Pancreatic polypeptide, glucagon and insulin secretion from the isolated perfused canine pancreas

TE Adrian, SR Bloom, K Hermansen, J Iversen - Diabetologia, 1978 - Springer
TE Adrian, SR Bloom, K Hermansen, J Iversen
Diabetologia, 1978Springer
The release of pancreatic polypeptide (PP) by gut hormones, acetyl choline and adrenaline
was investigated in an isolated perfused pancreas preparation. PP was potently released by
1 nmol/l caerulein (186±12%, p< 0.001) and gastric inhibitory peptide (GIP)(211±31%, p<
0.005) as well as by 1 [νmol/l acetyl choline (1097±59%, p< 0.001). A significant two-fold
release of PP was also evoked by 1 nmol/l vasoactive intestinal peptide (VIP)(129±38%, p<
0.02 and gastrin (108±25% p< 0.01). Insulin release, induced by high glucose concentration …
Summary
The release of pancreatic polypeptide (PP) by gut hormones, acetyl choline and adrenaline was investigated in an isolated perfused pancreas preparation. PP was potently released by 1 nmol/l caerulein (186±12%, p<0.001) and gastric inhibitory peptide (GIP) (211±31%, p<0.005) as well as by 1 [νmol/l acetyl choline (1097±59%, p<0.001). A significant two-fold release of PP was also evoked by 1 nmol/l vasoactive intestinal peptide (VIP) (129±38%, p<0.02 and gastrin (108±25% p<0.01). Insulin release, induced by high glucose concentration was enhanced by both GIP (210 ±38%, p<(0.01) and VIP (48±5%, p<0.001). In addition GIP enhanced the release of glucagon by 179±18% (p<0.001) at 1.4 mmol/l glucose and by 127±24% (p<0.005) at 8.3 mmol/l glucose. Thus no simple inter-relationship appears to exist between the control of the three circulating islet hormones.
Springer