J. Vonschonfeld et al., RAT PANCREAS AFTER LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOG OCTREOTIDE, Experimental physiology, 80(6), 1995, pp. 1031-1038
Somatostatin is a potent inhibitor of endocrine and exocrine pancreati
c secretion. However, it is not clear whether it also inhibits pancrea
tic growth. Therefore we treated male Wistar rats with a somatostatin
analogue, octreotide (12-192 mu g/(kg body wt.day)), over a period of
14 days. In a dose-dependent manner, this potent and long-acting analo
gue caused a reduction in weight of the pancreas and a reduction in pa
ncreatic content of protein, DNA, trypsin, chymotrypsin, amylase and l
ipase, as well as pancreatic content of insulin-, glucagon- and somato
statin-like immuno-reactivities. When growth of rat pancreas was induc
ed by oral administration of camostate (200 mg/(kg body wt.day) or by
subcutaneous administration of cholecystokinin (2 x 10 mu g/(kg body w
t.day)) over a period of 14 days, octreotide (12-192 mu g/(kg body wt.
day)) had the same effects, but these were even more pronounced. We co
nclude that somatostatin is an important regulator of pancreatic growt
h.