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Autonomic function and control of pancreatic somatostatin
E Samols1,2, J I Stagner1,2, G C Weir1,2
1Veterans Administration Medical Center and Department of Medicine, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Canine pancreatic D cells have alpha-adrenergic receptors that inhibit somatostatin release and beta-adrenergic receptors that increase it. Muscarinic receptor stimulation mildly inhibits secretion, with no dopaminergic receptors present.
Area of Science:
- Endocrinology
- Neuroscience
- Gastroenterology
Background:
- D cells in the canine pancreas secrete somatostatin, a key hormone regulating gastrointestinal function.
- Autonomic nervous system regulation of pancreatic hormone secretion is crucial for maintaining homeostasis.
- Previous research has not fully elucidated the specific autonomic receptor subtypes on canine pancreatic D cells.
Purpose of the Study:
- To investigate the presence and function of alpha and beta adrenergic receptors on canine pancreatic D cells.
- To determine the effect of muscarinic and dopaminergic receptor stimulation on somatostatin release from D cells.
- To understand the potential physiological role of autonomic receptor stimulation in vivo.
Main Methods:
- Utilized canine pancreatic tissue preparations.
- Performed pharmacological stimulations to assess receptor activity.
- Measured somatostatin release in response to various autonomic receptor agonists and antagonists.
Main Results:
- Alpha-adrenergic receptor stimulation was found to inhibit somatostatin release.
- Beta-adrenergic receptor stimulation was found to increase somatostatin release.
- Muscarinic receptor stimulation resulted in mild inhibition of somatostatin secretion, and no dopaminergic receptors were detected on D cells.
Conclusions:
- Canine pancreatic D cells possess functional alpha and beta adrenergic receptors that modulate somatostatin secretion.
- Autonomic control of D cells involves adrenergic and muscarinic pathways, but not dopaminergic.
- These findings suggest that local ganglionic or central autonomic pathways may physiologically regulate D cells in vivo.
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