[quote=“RapAdmin, post:1, topic:3696”]
The bigger issue for rapamycin users is the impact of Tumeric / Curcumin on rapamycin blood levels. People need to be aware of how Curcumin significantly impacts the rapamycin bioavailability (greatly lowering it) - see details at bottom of this post.

Would a person not taking any curcumin for a day before and on the day that he takes his rapamycin avoid this negative effect on bioavailability if curcumin is taken on other days?

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Turmeric/curcumin is one of those supplements where a small amount is good but megadosing causes all kinds of potential problems.

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Google “half life of turmeric” and that will be your answer.

Well I feel like a dumbass… I take Longvida daily and have not paid any attention to skipping doses around my weekly rapamycin. The fact that even the lower dose seemed to markedly suppress AUC is quite striking. Strange that I definitely still seem to be absorbing a considerable amount of rapa given that my WBC count has been borderline low since starting.

Has this discussion been continued in any other threads? With a half-life of roughly 7 hours it would seem that 24-36 hours between curcumin and rapamycin would probably be enough to avoid this effect.

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This is good information. Thank you.

Someone on this site found that the half-life of rapamycin in his blood was roughly 41 hours. So it would be best to wait 24-36 hours after taking curcumin (half-life 7.5 hours) before consuming rapamycin, and then waiting roughly 3-5 half lives of rapamycin (123 to 205 hours) before taking any more curcumin. Although since the benefits from rapamycin come from alternating periods of “cleanup” and “growth” maybe you don’t have to wait 123-205 hours after consuming rapamycin - a shorter “cleanup” period may be fine.

The 41-hour half-life of rapamycin may differ from person to person. See Rapamycin Half Life Calculations and Graphing - Spreadsheet

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My thoughts, as someone who takes curcurmin, are that if I take Rapamycin 2 hours before curcurmin then I should get most of the Rapamycin into my blood before the curcurmin has an effect in the intestines.

That may be wrong, however.

I have also read the above papers to get a better understanding of the liver issues. I have recently reduced my daily consumption of curcumin from 1.5g to 1g because in certain circumstances (mainly with alcohol) it appeared to cause digestion problems. I note in the papers above that if there are liver issues they are seen with high ALT over 1000 IU/L. My ALT has come down over the past year and a bit from around 20 to around 15. I have had as low as 11. My highest was 24. Hence as far as I am concerned I am going to stick to 1g per day. The papers that research overdose on this have pointed at a threshold of 1.5g/d being tolerable. I think, however, that I am going to stick to 1g.

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The trouble with that approach is that it’s not curcumin per se that increases the metabolism of Rapamycin, it’s the curcumin metabolites that do so! In other words whatever curcumin is broken down into is what activates CYP4A (not bothering to look up, that might be wrong, but whatever the relevant one is), causing Rapa to be broken down more. Curcumin itself actually inhibits CYP4A so would increase absorption of Rapa, if not for its metabolites.

At least that’s my understanding from reading the papers.

So, to correctly do the analysis your are postulating, I think you need to know both the half life of Curcumin, AND the half life of whatever the relevant metabolites are, and maybe to a lesser degree the relative activation/inhibition of curcumin v its metabolite!

Plus everyone metabolizes everything differently anyway, so wtf knows?

Anyway, that’s my understanding, but I could be wrong.

I tested my Rapa blood levels and they were quite low, much lower given the dose than reported by several on this site (Thanks @Agetron ). I finally got them up with a combo of quitting curcumin (Theracumin), eating a grapefruit the night before and concurrent with dosing Rapa, as well as a big swig of olive oil. Even after all that, my (dose adjusted) blood levels are lower than most, so I’ve been taking 12 or 14 mg weekly in recent weeks, with no side effects I’m aware of.

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I have been working on my plan for when I next take Rapamycin and I am getting quite confused as to the situation with Curcumin. Curcumin is argued to be an activator of CYP3a4. I have found references to it inhibiting CYP3A4. I have looked at the metabolites of Feruilic Acid and Vanillin and both of these seem to either inhibit CYP3A4 or have no effect. These are, however, supposed to be minor metabolites.

