| Autor: |
Montaner, Mireia, Denom, Jessica, Simon, Vincent, Jiang, Wanqing, Holt, Marie K., Brierley, Daniel I., Rouch, Claude, Foppen, Ewout, Kassis, Nadim, Jarriault, David, Khan, Dawood, Eygret, Louise, Mifsud, Francois, Hodson, David J., Broichhagen, Johannes, Van Oudenhove, Lukas, Fioramonti, Xavier, Gault, Victor, Cota, Daniela, Reimann, Frank |
| Předmět: |
|
| Zdroj: |
Nature Communications; 8/13/2024, Vol. 15 Issue 1, p1-14, 14p |
| Abstrakt: |
Glucagon-like peptide 1 (GLP-1) stimulates insulin secretion and holds significant pharmacological potential. Nevertheless, the regulation of energy homeostasis by centrally-produced GLP-1 remains partially understood. Preproglucagon cells, known to release GLP-1, are found in the olfactory bulb (OB). We show that activating GLP-1 receptors (GLP-1R) in the OB stimulates insulin secretion in response to oral glucose in lean and diet-induced obese male mice. This is associated with reduced noradrenaline content in the pancreas and blocked by an α2-adrenergic receptor agonist, implicating functional involvement of the sympathetic nervous system (SNS). Inhibiting GABAA receptors in the paraventricular nucleus of the hypothalamus (PVN), the control centre of the SNS, abolishes the enhancing effect on insulin secretion induced by OB GLP-1R. Therefore, OB GLP-1-dependent regulation of insulin secretion relies on a relay within the PVN. This study provides evidence that OB GLP-1 signalling engages a top-down neural mechanism to control insulin secretion via the SNS. The regulation of energy homeostasis by centrally-produced GLP-1 is not yet fully understood. Here, authors show that GLP-1 neuronal circuitry in the olfactory bulb reduces food intake and enhances insulin secretion in obese mice. The increase in insulin secretion is mediated by a GABA-dependent relay in the paraventricular hypothalamus and decreased sympathetic nerve activity. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
Full text from SpringerLink