| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Original Studies |
Divisione di Medicina Interna (R.L., G.M.), Unitá di Malattie Metaboliche (A.E.P.), Divisione di Neurochirurgia (M.L.), Unitá di Epidemiologia (A.C.), Istituto Scientifico Ospedale San Raffaele and Universitá degli Studi di Milano, 20132 Milano, Italy
Address all correspondence and requests for reprints to: Roberto Lanzi, M.D., Division of Internal Medicine, Istituto Scientifico Ospedale San Raffaele, Via Olgettina 60, 20132 Milano, Italy. E-mail: lanzi.roberto{at}hsr.it
Free fatty acids (FFA) physiologically regulate GH release via a
negative feedback. The aim of this study was to examine whether such
feedback is preserved in acromegaly, a condition in which alterations
in other regulatory mechanisms of GH release occur. Eight acromegalic
patients (group 1: five women and three men, 43.0 ± 4.2 yr old,
mean ± SE) received per os on two different
days, at a 3 day-interval, in a random order, placebo or 250 mg of
acipimox, an inhibitor of lipolysis analogous to nicotinic acid, at
0700 and 1100 h. In both tests GHRH (129 NH2), 50
µg, was administered iv at 1300 h. Blood samples for GH, FFA,
immunoreactive insulin (IRI), and glucose were taken from 0900 to
1500 h, and the time period considered for statistical analysis
was 12001500 h, representative of steady-state condition for FFA,
IRI, and glucose. Mean plasma FFA levels (12001500 h) were
significantly lower after acipimox than after placebo (0.05 ±
0.01 vs. 0.17 ± 0.01 g/L, P <
0.01). In contrast, both mean basal GH levels (12001300 h) and the
mean GH response to GHRH (GH
area, 13001500 h) were significantly
higher after acipimox than after placebo (12.0 ± 1.9
vs. 7.8 ± 1.2 µg/L, P <
0.01; 2937 ± 959 vs. 1154 ± 432 µg/L·120
min, P < 0.01). The increase in both basal GH
levels and GH
area occurred in all eight patients. Acipimox also
reduced mean serum IRI (83 ± 12 vs. 112 ± 14
pmol/L) and blood glucose (5.1 ± 0.1 vs. 5.7
± 0.1 mmol/L) levels, as compared with placebo (P
< 0.03 or less). Eight acromegalic patients (group 2: six women and
two men, 46.6 ± 5.7 yr old) underwent a constant iv 10% lipid
infusion (150 mL/h), started at 0900 h and continued until
1500 h. Mean plasma FFA levels (12001500 h) were significantly
higher during lipid infusion than after placebo (0.27 ± 0.01
vs. 0.16 ± 0.01 g/L, P <
0.02); in contrast, mean basal GH levels (12001300 h) were reduced by
lipid infusion, as compared with placebo (9.9 ± 3.1
vs. 16.6 ± 4.4 µg/L, P <
0.01), and the same occurred for the GH
area after GHRH (2498
± 1643 vs. 4512 ± 1988 µg/L·120 min,
P < 0.01). Serum IRI and blood glucose levels were
similar after placebo and during lipid infusion.
These data indicate that, in acromegaly, the acute reduction of circulating FFA levels results in increased GH release, whereas the increase in circulating FFA levels is accompanied by a reduced GH release. Taken together, these findings suggest that, in acromegaly, the control of FFA on GH release is preserved.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |