It is known that in adult rats, GH by itself and by promoting secretion of the somatomedins acts at the level of the hypothalamus to trigger release of somatostatin and decrease output of GH-releasing hormone (GHRH), thereby inhibiting further secretion of GH. To assess whether these mechanisms are already operative in the early postnatal period, we have evaluated the effect of short-term administration of GH in 10-day-old rats. Twice-daily s.c. administration of 25 micrograms human GH/rat, from days 5 to 9 of life, significantly reduced pituitary content of GH, decreased hypothalamic levels of GHRH mRNA and abolished the in-vivo GH response to a challenge dose of GHRH (20 ng/100 g body weight, s.c.). GHRH (20 ng/100 g body weight, twice daily, s.c.) given concomitantly with the GH treatment, completely counteracted the inhibitory effect of the latter on pituitary content of GH and restored to normal the in-vivo GH response to the GHRH challenge. These data indicate that impaired secretion of GHRH is involved in the inhibitory effect elicited by GH treatment in infant rats. However, concomitant involvement of hypothalamic somatostatin as a result of GH treatment cannot be ruled out. In fact, pituitaries from rats pretreated with GH responded in the same manner as pituitaries from control rats to the GHRH challenge in vitro.

Growth hormone (GH) autofeedback action in the neonatal rat : involvement of GH-releasing hormone and somatostatin / S.G. Cella, V. De Gennaro Colonna, V. Locatelli, V. Moiraghi, S. Loche, W.B. Wehrenberg, E.E. Müller. - In: JOURNAL OF ENDOCRINOLOGY. - ISSN 0022-0795. - 124:2(1990 Feb), pp. 199-205.

Growth hormone (GH) autofeedback action in the neonatal rat : involvement of GH-releasing hormone and somatostatin

S.G. Cella;V. De Gennaro Colonna;
1990

Abstract

It is known that in adult rats, GH by itself and by promoting secretion of the somatomedins acts at the level of the hypothalamus to trigger release of somatostatin and decrease output of GH-releasing hormone (GHRH), thereby inhibiting further secretion of GH. To assess whether these mechanisms are already operative in the early postnatal period, we have evaluated the effect of short-term administration of GH in 10-day-old rats. Twice-daily s.c. administration of 25 micrograms human GH/rat, from days 5 to 9 of life, significantly reduced pituitary content of GH, decreased hypothalamic levels of GHRH mRNA and abolished the in-vivo GH response to a challenge dose of GHRH (20 ng/100 g body weight, s.c.). GHRH (20 ng/100 g body weight, twice daily, s.c.) given concomitantly with the GH treatment, completely counteracted the inhibitory effect of the latter on pituitary content of GH and restored to normal the in-vivo GH response to the GHRH challenge. These data indicate that impaired secretion of GHRH is involved in the inhibitory effect elicited by GH treatment in infant rats. However, concomitant involvement of hypothalamic somatostatin as a result of GH treatment cannot be ruled out. In fact, pituitaries from rats pretreated with GH responded in the same manner as pituitaries from control rats to the GHRH challenge in vitro.
Rats, Inbred Strains ; Rats ; Animals ; Hypothalamus ; Antibodies ; Pituitary Gland ; Gene Expression ; Feedback ; Growth Hormone-Releasing Hormone ; Somatostatin ; Growth Hormone
Settore BIO/14 - Farmacologia
Settore MED/13 - Endocrinologia
feb-1990
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/206114
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