Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Mod GRF 1-29

Sermorelin, Growth Hormone Releasing Hormone (1-29), hGRF(1-29)NH2

Quick Stats
Studies 227
Trials 47
Score 2
1990 pubmed

Perinatal growth hormone (GH) physiology: effect of GH-releasing factor on maternal and fetal secretion of pituitary and placental GH.

de Zegher. F F; Vanderschueren-Lodeweyckx. M M; Spitz. B B; Faijerson. Y Y; Blomberg. F F; Beckers. A A; Hennen. G G; Frankenne. F F

Key Findings

  • A single dose of GRF‑1‑29 caused a small, borderline‑significant increase in maternal pituitary GH (p = 0.08).
  • Placental GH levels were unchanged after GRF‑1‑29 administration.

Practical Outcomes

  • For self‑experimenters, this study suggests that short‑term GRF‑1‑29 use in late pregnancy is unlikely to boost fetal growth hormone or affect placental hormone production. The modest maternal GH rise is not robust enough to be considered a reliable performance or longevity benefit, and the peptide does not cross to the fetus, limiting any direct fetal effects.

Summary

Giving the GH‑releasing peptide Sermorelin (GRF‑1‑29) to women right before a C‑section caused only a tiny, not statistically solid, rise in the mother's own growth hormone, didn’t change the placenta’s growth hormone, and didn’t reach the baby at all. In short, the peptide stays with the mother and doesn’t affect the fetus.

Abstract

To study regulation of the secretion of human pituitary GH (hGH) and placental GH (hPGH) in the pregnant woman and human fetus, the GH-releasing factor Sermorelin [GRF-(1-29)-NH2] was administered to pregnant women at term (n = 5), just before elective cesarean section; saline was administered in control studies (n = 5). The effects of GRF-(1-29)-NH2 administration on maternal and fetal serum concentrations of hGH and GRF-(1-29)-NH2 and maternal serum levels of hPGH were evaluated at birth. The mean time span between injection and birth was 20 min (range, 15-25 min). Cord serum hGH concentrations were similar in infants of GRF-(1-29)-NH2-injected mothers and control infants. GRF-(1-29)-NH2 elicited a consistent but small rise in maternal hGH serum concentrations (P = 0.08), whereas hPGH concentrations remained unaltered. Finally, GRF-(1-29)-NH2 concentrations were undetectable in cord serum, but readily detectable in concomitantly obtained maternal serum. In conclusion, these data suggest that hGH secretion in the pregnant woman at term is suppressed at the pituitary level, that GRF does not affect hPGH secretion, and that fetal hGH secretion is independent of circulating maternal GRF, probably because of lack of transplacental GRF passage.

Study Information

Provider

pubmed

Year

1990

DOI

10.1210/jcem-71-2-520