Acute stimulation of brain mu opioid receptors inhibits glucose-stimulated insulin secretion via sympathetic innervation. (November 2016)

• Record Type: Journal Article
• Authors: Tudurí, Eva; Beiroa, Daniel; Stegbauer, Johannes; Fernø, Johan; López, Miguel; Diéguez, Carlos; Nogueiras, Rubén
• Is Part Of: Neuropharmacology. Volume 110(2016) Part A
• Page Start: 322
• Page End: 332
• Publication Date: 2016-11
• Subjects: β-Cells -- DAMGO -- Islets -- Glucose metabolism; DAMGO (PubChem CID: 5462471) -- U-50.488 (PubChem CID: 6604724) -- SNC-80 (PubChem CID: 123924) -- β-FNA (PubChem CID: 57339687); Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2016.08.005
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Pancreatic insulin-secreting β-cells express opioid receptors, whose activation by opioid peptides modulates hormone secretion. Opioid receptors are also expressed in multiple brain regions including the hypothalamus, where they play a role in feeding behavior and energy homeostasis, but their potential role in central regulation of glucose metabolism is unknown. Here, we investigate whether central opioid receptors participate in the regulation of insulin secretion and glucose homeostasis in vivo . C57BL/6J mice were acutely treated by intracerebroventricular (i.c.v.) injection with specific agonists for the three main opioid receptors, kappa (KOR), delta (DOR) and mu (MOR) opioid receptors: activation of KOR and DOR did not alter glucose tolerance, whereas activation of brain MOR with the specific agonist DAMGO blunted glucose-stimulated insulin secretion (GSIS), reduced insulin sensitivity, increased the expression of gluconeogenic genes in the liver and, consequently, impaired glucose tolerance. Pharmacological blockade of α2A -adrenergic receptors prevented DAMGO-induced glucose intolerance and gluconeogenesis. Accordingly, DAMGO failed to inhibit GSIS and to impair glucose tolerance in α2A -adrenoceptor knockout mice, indicating that the effects of central MOR activation on β-cells are mediated via sympathetic innervation. Our results show for the first time a new role of the central opioid system, specifically the MOR, in the regulation of insulin secretion and glucose metabolism. Graphical abstract: Highlights: Acute activation of central MOR, but not DOR or KOR, induces glucose intolerance. Stimulation of central MOR reduces insulin sensitivity and increases the expression of gluconeogenic genes in the liver. Central MOR activation impedes insulin release via a2α-adrenergic receptors.