All articles
Articlebeginnersemaglutidetirzepatide

What Are GLP-1 Peptides? A Plain-English Guide

GLP-1 peptides like semaglutide and tirzepatide are reshaping weight loss and metabolic health. What they are, how they work, and what to know before starting.

April 28, 2026 · 3 min read · By GLP-FAQ Editors


If you've spent any time on the internet in the last two years, you've heard the names: Ozempic. Wegovy. Mounjaro. Zepbound. They're prescribed for type 2 diabetes and weight loss, and behind every brand sits a class of molecules called GLP-1 receptor agonists — peptides that mimic a hormone your gut already makes.

This guide is the orientation we wish we'd had when we first tried to figure out what these drugs do, who they're for, and why they've become a generational shift in metabolic medicine.

What does "GLP-1" actually mean?

GLP-1 stands for glucagon-like peptide-1, a hormone secreted by your intestines after you eat. Its job is to:

  • Tell your pancreas to release insulin (so blood sugar comes down)
  • Slow gastric emptying (so food sits longer in your stomach)
  • Signal fullness to your brain (so you stop eating)

A GLP-1 receptor agonist is a synthetic peptide that binds to the same receptors as natural GLP-1 — but lasts much longer in your body. Where natural GLP-1 is broken down in minutes, modern peptides like semaglutide can stick around for about a week per dose.

The peptides you'll actually hear about

PeptideBrand namesTargetsNotes
SemaglutideOzempic, Wegovy, RybelsusGLP-1The original blockbuster
TirzepatideMounjaro, ZepboundGLP-1 + GIPDual-agonist; tends to outperform semaglutide on weight loss
LiraglutideSaxenda, VictozaGLP-1Older, daily injection
Retatrutide(in trials)GLP-1 + GIP + glucagonTriple-agonist; promising trial data, not yet FDA-approved

How they work for weight loss

Three mechanisms compound on each other:

  1. Reduced appetite. The "food noise" — that low-grade preoccupation with what to eat next — quiets down for most people within the first week.
  2. Slower digestion. Meals satisfy you for longer because they're physically still in your stomach.
  3. Better blood sugar control. Stable glucose means fewer insulin spikes, fewer cravings, and a metabolism that prefers fat for fuel.

In trials, semaglutide users lost roughly 15% of body weight over 68 weeks. Tirzepatide users lost up to 22% at the highest dose. For context, that's well past what bariatric surgery achieves for many patients.

What about side effects?

Most are GI: nausea, constipation, occasional vomiting — usually worst in the first week after a dose increase, then fading. Less common but worth knowing about: pancreatitis, gallbladder issues, and (in animal studies, not yet confirmed in humans) thyroid C-cell tumors. This is why titration matters — you start at a sub-therapeutic dose and ramp up over weeks.

Should you consider one?

That's a conversation for you and a clinician — but the candidates who tend to do best are people with:

  • BMI ≥ 27 with a comorbidity (high blood pressure, sleep apnea, prediabetes)
  • BMI ≥ 30 regardless
  • Type 2 diabetes that's not well-controlled on metformin alone

Where to go from here

The science is moving fast, but the fundamentals haven't changed: GLP-1 peptides work by amplifying a signal your body already sends. Used thoughtfully, with a clinician in the loop, they're one of the most effective metabolic tools we've ever had.

Free weekly newsletter

Get the GLP-1 highlights, weekly.

One short email a week — new FAQs, trial readouts, supply updates, and dosing tips. Plain-English, no spam.

Unsubscribe anytime. We never share your email.