Update on Brad Stanfield's Rapamycin Clinical Study in NZ

I think people are reading too much into this trial. I don’t think the results suggest that rapamycin is detrimental at all. For short term exercise gain it may be detrimental, and if that’s all you care about then you might want to stay away from it. But the trial couldn’t possible answer whether it has beneficial effects on aging in humans.

Effects on aging would take much longer to show up and wouldn’t show up as changes in exercise performance in the short term. It’s entirely possible that muscle strength and size gains are somewhat reduced in the short term, while over the long run, rapamycin would have protective effects on muscle quality, which would leads to improvements that won’t be detected until someone has taken it for many years, if not decades.

Note that calorie restriction reduces muscle mass for obvious reasons, but when done over the long run it actually prevents sarcopenia and improves muscle quality in rodents. It’s a case of a shorter term sacrifice (in strength and mass) for long term benefits.

The fact that rapamycin slightly blunted gains from exercise might actually be considered somewhat of a confirmation that it’s effectively doing what we want it to do, which is inhibit mTOR.

Btw I recall seeing evidence that blocking mTOR only blocks some of the muscle gain stimulation because some of it is independent of mTOR inhibition. Anecdotally, rapamycin doesn’t appear to have much of an effect on the ability to gain muscle, so the effect is at best small in most people. It’s possible of course that it is more significant in older more frail people.

My hope is that this study doesn’t give rapamycin a negative publicity. People must realize that this study does in no way indicate that rapamycin doesn’t work for slowing down aging. To detect the effects of rapamycin on aging requires much longer trials, and so far we only have animal studies to go by in that regard.

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It would be interesting to see if like a year or two later the people who took Rapamycin are in better health, compared to the placebo group. i.e. it might be that a couple weeks of Rapamycin triggers long-term improvements in health.

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That, of course, is the key issue. A proper test of Rapamycin in Homo sapiens would take quite a long time.

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Instinctively this seems right. At least fasting “well” can be beneficial for sarcopenia in the long. The big question with both fasting and rapamycin is what constitutes an optimal dose.

I wonder, given this research and given the recent paper indicating that rapamycin’s benefits largely derive from autophagy…whether we should be inspired by fasting research when deciding the best rapa dosing schedule.

For example I’m disinclined to calorie restrict to the point/edge of side effects - Ive always been disinclined to dose rapa that way.

Instead, here’s my attempt to translate fasting recommendations into rapamycin recommendations…

A weekly “monk” fast for 24 to 36 hours is often cited as the optimal balance for deep cellular benefits without significant muscle catabolism - could this translate to a weekly everolimus dosing?
And a deeper quarterly or bi-monthly 48-72 Hour Fast could use sirolimus with its longer half life?

Either way, as you say, we have easy ability to increase resistance exercise and protein consumption when not in the rapa window to compensate for any negative impact in muscle from either fasting or rapamycin

Looking back at my rapamycin dosing records I decided on dosing having read this forum and read various research papers. The most frequently I have taken rapamycin has been every 21 days. I am now settled on a minimum break of 42 days.

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Agreed, there are some studies that show that although rapamycin seems to have a deleterious effect, after time has passed we find out that it has improved function. Here’s one example: https://www.sciencedirect.com/science/article/abs/pii/S0014299925007149

Yes, there are several, and it’s a fascinating subject : The role of mTOR signalling in the regulation of skeletal muscle mass in a rodent model of resistance exercise | Scientific Reports

in this study, we investigated the role of rapamycin-sensitive mTOR in the RE-induced activation of muscle protein synthesis, ribosome biogenesis, PGC-1α expression and hypertrophy. The results indicated that the inhibition of rapamycin-sensitive mTOR could prevent the induction of ribosome biogenesis by RE, but it only partially inhibited the activation of muscle protein synthesis. Likewise, the inhibition of rapamycin-sensitive mTOR only partially blocked the hypertrophic effects of chronic RE. Furthermore, both acute and chronic RE promoted an increase in PGC-1α expression and these alterations were not affected by the inhibition of rapamycin-sensitive mTOR. Combined, the results from this study not only establish that rapamycin-sensitive mTOR plays an important role in the RE-induced activation of protein synthesis and the induction of hypertrophy, but they also demonstrate that additional (rapamycin-sensitive mTOR-independent) mechanisms contribute to these fundamentally important events.

