Methylprednisolone does not inhibit the release of growth hormone after intravenous injection of a novel growth hormone secretagogue in rats.
Malmlöf. K K; Johansen. P B PB; Haahr. P M PM; Wilken. M M; Oxlund. H H
Key Findings
- Methylprednisolone lowers body‑weight gain but does not blunt the immediate GH surge from ipamorelin.
- Co‑administration of ipamorelin with methylprednisolone reduces steroid‑induced weight loss.
- Combined treatment raises IGF‑1 levels, indicating enhanced growth‑axis activity.
Practical Outcomes
- For biohackers using glucocorticoids (e.g., for inflammation or performance), ipamorelin may still work and could help offset catabolic effects. While the study is in rats, it suggests that ipamorelin dosing (roughly 0.4–1.6 mg/kg in rats) does not need to be reduced when steroids are present, but human dosing should be approached cautiously and under medical guidance.
Summary
In rats, the steroid methylprednisolone cuts weight gain but doesn’t stop the quick rise in growth hormone that ipamorelin causes. When ipamorelin is given together with the steroid, the animals lose far less weight and their IGF‑1 (a growth‑promoting hormone) goes up, showing a net anabolic effect.
Abstract
The present study was undertaken to study the growth hormone-releasing properties and growth-promoting effect of a GH secretagogue ipamorelin (IPA) in rats given the synthetic glucocorticoid methylprednisolone (MP). In a first experiment, rats received either saline or MP (5.0 mg/kg) for 8 days. Treatment with MP significantly (P< 0.001) decreased body weight gain, but the acute response to either IPA or growth hormone releasing hormone (GHRH) in terms of plasma GH was not changed. In a second experiment, venous catheters were surgically implanted. On the next day, rats were randomly allocated to receive saline alone, MP alone (5.0 mg/kg) or MP plus IPA in doses of 0.4 or 1.6 mg/kg/day for 10 days. IPA was administered intravenously four times a day.MP treatment significantly (P< 0.05) retarded recovery from surgery in terms of body weight. Thus, saline treated animals lost 4.0 +/- 3.5 g over the entire experimental period, whereas animals receiving MP lost 13. 6 +/- 2.9 g. When IPA was given together with MP, losses in body weight were significantly (P< 0.05) reduced to 2.3 +/- 2.0 and 1.6 +/- 2.0 g in animals given the high and low dose of IPA, respectively. In parallel with this IGF-I levels increased. In conclusion, this work shows that MP does not disrupt the response of the GH-IGF-I axis to an exogenous stimulus like IPA, and repeated stimulation leads to increases in IGF-I and of body weight gain.
Study Information
pubmed
1999
10.1054/ghir.1999.0128