Sixteen weeks of hexarelin therapy in aged dogs: effects on the somatotropic axis, muscle morphology, and bone metabolism.
Cella. S G SG; Cerri. C G CG; Daniel. S S; Sibilia. V V; Rigamonti. A A; Cattaneo. L L; Deghenghi. R R; Müller. E E EE
Key Findings
- Hexarelin repeatedly increased GH peak responses in old dogs, though IGF‑1 stayed unchanged.
- Urinary lysylpyridinoline, a bone‑resorption marker, was significantly reduced, suggesting less bone loss.
- Three of six old dogs showed modest improvements in muscle morphology and biochemistry, whereas young controls did not change.
Practical Outcomes
- Hexarelin may be useful for stimulating GH pulses and modestly supporting muscle and bone health in older individuals, but human data are lacking. The study used 500 µg/kg subcutaneous daily in on/off cycles, which is not a proven human protocol. Biohackers should treat these findings as preliminary and consider safety, dosing, and species differences before experimenting.
Summary
In a small study of old beagle dogs, daily injections of hexarelin (500 µg per kg) for 16 weeks repeatedly boosted growth‑hormone spikes but didn’t raise IGF‑1 levels. The peptide also lowered a urine marker of bone breakdown and, in half the dogs, showed modest improvements in muscle tissue, while young untreated dogs showed no changes. These results hint that hexarelin can revive GH activity and may help muscle and bone health in aging, but the evidence is limited to dogs and may not translate directly to people.
Abstract
Hexarelin (HEXA; 500 micrograms/kg/die, s.c.) was administered for 16 weeks to six old beagle dogs. The treatment consisted of three on-drug periods spaced by two off-drug periods. During each on period, the growth hormone (GH) peak response to HEXA initially increased and then dropped to pretreatment values. Each time, a wash-out interval restored the same pattern of GH responsiveness. HEXA significantly augmented the indices of spontaneous pulsatility of GH, but plasma insulin-like growth factor I levels did not change during treatment. HEXA apparently reduced bone resorption since it significantly decreased the urinary concentration of lysylpyridinoline, a bone matrix component. Bone formation apparently was not affected since unchanged levels of alkaline phosphatase were recorded. In three of six old dogs, HEXA induced an improvement of some morphological and biochemical muscular indices, evaluated in muscle specimens that, instead, remained unchanged in a group of young untreated controls. These findings indicate that HEXA effectively releases GH and primes the pituitary of old dogs, and strengthen the view that in aging, GH secretion may be restored by pharmacological means. It would also appear that HEXA-induced GH release improves some indices of body composition in old dogs.
Study Information
pubmed
1996
10.1093/gerona/51a.6.b439