Here’s another one, interesting because it focuses on exercises that lengthen the muscle by mechanical loading:

Here, we show that an increase in mechanical loading induces muscle fiber growth through two distinct mechanisms. Radial growth, reflected by an increase in fiber cross-sectional area, is mediated through an mTORC1-dependent signaling pathway, whereas longitudinal growth, marked by the in-series addition of sarcomeres, is mediated through an mTORC1-independent signaling pathway. To gain further insight into the events that drive longitudinal growth, we combined BONCAT-based labeling of newly synthesized proteins with high-resolution imaging and determined that the in-series addition of sarcomeres is mediated by a process that involves transverse splitting at the Z-lines of pre-existing sarcomeres. Collectively, our findings not only challenge the long-standing view that mechanically induced growth is uniformly governed by mTORC1, but they also lay the framework for a new understanding of the molecular and structural events that drive this process.

To me, the Stanfield study further shows that there is an mtor-indenpendent component to muscle protein synthesis.

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No, both groups actually did train the exact same amount so it was a well designed study.

In this study, the proposed mechanism actually showed itself to be true.

And unfortunately, I took my weekly 5mg dose this morning before reading these results. I will not be taking Rapamycin anymore unless I don’t plan to train for a few days after dosing it, which is basically never. This is enough to remove it from my stack. Hopefully I reaped some rewards from it over the last five years I have been taking it though.

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I never really understood your dosing protocol but after these new results, I admit you were right all along.



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For someone like me, that is mostly focused on metabolic health (which includes muscle building/retention) at this time, the prospect of weekly dosing started to look more and more suboptimal to me. The long half-life makes weekly dosing too frequent for my purposes. I prefer to do short cycles now: taking 3-6mg of rapamycin every 2 weeks, for at most 2 months out of the year. My intuition is that measurable inhibition should be acute, short, and infrequent. The inhibition is only half of the equation, giving the body enough time to recover is the other half.

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Thank you for this. My basic argument is that we need an anabolic period as well as a catabolic period. All of these things are variable. It is not a switch between anabolic 100% and catabolic 100%, but variations between the two. I also argue that increasing the level of catabolism is better up to a point. Hence two mild periods of catabolism are not as good as one more serious period of catabolism. There will, of course, be a point where systemic damage could occur from catabolism. Hence care is required.

That is because the mitophagy that occurs is selective mitophagy that destroys the least functional mitochondria.

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It’s your decision but you are wrong in my opinion. This study showed/told us exactly what we knew all along that Mtorc inhibition while good (maybe even great) for longevity, it is detrimental to exercising and muscle growth. Last time I checked calorie restriction (which has been shown to have the highest impact in longevity in mammals to date) is not so good if you want to gain muscle either. If you are after longevity, you MUST keep doing Rapa. If you only care for big muscles, then you most likely will do better if you stop it. IMO you can either chose big muscles and an average lifespan, or average muscles (think of a swimmer’s body) and live much longer (like at least 20 years longer than with big muscles). Of course, it is way more nuanced (and when I say big muscles I mean huge like the body builder types) but at the end of day not too many bodybuilders seem to be reaching the supercentenarian status. To each their own, but IMO this study proved once again that RAPA is great for longevity.

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I am not sure that the study says anything about longevity.

I am open to be persuaded otherwise, but I don’t think it was designed to test longevity.

What the study does say is that if you exercise you get stronger (well we knew that). Also if you exercise and take rapamycin you get stronger, but not necessarily as much as if you exercise and don’t take rapamycin. (weekly)

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Someone else alluded to this I think, but doesn’t Rapa often cause some weight loss at the onset. That would not be helpful for building strength
And this calorie reduction would be particularly an issue for someone a bit older.

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Ask yourself a question. How often do you want a period of enhanced catabolism?

