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Evidence-based GLP-1 & peptide discussion since 2023
ForumsOther Peptides & Research CompoundsHas anyone dealt with selank and semax?

Has anyone dealt with selank and semax?

Dr.GutHealth Mon, Apr 13, 2026 at 9:22 PM 9 replies 644 viewsPage 1 of 2
Dr.GutHealth
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Apr 13, 2026 at 9:22 PM#1

Reading about receptor desensitisation and trying to work out which of the effects adapt over time and which do not, because people clearly experience both.

What I am after is which effects tachyphylax and which persist, because the answer explains why tolerability improves while the appetite effect keeps working.

Practical detail welcome, however dull — the duller the better.

38 8VanRx_Mike, steve_okc, dave_SLC and 35 others
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mike.trainer_LA
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Apr 13, 2026 at 10:00 PM#2
Dr.GutHealth said:
Reading about receptor desensitisation and trying to work out which of the effects adapt over time and which do not, because people clearly experience…

PK/PD modeling for the pharmacology: understanding the pharmacokinetics helps optimize dosing. Semaglutide:

  • Tmax: 24-72 hours post-injection
  • T½: ~168 hours (7 days) — enables weekly dosing
  • Steady state: reached at 4-5 weeks
  • Bioavailability (SubQ): ~89%
  • Volume of distribution: ~12.5L (primarily plasma)

The albumin binding (>99%) is the key pharmacological innovation — creating a sustained-release effect from a single injection. Previous GLP-1 agonists (exenatide) required BID dosing due to rapid clearance.

37 7newstart_MO, mia_MS2, LeilaHI and 34 others
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A1cHero_PHX
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Apr 13, 2026 at 10:38 PM#3
mike.trainer_LA said:
PK/PD modeling for the pharmacology: understanding the pharmacokinetics helps optimize dosing.

No disagreement with mike.trainer_LA. One condition attached. The pharmacokinetics explain nearly every practical question asked here. Albumin binding above 99% slows clearance enough to make weekly dosing possible; a terminal half-life near a week means four to five weeks to steady state and therefore a four-week titration interval; subcutaneous bioavailability around 89% means injection site barely matters. Those three facts answer most timing questions before they are asked.

36 6tampaLisa73, KarenAZ_mom, zoe_NC and 33 others
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JakeBK_lifts
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Apr 13, 2026 at 11:16 PM#4
Dr.GutHealth said:
Reading about receptor desensitisation and trying to work out which of the effects adapt over time and which do not, because people clearly experience…

Same pattern here, and in the same order.

Last edited: Apr 14, 2026 at 1:16 AM
35 5kate.chem, DataDave, Dr.GutHealth and 32 others
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Dr.BariatricHTX
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Apr 14, 2026 at 2:47 AM#5

From the other side of the consultation, briefly.

Amycretin (AMY/GLP-1 dual agonist) emerging data relevant to the pharmacology: Phase 1 showed -13.1% body weight at only 12 weeks, the fastest trajectory ever seen for an anti-obesity agent[1].

Amylin receptor agonism enhances satiety signaling through the area postrema and reduces glucagon secretion. Combined with GLP-1R agonism, this dual mechanism may produce even greater efficacy than current agents.

Early-stage data — interpret with caution. But the trajectory is extraordinary.

References:
[1] Novo Nordisk investor presentation, September 2023.
34 4maya_sedona, stefan_berlin, Dr.EM_Chicago and 31 others
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