Effects of calcitonin on GH response to pyridostigmine in combination with hGHRH (1-29) NH2 in normal adult subjects.
Giustina. A A; Bodini. C C; Bossoni. S S; Doga. M M; Girelli. A A; Pizzocolo. G G; Wehrenberg. W B WB
Key Findings
- Salmon calcitonin significantly suppresses GH release triggered by GHRH (sermorelin).
- Pyridostigmine enhances GH response to GHRH in normal subjects.
- Pyridostigmine does not reverse the inhibitory effect of calcitonin on GH release.
Practical Outcomes
- If you’re using sermorelin or other GHRH peptides for GH boosting, avoid taking calcitonin concurrently as it will blunt the effect. Pyridostigmine might be used to modestly enhance GH response, but it won’t help if calcitonin is present. Plan your supplement/medication schedule accordingly.
Summary
The study shows that salmon calcitonin (a hormone used for bone health) reduces the growth hormone boost you get from a GHRH peptide like sermorelin. Taking pyridostigmine, a drug that raises acetylcholine, can increase the GH response to GHRH, but it doesn’t counteract the calcitonin effect. In short, calcitonin can blunt the benefits of GHRH, while pyridostigmine may help a bit if calcitonin isn’t involved.
Abstract
Studies in man demonstrated that salmon calcitonin (sCT) administration blunts the pituitary GH response to GH-releasing hormone (GHRH). However, the mechanisms underlying this inhibitory action of CT in man are unclear. Pyridostigmine (PD), an acetylcholinesterase inhibitor, is hypothesized to enhance the GH response to GHRH in normal subjects probably via a decrease in the somatostatinergic tone. The aim of the present study was to investigate the mechanism of the inhibitory action of sCT on the GH response to human GHRH (1-29) NH2 by concomitant PD administration in normal humans. The GH response to GHRH was significantly suppressed by prior administration of sCT. Pretreatment of subjects with PD significantly enhanced the GH response to GHRH but did not alter the inhibitory actions of sCT. We conclude that sCT is able to inhibit GHRH-stimulated GH secretion in man without influencing the hypothalamic somatostatinergic tone.
Study Information
pubmed
1990
1990-09-01T00:00:00.000Z
10.1111/j.1365-2265.1990.tb00502.x
9
26