V. Martina et al., BLUNTED GH RESPONSE TO GROWTH HORMONE-RELEASING HORMONE (GHRH) ALONE OR COMBINED WITH ARGININE IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS, Hormone and Metabolic Research, 27(1), 1995, pp. 26-30
An increased spontaneous and stimulated growth hormone (GH) secretion
is well documented in insulin-dependent diabetes mellitus. On the cont
rary, in non-insulin-dependent diabetes mellitus (NIDDM) conflicting r
esults arise from literature. In 14 patients with NIDDM, 7 normal weig
ht (NWD) and 7 obese (OD), we investigated the somatotrope responsiven
ess to GHRH (1 mu g/kg) alone or combined with arginine (ARC, 0.5 g/kg
), which is able to enhance the GH response to GHRH, probably by inhib
iting somatostatin release from hypothalamus. Baseline ICF-I, IRI, FFA
and glucose levels were also determined. Twelve healthy normal subjec
ts (NS) and 12 obese patients (OP) were evaluated as control groups. G
H but not IGF-I levels were higher (p<0.05) in NS than in OP (1.5+/-0.
5 vs 0.5+/-0.2 mu g/l). Insulin levels were higher (p<0.05) in OP than
in NS, NWD and OD (18.7+/-1.8 vs 8.7+/-0.5, 6.4+/-1.9 and 11.8+/-1.2
mu U/l). FFA were higher (p<0.05) in NWD, OD and OP than in NS (0.69+/
-0.04, 0.70+/-0.04 and 0.65+/-0.06 vs 0.39+/-0.03 mmol/l). Plasma gluc
ose was higher (p<0.05) in diabetic patients than in normal and obese
subjects. CH responses to GHRH in NWD, OD and OP were similar (AUG: 22
1.6+/-33.3, 206.0+/-35.9 and 177.2+/-57.3 mu g/I/min, respectively) an
d all lower (p<0.05) than that in NS (776.7+/-206.5 mu g/l/min). ARG d
etermined a significant increase of GHRH-induced GH release in all gro
ups (p<0.01). Again the GH responses to ARC + GHRH in NWD, OD and OP w
ere lower (p<0.05) than that observed in NS. In conclusion, our result
s demonstrate that, irrespective of body weight, patients with non-ins
ulin-dependent diabetes mellitus had an impairment of CH responses to
GHRH alone or combined with arginine. This finding may be explained by
the presence of high FFA levels which are known to inhibit GH secreti
on.