, and that vendor had actually done it properly without turning it dirt brown. The vein color itself is irrelevant since the same plant can have different colored stems. At the end of the day there's just good or bad kratom, it's not as diverse as cannabis or even kava.
from the study you replied to "Our results in rats demonstrate that cytochrome P450 3A (CYP3A) inhibition can increase the systematic exposure of both mitragynine and 7-hydroxymitragynine and their potency to produce MOR-mediated behavioral effects."but wouldn't inhibition stop the CYP from converting the mitragynine to the more powerful 7-OH thus rendering it weaker.
I sure did! My bad, mateI think you quoted the wrong post, I didn’t say anything about nigella sativa. But now I’m going to look it up
Edit: I didn’t realize it was just black seed oil![]()
No need to be snarky. I'm aware it's a calcium channel blocker, but my point still stands that it does have some involvement with the mu-opioid receptor at least as far as I can tell. If you wanted to correct me you could've done so in a more congenial way.Because it is a calcium channel blockerLet me just link this again https://onlinelibrary.wiley.com/doi/full/10.1002/jppr.1769
LOL Im trying to show you that blocked calcium (ligand or voltage-gated) channels can modulate opioid receptors.No need to be snarky. I'm aware it's a calcium channel blocker, but my point still stands that it does have some involvement with the mu-opioid receptor at least as far as I can tell. If you wanted to correct me you could've done so in a more congenial way.
Still not sure about kratom yet.
Yeah here's the problem with Kratom, take it on empty stomach and you'll get this great high that gives you the munchies. Then all you can think about is eating, but as soon as you do your high goes away. The only kind of workaround is to fill your stomach with coffee.How much are you taking? There's a lot of bunk stuff out there too. If it looks brown and all it's as good as garbage. This is what most "red vein strains" are, overly sun dried kratom. Good kratom dosed well will give you a VERY nice opioid high, but unlike other opioids eating tends to kill the effects and taking it on a full stomach won't yield much, but it still works for some people.
To my knowledge the amount of 7oh in kratom is so small that its content cannot be reliably estimated in a usual lab analysis.Reds are fermented. They are tied up wet into plastic bags air tight and left to rot in the sun for 3 days. However, when you compare alkaloid profile C of A's of the 3 main colors. the 7oh really doesnt differ, you are spot on there
I wonder if this supplement also potentiates 7oh. Or does it facilitate the conversion from mitragynine to 7oh? Hmm....2025 and now there's crazy 7-oh and pseudoindoxyl isolated. At least Dougie Doozer didn't jump out from behind another windmill and blow paprika extract into everybody's dang eyeballs again...