Growth hormone secretion in the guinea-pig.
Gabrielsson. B B; Fairhall. K M KM; Robinson. I C IC
Key Findings
- Guinea‑pig GH is secreted in episodic pulses, similar to rats, with males pulsing every 3‑4 h and females every 1‑2 h.
- Intravenous GRF‑1‑29 (2‑20 µg) stimulates GH release in a dose‑dependent manner.
- Somatostatin infusion suppresses spontaneous GH pulses, and stopping the infusion triggers a rebound surge of GH.
Practical Outcomes
- For biohackers, the data confirms that GRF‑1‑29 can act as a GH‑releasing agent in mammals, supporting its use as a secretagogue. However, because the work is in guinea‑pigs, the dosing and timing may not translate directly to humans. The study suggests that intermittent dosing could mimic natural GH pulses, but further human research is needed before applying these protocols.
Summary
In guinea‑pigs, growth hormone (GH) is released in bursts that can be triggered by a synthetic peptide called GRF‑1‑29. The study shows that giving GRF‑1‑29 in increasing doses makes the animals secrete more GH, and that blocking somatostatin (a GH‑inhibiting hormone) stops the bursts but causes a rebound when the block is lifted.
Abstract
The guinea-pig is unusual in that it continues to grow at a normal rate after hypophysectomy. Although its pituitary gland appears to contain a GH, this has not been isolated or characterized, and nothing is known about its secretion or physiological control. We have identified guinea-pig GH, established a sensitive heterologous radioimmunoassay and adapted our automatic blood microsampling method to study spontaneous GH secretion in this species. In male guinea-pigs, GH is released in an episodic pattern, reminiscent of the rat. Large multicomponent pulses of GH secretion occur every 3-4 h between periods of low or undetectable GH release, whereas most females showed a more uniform pulsatile pattern with pulses every 1-2 h. GH was released in response to GH-releasing factor (GRF) injections (2, 10 or 20 micrograms [Nle27]-GRF(1-29)NH2) in a dose-dependent fashion, and i.v. infusion of somatostatin (50 micrograms/h) blocked spontaneous GH pulses, eliciting a rebound release (from 2.0 +/- 0.8 (S.E.M.) to 36 +/- 17 micrograms/l 30 min after stopping the infusion). Infusions of a GH-releasing hexapeptide (100 or 400 micrograms/h for 4 h) also released GH. These results provide the first description of the pattern of GH release in the guinea-pig, and suggest that the striking episodic pattern is controlled by the same hypothalamic peptides that regulate GH in other species. Since the guinea-pig grows well in the absence of GH, this species may use GH for its metabolic, rather than growth-promoting actions. The guinea-pig may well prove a useful model, now that methods are available for studying its endogenous GH secretion.
Study Information
pubmed
1990
10.1677/joe.0.1240371