Wilfrid Mazier (Equipe Cota) & al. dans Molecular Metabolism

mTORC1 and CB1 receptor signaling regulate excitatory glutamatergic inputs onto the hypothalamic paraventricular nucleus in response to energy availability Wilfrid Mazier, Nicolas Saucisse, Vincent Simon, Astrid Cannich, Giovanni Marsicano, Federico Massa, Daniela Cota*


*Corresponding author. Group“Energy Balance and Obesity”, INSERM U1215, Neurocentre Magendie, 146 Rue Léo Saignat, 33077 Bordeaux, France. E-mail:


mTORC1 and CB1R signaling regulate the POMC-PVN parvocellular glutamatergic synapse. mTORC1 blockade with rapamycin (RAPA) at POMC neurons (1) favors endocannabinoid (eCB) synthesis from parvocellular neurons through an unknown mechanism possibly involving reduced α-MSH and decreased MC4R activation (2). Increase eCB levels, and in particular 2-AG, then activate presynaptic CB1R on POMC neurons (3), resulting in decreased glutamate release and glutamatergic input onto parvocellular neurons of the PVN (4).


The hypothalamic paraventricular nucleus (PVN) is a key target of the melanocortin system, which orchestrates behavioral and metabolic responses depending on energy availability. The mechanistic target of rapamycin complex 1 (mTORC1) and the endocannabinoid type 1 receptor (CB1R) pathways are two key signaling systems involved in the regulation of energy balance whose activity closely depends upon energy availability. Here we tested the hypothesis that modulation of mTORC1 and CB1R signaling regulates excitatory glutamatergic inputs onto the PVN.


Patch-clamp recordings in C57BL/6J mice, in mice lacking the mTORC1 component Rptor or CB1R in pro-opio-melanocortin (POMC) neurons, combined with pharmacology targeting mTORC1, the melanocortin receptor type 4 (MC4R), or the endocannabinoid system under chow or a hypercaloric diet.


Acute pharmacological inhibition of mTORC1 in C57BL/6J mice decreased glutamatergic inputs onto the PVN via a mechanism requiring modulation of MC4R, endocannabinoid 2-AG mobilization by PVN parvocellular neurons, and retrograde activation of presynaptic CB1R. Further electrophysiology studies using mice lacking mTORC1 activity or CB1R in POMC neurons indicated that the observed effects involved mTORC1 and CB1R-dependent regulation of glutamate release from POMC neurons. Finally, energy surfeit caused by hypercaloric high-fat diet feeding, rapidly and time-dependently altered the glutamatergic inputs onto parvocellular neurons and the ability of mTORC1 and CB1R signaling to modulate such excitatory activity.


These findings pinpoint the relationship between mTORC1 and endocannabinoid-CB1R signaling in the regulation of the POMC-mediated glutamatergic inputs onto PVN parvocellular neurons and its rapid alteration in conditions favoring the development of obesity.


Comment by Daniela Cota :

Publication: 16/10/19
Mise à jour: 22/10/19