TY - JOUR
T1 - Growth hormone-releasing activity of hexarelin, a new synthetic hexapeptide, before and during puberty
AU - Bellone, J.
AU - Aimaretti, G.
AU - Bartolotta, E.
AU - Benso, L.
AU - Imbimbo, B. P.
AU - Lenhaerts, V.
AU - Deghenghi, R.
AU - Camanni, F.
AU - Ghigo, E.
PY - 1995/4
Y1 - 1995/4
N2 - The objective of this study was to verify the GH-releasing activity of a synthetic hexapeptide, hexarelin (HEX), before and during puberty. Ninety- six children (54 boys and 42 girls, aged 4.1-17.4 yr) were studied. Fifty- two of the children were prepubertal, and the other 44 were in pubertal stage II-IV. The GH response to 2 μg/kg HEX, iv (n = 56), was higher (P < 0.001) than that induced by 1 μg/kg GHRH, iv (n = 33). The iv dose of 2.0 μg/kg HEX induced a greater GH increase (P < 0.02) than the 1.0 μg/kg dose. The GH-releasing effect of 10 mg HEX, orally, was greater (P < 0.03) than that of 1.0 μg/kg GHRH, iv (n = 7). The iv dose of 2 μg/kg HEX elicited an increase in GH levels that was higher in pubertal children than in prepubertal children (77.5 ± 8.5 vs. 39.4 ± 4.4 μg/L; P < 0.001). Before puberty, there was no sex-dependent difference in the GH response to HEX. It increased during puberty (P < 0.05 and P < 0.002 for boys and girls, respectively), when it was higher (P < 0.05) in girls than in boys. In contrast, GH responses to GHRH were not related to sex differences and/or puberty. In conclusion, HEX is a potent and reproducible stimulus of GH secretion in children. The effect of HEX increases in puberty, with girls showing a more marked GH response.
AB - The objective of this study was to verify the GH-releasing activity of a synthetic hexapeptide, hexarelin (HEX), before and during puberty. Ninety- six children (54 boys and 42 girls, aged 4.1-17.4 yr) were studied. Fifty- two of the children were prepubertal, and the other 44 were in pubertal stage II-IV. The GH response to 2 μg/kg HEX, iv (n = 56), was higher (P < 0.001) than that induced by 1 μg/kg GHRH, iv (n = 33). The iv dose of 2.0 μg/kg HEX induced a greater GH increase (P < 0.02) than the 1.0 μg/kg dose. The GH-releasing effect of 10 mg HEX, orally, was greater (P < 0.03) than that of 1.0 μg/kg GHRH, iv (n = 7). The iv dose of 2 μg/kg HEX elicited an increase in GH levels that was higher in pubertal children than in prepubertal children (77.5 ± 8.5 vs. 39.4 ± 4.4 μg/L; P < 0.001). Before puberty, there was no sex-dependent difference in the GH response to HEX. It increased during puberty (P < 0.05 and P < 0.002 for boys and girls, respectively), when it was higher (P < 0.05) in girls than in boys. In contrast, GH responses to GHRH were not related to sex differences and/or puberty. In conclusion, HEX is a potent and reproducible stimulus of GH secretion in children. The effect of HEX increases in puberty, with girls showing a more marked GH response.
UR - http://www.scopus.com/inward/record.url?scp=0028967983&partnerID=8YFLogxK
U2 - 10.1210/jc.80.4.1090
DO - 10.1210/jc.80.4.1090
M3 - Article
SN - 0021-972X
VL - 80
SP - 1090
EP - 1094
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 4
ER -