Delta sleep-inducing peptide in spontaneously hypertensive rats.
Graf. M V MV; Kastin. A J AJ; Schoenenberger. G A GA
Key Findings
- Spontaneously hypertensive rats have about 25% higher plasma DSIP levels than normal rats.
- Continuous DSIP infusion (200 µg/kg/day) prevented the usual rise in blood pressure over 10 days.
- A 5‑day course of daily DSIP injections produced a comparable blood‑pressure‑stabilizing effect.
Practical Outcomes
- The data suggest DSIP could influence blood‑pressure regulation, but the evidence is limited to rats and uses invasive delivery methods. For biohackers, it’s not yet a ready‑to‑use protocol for humans, but it may warrant watching future research on DSIP’s cardiovascular effects.
Summary
In a study with rats that naturally have high blood pressure, researchers found that a peptide called DSIP was a bit higher in these rats than in normal ones. Giving the rats extra DSIP for 10 days kept their blood pressure from climbing as much as it did in rats that got a salt solution. A short five‑day injection schedule gave a similar result. This hints that DSIP might play a role in controlling blood pressure, at least in this animal model.
Abstract
Delta sleep-inducing peptide has been shown to exert extra-sleep effects as well as effects on sleep. In this study, the concentrations of DSIP-like immunoreactivity were measured by radioimmunoassay in the plasma of spontaneously hypertensive rats (SHR). They were found to be about 25% higher in SHR plasma than in the plasma of the normotensive Wistar-Kyoto (WK) controls. DSIP was then infused for 10 days by osmotic minipump (200 micrograms/kg/day) into SHR. This resulted in in maintenance of BP at a level of about 200 mm Hg as compared with the significant increase to about 220 mm Hg after 10 days in the SHR controls infused with 0.9% NaCl. After daily SC injection of a single dose of 200 micrograms/kg DSIP for each of 5 days in SHR, findings were similar. The results raise the possibility of an involvement of DSIP in the regulation of BP in SHR.
Study Information
pubmed
1986
1986-06-01T00:00:00.000Z
10.1016/0091-3057(86)90524-1
14
12