4.3 Article

Mechanism of Orexin B-Stimulated Insulin and Glucagon Release From the Pancreas of Normal and Diabetic Rats

Journal

PANCREAS
Volume 40, Issue 1, Pages 131-136

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MPA.0b013e3181f74b4b

Keywords

orexin; diabetes; islet; hormone; immunohistochemistry; radioimmunoassay

Funding

  1. Faculty of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates

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Objectives: To examine the pattern of distribution and effect of orexin B in the islets of normal and diabetic rats. Methods: Pancreatic tissue fragments collected from normal and diabetic (4 weeks after the onset of diabetes) rats were either processed for immunohistochemistry or treated with different concentrations (10(-12) to 10(-6) mol/L) of orexin B. Results: Orexin B-positive nerves were observed in the wall of blood vessels of both normal and diabetic rat pancreas. Orexin B is abundant in the islets of normal rats and colocalized with insulin in A cells. The number of orexin B-positive cells decreased after the onset of diabetes. Orexin B evoked significant (P < 0.05) increases in insulin release from the pancreas of normal and diabetic rats. Propranolol, a A-adrenergic receptor antagonist, significantly (P < 0.04) reduced the stimulatory effect of orexin B on insulin secretion. Orexin B also induced significant (P < 0.05) increases in glucagon release from the pancreas of normal rats but failed to stimulate glucagon secretion from the pancreas of diabetic rats. Conclusions: Orexin B stimulated insulin secretion in normal and diabetic rat pancreas through the beta-adrenergic pathway. Orexin B may have an important role in the regulation of islet function.

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