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GlossaryMechanismGHRH Analog
Mechanism

GHRH Analog

Also known as: GHRH mimetic · growth hormone releasing hormone analog

A GHRH analog is a modified growth hormone-releasing hormone that activates the GHRH receptor on the pituitary to release the body's own growth hormone.

Growth hormone-releasing hormone (GHRH) is a peptide from the hypothalamus that acts on somatotroph cells in the pituitary to stimulate the production and pulsatile release of growth hormone. Growth hormone is both anabolic and fat-mobilizing, and many of its effects run through IGF-1 made in the liver and other tissues. GHRH analogs mimic the natural hormone at its receptor: in lab testing, tesamorelin binds and stimulates human GHRH receptors with potency similar to native GHRH. Sermorelin is a 29-amino-acid analog of human GHRH. These act on a different receptor from ghrelin-receptor agonists such as ipamorelin and MK-677.

The biggest practical difference between GHRH analogs is how long they last. The label gives tesamorelin a mean elimination half-life of 8 minutes after a subcutaneous (SubQ) injection. The long-acting CJC-1295 tested in healthy adults had an estimated half-life of 5.8 to 8.1 days; a single injection raised growth hormone 2- to 10-fold for 6 days or more and IGF-1 1.5- to 3-fold for 9 to 11 days. Research-market products labeled "CJC-1295 no DAC" are sold as a shorter-acting variant, so do not assume that trial's half-life applies to them.

Why it matters

Tesamorelin is the FDA-approved member of the class. Egrifta SV is indicated to reduce excess abdominal fat in adults with HIV and lipodystrophy; its label states it is not indicated for weight loss and is weight neutral. Its effectiveness rests on two randomized, double-blind, placebo-controlled 26-week studies that measured visceral fat by CT scan.

The label also shows what raising growth hormone and IGF-1 involves. Tesamorelin is contraindicated in active malignancy, pregnancy and disruption of the hypothalamic-pituitary axis. Warnings include fluid retention (swelling, joint pain, carpal tunnel syndrome), glucose intolerance or diabetes, and elevated IGF-1: after 26 weeks, 47% of treated patients had IGF-1 above 2 standard deviation scores and 36% above 3. Sermorelin's clinical data are limited and come mainly from children with growth hormone deficiency.

How to work out a label dose volume

  1. Find the vial strength and the diluent volume on the label.
  2. Concentration = vial amount divided by diluent volume.
  3. Volume to inject = prescribed dose divided by concentration.
  4. Use only the formulation the numbers came from; the Egrifta label warns that its two vial strengths have different dosing and reconstitution. The DoseCraft reconstitution calculator at /tools/reconstitution does the same arithmetic.

Volume to draw (mL) = dose (mg) / concentration (mg/mL)

Worked example

Egrifta SV label: a 2 mg vial reconstituted with 0.5 mL gives 2 / 0.5 = 4 mg/mL. The labeled 1.4 mg dose is 1.4 / 4 = 0.35 mL, which is exactly the volume the label specifies.

Common mistakes

  • Mixing up GHRH analogs and ghrelin-receptor agonists; they act on different receptors.
  • Assuming every product called CJC-1295 has the 5.8 to 8.1 day half-life measured in the trial.
  • Treating tesamorelin as a weight-loss drug; its label says it is weight neutral and not indicated for weight loss.
  • Skipping IGF-1 and glucose monitoring, which the tesamorelin label calls for.
  • Applying one formulation's dose and volume to another formulation or vial strength.

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