RAT PANCREAS AFTER LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOG OCTREOTIDE

Citation
J. Vonschonfeld et al., RAT PANCREAS AFTER LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOG OCTREOTIDE, Experimental physiology, 80(6), 1995, pp. 1031-1038
Citations number
23
Categorie Soggetti
Physiology
Journal title
ISSN journal
09580670
Volume
80
Issue
6
Year of publication
1995
Pages
1031 - 1038
Database
ISI
SICI code
0958-0670(1995)80:6<1031:RPALTW>2.0.ZU;2-U
Abstract
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.