Hence I am not quite sure where the original research is that points to Curcumin activating CYP3A4.

Can anyone find the original papers or references to them.

It happens that I tend to take Ferulic Acid and vanillin separately.

Ferlic Acid is possibly a metabolite of the anthacyanins and potentially the active molecule.

Check out the paper in the first post in this topic Rapadmin posted showing Curcumin lowing blood Rapa levels. Pretty sure that’s where I got most of the info.

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Thanks for highlighting

https://www.nature.com/articles/srep06587

Which looks at coadministratiion in rats at 50 and 100mg kg. That would be 4 or 8g for me and i normally take 0.5g twice.

I will avoid curcumin to start as last time

The fact that the activation of cytochrome P450 3A4 or whatever might be due to the metabolites of curcumin itself, rather than curcumin, never occurred to me. Thanks.
That raises the question, “what are the half-lives of curcumin metabolites?” I found this paper:

Shaiju K. Vareed et al., “Pharmacokinetics of Curcumin Conjugate Metabolites in Healthy Human Subjects,” Cancer Epidemiol Biomarkers Prev. 2008 Jun; 17(6): 1411–1417.

The paper says “Cmax, t_sub_1/2 and AUC of total curcumin conjugates calculated from the raw data are presented in [Table 2] (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4138955/table/T2/). One subject on the 10g dose level had a Tmax of 10 hr, but no curcumin conjugates were detected in this subject before 2 hr and after 48 hours of drug intake. When the Tmax was within the range of 1 to 4 hr, curcumin conjugates were completely eliminated from plasma at the 24 hr time point.”

I’ve been helped by taking Meriva, which is turmeric or curcuminoids bound to phospholipids. I wonder how long the metabolites of Meriva would last in me.

A lower dose of curcumin (0.5, 2.5 and 10 mg/kg bodyweight orally) actually inhibited CYP3A4 and increased the bioavailability of tamoxifen in rats by roughly 30-70%. http://pmid.us/22512082

This whole situation appears very complicated. It’s hard to predict what the overall effect will be. Has anyone taken a blood test while taking curcumin regularly and when taking a break from curcumin?

Could you please report on what your blood levels were and at what dose? Thanks

Sorry if I am waking up a topic that people feel is closed, but I am wondering if taking the Longvida form of curcumin would have the same effect on rapamycin as has been reported for most forms of curcumin/turmeric.
If I understand the attached description of Longvida, it is not metabolized in the same way?
https://www.protocolforlife.com/wp-content/uploads/2018/10/P2395-Cogumin-SLPC-Tech-Sheet-New-Design-.pdf

I would recommend you contact Longvida customer service and ask them the impact on CYP3A4 from their curcumin product. They are the only people who would likely know. Its their product, and this is their area of expertise. Please post their response, if you think it would be helpful to others here.

Here is a related thread: Curcumin Does Not Appear to Meaningfully Inhibit CYP3A4

The absolute dose of curcumin in Longvida is a small fraction of the doses typically given: that alone should reduce the risk. Plus, its higher systemic bioavailability is due to avoiding metabolism in the liver (and also the intestine), which I would think would mean a further reduction in hepatic exposure and therefore tox potential.

I just tried Theracurmin for past few days and took my rapamycin yesterday. It hit me hard. Lots of fatigue and trouble sleeping.
I am so confused reading this thread because from what I read - multiple studies, curcumins can inhibit cytochrome p450 and thus increase rapa level. Also increased tamoxifen, steroids, etc.
Unfortunately I don’t have the time to get my blood levels checked.

I stopped curcumin/turmeric supplementation a couple of months before taking rapamycin, because I read that c/t affects rapa, but there are conflicting claims about in what way and in what direction. I therefore stopped c/t, because there’s too much confusion here. Rapa is the intervention I’m interested in, so anything that strongly affects it, but nobody can clearly explain in what way, is not worth the risk of unfavorable interference. YMMV.

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I take both Berberine and Curcumin which have effects in both directions. Hence I take Rapamycin a few hours before them.

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