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Growth hormone status during long-term hexarelin therapy
A Rahim1, P A O'Neill, S M Shalet
1Department of Endocrinology, Christie Hospital, Withington, Manchester, United Kingdom.
The Journal of Clinical Endocrinology and Metabolism
|May 20, 1998
Summary
Long-term hexarelin therapy in adults causes a temporary decrease in growth hormone (GH) response, which recovers after treatment stops. The study found minimal impact on the GH-IGF-I axis and body composition.
Area of Science:
- Endocrinology
- Pharmacology
Background:
- Hexarelin is a potent growth hormone (GH)-releasing peptide with known efficacy via various administration routes.
- The long-term effects of hexarelin on GH levels in adults remained uncharacterized.
Purpose of the Study:
- To investigate the impact of 16 weeks of twice-daily subcutaneous hexarelin administration on GH response in adults.
- To assess the reversibility of GH response attenuation after hexarelin cessation.
- To evaluate chronic hexarelin effects on the GH-IGF-I axis, bone metabolism, body composition, and bone mineral density.
Main Methods:
- 16 weeks of twice-daily subcutaneous hexarelin (1.5 µg/kg BW) administration.
- GH response measured via area under the curve (AUCGH) at baseline, weeks 1, 4, 16, and 20 (4 weeks post-therapy).
- Assays for serum IGF-I, IGFBP-3, bone formation/resorption markers, body composition, and bone mineral density.
Main Results:
- Significant decrease in AUCGH at weeks 4 and 16 compared to baseline (P < 0.05 and P < 0.01).
- AUCGH significantly recovered by week 20 (P < 0.05 vs. week 16) and was not different from baseline.
- No significant changes in serum IGF-I, IGFBP-3, body composition, or bone mineral density.
- Increased serum C-terminal propeptide of type I collagen at week 16 (P = 0.019).
Conclusions:
- Chronic hexarelin therapy leads to a partial and reversible attenuation of GH response.
- The studied hexarelin regimen demonstrated minimal biological impact on the GH-IGF-I axis.
- Further research is warranted to explore the therapeutic potential of chronic hexarelin administration.