BPC-157: what the rodent literature actually shows, and what it does not — a second dataset
Taking post #6 at face value and following it one step further.
The pentadecapeptide sequence is short and stable enough to survive conditions that would degrade a larger peptide, which is one of the few things about it that is well characterised.
Dose-response is unstudied in humans for essentially everything in this family, which means the confident numbers in circulation came from somewhere other than a trial.
It is one reading of the data and not the only reasonable one.
Where I part company with post #44, and it is a narrow parting.
Where the BPC-157 reasoning breaks down for me is the step from the group result to the individual case. That step is almost never argued for.
BPC-157's published evidence is overwhelmingly preclinical and mostly rodent. That is not a dismissal — it is the state of the literature, and any discussion that starts elsewhere is starting from something that is not there.
I am describing what is, rather than arguing for what should be.
Reading a preclinical wound-healing model: the model shows whether a mechanism is plausible in a specific context. It does not show magnitude of effect in humans, does not show safety profile in humans, and does not show whether the effect survives in a more complex biological system. That is not a criticism of preclinical work — it is what preclinical work is for.
Someone should write this up properly, and it should probably not be me.
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- What would change my mind about repair peptides: a specific answer — one year onCompounds › Repair & healing peptides · 13 replies
- BPC-157: what the rodent literature actually shows, and what it does not — does this still hold?Compounds › Repair & healing peptides · 10 replies
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