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DSIP

Emideltide, DSIP nonapeptide, Delta sleep-inducing peptide

Quick Stats
Studies 458
Trials 82
Score 2
1995 pubmed 18 citations

Delta-sleep-inducing peptide sequels in the mechanisms of resistance to emotional stress.

Sudakov. K V KV; Coghlan. J P JP; Kotov. A V AV; Salieva. R M RM; Koplik. E V EV

Key Findings

  • DSIP administration significantly altered hypothalamic and plasma levels of substance P, beta‑endorphin, and corticosterone.
  • The timing of DSIP injection (1 hour vs 24 hours before measurement) affected the magnitude of hormone changes.
  • Wistar rats showed a larger DSIP‑induced stress‑coping response than August rats, indicating strain‑dependent effects.

Practical Outcomes

  • DSIP appears to modulate stress‑related hormones in animals, hinting it could influence stress resilience. However, the study is limited to rats, uses high doses, and provides no human dosing guidance, so biohackers should treat it as preliminary evidence and await human trials before incorporating DSIP into stress‑management protocols.

Summary

In rats, giving the peptide delta‑sleep‑inducing peptide (DSIP) changes key stress‑related chemicals like substance P, beta‑endorphin and cortisol. The changes depend on when DSIP is given and are stronger in a strain of rats that handles stress better (Wistar) than in a more stress‑sensitive strain (August).

Abstract

The aim of this study is to investigate time-related changes in substance P (SP), beta-endorphin (BE), and corticosterone (CORT) levels due to DSIP aftereffects in the control and stress rats. Experiments were carried out on male Wistar and August rats. The SP and BE immunoreactivity in the hypothalamus and plasma samples was determined radioimmunologically. Blood CORT level was determined radioimmunologically. The rats were stressed at nighttime in special cages and tied by tails to the back side of the cage. The stress experiments were repeated for 12 hours for 5 days. There were 6 groups: 1. control animals, 2. stress animals, 3. rats that received DSIP in a dose of 60 nmol/kg one hour before decapitation, 4. rats in which DSIP was injected 24 hour before decapitation, 5. stressed rats in which DSIP was injected one hour before decapitation during the 5th exposure to stress, 6. stressed rats to which DSIP was injected 12 hours before the 5th exposure to stress, i.e., 24 hours before decapitation. Our experiments showed that DSIP administration induced marked changes in SP, BE, and CORT levels in hypothalamus and blood plasma. This suggests that the long-term stress-coping effect of DSIP depends on considerable changes in the level of other oligopeptides and hormones induced by DSIP. Evidently, DSIP triggers these processes inducing a cascade of interrelated molecular reactions radically different in animals with different resistance to emotional stress. This cascade of sequential reactions is different in Wistar and August rats differing by their resistance to emotional stress. DSIP administration stimulates the mechanism of resistance in August rats to a lesser extent than in Wistar animals.

Study Information

Provider

pubmed

Year

1995

Date

1995-12-29T00:00:00.000Z

DOI

10.1111/j.1749-6632.1995.tb44685.x

Citations

18

References

3