[Effect of newly developed analogue of growth hormone releasing peptide [D-Ala-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2 (KP-102)] on growth hormone secretion in adult male rats].
Sawada. H H
Key Findings
- KP‑102 alone caused a strong GH spike at a very low dose (0.5 µg/kg) in awake rats.
- When combined with GRF, KP‑102 produced an even larger GH response, showing a synergistic effect.
- Pre‑treatment with cysteamine amplified the GH‑boosting action of KP‑102, turning synergy into an additive effect.
Practical Outcomes
- For biohackers, the study suggests that a GHRP‑like peptide can effectively raise GH levels, especially when paired with a GHRH analog or cysteamine. However, the data are limited to rats and specific experimental conditions, so direct dosing or protocol recommendations for humans are not yet supported.
Summary
In male rats, a new six‑amino‑acid peptide called KP‑102 can trigger a big release of growth hormone, especially when it’s given together with a growth‑hormone‑releasing factor (GRF) or after a drug called cysteamine. The effect depends a lot on the timing of the body’s natural hormone cycles.
Abstract
The effect of a newly developed hexapeptide; D-Ala-D-beta Nal-Ala-Trp-D-Phe-Lys-NH2 (KP-102) on GH secretion was studied in adult male rats. KP-102 induced a large plasma GH response at a dose of 0.5 micrograms/kg BW in conscious rats, although GH-releasing abilities of KP-102 varied markedly depending on the phase of GH secretion. Among urethan-anesthetized rats, KP-102 alone exerted a small influence on GH secretion, but it produced a large plasma GH response in the presence of exogenous GH-releasing factor (GRF). The rest of studies were performed on urethan anesthetized rats. During intermittent administration of GRF, the somatotropes became refractory to a large bolus dose of GRF, but KP-102 induced a marked increase of plasma GH. The GH response to KP-102 alone or KP-102 with GRF was significantly augmented when cysteamine HCl was previously administered. Although KP-102 and GRF acted synergistically on GH secretion in control animals, they acted additively in cysteamine-administered rats. Taken together, these findings suggest that the KP-102-induced GH secretion largely depends on GRF and the secretagogue potentiates the GRF effect by antagonizing the SS action at the level of somatotropes. It is concluded that KP-102 alone or in combination with GRF provides a means of stimulating GH secretion in the face of elevated inhibitory tone mediated by SS.
Study Information
pubmed
1995
10.1272/jnms1923.62.142