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GHRP-6 is able to stimulate cortisol and ACTH release in patients with Cushing's disease: comparison with DDAVP
J H A Oliveira1, J G H Vieira, J Abucham
1Division of Endocrinology, Universidade Federal de São Paulo-UNIFESP, São Paulo, Brazil.
Insights
Growth hormone-releasing peptide-6 (GHRP-6) stimulates adrenocorticotropic hormone (ACTH) and cortisol release in Cushing's disease patients. The effects of GHRP-6 were comparable to those of desmopressin (DDAVP), suggesting similar mechanisms of action.
Area of Science:
- Endocrinology
- Neuroendocrinology
- Pharmacology
Background:
- Hexarelin is known to stimulate ACTH and cortisol secretion in Cushing's disease.
- The precise mechanism of hexarelin's action on the hypothalamic-pituitary-adrenal axis is not fully understood, but may involve arginine vasopressin (AVP).
Purpose of the Study:
- To investigate the ACTH and cortisol releasing effects of GHRP-6 in patients with Cushing's disease.
- To compare these effects with those induced by desmopressin (DDAVP) administration.
Main Methods:
- Ten patients with Cushing's disease (9 with microadenomas) received intravenous bolus injections of GHRP-6 (2 μg/kg) and DDAVP (10 μg) on separate occasions.
- Adrenocorticotropic hormone (ACTH) and cortisol levels were measured using immunochemiluminometric assay and radioimmunoassay, respectively.
Main Results:
- GHRP-6 significantly increased both ACTH and cortisol levels in patients with Cushing's disease.
- The ACTH and cortisol responses to GHRP-6 were not significantly different from those observed after DDAVP administration.
- A significant positive correlation was found between peak cortisol levels following GHRP-6 and DDAVP administration.
Conclusions:
- GHRP-6 stimulates ACTH and cortisol release in Cushing's disease patients.
- The similar responses to GHRP-6 and DDAVP suggest potential shared mechanisms of action at the hypothalamic or pituitary level.
Abstract:
It has been shown that hexarelin stimulates ACTH and cortisol secretion in patients with Cushing's disease. The ACTH release induced by this peptide is 7-fold greater than that obtained by hCRH. The mechanism of action of hexarelin on the hypothalamic-pituitary-adrenal axis has not been fully elucidated. Although controversial, there is evidence that it might be mediated by arginine vasopressin (AVP). The aim of this study was to evaluate the ACTH and cortisol releasing effects of GHRP-6 in patients with Cushing's disease and to compare them with those obtained with DDAVP administration. We studied 10 patients with Cushing's disease (8 female, 2 male; age: 36.7 +/- 4.2 yr), 9 with microadenomas, who were submitted to both GHRP-6 (2 microg/kg iv) and DDAVP (10 micro g i.v.) in bolus administration on 2 separate occasions. ACTH was measured by immunochemiluminometric assay and cortisol by radioimmunoassay. The sensitivities of the assays are 0.2 pmol/l for ACTH, and 11 nmol/l for cortisol. GHRP-6 was able to increase significantly both ACTH (pmol/l, mean +/- SE; basal: 15.5 +/- 1.7 vs peak: 45.1 +/- 9.3) and cortisol values (nmol/l, basal: 583.0 +/- 90.8 vs peak: 1013.4 +/- 194.6). ACTH AUC (pmol/l min(-1)) and cortisol AUC (nmol/l min(-1)) values were 1235.4 and 20577.2, respectively. After DDAVP administration there was a significant increase in ACTH (basal: 13.0 +/- 1.4 vs peak: 50.5 +/- 16.2) and cortisol levels (basal: 572.5 +/- 112.7 vs peak: 860.5 +/- 102.8. AUC values for ACTH and cortisol were 1627.6 +/- 639.8 and 18364.7 +/- 5661.4, respectively. ACTH and cortisol responses to GHRP-6 and DDAVP did not differ significantly (peak: 45.1 +/- 9.3 vs 50.5 +/- 16.2; AUC: 1235.4 +/- 424.8 vs 1627.6 +/- 639.8). There was a significant positive correlation between peak cortisol values after GHRP-6 and DDAVP administration (r = 0.87, p = 0.001). Our results show that GHRP-6 is able to stimulate ACTH and cortisol release in patients with Cushing's disease. These responses are similar to those obtained after DDAVP injection. These findings could suggest the hypothesis that both peptides act by similar mechanisms, either at hypothalamic or pituitary level.
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