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- Title
Evidence for a Direct Pituitary Inhibition by Free Fatty Acids of in vivo Growth Hormone Responses to Growth Hormone-Releasing Hormone in the Rat.
- Authors
Alvarez, Clara V.; Mallo, Federico; Burguera, Bartolome; Cacicedo, Luanda; Dieguez, Carlos; Casanueva, Felipe F.
- Abstract
The aim of this study was to determinate whether elevations in circulating free fatty acids (FFA) inhibit in vivo growth hormone (GH) responses to GH-releasing hormone (GHRH) by increasing hypothalamic somatostatin release or by acting directly on the pituitary. Thus, we have studied the effect of an Intralipid-heparin infusion on in vivo GH responses to GHRH in normal rats, normal rats passively immunized with antisomatostatin antiserum, rats with medial hypothalamic ablation, and hypophysectomized rats bearing two hypophyses under the renal capsule. Administration of 1 ml of Intralipid (500 μl at -30 min and 500 μl at -25 min) plus heparin (50 IU at-15 min) induced a marked decrease in GH responses to both 1 and 5 μg/kg of GHRH (p < O.Ol at 5, 10 and 15 min for GHRH alone vs. GHRH plus Intralipid). A similar degree of inhibition was obtained after the administration of antisomatostatin antiserum (750 μl i.v. at-60 min) previous to a challenge with 5 μg/kg of GHRH plus 1 ml of Intralipid (p < 0.05 at 5 and 15 min, and p < 0.01 at 10 min for GHRH plus normal rabbit serum vs. GHRH plus Intralipid plus antisomatostatin antiserum). Furthermore, administration of 1 ml of Intralipid also markedly reduced GH responses to GHRH in rats with medial hypothalamic ablation (p < 0.01 at 5, 10, 15 and 30 min for GHRH alone vs. GHRH plus Intralipid) as well as in hypophysectomized rats bearing two hypophyses under the renal capsule (p < 0.01 at 5, 10 and 15 min for GHRH alone vs. GHRH plus Intralipid). In brief, our data show that elevations in circulating FFA levels inhibit in vivo GH responses to GHRH by acting directly at the pituitary level. Copyright © 1991 S. Karger AG, Basel
- Publication
Neuroendocrinology, 1991, Vol 53, Issue 2, p185
- ISSN
0028-3835
- Publication type
Article
- DOI
10.1159/000125716