The distribution and biologic activity of somatostatin receptor subtypes (S
STR) in pituitary adenomas is not clarified, especially regarding clinicall
y non-functioning adenomas (NFPA). We therefore characterized SSTR in human
pituitary adenomas by combining molecular biology and in vivo scintigraphy
. Go-expression of gonadotropin-releasing hormone receptor (GnRH-R) mRNA wa
s also assessed to see whether this feature was associated with adenoma sub
type and SSTR status. Pituitary tumor biopsies were obtained during transsp
henoidal adenomectomy from 21 patients (11 NFPA, 7 acromegalics, 2 prolacti
nomas, 1 Gushing's disease). Expression of mRNA encoding the 5 known SSTR s
ubtypes and the GnRH-R was determined by RT-PCR. Twelve patients also under
went a pre-operative somatostatin receptor scintigraphy. Most adenomas (no.
= 18) expressed mRNA for more than one SSTR. SSTR2 mRNA was expressed in 1
8 cases, whereas SSTR4 was absent in all but one. SSTR3 was frequently expr
essed in NFPAs. Somatostatin receptor scintigraphy was positive in most cas
es, and with a significantly higher uptake index in GH-producing adenomas a
ll of which expressed SSTR2 mRNA. The uptake index appeared to be related t
o receptor density rather than tumor volume. Expression of GnRH-R mRNA was
found in both NFPAs and GH-producing adenomas and was not significantly ass
ociated with a particular SSTR subtype population. In conclusion: 1) the di
stribution of SSTR is not significantly different between NFPA and GH-produ
cing adenomas; and 2) somatostatin receptor scintigraphy reveals a higher u
ptake in GH-producing adenomas which is not significantly related to either
SSTR distribution or tumor volume. (J. Endocrinol. Invest. 24: 430-437, 20
01) (C) 2001, Editrice Kurtis.