Inhibition of Polyamine Synthesis by α-Difluoromethylornithine and its Effects on Pancreatic Secretion and Growth in the Rat

The role played by the polyamines in mediating the pancreatic growth and secretory responses to hormonal stimulation is uncertain. The effect of an inhibitor of ornithine decarboxylase (ODC), α-difluoromethylornithine (DFMO), on rat pancreatic protein secretion and synthesis and on growth in respons...

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Veröffentlicht in:Scandinavian journal of gastroenterology 1989, Vol.24 (6), p.733-744
Hauptverfasser: Haarstad, H., Skei, T., Petersen, H.
Format: Artikel
Sprache:eng
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Zusammenfassung:The role played by the polyamines in mediating the pancreatic growth and secretory responses to hormonal stimulation is uncertain. The effect of an inhibitor of ornithine decarboxylase (ODC), α-difluoromethylornithine (DFMO), on rat pancreatic protein secretion and synthesis and on growth in response to hormonal stimulation was therefore studied. Anesthetized rats were given an intravenous injection of DFMO (50,100, or 150 mg/kg), followed by a 7-h continuous infusion (15, 25, or 35 mg/kg/ h, respectively). After a basal 1-h period an intravenous infusion of 2.5 μg/kg/h of the cholecystokinin-like peptide Thr28Nle31CCK25-33 (CCK-LP) was added and continued for 6 h. The control rats received CCK-LP only. The ODC activity in the pancreas was markedly reduced by DFMO, but DFMO did not affect pancreatic juice volume or protein output. In another series conscious rats were given a continuous intravenous infusion of 2.5 μg/kg/h of CCK-LP for 8, 24, and 48 h or 5.0μg/kg/h of secretin for 8 and 48 h, with or without DFMO (100 mg/kg as an injection initially and thereafter 25mg/kg/h). The ODC activity and putrescine concentration in the pancreas were significantly reduced by DFMO at 8 and 24 h but not at 48 h. DFMO also significantly reduced the activities of RNA polymerase, DNA polymerase, and thymidine kinase at 24 h, but not at 48 h. The present study thus indicates that polyamines play a role in the initiation of the growth response to hormonal stimulation but does not support a similar dependence for early pancreatic protein synthetic and secretory responses.
ISSN:0036-5521
1502-7708
DOI:10.3109/00365528909093115