Splanchnic Neural Regulation of Somatostatin Secretion in the Isolated Perfused Human Pancreas

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Abstract

Objective

The somatostatin-secreting delta cells in the islets of Langerhans appear to be regulated by neural mechanisms that have not been defined clearly. In this study, the celiac neural bundle of the human pancreas was electrically stimulated in the presence and absence of selective neural antagonists.

Summary Background Data

The authors previously reported on studies of the splanchnic neural regulation of insulin, glucagon, and pancreatic potypeptide secretion. In these studies, alpha-adrenergic fibers appeared to have a predominant effect, strongly inhibiting the secretion of insulin, glucagon, and pancreatic polypeptide secretion. Cholinergic fibers appeared to stimulate strongly, although beta-adrenergic fibers weakly stimulated, the secretion of these hormones. Investigations of neural regulatory mechanisms governing human somatostatin release in vitro have not been previously reported.

Methods

Pancreata were obtained from eight cadaveric organ donors. The isolated perfused human pancreas technique was used to assess the regulation of somatostatin secretion by the various neural fibers contained within the celiac plexus. The secretory response of somatostatin was examined in the presence of 16.7 mmol/L glucose, with and without neural stimulation, and specific neural antagonists.

Results

The basal somatostatin secretion was 88 ± 26 fmol/g/min and increased 131 ± 23%(n = 8,p <> 0.01) in response to 16.7 mmol/L glucose. The augmentation seen with glucose was inhibited 66 ± 22% (n = 8, p < 0.05) during celiac neural bundle stimulation. Alpha-adrenergic blockade resulted in a 90 ± 30% (n = 6, p < 0.01) augmentation of somatostatin release. Beta-adrenergic blockade caused a 13 ± 2% (n = 6, p > 0.05) suppression of somatostatin release. Complete adrenergic blockade resulted in a 25 ± 23% (n = 5, p = not significant) inhibition of somatostatin release. Cholinergic blockade resulted in a 40 ± 10% (n = 6, p < 0.02) suppression of somatostatin release.

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