The delta EEG (sleep)-inducing peptide (DSIP). XI. Amino-acid analysis, sequence, synthesis and activity of the nonapeptide.
Schoenenberger. G A GA; Maier. P F PF; Tobler. H J HJ; Wilson. K K; Monnier. M M
Key Findings
- DSIP’s exact amino‑acid sequence is Trp‑Ala‑Gly‑Gly‑Asp‑Ala‑Ser‑Gly‑Glu.
- Synthetic DSIP given intracerebroventricularly increased delta EEG activity ~35% in rabbits, unlike control solutions or other related peptides.
- The active form is the alpha‑aspartyl isomer; the beta‑Asp version is inactive.
Practical Outcomes
- DSIP shows promise as a sleep‑promoting molecule, but the effective delivery in this study required direct brain infusion, which isn’t feasible for everyday use. For biohackers, the data suggest that peripheral or oral formulations (if they exist) may not replicate the effect, and more research is needed before practical dosing protocols can be recommended.
Summary
Researchers identified a 9‑amino‑acid peptide called DSIP that, when directly injected into the brain of rabbits, boosts deep‑sleep brain waves (delta activity) by about 35%. Only the natural form of the peptide works; a slightly different version does not.
Abstract
A peptide which induces slow-wave EEG (sleep) after intraventricular infusion into the brain has been isolated from the extracorporeal dialysate of cerebral venous blood in rabbits submitted to hypnogenic electrical stimulation of the intralaminar thalamic area. It was shown by amino-acid analysis and sequence determination to be Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu and named "Delta Sleep-Inducing Peptide" (DSIP). This compound was synthesized as well as 5 possible metabolic products (1--8, 2--9, 2--8, 1--4 and 5--9), 2 nonapeptide analogues (with one and two amino-acids exchanged) and a related tripeptide (Trp-Ser-Glu). All 9 synthetic peptides were infused intraventricularly in rabbits (6 nmol/kg in 0.05 ml of CSF-like solution over 3.5 min) and tested under double-blind conditions. A total of 61 rabbits including controls were used. The EEG from the frontal neocortex and the limbic archicortex were subjected to direct fast-Fourier transformation and analyzed by an 1108 computer system. A highly specific delta and spindle EEG-enhancing effect of the synthetic DSIP could be demonstrated. The mean increase of EEG delta activity reached 35% in the neocortex and limbic cortex as compared to control animals receiving CSF-like solution or any of the other 8 peptides. The final chemical characterization of the synthetic DSIP revealed that only the pure alpha-aspartyl peptide is highly active in contrast to its beta-Asp isomer. A neurohumoral modulating and programming activity was suggested.
Study Information
pubmed
1978
1978-09-06T00:00:00.000Z
10.1007/bf00581575