Library / Peptides / Gut & Inflammation / KPV
Theoretical · Grade C

KPV

KPV (Lys-Pro-Val, alpha-MSH Fragment 11-13)
Evidence
Theoretical
Route
Oral, Subcutaneous injection, or Topical
Frequency
1-2x daily
Category
Gut & Inflammation
TL;DR
KPV is a naturally occurring tripeptide (Lysine-Proline-Valine) derived from the C-terminal end of alpha-melanocyte-stimulating hormone (alpha-MSH). It retains the potent inflammation-modulating properties of the parent hormone without its melanogenic (skin-darkening) effects.
Part 01 · How it works

Mechanism.

KPV is a naturally occurring tripeptide (Lysine-Proline-Valine) derived from the C-terminal end of alpha-melanocyte-stimulating hormone (alpha-MSH). It retains the potent inflammation-modulating properties of the parent hormone without its melanogenic (skin-darkening) effects. KPV has been studied primarily in preclinical models for inflammatory bowel disease, skin inflammation, and wound healing.

Alpha-MSH is like a Swiss Army knife with many tools — inflammation-modulating action, skin tanning, appetite effects. KPV is just the inflammation-modulating blade extracted from that knife, doing one job very well without the other effects.

Mechanism · technical
KPV exerts inflammation-modulating effects primarily by entering cells and directly interacting with inflammatory signaling pathways. It inhibits NF-kB activation, reducing the transcription of pro-inflammatory cytokines (TNF-alpha, IL-1beta, IL-6). KPV has been shown to penetrate intestinal epithelial cells and interact with intracellular inflammatory mediators. Unlike full-length alpha-MSH, KPV does not significantly activate melanocortin receptors responsible for pigmentation, allowing it to deliver inflammation-modulating benefits without skin darkening.
Part 02 · Dosing & administration

How it's taken.

Values below describe how KPV has been administered in published trials and labeling. Provided for educational purposes only — this is not medical advice and not instructions for self-administration. Consult your healthcare provider before making any health decision.

Standard dose
200-500 mcg
Oral, Subcutaneous injection, or Topical · 1-2x daily
Duration
4-8 weeks typical cycle

C-terminal fragment of alpha-MSH (11-13). Inflammation-modulating without melanogenic effects. Oral/capsule form often used for GI applications. Not FDA-approved; published research protocols.

Need help with reconstitution?

Use the free peptide calculator for dilution, unit conversion, and injection volume.

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Part 03 · Safety

Side effects, rare serious events, who shouldn't.

Reported side effects
KPV has shown a very favorable safety profile in preclinical studies with no significant toxicity reported. Human safety data is extremely limited. Theoretical side effects may include injection site reactions and mild GI symptoms with oral use. No known serious adverse effects have been identified in the published literature.
Absolute · do not use
×
Active systemic infection (may suppress needed inflammatory response)
×
Pregnancy or breastfeeding
×
Children under 18
×
Known hypersensitivity to KPV, alpha-MSH fragments, or any component
Interactions
Immunosuppressants (tacrolimus, cyclosporine, biologics)
Additive immunosuppressive/inflammation-modulating effects; may increase infection risk
Moderate
NSAIDs
Additive inflammation-modulating effects; generally favorable but monitor for excessive immune suppression in vulnerable patients
Minor
TNF inhibitors (adalimumab, infliximab)
KPV inhibits NF-kB and TNF pathways; additive immunosuppression risk
Moderate
Labs to monitor
CRP / ESR
Baseline and monthly
Track inflammatory markers (primary indication is inflammation-modulating)
CMP (Comprehensive Metabolic Panel)
Baseline and every 3 months
Liver and kidney function
CBC with Differential
Baseline and every 3 months
Monitor immune parameters
Fecal Calprotectin
Baseline and monthly
If used for GI inflammation/IBD
Part 04 · Research log

Every study we cite.

Each study with its published finding and a plain-language note on limitations or funding.

01
2008
0
KPV peptide suppresses colitis in animal models
Oral KPV reduced colonic inflammation and TNF-alpha in murine colitis models
Preclinical; well-designed animal study
PMID 18200040 ↗
02
2006
0
Alpha-MSH fragments as inflammation-modulating agents
KPV retained inflammation-modulating activity of alpha-MSH without melanocortin receptor-mediated side effects
In vitro and in vivo mechanistic studies
Part 05 · Cost & access

Where you can get it.

Regulatory status
KPV is not FDA-approved for any indication. It is available through some compounding pharmacies with a prescription and as a research peptide. It has no formal regulatory designation and remains primarily investigational.
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Part 06 · Your appointment

Questions to bring.

01
Is KPV appropriate for my inflammatory condition given the limited human data?
02
What is the difference between oral, topical, and injectable KPV?
03
How does KPV compare to established inflammation-modulating treatments for my condition?
04
Are there any drug interactions I should be aware of with KPV?
05
What would a reasonable trial period look like to evaluate KPV's effects?
06
Is there clinical trial data in humans supporting KPV for gut inflammation?