Effects of psychoactive drugs on delta sleep-inducing peptide concentrations in rat brain.
Wahlestedt. C C; Ekman. R R; Heilig. M M; Widerlöv. E E
Key Findings
- Antidepressants (imipramine, zimeldine) reduce DSIP levels in hypothalamus, frontal cortex, and cerebellum
- Repeated haloperidol increases DSIP in hypothalamus but not cortex
- A single pentobarbital dose raises hypothalamic DSIP; repeated doses do not
- Adrenalectomy elevates hypothalamic DSIP
Practical Outcomes
- The study hints that drugs affecting mood or sedation can alter DSIP, a peptide some biohackers use for sleep support. However, because the data are from rats and focus on brain concentrations, there’s no clear protocol change for humans. It mainly serves as a caution that certain medications might interfere with DSIP‑related sleep effects.
Summary
In rats, the brain levels of the sleep‑related peptide DSIP change when certain drugs are given. Antidepressants like imipramine and zimeldine lower DSIP in several brain areas, while the antipsychotic haloperidol and a single dose of the barbiturate pentobarbital raise DSIP in the hypothalamus. Removing the adrenal glands also boosts DSIP there. These effects are seen in animal brains and may not translate directly to humans.
Abstract
The concentration of delta sleep-inducing peptide-like immunoreactivity (DSIP-LI) in rat brain regions was determined by radioimmunoassay following treatment with various psychoactive drugs or adrenalectomy. The antidepressant drugs imipramine and zimeldine, given orally twice daily for three weeks, reduced the concentrations of DSIP-LI in the hypothalamus, frontal cortex and cerebellum. The effects of zimeldine were similar but somewhat less pronounced than those of imipramine. The neuroleptic drug haloperidol, given i.p. once daily for two weeks, increased the concentration of DSIP-LI in the hypothalamus, but not in the frontal cortex. A single dose of haloperidol did not affect the concentration of DSIP-LI in either region. Like haloperidol, pentobarbital elevated the concentration of DSIP-LI in the hypothalamus; however, this effect of the barbiturate was seen after single but not after repeated administration. Cortical concentrations of DSIP-LI were unaffected following both single and repeated pentobarbital administration. Finally, adrenalectomy increased the concentration of DSIP-LI in the hypothalamus, but not in the other brain regions. In conclusion, the DSIP concentration in rat brain regions may be altered by a variety of interventions. The most profound and general alterations were observed following administration of antidepressant drugs.
Study Information
pubmed
1989
1989-01-17T00:00:00.000Z
10.1016/0014-2999(89)90159-3
2
16