Endogenous GLP-1 acts on paraventricular nucleus to suppress feeding: projection from nucleus tractus solitarius and activation of corticotropin-releasing hormone …

K Katsurada, Y Maejima, M Nakata, M Kodaira… - Biochemical and …, 2014 - Elsevier
K Katsurada, Y Maejima, M Nakata, M Kodaira, S Suyama, Y Iwasaki, K Kario, T Yada
Biochemical and biophysical research communications, 2014Elsevier
Abstract Glucagon-like peptide-1 (GLP-1) receptor agonists have been used to treat type 2
diabetic patients and shown to reduce food intake and body weight. The anorexigenic
effects of GLP-1 and GLP-1 receptor agonists are thought to be mediated primarily via the
hypothalamic paraventricular nucleus (PVN). GLP-1, an intestinal hormone, is also localized
in the nucleus tractus solitarius (NTS) of the brain stem. However, the role of endogenous
GLP-1, particularly that in the NTS neurons, in feeding regulation remains to be established …
Abstract
Glucagon-like peptide-1 (GLP-1) receptor agonists have been used to treat type 2 diabetic patients and shown to reduce food intake and body weight. The anorexigenic effects of GLP-1 and GLP-1 receptor agonists are thought to be mediated primarily via the hypothalamic paraventricular nucleus (PVN). GLP-1, an intestinal hormone, is also localized in the nucleus tractus solitarius (NTS) of the brain stem. However, the role of endogenous GLP-1, particularly that in the NTS neurons, in feeding regulation remains to be established. The present study examined whether the NTS GLP-1 neurons project to PVN and whether the endogenous GLP-1 acts on PVN to restrict feeding. Intra-PVN injection of GLP-1 receptor antagonist exendin (9–39) increased food intake. Injection of retrograde tracer into PVN combined with immunohistochemistry for GLP-1 in NTS revealed direct projection of NTS GLP-1 neurons to PVN. Moreover, GLP-1 evoked Ca2+ signaling in single neurons isolated from PVN. The majority of GLP-1-responsive neurons were immunoreactive predominantly to corticotropin-releasing hormone (CRH) and nesfatin-1, and less frequently to oxytocin. These results indicate that endogenous GLP-1 targets PVN to restrict feeding behavior, in which the projection from NTS GLP-1 neurons and activation of CRH and nesfatin-1 neurons might be implicated. This study reveals a neuronal basis for the anorexigenic effect of endogenous GLP-1 in the brain.
Elsevier