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Six-week treatment with hexarelin in young dogs: evaluation of the GH responsiveness to acute hexarelin or GHRH administration, and of the orexigenic effect of hexarelin

Study · animal · European journal of endocrinology · 1999 · DOI 10.1530/eje.0.1410313 · PMID 10474131

Plain-language summary

Paraphrased from the published abstract below — not a verdict on whether anything works.

This study evaluated a 6-week administration of hexarelin (250 microg/kg subcutaneously twice daily) in six young beagle dogs, assessing GH responses to acute hexarelin or GHRH challenge (2 microg/kg) before and after 3 and 6 weeks. The authors report the GH peak response to acute hexarelin or GHRH initially increased, peaking at the 3rd week, then decreased to basal values for GHRH or lower for hexarelin by the 6th week, indicating initial priming followed by downregulation of the hexarelin response with preservation of the GHRH response. They also studied rebound GH secretion after withdrawal of a somatostatin infusion. An acute feeding response to hexarelin was abolished at the 3rd week and returned at the 6th week. The authors suggest different central GH-releasing peptide receptor subtypes.

Abstract

In this study we evaluated, in six young (5-7 year-old) beagle dogs, the effects of a 6-week administration of hexarelin (250 microg/kg s. c. twice daily) on the GH response to an acute challenge with hexarelin or GHRH (2 microg/kg i.v.), delivered before and after 3 and 6 weeks of treatment. The GH peak response to acute hexarelin or GHRH initially increased, with a maximum observed at the 3rd week, and then decreased to basal values (GHRH) or less (hexarelin) at the 6th week. These data would indicate that hexarelin initially primed the pituitary to acute administration of further hexarelin or of GHRH, followed by downregulation of the GH response to hexarelin and preservation of the response to GHRH. We then studied the rebound increase in GH secretion after withdrawal of an infusion of somatostatin (4 microg/kg per h for 1.5 h), a likely stimulus of endogenous GHRH function. The pattern obtained was similar to, though not superimposable upon, that ensuing after acute hexarelin or GHRH administration. Parallel evaluation of the acute orexigenic effect of hexarelin evinced a different time-course of the behavioural response, namely an acute feeding response to hexarelin that was abolished at the 3rd week and returned to normal at the 6th week. The differing timing of the neuroendocrine or behavioural response to hexarelin would suggest the existence of different subtypes of central nervous system GH-releasing peptide receptors.

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