I read post #27 twice before replying, because I had assumed the opposite.
The most useful reply I ever got about reading a rodent study was a request to state my units. It sounds like pedantry and it has saved me twice.
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1.
I read post #27 twice before replying, because I had assumed the opposite.
The most useful reply I ever got about reading a rodent study was a request to state my units. It sounds like pedantry and it has saved me twice.
Since reading a rodent study keeps coming up, it should probably be a maintained page rather than a recurring thread. I am happy to draft it if someone with more direct experience will review it.
Storage: these are lyophilised short peptides and are generally reasonably stable dry and considerably less so in solution. Reconstituting only what will be used within the period the supplier's own data covers is the conservative approach.
The step people skip is the one I have spelled out.
On reading a rodent study I would separate what is worth knowing from what is worth acting on. The first list is long and the second is short, and conflating them is how threads get heated.
What a well-designed human trial of a secretagogue would look like: randomised, placebo-controlled, adequate sample size, IGF-1 as primary outcome, muscle and strength as secondary outcomes, adequate follow-up duration. Very few secretagogue trials meet that description.
Genuine question rather than a rhetorical one: has anyone here actually observed reading a rodent study, as opposed to read about it? The thread is long and I cannot tell.
Evidence quality in the secretagogue literature is honestly weaker than in the incretin literature. Large randomised controlled trials are rare. Most evidence is mechanistic or from small studies. This is why this subcategory has higher sourcing standards than most.
I read post #42 twice before replying, because I had assumed the opposite.
What I want from this reading a rodent study thread is the list of things that would need to be true for the claim to hold. If we can write that list, we can check it.
Narrowing post #44, because the general version has more than one answer.
CJC-1295 exists in two forms in circulation — with and without the drug affinity complex — and they have very different half-lives. Product descriptions frequently do not say which, and the difference is not cosmetic.
I have left out the parts I could not verify.
Everything in post #46 holds. The case it does not cover is the one I have.
The thing about reading a rodent study that took me longest to accept is that a plausible mechanism is not evidence of an effect. It is a reason to look, not a result.
Where I part company with post #46, and it is a narrow parting.
Effects reported at the level of appetite are the most consistently described and the most mechanistically direct for the ghrelin-receptor compounds, which is not what most people are taking them for.
This has been discussed before and I could not find the thread, so, again.
CJC-1295 with and without DAC: the version with a drug affinity complex binds albumin covalently and persists for days. The version without it does not persist. Supplier labelling frequently does not distinguish them clearly, so confirming which you have is important.
I changed my mind about reading a rodent study after someone here asked me for the source and I could not produce one. That is worth saying out loud because it is the ordinary way it happens.
Post #49 describes the usual case. This is about the unusual one.
Speaking only to reading a rodent study as I have actually seen it, rather than as it is usually described: the effect is real, it is smaller than the thread suggests, and the variance between people is larger than the effect.
A mass result for a short peptide is more discriminating than for a long one, because a single residue difference is a larger proportion of the total. That makes identity confirmation genuinely useful here.
Nothing above should be read as advice about what anyone else should do.
| Topic | Participants | Replies | Views | Activity |
|---|---|---|---|---|
|
IGF-1 as a surrogate endpoint and its limitations — the long version
On the subject in the title: IGF-1 as a surrogate endpoint and its limitations — the long version Working notes rather than a conclusion. A narrow question about IGF-1, deliberately narrow, because the broad…
|
+14 | 18 | 53k | 12mo |
|
Revisiting: What a well-designed human trial of a secretagogue would look like
On the subject in the title: Revisiting: What a well-designed human trial of a secretagogue would look like Working notes rather than a conclusion. Something about well-designed human trial does not reconcile…
|
+69 | 74 | 25k | 18mo |
|
Why pulsatile secretion matters for interpreting secretagogue claims — a second dataset
The question in the title: Why pulsatile secretion matters for interpreting secretagogue claims — a second dataset I will give what I have already checked below so nobody repeats it. Posting a small dataset…
|
+60 | 64 | 25k | 15mo |
|
Ipamorelin selectivity claims and where they came from — a second dataset
Posting this under the heading it deserves: Ipamorelin selectivity claims and where they came from — a second dataset Everything below is what sits behind that. Posting a small dataset on Ipamorelin…
|
2 | 27k | 14mo | |
|
CJC-1295 with and without DAC: what the modification does — what changed since
CJC-1295 with and without DAC: what the modification does — what changed since Writing it up because I had to work it out twice and would rather nobody else did. What changes if the standard account of…
|
4 | 5.1k | 7mo |
| Topic | Participants | Replies | Views | Activity |
|---|---|---|---|---|
|
Revisiting: Why the absence of controlled human data on BPC-157 matters more than people admit
Revisiting: Why the absence of controlled human data on BPC-157 matters more than people admit Writing it up because I had to work it out twice and would rather nobody else did. A follow-up question about…
|
+50 | 55 | 7.8k | 2d |
|
Critiquing an observational claim about a class effect
Posting this under the heading it deserves: Critiquing an observational claim about a class effect Everything below is what sits behind that. I was wrong about critiquing an observational claim in a thread…
|
2 | 6.9k | 14mo | |
|
Sample size in a voluntary survey: the selection problem
Posting this under the heading it deserves: Sample size in a voluntary survey: the selection problem Everything below is what sits behind that. Sample size: setting out the arithmetic in full, because I have…
|
+1 | 5 | 12k | 15mo |
|
Criticising the method without criticising the authors
Criticising the method without criticising the authors Writing it up because I had to work it out twice and would rather nobody else did. I was wrong about criticising the method without criticising in a…
|
+55 | 61 | 60k | 15mo |
|
Selection into a registry and what it does to the estimate
Selection into a registry and what it does to the estimate — setting out what I have, and where I think it stops being reliable. Working notes on selection rather than a conclusion. I would rather post the…
|
2 | 55k | 7mo |