Hypothalamic control of growth hormone (GH) secretion in type I diabetic men: effect of the combined administration of GH-releasing hormone and hexarelin, a novel GHRP-6 analog
| Autor: | William B. Wehrenberg, P. Desenzani, Giovanna Bugari, Andrea Giustina, Gianni Giustina, P. Perini, Romano Deghenghi |
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| Přispěvatelé: | Giustina, Andrea, Desenzani, P, Perini, P, Deghenghi, R, Bugari, G, Wehrenberg, Wb, Giustina, G. |
| Jazyk: | angličtina |
| Rok vydání: | 1996 |
| Předmět: |
Adult
Blood Glucose Male endocrine system medicine.medical_specialty Hypothalamus Growth hormone Growth Hormone-Releasing Hormone chemistry.chemical_compound Endocrinology Bolus (medicine) Internal medicine medicine Humans Secretion GHRP-6 business.industry Human Growth Hormone Drug Synergism General Medicine Growth hormone secretion Abnormal Growth Hormone Kinetics Somatostatin Diabetes Mellitus Type 1 chemistry business Oligopeptides hormones hormone substitutes and hormone antagonists Hormone |
| Popis: | Insulin dependent (type I) diabetic patients show abnormal growth hormone (GH) secretion. Hexarelin is an analog of GHRP-6 which releases GH in part via somatostatin inhibition. The aim of our study was to evaluate the effects of hexarelin and GHRH, administered either alone or in combination, on GH secretion in 10 type I diabetic and 7 normal men. All the subjects were administered: 1) human GHRH (1-29) NH2 100 micrograms i.v. bolus at 0 min; 2) hexarelin 100 micrograms i.v. bolus at 0 min; 3) hexarelin 100 micrograms + hGHRH 100 micrograms i.v. bolus at 0 min. In type I diabetic patients significantly greater GH responses to GHRH and hexarelin have been observed with normal subjects. Hexarelin caused a significantly (p0.05) greater GH response as compared to GHRH in both diabetic and control subjects. After the administration of hexarelin+GHRH, a significant increase in both GH absolute and peak levels as compared to hexarelin or GHRH alone was found in all the subjects. However, the GH responses to the combined stimuli were not significantly different in diabetics as compared to normals; moreover, the interaction of GHRH and hexarelin was synergistic in controls and additive in diabetics. We hypothesize that a reduction in the hypothalamic somatostatin inhibitory tone combined with increased pituitary GH production may be responsible for the pattern of the GH responses to hexarelin and GHRH observed in our type I diabetic patients. |
| Databáze: | OpenAIRE |
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