We know that weekly is probably too frequent.

What about annually?

What about every 6 months?

I am going for a period of 6 weeks or longer, but there is an interesting question as to where the threshold of benefit lies.

Incidentally I know that my 3 day a week water fast also enhances catabolism and hence reduces muscle gain (although I am still gaining slightly). Muscle gain is not my priority although I would not want any loss. At the moment I am aiming to reduce my weight, but the additional catabolism is good as well.

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First, we can’t ignore the fact that Rapamycin was shown to improve muscle gain in animals. Yes, the mechanism would suggest otherwise and we now finally have proof of that in humans. It makes sense I suppose since animals aren’t strength training the same way that humans are.

You actually bring up something important as far as longevity vs muscles is concerned. It does appear that we must have to choose one or the other when it comes to Rapamycin. I was hopeful that Rapamycin wouldn’t interfere with muscle based on the outcomes of all the animal studies showing that it didn’t.

Since we now know it does in humans (at least for once weekly dosing at 6mg), I personally would rather have big muscles while just continuing all other longevity interventions I’m already doing, even if there is a minor trade off in longevity. Just my personal choice.

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Sounds like cope. Rapamycin, at low to moderate doses, does pretty much nothing even when taken daily. You need full body penetration and saturation at very high doses to have any sort of lifespan extension effect which works even when taken infrequently or only for a ““short”” duration.
Imo 20-100mg taken once every three months while you don’t go outside probably has the best chances of improving your overall health and give you lifespan extension effects.

exactly but that is the point. It implies it by proving that it is not good for muscle building (I’m staying away from the scientific terms and just reading the layman version of it) which is to say that to date most interventions that mimic calorie restriction which is basically mtorc inhibition have shown positive effects on longevity. Even Sglt2i are being argued to provide the longevity benefit via similar mechanics, apart from the glucose impact. I tend to discount this study as anything other than proving the obvious which we knew (or was known) all along which is to say mtorc inhibition is bad for exercise and muscles. Not much new here IMO.
I don’t mean it to say it to be controversial, but I’m a bit more comfortable now (meaning Rapa will help with longevity) than I was last night (pre this study) because as I mentioned above it is exactly what we thought it would do (negatively (mildly) effect exercise) and this study did seem to prove it.

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@John_Hemming and everyone…

If one wants to consider dosing every two weeks vs weekly, how do we begin to figure out the right dose to try?

In the US, it’s easy and cheap ($17) to test rapa blood levels, so it’s an experiment I can easily track.

I’ll think out loud l…

I currently take 8mg each sat

My workout schedule is:

Monday- resistance training (RT)

Wednesday- RT

Friday- pilates

Saturday- rapa day.
I was taking rapa on Saturdays so it was after pilates and 2 days prior to Monday RT.

Until I figure out the pro and con of a two week dosing schedule, would someone recommend I take rapa on Thursday? That is the day after my RT on Wed, and then I have many days before Mon, and I just sacrifice the less important pilates? Or is Friday night a better call?

On pros and cons of dosing schedule:

Every two weeks might be better for muscles… that is good for my puny self.
But, if I’m taking a higher dose, then I’m probably blunting that week’s RT even more, so maybe the extra blunting of one week vs less blunting of one week is a wash?

Rapa cured my insomnia which is the biggest health promoting thing it could ever do for me. I assume skipping one extra week won’t make a difference, but if it did, better I just workout harder.

Does a larger dose make us more vulnerable to negative consequences… greater chances of infection etc… I assume so?

Larger dose might give a boost to some of the health promoting effects… I assume so?

Would just adding one day of RT make all this a moot point… or maybe I should take it every two weeks, and I could add that extra day on my off week and then turn into the @agetron of old ladies

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hope you don’t take this as arguing, but haven’t you been taking RAPA for a while now? And if you are relatively content with your physical appearance (I only wish my body was about 30% as good a shape as yours LOL) then why go for perfection, when we all know that perfection is the enemy of anything and everything. Again, not trying to change your mind, but the marginal effect on muscles I think is compensated by longevity effect of RAPA. Just my opinion.

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