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KPV

When your gut starts running the day.

KPV is a three-amino-acid peptide studied in intestinal cells and mouse colitis models. The studies measured inflammatory pathways, colon-tissue damage, and recovery.

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Why people are watching KPV

Gut-barrier biology, measured one small peptide at a time.

KPV is lysine-proline-valine, the three-amino-acid tail of α-MSH. The studies tracked how intestinal cells transported it, what happened to inflammatory signaling inside those cells, and how colon tissue changed in two mouse models.

Close portrait through moving water with visible natural skin texture.Barrier questions show up in more than one place.

Gut and skin irritation

You want calm—not another vague wellness promise.

People looking into KPV often arrive with the same two frustrations: a gut that can derail the day and skin that keeps looking visibly irritated. Gut and skin are both barrier tissues, but the published work on this page is intestinal.

The published work follows intestinal-cell transport and signaling, then weight recovery, MPO activity, and colon histology in mouse colitis models.

Clear vial labeled KPV 10 mg injection on white.

The KPV vial

10 mg KPV injection. One 20-day vial.

The planned product is a 5 mL vial filled by a licensed U.S. compounding pharmacy. The patient-specific label identifies the formulation, strength, storage, and beyond-use date.

Strength
10 mg
Package
5 mL vial
Planned supply
20 days
Route
Prescription injection
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KPV product details

Formulation, directions, price, and supply.

Study notes, product details, and sources in one Rebody account.

  1. 01KPV evidence

    Intestinal-cell, immune-cell, and inflammatory-signaling studies.

  2. 02Product details

    Formulation, directions, price, supply, pharmacy, and states served.

  3. 03Injection routine

    Directions, storage, supply, and refill timing.

Glass intestinal epithelium showing KPV crossing a PepT1 transporter.

The transport step

PepT1

Intestinal cells can transport KPV.

Investigators identified PepT1-mediated uptake in intestinal and immune cells. Blocking PepT1 blocked the anti-inflammatory response in the experiment.

Mouse colitis studies

Earlier recovery. Lower MPO. Less inflammatory damage.

Across DSS colitis and transfer colitis, KPV-treated mice regained weight earlier and showed less inflammation in colon tissue. One oral experiment used five mice per group and measured weight, myeloperoxidase activity, and histology.

Read the Gastroenterology study ↗
Translucent colon tissue specimens illustrating inflammation measured in mouse models.

KPV study map

Transport. Signaling. Weight. Colon tissue.

The studies tracked PepT1 transport in intestinal and immune cells, NF-κB and MAPK signaling under TNF-α stimulation, and weight, MPO activity, and histology across mouse colitis models.

Read the evidence review ↗

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