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Carbohydrates modulate opiate receptor mediated mechanisms during postprandial endocrine function
Regulatory Peptides
|November 1, 1983
Summary
Carbohydrates modulate how endogenous opiates affect digestive hormone release after meals in dogs. This study shows carbohydrates can inhibit or stimulate somatostatin, insulin, and pancreatic polypeptide release via opiate receptors.
Area of Science:
- Gastroenterology
- Endocrinology
- Neuroscience
Background:
- Endogenous opiates play a role in regulating gastrointestinal hormone release.
- The influence of carbohydrates on opiate receptor-mediated hormonal responses is not fully understood.
Purpose of the Study:
- To investigate the role of carbohydrates in naloxone-induced opiate receptor blockade.
- To determine the effect of carbohydrates on postprandial somatostatin, insulin, and pancreatic polypeptide levels in response to protein and fat meals.
Main Methods:
- Conscious dogs were fed test meals containing protein (liver extract) or fat (corn oil) with or without carbohydrates (sucrose or intravenous glucose).
- Naloxone (an opiate receptor antagonist) or saline was administered with the test meals.
- Plasma levels of somatostatin, insulin, and pancreatic polypeptide were measured postprandially.
Main Results:
- Carbohydrates abolished naloxone's inhibitory effect on postprandial somatostatin in protein meals but stimulated somatostatin in fat meals.
- Naloxone augmented insulin secretion when carbohydrates were given with fat meals.
- Pancreatic polypeptide release was enhanced by naloxone when carbohydrates were combined with either protein or fat meals.
Conclusions:
- Oral or intravenous carbohydrates modulate the effects of endogenous opiates on postprandial somatostatin, insulin, and pancreatic polypeptide release in dogs.
- Carbohydrates appear to induce inhibitory mechanisms mediated via endogenous opiate receptors in this context.