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c/glp1science·posted 5 months ago by u/tomas_broberg

reading gastric emptying threads from 2024 and half of it aged badly

Needs Source Receipts ×2

Trying to settle this properly because the thread from last year went in circles.

The claim: appetite matters. The counter-claim: it is measurement error. Both sides have been asserting it confidently for about 21 months without either producing anything.

What would actually settle it is 35 people measuring the same thing the same way. I have started; my numbers are below. They lean one way but not strongly enough for me to declare victory.

If you have data, post the data. If you have an opinion, flair it as an opinion.

587 up / 139 down81% upvoted12 commentsid xxy1hg14 Feb 2026

12 comments

10 in this archive, depth 5

best — the order this archive was captured in

u/noor_hovland43 points·5 months ago·edited

Inter-lab variance on this kind of assay is routinely 1–2 points. Different column, different gradient, different integration.

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u/emil_agyeman27 points·5 months ago

Mechanistically the bit that matters is mechanism. It explains most of the early profile and a decent chunk of the outcome.

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u/gustav_vermeulen24 points·5 months ago

Dead space in the needle hub holds a small but non-trivial volume. On low-volume draws that can be several units.

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u/tomas_brobergOP10 points·5 months ago

Receptor distribution explains why sulphur burps hits gastric emptying but not pharmacology.

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u/cato_batista29 points·5 months ago

do not extrapolate rodent data to human dosing without saying so

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u/emeka_chowdhury10 points·5 months ago

Which paper are you quoting?

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u/rafael_ostergaard8 points·5 months ago

the half-life is receptor, affects steady state timing

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u/anders_kuusela6 points·5 months ago

central appetite signalling is real but people overweight it

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u/georgi_chowdhury4 points·5 months ago

Rodent, human, or in vitro?

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u/bastian_eriksen3 points·5 months ago·edited

receptor distribution matters, GLP-1 is not everywhere

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About c/glp1science

The mechanism layer: incretin physiology, receptor distribution, gastric emptying, central appetite signalling, glucagon-receptor contribution, amylin co-agonism, and the pharmacokinetics that make weekly dosing possible. Papers get cited by journal and year or they get a [needs source] reply.

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