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DSIP

Emideltide, DSIP nonapeptide, Delta sleep-inducing peptide

Quick Stats
Studies 458
Trials 82
Score 2
1991 pubmed 25 citations

Colocalization of delta sleep inducing peptide and luteinizing hormone releasing hormone in neurosecretory vesicles in rat median eminence.

Vallet. P G PG; Charnay. Y Y; Boura. C C; Kiss. J Z JZ

Key Findings

  • DSIP and LH‑RH are found in the same axons and dense‑core vesicles in the rat median eminence.
  • Both peptides show similar distribution patterns and often contact tanycyte processes but not blood vessels directly.
  • No DSIP or LH‑RH staining was seen in glial or ependymal cells, indicating neuron‑specific storage.

Practical Outcomes

  • For biohackers, this study suggests DSIP might have effects beyond sleep, potentially modulating reproductive hormone pathways. However, the work is purely anatomical in rats, with no dosage or human data, so it doesn’t translate into a concrete protocol yet. Use this as background knowledge, not a direct supplement recommendation.

Summary

In rats, the sleep‑related peptide DSIP and the hormone‑releasing peptide LH‑RH are packed together in the same nerve endings in the brain area that controls hormone release. This means they are likely released at the same time, hinting that DSIP could influence reproductive hormone signaling.

Abstract

The colocalization of immunoreactivities similar to delta sleep inducing peptide (DSIP) and luteinizing hormone releasing hormone (LH-RH) was investigated by light and electron microscopic immunocytochemistry in the rat median eminence. At the light microscopic level, DSIP and LH-RH immunostained fibers, and varicosities exhibited a similar distribution pattern throughout the median eminence. Immunoreactive axons were mainly found in the lateral part of the external layer. Using an elution-restaining technique, the coexistence of LH-RH and DSIP immunoreactivities was observed in most labelled axons. To determine the intracellular localization of DSIP and LH-RH, we used double immunocytochemical labelling with species-specific antibodies and secondary antibodies conjugated to different sizes of gold particles. The two peptides were found colocalized in single axons. Immunoreactive terminals frequently showed direct membrane apposition with tanycyte processes but rare contacts with portal capillaries. No staining was observed in tanycytes and ependymal or glial elements. Moreover, we could demonstrate that LH-RH and DSIP (or a closely related molecular form) are contained not only in the same axons, but also in the same approximately 100-nm dense-core vesicles, suggesting cosecretion of these peptides.

Study Information

Provider

pubmed

Year

1991

DOI

10.1159/000125705

Citations

25