PinealonWhat the studies show

A three-amino-acid peptide from a St Petersburg laboratory, studied almost entirely in cell dishes and rats by the group that designed it.

4 min read · Animal and lab studies · Updated November 2026

In short

Name
pinealon
Evidence
Animal and lab studies
Bottom line
Cell-culture and single rat studies from the laboratory that designed the peptide, with no published trial in people and no independent replication.

Before you read this

This guide explains what published studies found. That is all it is.

It is not medical advice and it is not instructions for using anything. Where a dose appears, we are reporting what a named study gave the people or animals in it — a fact about the study, not an instruction to you.

The compounds here are not approved by the FDA for use in people and are sold for laboratory research only. A study tells you what happened to the subjects in it; it does not tell you what would happen to you. Talk to a doctor first.

What it is

Pinealon is a chain of three amino acids: glutamate, aspartate and arginine (Glu-Asp-Arg). It is one of a family of very short peptides designed by Vladimir Khavinson's group at the St Petersburg Institute of Bioregulation and Gerontology, which began with extracts of animal organs in the 1980s and later moved to synthetic two-, three- and four-amino-acid chains meant to stand in for them. Each is named for the organ it was derived from, pinealon for the pineal gland, and the group's central claim is that these tiny peptides enter cells, bind DNA and switch nearby genes on or off 1. In Russia it is classified as a dietary supplement rather than a medicine, and it is not approved as a drug anywhere.

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Terms

These guides explain what published studies found. That is all they are. They are not medical advice, and they are not instructions for using anything. Nothing here is meant to diagnose, treat, cure or prevent any illness. The compounds discussed on this site are not approved by the FDA for use in people. Research compounds are sold for laboratory use only, not for use in humans or animals. A study tells you what happened to the people or animals in it. It does not tell you what would happen to you. What you do with what you read here is your responsibility, so talk to a doctor first. This site is published by Progression Labs, which sells research compounds.

Cell studies

The most cited paper is from 2011 in Rejuvenation Research. The group grew cells in culture, exposed them to oxidative stress, and found that cells pre-treated with pinealon had lower levels of reactive oxygen species, less cell death, and a larger share of cells dividing than among untreated cells 2. The authors read this as a protective, pro-proliferative effect. A 2007 paper from the same institute had already reported antioxidant activity for several of these pineal-derived peptides in test-tube assays 3. In 2014 the group reported that pinealon and related tripeptides increased the amount of serotonin produced in cultured cells from rat brain cortex 4.

All of this is in dishes. A cell-culture result tells you a molecule can do something to a cell when it is placed directly on it; it does not tell you the molecule reaches that cell in a living animal, or what happens when it does.

Rats

The one animal study that stands out gave pinealon to pregnant rats whose homocysteine had been artificially raised, a condition that damages the developing brain, and reported that the offspring had better spatial learning and less oxidative damage in brain tissue than the offspring of untreated mothers 5. It is a single study, with small groups, from the same institute, and it has not been repeated.

The DNA-binding idea

The group's explanation for how a three-amino-acid peptide could do anything is unusual. In a 2013 paper they proposed that these short peptides pass through the cell and nuclear membranes and settle into the groove of the DNA double helix at particular sequences, nudging the genes nearby on or off; the evidence was computer modelling of the peptide-to-DNA fit, plus experiments in which the peptides changed gene expression in cultured cells 1. It is an interesting hypothesis. It has not been tested by anyone outside the institute, and the usual view in peptide chemistry is that a chain this short has no stable shape of its own, which makes specific DNA recognition hard to picture.

What is not known

There is no published, placebo-controlled trial of pinealon in people in the PubMed-indexed literature, and no pharmacokinetic study showing that a three-amino-acid chain survives digestion and reaches the brain intact; the default expectation for a peptide this small is that the gut breaks it into its component amino acids, which are the same amino acids found in any protein meal. Every study above comes from one laboratory, the one that designed the molecule and holds the patents. That does not make the findings wrong, but it does mean nobody has checked them. In short: the evidence base is small, comes from one source, and stops at cells and rats.

What these studies are, and aren't

Animal and lab studies. Cell-culture and single rat studies from the laboratory that designed the peptide, with no published trial in people and no independent replication.

Sources

  1. 1Khavinson VKh, Tarnovskaya SI, Linkova NS, et al. Short cell-penetrating peptides: a model of interactions with gene promoter sites. Bulletin of Experimental Biology and Medicine, 2013.
  2. 2Khavinson V, Ribakova Y, Kulebiakin K, et al. Pinealon increases cell viability by suppression of free radical levels and activating proliferative processes. Rejuvenation Research, 2011.
  3. 3Kozina LS, Arutjunyan AV, Khavinson VKh. Antioxidant properties of geroprotective peptides of the pineal gland. Archives of Gerontology and Geriatrics, 2007.
  4. 4Khavinson VKh, Lin'kova NS, Tarnovskaya SI, et al. Short peptides stimulate serotonin expression in cells of brain cortex. Bulletin of Experimental Biology and Medicine, 2014.
  5. 5Arutjunyan A, Kozina L, Stvolinskiy S, et al. Pinealon protects the rat offspring from prenatal hyperhomocysteinemia. International Journal of Clinical and Experimental Medicine, 2012.

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