The Longevity Desk
Compound reference

Cognitive and neuro

DSIP

Named for sleep, then matched by saline in rabbits

What circulates
100 to 300 mcg under the skin, once in the evening
What was studied
About 1,485 mcg into a vein, for a 70 kg adult
The gap
Convention runs below the studied dose
How long it lasts
FDA states a short plasma half life of 8 minutes, citing a 2001 review rather than a primary measurement, and I could not trace that figure back to a primary human study. Kato and colleagues, measuring how fast it disappeared after an injection into a vein, got 4.0 minutes in 4 anaesthetised dogs, 2.9 in a monkey and 2.0 in 3 rats. All of those numbers are for a vein. Fast clearance from a vein does not by itself sink a nightly injection under the skin, since absorption out of the tissue can be the slow step, and neither FDA nor I found a study measuring that in any species. Untested, not refuted.

What it actually is

DSIP is short for delta sleep inducing peptide. It is a chain of nine amino acids, the small units proteins are built from, and short chains like that are called peptides. Guido Schoenenberger and Marcel Monnier, in Basel, pulled it out of the blood leaving the brains of rabbits in 1977, and named it for what it did to the rabbits' brainwave trace when it was dripped straight into the fluid filled chambers inside the brain. The American regulator's name for it is emideltide. What is sold is injected under the skin in the evening, and the name is the strongest claim anyone has made for it.

What it is supposed to do

There is no established mechanism. Kovalzon and Strekalova's 2006 review says the link between DSIP and sleep has never been further characterised, in part because no DSIP gene, protein or related receptor has been isolated, and calls the sleep factor hypothesis extremely poorly documented and still weak. A 2011 search of mammalian gene and protein databases reported that nothing is known of any precursor protein or encoding gene for it. Every human study of DSIP in blood that I read measures DSIP-like immunoreactivity, meaning whatever the antibody stuck to rather than DSIP itself, and it tracks body temperature, sits lower in REM sleep, the rapid eye movement stage, than in waking, and falls at the moment of falling asleep. The 2006 review proposes that a different, unidentified peptide is at least partly responsible for both.

What people take it for

People take it for sleep, which is what the name promises, usually as a single evening injection 1 to 3 hours before intended sleep. That is the convention that circulates and it is reported here as observation, not as a recommendation. The three uses FDA evaluated it for in 2026 were chronic insomnia, narcolepsy and opioid withdrawal, and the older human record splits along those lines too: sleep laboratory studies in chronic insomniacs, and one series in 107 inpatients in alcohol or opiate withdrawal, every one of them whose route I could establish given into a vein.

The dose question

What circulates
100 to 300 mcg under the skin, once in the evening
What was studied
About 1,485 mcg into a vein, for a 70 kg adult
25 nmol/kg, or 21.2 mcg/kg, the dose most of the human sleep trials used

Below the studied dose

The circulating figure is roughly 5 to 15 times smaller per kilogram than the trial dose, and it goes in by a route neither FDA's reviewers nor I found a human trial for. Every human administration whose route I could establish went into a vein, apart from one study up the nose that carries no abstract. I could find no published derivation for the 100 to 300 mcg number, and the dosing page I opened describes those figures as coming from research write ups rather than clinical trials. Against the two cat experiments, both near 100 mcg/kg under the skin, it is 24 to 71 times smaller.

Reported because it is what people use. Nothing here recommends any amount.

How long it lasts

FDA states a short plasma half life of 8 minutes, citing a 2001 review rather than a primary measurement, and I could not trace that figure back to a primary human study. Kato and colleagues, measuring how fast it disappeared after an injection into a vein, got 4.0 minutes in 4 anaesthetised dogs, 2.9 in a monkey and 2.0 in 3 rats. All of those numbers are for a vein. Fast clearance from a vein does not by itself sink a nightly injection under the skin, since absorption out of the tissue can be the slow step, and neither FDA nor I found a study measuring that in any species. Untested, not refuted.

Route studied

Into a vein, in every human administration whose route I could establish, apart from one study given up the nose that carries no abstract. In animals, infused into the fluid filled chambers inside the brain, and under the skin in two cat experiments and in rabbits at 1 mg/kg.

Route used

Injected under the skin, once in the evening, 1 to 3 hours before intended sleep.

How to check you have the right molecule

Two numbers to hold a batch report against. The mass should come back near 848.8, and the sequence should read Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu, nine amino acids long. Then two names. Emideltide is the American regulator's word for the same molecule, so that one is not a substitution. Deltaran is: FDA describes it as a freeze dried mixture of DSIP and glycine at one part to ten by weight, and the mouse life span result that circulates as a DSIP finding was run on that two component preparation rather than on DSIP alone. The same substitution runs through the animal sleep record, where the steadiest effects belong to modified versions of the molecule with one piece swapped out, and not to the parent.

Walked through on two real certificates in how to read a certificate of analysis.

What people get wrong

Reading the abstract and stopping there. Everyone quoting DSIP safety, including this site until FDA's 2026 document was read, has been quoting the abstract of that 1984 withdrawal series, which records only headaches in a few patients, while the full paper records three serious adverse effects. The abstract is the part that is free. The second mistake is the name. DSIP was named on a rabbit brainwave result from 1977, and when a Moscow group put DSIP and thirteen modified versions back into rabbits by that same route into the brain, DSIP itself did nothing to sleep that a saline injection into the same animals did not do, while two of the modified versions raised slow wave sleep by 10 to 15 percent and a third suppressed it.

What is known about harm

The safety record is thin, old, almost entirely by vein, and its largest item is not in the abstracts. Dick and colleagues gave DSIP into a vein to 107 inpatients in alcohol or opiate withdrawal, with no control group and no blinding, and the published abstract says tolerance was good aside from headaches reported by a few patients. FDA's 2026 reviewers read the full paper and report that 95 of the 107 had no significant adverse events, 9 had minor transient effects including perspiration, headache, nausea and vertigo, and 3 had serious adverse effects, two of them low blood pressure at the start of the first injection, with one of those going on to worsening low blood pressure after a second injection. Separately, in a 2009 randomised trial in 24 women having surgery, the 12 who received DSIP had a raised heart rate, lowered heart rate variability and lighter rather than deeper anaesthesia. For the route people actually use, FDA reports no nonclinical or clinical safety data and no effectiveness data at all.

Others in Cognitive and neuro

Everything on this page is a summary. The citations, the studies and the reasoning live in the full entry.

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